Document and Entity Information
Document and Entity Information - USD ($) $ in Millions | 12 Months Ended | ||
Dec. 31, 2021 | Jan. 31, 2022 | Jun. 30, 2021 | |
Cover [Abstract] | |||
Document Type | 10-K/A | ||
Amendment Flag | true | ||
Document Period End Date | Dec. 31, 2021 | ||
Document Fiscal Year Focus | 2021 | ||
Document Fiscal Period Focus | FY | ||
Trading Symbol | CTMX | ||
Entity Registrant Name | CytomX Therapeutics, Inc. | ||
Entity Central Index Key | 0001501989 | ||
Current Fiscal Year End Date | --12-31 | ||
Entity Well-known Seasoned Issuer | No | ||
Entity Voluntary Filers | No | ||
Entity Current Reporting Status | Yes | ||
Entity Filer Category | Accelerated Filer | ||
Entity Small Business | false | ||
Entity Emerging Growth Company | false | ||
ICFR Auditor Attestation Flag | true | ||
Entity Shell Company | false | ||
Entity File Number | 001-37587 | ||
Entity Tax Identification Number | 27-3521219 | ||
Entity Address, Address Line One | 151 Oyster Point Boulevard, | ||
Entity Address, Address Line Two | Suite 400 | ||
Entity Address, City or Town | South San Francisco | ||
Entity Address, State or Province | CA | ||
Entity Address, Postal Zip Code | 94080 | ||
City Area Code | 650 | ||
Local Phone Number | 515-3185 | ||
Entity Interactive Data Current | Yes | ||
Title of 12(b) Security | Common Stock, $0.00001 par value | ||
Security Exchange Name | NASDAQ | ||
Entity Incorporation, State or Country Code | DE | ||
Document Annual Report | true | ||
Document Transition Report | false | ||
Entity Public Float | $ 408.3 | ||
Entity Common Stock, Shares Outstanding | 65,392,758 | ||
Documents Incorporated by Reference | Portions of the registrant’s definitive proxy statement to be filed for its 2022 Annual Meeting of Stockholders are incorporated by reference into Part III hereof. Such proxy statement will be filed with the Securities and Exchange Commission within 120 days of the end of the fiscal year covered by this Amended Annual Report on Form 10-K/A . | ||
Auditor Name | Ernst & Young LLP | ||
Auditor Firm Id | 42 | ||
Auditor Location | California | ||
Amendment Description | Amendment No. 1 |
BALANCE SHEETS
BALANCE SHEETS - USD ($) $ in Thousands | Dec. 31, 2021 | Dec. 31, 2020 |
Current assets: | ||
Cash and cash equivalents | $ 205,530 | $ 191,859 |
Short-term investments | 99,696 | 124,260 |
Accounts receivable | 790 | 798 |
Prepaid expenses and other current assets | 4,285 | 7,096 |
Total current assets | 310,301 | 324,013 |
Property and equipment, net | 5,960 | 6,950 |
Intangible assets, net | 1,021 | 1,167 |
Goodwill | 949 | 949 |
Restricted cash | 917 | 917 |
Operating lease right-of-use asset | 19,362 | 22,495 |
Other assets | 901 | 2,172 |
Total assets | 339,411 | 358,663 |
Current liabilities: | ||
Accounts payable | 2,818 | 2,996 |
Accrued liabilities | 34,236 | 23,059 |
Deferred revenues, current portion | 40,816 | 42,056 |
Total current liabilities | 77,870 | 68,111 |
Deferred revenue, net of current portion | 243,944 | 276,651 |
Operating lease liabilities - long term | 18,056 | 21,675 |
Total liabilities | 339,870 | 366,437 |
Commitments and contingencies (Note 11) | ||
Stockholders' equity (deficit) | ||
Common stock, $0.00001 par value; 150,000,000 and 150,000,000 shares authorized at December 31, 2021 and 2020, respectively; 48,251,819 and 48,251,819 shares issued and outstanding at December 31, 2021 and 2020, respectively | 1 | 1 |
Additional paid-in capital | 623,344 | 499,964 |
Accumulated other comprehensive income (loss) | (242) | (47) |
Accumulated deficit | (623,562) | (507,692) |
Total stockholders' equity (deficit) | (459) | (7,774) |
Total liabilities and stockholders' equity (deficit) | 339,411 | 358,663 |
Convertible Preferred Stock | ||
Stockholders' equity (deficit) | ||
Convertible preferred stock, $0.00001 par value; 10,000,000 shares authorized and no shares issued and outstanding at December 31, 2021 and 2020 | $ 0 | $ 0 |
BALANCE SHEETS (Parenthetical)
BALANCE SHEETS (Parenthetical) - $ / shares | Dec. 31, 2021 | Dec. 31, 2020 |
Common stock, par value | $ 0.00001 | $ 0.00001 |
Common stock, shares authorized | 150,000,000 | 150,000,000 |
Common stock, shares issued | 65,392,758 | 48,251,819 |
Common stock, shares outstanding | 65,392,758 | 48,251,819 |
Convertible Preferred Stock | ||
Convertible Preferred stock, par value | $ 0.00001 | $ 0.00001 |
Convertible Preferred stock, shares authorized | 10,000,000 | 10,000,000 |
Convertible Preferred stock, shares issued | 0 | 0 |
Convertible Preferred stock, shares outstanding | 0 | 0 |
STATEMENTS OF OPERATIONS AND CO
STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||||||||
Dec. 31, 2021 | Sep. 30, 2021 | Jun. 30, 2021 | Mar. 31, 2021 | Dec. 31, 2020 | Sep. 30, 2020 | Jun. 30, 2020 | Mar. 31, 2020 | Jun. 30, 2021 | Jun. 30, 2020 | Sep. 30, 2021 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Statement of Comprehensive Income [Abstract] | |||||||||||||||
Revenues | $ 11,132 | $ 9,189 | $ 8,795 | $ 8,197 | $ 7,078 | $ 7,466 | $ 6,988 | $ 46,895 | $ 16,992 | $ 53,883 | $ 26,181 | $ 61,349 | $ 37,312 | $ 68,427 | $ 26,902 |
Type of Revenue [Extensible List] | us-gaap:LicenseAndServiceMember | us-gaap:LicenseAndServiceMember | us-gaap:LicenseAndServiceMember | ||||||||||||
Operating expenses: | |||||||||||||||
Research and development | 36,580 | 29,143 | 26,100 | 22,371 | 22,007 | 24,049 | 24,066 | 42,814 | 48,471 | 66,880 | 77,614 | 90,929 | $ 114,194 | $ 112,936 | $ 131,619 |
General and administrative | 9,455 | 11,085 | 9,393 | 9,227 | 9,145 | 8,634 | 8,680 | 9,572 | 18,620 | 18,252 | 29,705 | 26,886 | 39,160 | 36,031 | 36,765 |
Total operating expenses | 46,035 | 40,228 | 35,493 | 31,598 | 31,152 | 32,683 | 32,746 | 52,386 | 67,091 | 85,132 | 107,319 | 117,815 | 153,354 | 148,967 | 168,384 |
Loss from operations | (34,903) | (31,039) | (26,698) | (23,401) | (24,074) | (25,217) | (25,758) | (5,491) | (50,099) | (31,249) | (81,138) | (56,466) | (116,042) | (80,540) | (141,482) |
Interest income | 73 | 70 | 44 | 68 | 107 | 200 | 454 | 1,075 | 112 | 1,529 | 182 | 1,729 | 255 | 1,836 | 8,365 |
Other expense, net | 7 | (13) | (82) | 5 | (29) | (15) | 5 | 12 | (77) | 17 | (90) | 2 | (83) | (27) | (135) |
Loss before income taxes | (34,823) | (30,982) | (26,736) | (23,328) | (23,996) | (25,032) | (25,299) | (4,404) | (50,064) | (29,703) | (81,046) | (54,735) | (115,870) | (78,731) | (133,252) |
Benefit from income taxes | (13,911) | (13,911) | (13,911) | 0 | (13,911) | (427) | |||||||||
Net income (loss) | (34,823) | (30,982) | (26,736) | (23,328) | (23,996) | (25,032) | (25,299) | 9,507 | (50,064) | (15,792) | (81,046) | (40,824) | (115,870) | (64,820) | (132,825) |
Other comprehensive income (loss): | |||||||||||||||
Unrealized gain (loss) on short-term investments, net of tax | (294) | 37 | 58 | 4 | (63) | (320) | 279 | 62 | (41) | 99 | (104) | (195) | (104) | 139 | |
Impact of adoption of new accounting pronouncement | 0 | 0 | 11 | ||||||||||||
Comprehensive income (loss) | $ (35,117) | $ (30,945) | $ (26,678) | $ (23,324) | $ (23,996) | $ (25,095) | $ (25,619) | $ 9,786 | $ (50,002) | $ (15,833) | $ (80,947) | $ (40,928) | $ (116,065) | $ (64,924) | $ (132,675) |
Net loss per share, basic | $ (0.53) | $ (0.48) | $ (0.41) | $ (0.38) | $ (0.51) | $ (0.54) | $ (0.55) | $ 0.21 | $ (0.79) | $ (0.34) | $ (1.27) | $ (0.89) | $ (1.81) | $ (1.40) | $ (2.93) |
Net loss per share, diluted | $ (0.53) | $ (0.48) | $ (0.41) | $ (0.38) | $ (0.51) | $ (0.54) | $ (0.55) | $ 0.20 | $ (0.79) | $ (0.34) | $ (1.27) | $ (0.89) | $ (1.81) | $ (1.40) | $ (2.93) |
Shares used to compute net loss per share, basic | 65,295,995 | 65,208,066 | 65,055,998 | 60,968,111 | 46,600,605 | 46,195,121 | 46,057,063 | 45,723,955 | 63,023,349 | 45,890,510 | 63,759,585 | 45,992,786 | 64,146,848 | 46,145,563 | 45,335,927 |
Shares used to compute net loss per share, diluted | 65,295,995 | 65,208,066 | 65,055,998 | 60,968,111 | 46,600,605 | 46,195,121 | 46,057,063 | 47,044,774 | 63,023,349 | 45,890,510 | 63,759,585 | 45,992,786 | 64,146,848 | 46,145,563 | 45,335,927 |
Statements of Stockholders' Equ
Statements of Stockholders' Equity (Deficit) - USD ($) $ in Thousands | Total | Common Stock | Additional Paid-in Capital | Accumulated Other Comprehensive Income/(Loss) | Accumulated Other Comprehensive Income/(Loss) Cumulative Effect, Period of Adoption, Adjustment | Accumulated Deficit | Accumulated Deficit Cumulative Effect, Period of Adoption, Adjustment |
Beginning balance at Dec. 31, 2018 | $ 135,828 | $ 1 | $ 445,956 | $ (93) | $ 11 | $ (310,036) | $ (11) |
Beginning balance, shares at Dec. 31, 2018 | 45,083,209 | ||||||
Accounting Standards Update [Extensible List] | us-gaap:AccountingStandardsUpdate201802Member | ||||||
Exercise of stock options | $ 633 | 633 | |||||
Exercise of stock options, shares | 146,930 | ||||||
Issuance of common stock under the Employee Stock Purchase Plan | 994 | 994 | |||||
Issuance of common stock under the Employee Stock Purchase Plan, shares | 142,949 | ||||||
Issuance of common stock in follow-on offering, net of issuance costs | 1,602 | 1,602 | |||||
Issuance of common stock in follow-on offering, net of issuance costs, shares | 150,000 | ||||||
Stock-based compensation | 19,100 | 19,100 | |||||
Other comprehensive income (loss) | 139 | 139 | |||||
Net loss (As Restated) | (132,825) | (132,825) | |||||
Ending balance at Dec. 31, 2019 | 25,471 | $ 1 | 468,285 | 57 | (442,872) | ||
Ending balance, shares at Dec. 31, 2019 | 45,523,088 | ||||||
Exercise of stock options | 4,876 | 4,876 | |||||
Exercise of stock options, shares | 1,064,830 | ||||||
Issuance of common stock under the Employee Stock Purchase Plan | $ 729 | 729 | |||||
Issuance of common stock under the Employee Stock Purchase Plan, shares | 128,684 | 128,684 | |||||
Issuance of common stock in follow-on offering, net of issuance costs | $ 11,288 | 11,288 | |||||
Issuance of common stock in follow-on offering, net of issuance costs, shares | 1,535,217 | ||||||
Stock-based compensation | 14,786 | 14,786 | |||||
Other comprehensive income (loss) | (104) | (104) | |||||
Net loss (As Restated) | (64,820) | (64,820) | |||||
Ending balance at Dec. 31, 2020 | (7,774) | $ 1 | 499,964 | (47) | (507,692) | ||
Ending balance, shares at Dec. 31, 2020 | 48,251,819 | ||||||
Other comprehensive income (loss) | 4 | ||||||
Net loss (As Restated) | (23,328) | ||||||
Ending balance at Mar. 31, 2021 | 80,671 | ||||||
Beginning balance at Dec. 31, 2020 | (7,774) | $ 1 | 499,964 | (47) | (507,692) | ||
Beginning balance, shares at Dec. 31, 2020 | 48,251,819 | ||||||
Other comprehensive income (loss) | 62 | ||||||
Net loss (As Restated) | (50,064) | ||||||
Ending balance at Jun. 30, 2021 | 58,109 | ||||||
Beginning balance at Dec. 31, 2020 | (7,774) | $ 1 | 499,964 | (47) | (507,692) | ||
Beginning balance, shares at Dec. 31, 2020 | 48,251,819 | ||||||
Other comprehensive income (loss) | 99 | ||||||
Net loss (As Restated) | (81,046) | ||||||
Ending balance at Sep. 30, 2021 | 30,432 | ||||||
Beginning balance at Dec. 31, 2020 | (7,774) | $ 1 | 499,964 | (47) | (507,692) | ||
Beginning balance, shares at Dec. 31, 2020 | 48,251,819 | ||||||
Exercise of stock options | $ 1,428 | 1,428 | |||||
Exercise of stock options, shares | 528,503 | 528,503 | |||||
Issuance of common stock under the Employee Stock Purchase Plan | $ 1,073 | 1,073 | |||||
Issuance of common stock under the Employee Stock Purchase Plan, shares | 183,865 | 183,865 | |||||
Issuance of common stock in follow-on offering, net of issuance costs | $ 107,712 | 107,712 | |||||
Issuance of common stock in follow-on offering, net of issuance costs, shares | 16,428,571 | ||||||
Stock-based compensation | 13,167 | 13,167 | |||||
Other comprehensive income (loss) | (195) | (195) | |||||
Net loss (As Restated) | (115,870) | (115,870) | |||||
Ending balance at Dec. 31, 2021 | (459) | $ 1 | 623,344 | (242) | (623,562) | ||
Ending balance, shares at Dec. 31, 2021 | 65,392,758 | ||||||
Beginning balance at Mar. 31, 2021 | 80,671 | ||||||
Other comprehensive income (loss) | 58 | ||||||
Net loss (As Restated) | (26,736) | ||||||
Ending balance at Jun. 30, 2021 | 58,109 | ||||||
Other comprehensive income (loss) | 37 | ||||||
Net loss (As Restated) | (30,982) | ||||||
Ending balance at Sep. 30, 2021 | 30,432 | ||||||
Other comprehensive income (loss) | (294) | ||||||
Net loss (As Restated) | (34,823) | ||||||
Ending balance at Dec. 31, 2021 | $ (459) | $ 1 | $ 623,344 | $ (242) | $ (623,562) | ||
Ending balance, shares at Dec. 31, 2021 | 65,392,758 |
STATEMENTS OF CASH FLOWS
STATEMENTS OF CASH FLOWS - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Cash flows from operating activities: | |||
Net loss | $ (115,870) | $ (64,820) | $ (132,825) |
Adjustments to reconcile net loss to net cash (used in) provided by operating activities: | |||
Amortization of intangible assets | 146 | 146 | 146 |
Depreciation and amortization | 2,560 | 2,427 | 2,459 |
Amortization of premium (accretion of discounts) on investments | 272 | (236) | (2,228) |
Stock-based compensation expense | 13,167 | 14,786 | 19,100 |
Non-cash lease expense | 3,133 | 2,887 | 2,672 |
Issuance of common stock in connection with UCSB sublicense fee | 0 | 0 | 1,602 |
Changes in operating assets and liabilities | |||
Accounts receivable | 8 | (785) | 84 |
Prepaid expenses and other current assets | 2,811 | 81 | 2,074 |
Other assets | 1,271 | (157) | (640) |
Accounts payable | (139) | (857) | (374) |
Accrued liabilities, income tax payable and other long-term liabilities | 7,558 | (11,039) | (15,396) |
Deferred revenue | (33,948) | 62,826 | (17,154) |
Net cash provided by (used in) operating activities | (119,031) | 5,259 | (140,480) |
Cash flows from investing activities: | |||
Purchases of property and equipment | (1,609) | (2,309) | (3,497) |
Purchases of investments | (99,898) | (199,108) | (174,992) |
Maturities of investments | 123,996 | 182,699 | 258,190 |
Net cash provided by (used in) investing activities | 22,489 | (18,718) | 79,701 |
Cash flows from financing activities: | |||
Proceeds from issuance of common stock, net of issuance costs | 107,712 | 11,288 | 0 |
Proceeds from employee stock purchase plan and exercise of stock options | 2,501 | 5,605 | 1,627 |
Net cash provided by financing activities | 110,213 | 16,893 | 1,627 |
Net increase (decrease) in cash, cash equivalents and restricted cash | 13,671 | 3,434 | (59,152) |
Cash, cash equivalents and restricted cash, beginning of year | 192,776 | 189,342 | 248,494 |
Cash, cash equivalents and restricted cash, end of year | 206,447 | 192,776 | 189,342 |
Supplemental disclosures of cash flow information: | |||
Cash paid for income taxes | 0 | 0 | 13,061 |
Supplemental disclosures of noncash investing items: | |||
Purchases of property and equipment in accounts payable and accrued liabilities | 83 | 122 | 428 |
Right of use assets obtained in exchange for operating lease obligations | $ 0 | $ 0 | $ 28,054 |
Description of the Business
Description of the Business | 12 Months Ended |
Dec. 31, 2021 | |
Disclosure Text Block [Abstract] | |
Description of the Business | 1. Description of the Business CytomX Therapeutics, Inc. (the “Company”) is a clinical-stage, oncology-focused biopharmaceutical company dedicated to destroying cancer differently. The Company aims to build a commercial enterprise to maximize its impact on the treatment of cancer. The Company is advancing potential first-in-class and best-in-class antibody-based therapeutics created using its Probody® therapeutic technology platform that could meaningfully improve outcomes for cancer patients. Its proprietary and unique Probody technology platform is designed to enable “conditional activation” of antibody-based drugs in the tumor microenvironment while minimizing drug activity in healthy tissues and in circulation. The Company is located in South San Francisco, California and was incorporated in the state of Delaware in September 2010. |
Basis of Presentation and Summa
Basis of Presentation and Summary of Significant Accounting Policies | 12 Months Ended |
Dec. 31, 2021 | |
Accounting Policies [Abstract] | |
Basis of Presentation and Summary of Significant Accounting Policies | 2. Basis of Presentation and Summary of Significant Accounting Policies Basis of Presentation The accompanying financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“U.S. GAAP”). Restatement of Financial Statements The Company re-evaluated its application of ASC Topic 606, Revenue from Contracts with Customers (“ASC 606”) for its prior collaboration and license agreements. The Company has historically recognized the revenue for certain arrangements ratably over the estimated research period, where the contract was treated as a single performance obligation. Upon reassessment, the Company has determined that certain revenue should be recognized over time using an input method as an appropriate measure of progress, rather than ratably over the estimated research period, with each research program as a separate combined performance obligation. In applying the input method, revenue is recognized based on actual full-time employee ("FTE") hours incurred as a percentage of total estimated FTE hours for completing the combined performance obligation over the estimated service period. The restatement affects the accounting for the Company’s agreements with Bristol-Myers Squibb Company, Astellas Pharma Inc., and certain agreements with AbbVie Ireland Unlimited Company, and Amgen, Inc. The error resulted in an overstatement of revenue in the statements of operations for the years ended December 31, 2021, 2020 and 2019, and an understatement of deferred revenue in the balance sheets as of December 31, 2021 and 2020. Impact of Restatement See below for a reconciliation from the previously reported to the restated amounts in the statements of operations for the years ended December 31, 2021, 2020 and 2019, and in the balance sheets as of December 31, 2021 and 2020. The previously reported amounts were derived from the Company's Annual Report on Form 10-K for the year ended December 31, 2021 filed with the SEC on March 1, 2022 (the “Original Report”). These amounts are labeled as “As Previously Reported” in the tables below. The amounts labeled “Restatement Adjustment” represent the effects of this restatement described above. The correction of this misstatement resulted in a decrease in revenue of $ 32.3 million, $ 31.9 million and $ 30.6 million in the statements of operations for the years ended December 31, 2021, 2020 and 2019, respectively, and a cumulative increase in total deferred revenue of $ 89.8 million and $ 57.6 million in the balance sheets as of December 31, 2021 and 2020, respectively. The following presents a reconciliation of the impacted financial statement line items as previously reported to the restated amounts as of December 31, 2021 and 2020, and for the years ended December 31, 2021, 2020 and 2019 (in thousands, except share and per share data): December 31, 2021 December 31, 2020 As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated Balance Sheets Deferred revenue, current portion $ 69,262 $ ( 28,446 ) $ 40,816 $ 74,869 $ ( 32,813 ) $ 42,056 Total current liabilities 106,316 ( 28,446 ) 77,870 100,924 ( 32,813 ) 68,111 Deferred revenue, net of current portion 125,660 118,284 243,944 186,261 90,390 276,651 Total liabilities 250,032 89,838 339,870 308,860 57,577 366,437 Accumulated deficit ( 533,724 ) ( 89,838 ) ( 623,562 ) ( 450,115 ) ( 57,577 ) ( 507,692 ) Total stockholders' equity (deficit) 89,379 ( 89,838 ) ( 459 ) 49,803 ( 57,577 ) ( 7,774 ) Total liabilities and stockholders' equity (deficit) 339,411 — 339,411 358,663 — 358,663 Year Ended December 31, 2021 Year Ended December 31, 2020 Year Ended December 31, 2019 As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated Statements of Operations Revenue $ 69,573 $ ( 32,261 ) $ 37,312 $ 100,362 $ ( 31,935 ) $ 68,427 $ 57,489 $ ( 30,587 ) $ 26,902 Operating expenses: Research and development 114,194 — 114,194 112,936 — 112,936 131,619 — 131,619 General and administrative 39,160 — 39,160 36,031 — 36,031 36,765 — 36,765 Total operating expenses 153,354 — 153,354 148,967 — 148,967 168,384 — 168,384 Loss from operations ( 83,781 ) ( 32,261 ) ( 116,042 ) ( 48,605 ) ( 31,935 ) ( 80,540 ) ( 110,895 ) ( 30,587 ) ( 141,482 ) Interest income 255 — 255 1,836 — 1,836 8,365 — 8,365 Other income (expense) ( 83 ) — ( 83 ) ( 27 ) — ( 27 ) ( 135 ) — ( 135 ) Loss before income taxes ( 83,609 ) ( 32,261 ) ( 115,870 ) ( 46,796 ) ( 31,935 ) ( 78,731 ) ( 102,665 ) ( 30,587 ) ( 133,252 ) Loss/(Benefit) from income taxes — — - ( 13,911 ) — ( 13,911 ) ( 427 ) ( 427 ) Net loss ( 83,609 ) ( 32,261 ) ( 115,870 ) ( 32,885 ) ( 31,935 ) ( 64,820 ) ( 102,238 ) ( 30,587 ) ( 132,825 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax ( 195 ) — ( 195 ) ( 104 ) — ( 104 ) 139 — 139 Impact of adoption of new accounting pronouncement - — — — — — 11 — 11 Comprehensive income (loss) $ ( 83,804 ) $ ( 32,261 ) $ ( 116,065 ) $ ( 32,989 ) ( 31,935 ) $ - $ ( 64,924 ) $ ( 102,088 ) $ ( 30,587 ) $ ( 132,675 ) Net loss per share, basic and diluted $ ( 1.30 ) $ ( 1.81 ) $ ( 0.71 ) $ ( 1.40 ) $ ( 2.26 ) $ ( 2.93 ) Shares used to compute net loss per share, basic and diluted 64,146,848 64,146,848 46,145,563 46,145,563 45,335,927 45,335,927 Year Ended December 31, 2021 Year Ended December 31, 2020 Year Ended December 31, 2019 As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated Statements of Stockholders' Equity (Deficit) Net loss ( 83,609 ) ( 32,261 ) ( 115,870 ) ( 32,885 ) ( 31,935 ) ( 64,820 ) ( 102,238 ) ( 30,587 ) ( 132,825 ) Accumulated deficit ( 533,724 ) ( 89,838 ) ( 623,562 ) ( 450,115 ) ( 57,577 ) ( 507,692 ) ( 417,230 ) ( 25,642 ) ( 442,872 ) Total stockholders' equity (deficit) 89,379 ( 89,838 ) ( 459 ) 49,803 ( 57,577 ) ( 7,774 ) 51,113 ( 25,642 ) 25,471 Year Ended December 31, 2021 Year Ended December 31, 2020 Year Ended December 31, 2019 As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated Statements of Cash Flow Net loss $ ( 83,609 ) $ ( 32,261 ) $ ( 115,870 ) $ ( 32,885 ) $ ( 31,935 ) $ ( 64,820 ) $ ( 102,238 ) $ ( 30,587 ) $ ( 132,825 ) Changes in operating assets and liabilities: Deferred revenue ( 66,209 ) 32,261 ( 33,948 ) 30,891 31,935 62,826 ( 47,741 ) 30,587 ( 17,154 ) Net cash used in operating activities ( 119,031 ) — ( 119,031 ) 5,259 — 5,259 ( 140,480 ) — ( 140,480 ) The remainder of the notes to the Company’s financial statements have been updated and restated, as applicable, to reflect the impacts of the restatement described above. Use of Estimates The preparation of the financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, disclosure of contingent assets and liabilities at the date of the financial statements and reported amounts of revenues and expenses during the reporting periods. Actual results could differ from those estimates. Concentration of Credit Risk and Other Risks and Uncertainties The Company is subject to a number of risks similar to other biopharmaceutical companies in the early stage, including, but not limited to, the need to obtain adequate additional funding, possible failure of preclinical testing or clinical trials, the need to obtain marketing approval for its product candidates, competitors developing new technological innovations, the need to successfully commercialize and gain market acceptance of the Company’s products, and protection of proprietary technology. If the Company does not successfully obtain regulatory approval, commercialize or partner any of its product candidates, it will be unable to generate revenue from product sales or achieve profitability. Financial instruments that potentially subject the Company to a concentration of credit risk consist of cash and cash equivalents, short-term investments and accounts receivable. Substantially all the Company’s cash is held by one financial institution. Such deposits may, at times, exceed federally insured limits. The Company invests its cash equivalents in highly rated money market funds and its short-term investments in U.S. Government Bonds. Customers and collaboration partners who represent 10% or more of the Company’s total revenue during each period presented or accounts receivable balance at each respective balance sheet date are as follows: Revenue Accounts Receivable, net Year Ended December 31, December 31, 2021 2020 2019 2021 2020 (As Restated) (As Restated) (As Restated) AbbVie Ireland Unlimited Company $ 11,546 $ 39,863 $ 5,305 $ — $ — Amgen, Inc. 8,488 8,522 4,087 — — Astellas Pharma Inc. 17,278 7,332 — 790 798 Bristol Myers Squibb Company — 12,710 17,510 — — Total revenue from customers who represent 10% or more $ 37,312 $ 68,427 $ 26,902 $ 790 $ 798 The Company’s customers are located in the United States of America, Ireland and Japan. Segments Management has determined that it has one business activity and operates as one operating segment as it only reports financial information on an aggregate basis to its chief executive officer and chief financial officer, who are the Company’s chief operating decision makers. All long-lived assets are maintained in the United States of America. Cash and Cash Equivalents The Company considers all highly liquid investments purchased with original maturities of three months or less at the date of purchase to be cash equivalents. Restricted Cash Restricted cash represents a standby letter of credit issued pursuant to an office lease. The following table provides a reconciliation of cash, cash equivalents, and restricted cash reported within the balance sheets that sum to the total of the amounts shown in the statement of cash flows: December 31 2021 2020 2019 (in thousands) Cash and cash equivalents $ 205,530 $ 191,859 $ 188,425 Restricted cash - non-current assets 917 917 917 Total $ 206,447 $ 192,776 $ 189,342 Investments All investments have been classified as available-for-sale (“AFS”) and are carried at fair value as determined based upon quoted market prices or pricing models for similar securities at period end. Investments that are required for use in current operations and that mature in less than 12 months are classified as short-term investments in the accompanying balance sheets. The amortized cost of securities is adjusted for amortization of premiums and accretion of discounts to maturity. Dividend and interest income are recognized when earned. Realized gains and losses are included in earnings and are derived using the specific identification method for determining the cost of securities sold. The Company assesses impairment of its AFS debt securities investments at each reporting period. Unrealized gains resulting from the excess of the fair value over the amortized cost basis of an investment are reported as a component of accumulated other comprehensive income (loss), net of tax. Unrealized losses or impairments resulting from the fair value of the AFS debt security being below the amortized cost basis are evaluated, using the discounted cash flow model, for identification of credit losses and non-credit related losses. Any credit losses are charged to earnings against the allowance for credit losses of the security, limited to the difference between the fair value and the amortized cost basis of the security. Any difference between the fair value of the security and the amortized cost basis, less the allowance for credit losses, are reported in other comprehensive income (loss). Expected cash inflows due to improvements in credit are recognized through a reversal of the allowance for credit losses subject to the total allowance previously recognized. In the event of impairment of any security, if management (i) has the intent to sell such security or (ii) will more-likely-than-not be required to sell such security before recovery of its amortized cost basis, such AFS debt security’s amortized cost basis will be written down to its fair value through earnings along with any existing allowance for credit losses. Property and Equipment, net Property and equipment are recorded at cost net of accumulated depreciation and amortization. Depreciation is provided using the straight-line method over the estimated useful lives of the respective assets. The useful lives of property and equipment are as follows: Machinery and equipment 5 years Computer equipment and software 3 years Furniture and fixtures 3 years Leasehold improvements Shorter of remaining lease term or estimated life of the assets Maintenance and repairs that do not extend the life or improve the asset are expensed when incurred. Goodwill and Intangible Asset s Goodwill represents the excess of the purchase price paid over the fair value of tangible and identifiable intangible assets acquired in business combinations. Goodwill and other intangible assets with indefinite lives are not amortized, but are assigned to reporting units and tested for impairment annually, or whenever there is an impairment indicator. Intangible assets are comprised of in-process research and development. The Company assesses impairment indicators annually as of December 31 or more frequently, if a change in circumstances or the occurrence of events suggests the remaining value may not be recoverable. Intangible assets that are not deemed to have an indefinite life are amortized over their estimated useful lives. There was no impairment of goodwill or intangible assets identified during the years ended December 31, 2021, 2020 and 2019. Impairment of Long-Lived Assets Long-lived assets are reviewed for impairment whenever events or changes in circumstances indicate that the carrying amount of an asset (or asset group) may not be recoverable and prior to any goodwill impairment test. An impairment loss is recognized when the total of estimated undiscounted future cash flows expected to result from the use of the asset (or asset group) and its eventual disposition is less than its carrying amount. Impairment, if any, would be assessed using discounted cash flows or other appropriate measures of fair value. There was no impairment of long-lived assets during the years ended December 31, 2021, 2020 and 2019. Revenue Recognition The Company’s revenues are primarily derived through its license, research, development and commercialization agreements. The terms of these types of agreements may include (i) licenses for the Company’s technology or programs, (ii) research and development services, and (iii) services or obligations in connection with participation in research or steering committees. Payments to the Company under these arrangements typically include one or more of the following: nonrefundable upfront and license fees, research funding, milestone and other contingent payments to the Company for the achievement of defined collaboration objectives and certain preclinical, clinical, regulatory and sales-based events, as well as royalties on sales of any commercialized products. The Company assesses whether the promises in its arrangements with customers are distinct performance obligations that should be accounted for separately. Judgment is required to determine whether the license to the Company’s intellectual property is distinct from the research and development services or participation on steering committees. The Company’s collaboration and license agreements may include contingent payments related to specified research, development and regulatory milestones. Such milestone payments are typically payable under the collaborations when the collaboration partner claims or selects a target, or initiates or advances a covered product candidate in preclinical or clinical development, upon submission for marketing approval of a covered product with regulatory authorities, or upon receipt of actual marketing approvals of a covered product or for additional indications. Milestone payments that are not within the control of the Company or the licensee, such as regulatory approvals, are not considered probable of being achieved until those approvals are received. At each reporting date, the Company re-evaluates whether the milestones are considered probable of being achieved and estimates the amount to be included in the transaction price by using the most likely amount method. If it is probable that a significant revenue reversal would not occur, the associated milestone value is included in the transaction price in such period of determination. The Company’s collaboration and license agreements may also include contingent payments related to sales-based milestones. Sales-based milestones are typically payable when annual sales of a covered product reach specified levels. Sales-based milestones are recognized at the later of when the associated performance obligation has been satisfied or when the sales occur. Unlike other contingency payments, such as regulatory milestones, sales-based milestones are not included in the transaction price based on estimates at the inception of the contract; instead, are included when the sales or usage occur. The transaction price in each arrangement is allocated to the identified performance obligations based on the relative standalone selling price (“SSP”) of each distinct performance obligation, which requires judgment. In instances where SSP is not directly observable, such as when a license or service is not sold separately, SSP is determined using information that may include market conditions and other observable inputs. Due to the early stage of the Company’s licensed technology, the license of such technology is typically combined with research and development services and steering committee participation as one performance obligation. In the event that the Company receives non-cash consideration such as consideration in the form of a research license and research support services from the counterparty, the transaction price of a non-monetary exchange that has commercial substance is estimated based on the fair value of the non-cash consideration received, which may be determined through a valuation analysis. In certain cases, the Company’s performance creates an asset that does not have an alternative use to the customer and the Company has an enforceable right to payment at all times for performance completed to date. In these cases, the Company utilizes judgment to assess the nature of the combined performance obligation to determine whether the combined performance obligation is satisfied over time or at a point in time and, if over time, the appropriate method of measuring progress for purposes of recognizing revenue. The Company evaluates the measure of progress each reporting period and, if necessary, adjusts the measure of performance and related revenue recognition. Any consideration payable to the Company’s customers is treated as a reduction to the transaction price and revenue, unless the payment to the customer is in exchange for distinct good and services. Comprehensive Income (Loss ) Comprehensive income (loss) represents all changes in stockholders’ equity (deficit) except those resulting from distributions to stockholders. The Company’s non-credit related unrealized gains and losses on investments and impact of adoption of new accounting pronouncements during the period represent the components of other comprehensive income (loss) that is excluded from the reported net loss. Contract Balances Customer payments are recorded as deferred revenue upon receipt or when due and may require deferral of revenue recognition to a future period until the Company satisfies its performance obligations under these arrangements. Amounts payable to the Company are recorded as accounts receivable when the Company’s right to consideration is unconditional. Research and Development Expenses The Company records accrued liabilities for estimated costs of research and development activities conducted by third-party service providers, which include the conduct of preclinical and clinical studies, and contract manufacturing activities. The Company records the estimated costs of research and development activities based upon the estimated amount of services provided but not yet invoiced, and includes these costs in accrued liabilities in the balance sheets and within research and development expense in the statements of operations. These costs are a significant component of the Company’s research and development expenses. The Company accrues for these costs based on factors such as estimates of the work completed and in accordance with agreements established with its third-party service providers under the service agreements. The Company makes significant judgments and estimates in determining the accrued liabilities balance in each reporting period. As actual costs become known, the Company adjusts its accrued liabilities. The Company has not experienced any material differences between accrued costs and actual costs incurred. However, the status and timing of actual services performed may vary from the Company’s estimates, resulting in adjustments to expense in future periods. Changes in these estimates that result in material changes to the Company’s accruals could materially affect the Company’s results of operations. Research and development expenses include costs directly attributable to the conduct of research and development programs, including the cost of salaries, payroll taxes, employee benefits, materials, supplies, depreciation on and maintenance of research equipment, the cost of services provided by outside contractors, and the allocated portions of facility costs, such as rent, utilities, insurance, repairs and maintenance, depreciation, and general support services. All costs associated with research and development are expensed as incurred. In January 2019, the Company acquired certain technology know-how that is complementary to the Company’s proprietary Probody technology from a third party for $ 5.0 million. The Company plans to use this technology in certain of the Company’s discovery stage projects, and has concluded that the technology acquired does not have an alternative future use. Accordingly, the $ 5.0 million has been recorded as research and development expense for 2019. Stock-based Compensation The Company measures compensation expense for all stock-based payment awards, including employee stock options, restricted stock units ("RSUs"), and employee stock purchases related to Employee Stock Purchase Plan ("ESPP") based on estimated fair values of the award at the grant date, and recognizes compensation expense over the requisite service vesting period. Stock options forfeitures are accounted for in the period in which they occur. To determine the fair value of a stock option award on the grant date, the Company uses the Black-Scholes option pricing model which consist of estimating variables such as: expected life, volatility, and risk-free interest rate. Expected life and volatility are estimated primarily from the Company's historical records, and the risk-free rate is based on the U.S. Treasury yield curve in effect at the time of grant commensurate with the expected life assumption. These estimates involve inherent uncertainties and the application of judgment. The Company measures its restricted stock unit awards based on the market price of the Company’s common shares on the date of grant. Share-based compensation expense for performance-based awards is recognized when it becomes probable that the performance condition will be met. The Company reassesses the estimated probability at each reporting period, and if it is determined at a future date that a performance condition is probable of being achieved, the Company will recognize a cumulative catch-up adjustment and record the remaining expense ratably over the remaining requisite service period. Income Taxes The Company accounts for income taxes using an asset and liability approach. Deferred tax assets and liabilities reflect the net tax effects of temporary differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The Company records a valuation allowance to reduce its deferred tax assets to reflect the net amount that it believes as more likely than not to be realized. Realization of the deferred tax assets is dependent on the generation of future taxable income, the amount and timing of which are uncertain. The valuation allowance requires an assessment of both positive and negative evidence when determining whether it is more likely than not that deferred tax assets are recoverable. Based upon the weight of available evidence at December 31, 2021, the Company continues to maintain a full valuation allowance against all of its deferred tax assets after management considered all available evidence, both positive and negative, including but not limited to its historical operating results, income or loss in recent periods, cumulative income in recent years, forecasted earnings, future taxable income, and significant risk and uncertainty related to forecasts. The Company recognizes the tax effects of an uncertain tax position only if it is more likely than not that it will be sustained based solely on its technical merits as of the reporting date and only in an amount more likely than not that it will be sustained upon review by the tax authorities. The Company evaluates uncertain tax positions on a quarterly basis and adjust the liability for changes in facts and circumstances, such as new regulations or interpretations by the taxing authorities, new information obtained during a tax examination, significant amendment to an existing tax law, or resolution of an examination. To the extent that the final tax outcome of these matters is different than the amounts recorded, such differences will impact the income tax provision in the period in which such determination is made. The resolution of its uncertain income tax positions is dependent on uncontrollable factors such as law changes, new case law, and the willingness of the income tax authorities to settle, including the timing thereof and other factors. Although the Company does not anticipate significant changes to its uncertain income tax positions in the next twelve months, items outside of its control could cause its uncertain income tax positions to change in the future, which would be recorded in its statements of operations. Interest and/or penalties related to income tax matters are recognized as a component of income tax expense. Leases The Company determines if an arrangement is or contains a lease at inception. Operating leases are recorded as operating lease right-of-use (“ROU”) assets and operating lease liabilities in the Company’s balance sheet. ROU assets represent the Company’s right to use an underlying asset for the lease term and lease liabilities represent its obligation to make lease payments arising from the lease. Operating lease ROU assets and liabilities are recognized at commencement date based on the present value of lease payments over the lease term. The Company uses an implicit rate when readily available, or its incremental borrowing rate based on the information available at lease commencement date in determining the present value of lease payments. The operating lease ROU assets also include any lease prepayments made and reduced by lease incentives. The Company’s lease terms may include options to extend the lease when it is reasonably certain that such option will be exercised. Lease expenses are recognized on a straight-line basis over the lease term. The Company elected the short-term lease recognition exemption. The Company’s operating lease arrangement includes lease and non-lease components which are generally accounted for separately. |
Adopted Accounting Pronouncemen
Adopted Accounting Pronouncements | 12 Months Ended |
Dec. 31, 2021 | |
Accounting Policies [Abstract] | |
Adopted Accounting Pronouncements | 3. Adopted Accounting Pronouncements In December 2019, the FASB issued ASU 2019-12, Income Taxes (Topic 740): Simplifying the Accounting for Income Taxes. The amendments in this ASU simplify the accounting for income taxes by removing certain exceptions to the general principles of ASC 740 in order to reduce cost and complexity of its application. The ASU removes the exception related to the incremental approach for intra-period tax allocation as well as two exceptions related to accounting for outside basis differences of equity method investments and foreign subsidiaries. The ASU also amends the scope of ASC 740 related to a franchise tax (or similar tax) that is partially based on income; clarifies when a step-up in the tax basis of goodwill should be considered part of the business combination in which the book goodwill was originally recognized and when it should be considered a separate transaction; specifies that an entity is not required to allocate income tax expense to a legal entity that is both not subject to tax and disregarded by the taxing authority; and clarifies that all tax effects, both deferred and current, should be accounted for in the interim period that includes the enactment date. The Company adopted this ASU on January 1, 2021 , and there was no material impact on the financial statements upon adoption of this ASU. |
Net Loss Per Share
Net Loss Per Share | 12 Months Ended |
Dec. 31, 2021 | |
Earnings Per Share [Abstract] | |
Net Loss Per Share | 4. Net Loss Per Share Basic net loss per share is calculated by dividing the net loss by the weighted-average number of shares of common stock outstanding for the period. Diluted net loss per share is calculated using the weighted-average number of common shares outstanding, plus potential dilutive common stock during the period. Diluted net loss per share is the same as basic net loss per share since the effect of the potentially dilutive securities is anti-dilutive. The following weighted-average outstanding shares of potentially dilutive securities are excluded from the computation of diluted net loss per share for the periods presented, because including them would have been anti-dilutive: Year Ended December 31, 2021 2020 2019 Options, RSUs and ESPP to purchase common stock 11,987,362 11,388,691 9,687,844 |
Fair Value Measurements and Inv
Fair Value Measurements and Investments | 12 Months Ended |
Dec. 31, 2021 | |
Fair Value Disclosures [Abstract] | |
Fair Value Measurements and Investments | 5. Fair Value Measurements and Investments In accordance with Accounting Standards Codification (“ASC”) 820-10, Fair Value Measurements and Disclosures, the Company determines the fair value of financial and non-financial assets and liabilities using the fair value hierarchy, which establishes three levels of inputs that may be used to measure fair value, as follows: • Level I: Inputs which include quoted prices in active markets for identical assets and liabilities. • Level II: Inputs other than Level I that are observable, either directly or indirectly, such as quoted prices for similar assets or liabilities; quoted prices in markets that are not active; or other inputs that are observable or can be corroborated by observable market data for substantially the full term of the assets or liabilities. • Level III: Unobservable inputs that are supported by little or no market activity and that are significant to the fair value of the assets or liabilities. The carrying amounts of the Company’s financial instruments, including restricted cash, accounts receivable, accounts payable and accrued liabilities approximate fair value due to their relatively short maturities. The Company’s financial instruments consist of Level I assets which consist primarily of highly liquid money market funds, some of which are included in restricted cash; and U.S. government bonds that are included in short-term investments. The following tables set forth the fair value of the Company’s investments subject to fair value measurements on a recurring basis and the level of inputs used in such measurements: December 31, 2021 Valuation Amortized Allowance for Credit Losses Gross Gross Aggregate (in thousands) Assets Money market funds Level I 165,736 $ — $ — $ — $ 165,736 Restricted cash (money market funds) Level I 917 — — — 917 U.S. Government bonds Level I 99,938 — — ( 242 ) 99,696 Total Securities 266,591 $ — $ — $ ( 242 ) $ 266,349 December 31, 2020 Valuation Amortized Allowance Gross Gross Aggregate (in thousands) Assets Money market funds Level I $ 131,121 $ — $ — $ — $ 131,121 Restricted cash (money market funds) Level I 917 — — — 917 U.S. Government bonds Level I 124,254 — 6 — 124,260 Total securities $ 256,292 $ — $ 6 $ — $ 256,298 No securities have contractual maturities of greater than twelve months . As of December 31,2021, the unrealized loss on the Company’s investment in US Government bonds were caused by interest rate changes and were not attributable to credit losses. The remaining contractual terms of those investments are less than a year. The Company does not intend to sell the investments and it is not more likely than not that the Company will be required to sell the investments before recovery of their amortized cost bases. |
Property and Equipment
Property and Equipment | 12 Months Ended |
Dec. 31, 2021 | |
Property, Plant and Equipment [Abstract] | |
Property and Equipment | 6. Property and Equipment Property and equipment, net consisted of the following: December 31 2021 2020 (in thousands) Machinery and equipment $ 15,086 $ 13,772 Computer equipment and software 1,608 1,600 Furniture and fixtures 1,054 1,024 Leasehold improvements 1,736 1,728 Construction in progress 308 252 19,792 18,376 Less: accumulated depreciation and amortization ( 13,832 ) ( 11,426 ) $ 5,960 $ 6,950 Depreciation and amortization expense was $ 2.6 million, $ 2.4 million and $ 2.5 million for the years ended December 31, 2021, 2020, and 2019, respectively. |
Intangible Assets
Intangible Assets | 12 Months Ended |
Dec. 31, 2021 | |
Goodwill and Intangible Assets Disclosure [Abstract] | |
Intangible Assets | 7. Intangible Assets The intangible asset is being amortized over the estimated lives of the patents which average 12 years. The amortization expense for the years ended December 31, 2021, 2020, and 2019 was $ 0.1 million, $ 0.1 million and $ 0.1 million, respectively. December 31, 2021 2020 (in thousands) Probody platform intangible asset $ 1,750 $ 1,750 Less accumulated amortization ( 729 ) ( 583 ) $ 1,021 $ 1,167 |
Accrued Liabilities
Accrued Liabilities | 12 Months Ended |
Dec. 31, 2021 | |
Accrued Liabilities, Current [Abstract] | |
Accrued Liabilities | 8. Accrued Liabilities Accrued liabilities consisted of the following: December 31, 2021 2020 (in thousands) Research and clinical expenses $ 18,861 $ 10,092 Payroll and related expenses 9,576 8,362 Legal and professional expenses 1,468 815 Operating lease liabilities - short term 3,618 3,195 Other accrued expenses 713 595 Total $ 34,236 $ 23,059 |
Collaboration and License Agree
Collaboration and License Agreements | 12 Months Ended |
Dec. 31, 2021 | |
Organization, Consolidation and Presentation of Financial Statements [Abstract] | |
Collaboration and License Agreements | 9. Collaboration and License Agreements The following table summarizes the revenue by collaboration partners (in thousands): Year Ended December 31, 2021 2020 2019 (As Restated) (As Restated) (As Restated) AbbVie $ 11,546 $ 39,863 $ 5,305 Amgen 8,488 8,522 4,087 Astellas 17,278 7,332 — Bristol Myers Squibb — 12,710 17,510 Total revenue $ 37,312 $ 68,427 $ 26,902 AbbVie Ireland Unlimited Company In April 2016, the Company and AbbVie entered into two agreements, a CD71 Co-Development and Licensing Agreement (the “CD71 Agreement”) and a Discovery Collaboration and Licensing Agreement (as amended and restated in June 2019, the “Discovery Agreement” and together with the CD71 Agreement the “AbbVie Agreements”). Under the terms of the CD71 Agreement, the Company and AbbVie will co-develop a conditionally activated antibody-drug conjugate (“ADC”) against CD71, with the Company responsible for preclinical and early clinical development. AbbVie will be responsible for later development and commercialization, with global late-stage development costs shared between the two companies. The Company will assume 35 % of the net profits or net losses related to later development and commercialization unless it opts out. If the Company opts-out from participation of co-development of the CD71 conditionally activated ADC, which includes CX-2029, AbbVie will have sole right and responsibility for the further development, manufacturing and commercialization of such CD71 conditionally activated ADC. Under the CD71 Agreement, the Company received an upfront payment of $ 20.0 million in April 2016, and was eligible to initially receive up to $ 470.0 million in development, regulatory and commercial milestone payments, a 35 % profit split on U.S. sales, and royalties on ex-U.S. sales at percentages in the high teens to low twenties if the Company participates in the co-development of the CD71 conditionally activated ADC subject to a reversion to a royalty on U.S. sales, and reduction in royalties on ex-U.S. sales, if the Company opts-out from the co-development of the CD71 conditionally activated ADC. The Company’s share of later stage co-development costs for each CD71 conditionally activated ADC is capped, provided that AbbVie may offset the Company’s co-development cost above the capped amounts from future payments such as milestone payments and royalties. In July 2017, the Company received a milestone payment of $ 14.0 million (net of payment of an associated sublicense fee of $ 1.0 million to Seagen Inc., formerly Seattle Genetics, Inc. (“SGEN”) under the Seattle Genetics Agreement) from AbbVie for achieving certain milestones required to be met to begin GLP toxicology studies under the CD71 Agreement. AbbVie had entered into a license agreement with SGEN to license certain intellectual property rights pursuant to which the Company was required to pay SGEN sublicense fees for certain milestone achievements and an annual maintenance fee. These sublicense fees were treated as reductions to the transaction price and combined with the performance obligation to which they relate. In May 2018, the United States Food and Drug Administration (“FDA”) cleared the IND application for CX-2029. As a result, the Company achieved the IND success criteria under the CD71 Agreement and received a $ 21.0 million milestone payment (net of the payment of an associated sublicense fee of $ 4.0 million to SGEN). In March 2020, the Company earned a $ 40.0 million milestone payment for satisfying the CD71 dose escalation success criteria under the CD71 Agreement. Inclusive of 2017, 2018 and 2020 milestone payments, as of December 31, 2021, the Company has received in aggregate $ 100.0 million in upfront and milestone payments under the CD71 Agreement. Under the terms of the Discovery Agreement, AbbVie received exclusive worldwide rights to develop and commercialize conditionally activated ADCs against up to two targets, one of which was selected in March 2017. AbbVie had the option to select a second target in exchange for a $ 10.0 million payment. The Company concluded that, at the inception of the agreement, AbbVie’s option to select the additional target was not a material right and did not represent a performance obligation of the agreement and would be accounted for as a separate arrangement upon exercise. The Company shall perform research services to discover the Probody therapeutics and create conditionally activated ADCs for the nominated collaboration targets. From that point, AbbVie shall have sole right and responsibility for development and commercialization of products comprising or containing such conditionally activated ADCs (“Discovery Licensed Products”). Under the Discovery Agreement, the Company received an upfront payment of $ 10.0 million for the first target in April 2016 and subsequently earned an additional $ 10.0 million payment triggered by selection of the second target by AbbVie in June 2019. The Company is also eligible to receive up to $ 265.0 million for each target, in development, regulatory and commercial milestone payments and royalties at percentages in the high single to low teens from commercial sales of any resulting conditionally activated ADCs. The second target was selected under the Discovery Agreement that allows AbbVie to select a target for developing a conditionally activated ADC or a Probody. The Company determined that the AbbVie Agreements should be combined and evaluated as a single arrangement in determining revenue recognition, because both agreements were concurrently negotiated and executed. Therefore, the Company concluded that there are two distinct performance obligations: (1) the CD71 Agreement performance obligation consisting of the CD71 Agreement research, development and commercialization license, related research services and participation in the joint research committee, and (2) the Discovery Agreement performance obligation consisting of the Discovery Agreement research, development and commercialization license, related research services and participation in the joint research committee. The total transaction price for the Discovery Agreement and CD71 Agreement, collectively, upon adoption of ASC 606 on January 1, 2018 of $ 39.8 million consists of $ 30.0 million in upfront payments, and a $ 14.0 million milestone payment received under the CD71 Agreement (net of the payment of an associated sublicense fee of $ 1.0 million to SGEN), less $ 4.2 million of estimated sublicense fees. The upfront payments under the AbbVie Agreements were allocated between the two performance obligations based on the estimated relative standalone selling prices. The $30.0 million of upfront payments was allocated $ 20.0 million to the CD71 Agreement, with the remaining $ 10.0 million allocated to the Discovery Agreement. The $ 14.0 million milestone payment received (net of the payment of an associated sublicense fee of $ 1.0 million to SGEN) and the estimated sublicense fees of $ 4.2 million were allocated to the CD71 Agreement performance obligation as they are directly related to the development of the CX-2029. Therefore, of the $ 39.8 million total initial transaction price discussed above, the Company allocated $ 29.8 million to the CD71 Agreement performance obligation and $ 10.0 million to the Discovery Agreement performance obligation and recognized revenue using an input measure for each performance obligation. In applying the input method, revenue is recognized based on actual FTE hours incurred as a percentage of total estimated FTE hours for completing the combined performance obligation over the estimated service period. The Company evaluates the measure of progress each reporting period and, if necessary, adjusts the measure of performance and related revenue recognition. The Company updated the transaction price for the CD71 Agreement performance obligation in May 2018, to include achievement of the $ 21.0 million milestone (net of the payment of an associated sublicense fee of $ 4.0 million to SGEN) and a revenue adjustment of $ 9.9 million was recognized in the second quarter of 2018 reflecting the percentage completed to-date on the project related to this milestone. The transaction price was updated again in March 2020 upon achievement of the $ 40.0 million milestone related to satisfaction of the CD71 dose escalation success criteria and $ 26.6 million was recognized as revenue related to this milestone reflecting the percentage completed to-date on the project as of March 2020. During 2019, as a result of ongoing dose escalation in the continued development program related to the CD71 Agreement performance obligation, there was a change in estimate of the research service period as well as an increase in the projected FTE hours-to-completion. As of December 31, 2021, the research service period for the CD71 Agreement performance obligation was extended during the course of the arrangement from April 2021 to March 2023. In June 2019, the Company received a $ 10.0 million payment for the second target selected by AbbVie under the Discovery Agreement. The $ 10.0 million payment is being recognized as revenue using the input method based on FTE hours incurred as a percentage of total estimated FTE hours for completing the related performance obligation over the estimated research service period of five years . The Company determined that the remaining potential milestone payments under the AbbVie agreements, if recognized, are probable of significant revenue reversal as their achievement is highly dependent on factors outside the Company’s control. Therefore, these payments continue to be fully constrained and are not included in the transaction price as of December 31, 2021. As of December 31, 2021 and 2020, deferred revenue related to the CD71 Agreement performance obligation was $ 16.1 million and $ 25.2 million, respectively, and deferred revenue related to the Discovery Agreement performance obligation was $ 6.5 million and $ 8.9 million, respectively. Amgen, Inc. On September 29, 2017, the Company and Amgen, Inc. (“Amgen”) entered into a Collaboration and License Agreement (the “Amgen Agreement”). Pursuant to the Amgen Agreement, the Company received an upfront payment of $ 40.0 million in October 2017. Concurrent with the Amgen Agreement, the Company and Amgen entered into a Share Purchase Agreement pursuant to which Amgen purchased 1,156,069 shares of the Company’s common stock at a price of $ 17.30 per share for total proceeds of $ 20.0 million. In October 2021, CytomX and Amgen executed an amendment to the Amgen Agreement primarily to (1) extend the target selection date for Amgen to select its additional targets for research and development, and (2) reduce the total number of milestone events and increase the total amount of milestone payments for EGFR Products. Under the terms of the Amgen Agreement, as amended, the Company and Amgen will co-develop a conditionally activated T-cell engaging bispecific therapeutic targeting epidermal growth factor receptor (the “EGFR Products”). The Company is responsible for early-stage development of EGFR Products and Amgen will be responsible for late-stage development and commercialization of EGFR Products. Following early-stage development, the Company will have the right to elect to participate financially in the global co-development of EGFR Products with Amgen, during which the Company would bear certain of the worldwide development costs for EGFR Products and Amgen would bear the rest of such costs (the “EGFR Co-Development Option”). If the Company exercises its EGFR Co-Development Option, the Company will share in somewhat less than 50 % of the profit and losses from sales of such EGFR Products in the U.S., subject to certain caps, offsets, and deferrals. If the Company chooses not to exercise its EGFR Co-Development Option, the Company will not bear any costs of later stage development. The Company is also eligible to receive up to $ 460.0 million in development, regulatory, and commercial milestone payments for EGFR Products, and royalties in the low-double-digit to mid-teen percentage of worldwide commercial sales, provided that if the Company exercises its EGFR Co-Development option, it shall receive a profit and loss split of sales in the United States and royalties in the low-double-digit to mid-teen percentage of commercial sales outside of the United States. Amgen also has the right to select a total of up to three targets, including the two additional targets discussed below. The Company and Amgen collaborate in the research and development of conditionally activated T-cell engaging bispecifics products directed against such targets. Amgen has selected one such target (the “Amgen Other Product”). If Amgen exercises its option within a specified period of time, it can select two such additional targets (the “Amgen Option Products” and, together with the Amgen Other Product, the “Amgen Products”). Except with respect to preclinical activities to be conducted by CytomX, Amgen will be responsible, at its expense, for the development, manufacture, and commercialization of all Amgen Products. If Amgen exercises all of its options and advances all three of the Amgen Products, CytomX was initially eligible to receive up to $ 950.0 million in upfront, development, regulatory, and commercial milestones and tiered high single-digit to low-teen percentage royalties. The Company concluded that, at the inception of the agreement, Amgen’s option to select the two additional targets is not a material right and does not represent a performance obligation of the agreement. At the initiation of the collaboration, CytomX had the option to select, from programs specified in the Amgen Agreement, an existing preclinical stage T-cell engaging bispecific product from the Amgen preclinical pipeline. In March 2018, CytomX selected the program. CytomX is responsible, at its expense, for converting this program to a conditionally activated T-cell engaging bispecific product, and thereafter, will be responsible for development, manufacturing, and commercialization of the product (“CytomX Product”). Amgen is eligible to receive up to $ 203.0 million in development, regulatory, and commercial milestone payments for the CytomX Product, and tiered mid-single digit to low double-digit percentage royalties. The Company considered the criteria for combining contracts in ASC 606 and determined that the Amgen Agreement and the Purchase Agreement should be combined into one contract. The Company accounted for the Amgen Agreement based on the fair values of the assets and services exchanged. The Company identified the following promised goods and services at the inception of the Amgen Agreement: (1) the research, development and commercialization license, (2) the research and development services for the EGFR Products and the Amgen Other Product, and (3) the obligation to participate in the joint steering committee (“JSC”) and the joint research committee (“JRC”). For each of the EGFR Products and the Amgen Other Products, the Company determined that the respective promised goods and services identified are not distinct from the related research and development services. Therefore the identified promised goods and services were combined into one single performance obligation for each of the EGFR Product and the Amgen Other Products. Furthermore, the Amgen Other Products are accounted for as a separate performance obligation from the EGFR Products as the nature of the services being performed is not the same and the value that Amgen can derive from one program is not dependent on the success of the other. The Company evaluates the measure of progress each reporting period using the cost input-method and, if necessary, adjusts the measure of performance and related revenue recognition. Concurrent with the execution of the Amgen Agreement, the Company entered into a sublicense agreement whereby the Company granted Amgen a sublicense of its rights to one patent family that it co-owns with UCSB, that is exclusively licensed to the Company under the UCSB Agreement covering Probody antibodies and other pro-proteins in the fields of therapeutics, in vivo diagnostics and prophylactics. This sublicense was incremental to the patents, patent applications and know-how covering conditionally activated T-cell engaging bispecific molecules that were developed and owned by the Company and licensed to Amgen. Under the UCSB Agreement, as amended, the Company is obligated to make a sublicense payment to UCSB equal to up to 7.5 % of certain upfront and milestone payments owed to or received by the Company. The total transaction price of $ 51.2 million, consisting of the $ 40.0 million upfront payment, an estimated fair value of $ 10.7 million for the CytomX Product and $ 0.5 million of premium on the sale of the Company’s common stock, was allocated between the two performance obligations based on the relative standalone selling price of each performance obligation. To determine the standalone selling price, the Company used the discounted cash flow method by calculating risk-adjusted net present values of estimated cash flows. The Company determined that the remaining potential milestone payments were fully constrained due to the uncertainty in achieving them as of December 31, 2021. Of the $ 51.2 million total transaction price, the Company allocated $ 46.4 million to the EGFR Products performance obligation and $ 4.8 million to the Amgen Other Product performance obligations. The transaction price of each performance obligation was recognized using an input measure. In applying the input method of revenue recognition, the Company uses actual FTE hours incurred relative to estimated total FTE hours expected to be incurred for the combined performance obligation over the research service period. At the end of the second quarter of 2019, the Company determined that it would undertake additional testing and assessment of the molecules being evaluated under the EGFR project. As a result, the estimated FTE hours-to-completion and research service period related to the EGFR project were increased to eight years . In the second quarter of 2020, the Company completed the clinical candidate characterization phase and has moved into the IND-enabling phase earlier than planned. As a result, the estimated FTE hours-to-completion and research service period related to the EGFR project were decreased from eight to approximately seven years . The $ 4.8 million transaction price allocated to the Amgen Other Product performance obligation is recognized using estimated FTE hours-to-completion over the estimated research service period of six years . As of December 31, 2021 and 2020 deferred revenue related to the EGFR Products performance obligation was $ 21.8 million and $ 29.8 million, respectively. As of December 31, 2021 and 2020, deferred revenue related to the Amgen Other Products performance obligation was $ 1.8 million and $ 2.3 million, respectively. Astellas Pharma Inc. The Company and Astellas Pharma, Inc. (“Astellas”) entered into a Collaboration and License Agreement (the “Astellas Agreement”) on March 23, 2020, the effective date, to collaborate on preclinical research activities to discover and develop certain antibody compounds for the treatment of cancer using the Company’s Probody therapeutic technology. Under the terms of the Astellas Agreement, the Company granted Astellas an exclusive, worldwide right to develop and commercialize Probody therapeutics for up to four collaboration targets including one initial target and three additional targets (“Additional Targets”). In addition, Astellas has the right to expand the number of Additional Targets from three up to five (the “Expansion Option”) before the third anniversary of the effective date. Furthermore, for a specified number of targets, at a pre-specified time prior to the initiation of the first pivotal study of a product against such target, the Company may elect to participate in certain development costs and share in the profits generated in the United States with respect to such product (“Cost Share Option”). The Cost Share Option, if exercised, will also provide the option for the Company to co-commercialize such product in the United States. The Company does not consider the Cost Share Option as a performance obligation at the inception of the agreement as the participation is at the Company’s discretion. Pursuant to the Astellas Agreement, the consideration from Astellas is comprised of an upfront fee of $ 80.0 million and contingent payments for development, regulatory and sales milestones of up to an aggregate of approximately $ 1.6 billion. If Astellas exercises its Expansion Option for the two Additional Targets, the Company would be eligible to receive additional upfront and milestone payments aggregating to approximately $ 0.9 billion. The Company is also entitled to tiered royalties from high-single digit to mid-teen percentage royalties from potential future sales. Astellas is responsible for all preclinical research costs incurred by either party as set forth in the preclinical research plan and the Company will receive research and development service fees based on a prescribed FTE rate. The Company determined that the license and expertise related to the development of product candidates should be combined with the research and development services and participation in the joint research committee as one combined performance obligation for each collaboration target. The Company concluded, that at the inception of the agreement, Astellas’ Expansion Option for two Additional Targets were not material rights and therefore not considered performance obligations. As such, each option will be accounted for as a separate arrangement upon exercise. The initial transaction price of $ 103.2 million consists of the upfront fee of $ 80.0 million and estimated research and development service fees of $ 23.2 million. The transaction price was allocated between the four performance obligations based on the relative standalone selling price of each performance obligation, which was deemed to be equal at the inception of the agreement. The Company determined that all potential milestone payments are constrained as of December 31, 2021 due to the significant uncertainty of achievement. The transaction price as allocated to the combined performance obligation for each target, is recognized using an input measure. In applying the input method of revenue recognition, the Company uses actual FTE hours incurred relative to estimated total FTE hours expected to be incurred of each target. As of December 31, 2021 and 2020, deferred revenue relating to the Astellas Agreement was $ 60.3 million and $ 74.2 million, respectively. The amount due from Astellas under the Astellas Agreement was $ 0.8 million and $ 0.8 million as of December 31, 2021 and 2020, respectively. Bristol Myers Squibb Company On May 23, 2014, the Company and Bristol Myers Squibb Company (“Bristol Myers Squibb”) entered into a Collaboration and License Agreement (the “BMS Agreement”) to discover and develop compounds for use in human therapeutics aimed at multiple immuno-oncology targets using the Company’s Probody therapeutic technology. The effective date of the BMS Agreement was July 7, 2014. Under the terms of the BMS Agreement, the Company granted Bristol Myers Squibb exclusive worldwide rights to develop and commercialize Probody therapeutics for up to four oncology targets. Bristol Myers Squibb had additional rights to substitute up to two collaboration targets within three years of the effective date of the BMS Agreement. These rights expired in May 2017. Each collaboration target had a two-year research term and the two additional targets had to be nominated by Bristol Myers Squibb within five years of the effective date of the BMS Agreement. The research term for each collaboration target could be extended in one year increments up to three times. Pursuant to the BMS Agreement, the financial consideration from Bristol Myers Squibb was comprised of an upfront payment of $ 50.0 million and estimated research and development service fees, and the Company was initially entitled to receive contingent payments of up to $ 25.0 million for additional targets and contingent payments for development, regulatory and sales milestones. In addition, the Company was entitled to royalty payments in the mid-single digits to low double-digit percentages from potential future sales. On March 17, 2017, the Company and Bristol Myers Squibb entered into Amendment Number 1 to Extend Collaboration and License Agreement (“Amendment 1”). Amendment 1 granted Bristol Myers Squibb exclusive worldwide rights to develop and commercialize Probody therapeutics for up to eight additional targets. The effective date of Amendment 1 was April 25, 2017 (“Amendment Effective Date”). Under the terms of Amendment 1, the Company continued to have obligations to Bristol Myers Squibb to discover and conduct preclinical development of Probody therapeutics against any targets they chose to select during the research period under the terms of Amendment 1. Pursuant to Amendment 1, the financial consideration from Bristol Myers Squibb was comprised of an upfront payment of $ 200.0 million, estimated research and development service fees, and contingent payments for development, regulatory and sales milestones for the eight targets. The Company was also entitled to tiered mid-single to low double-digit percentage royalties from potential future sales. Amendment 1 did not change the term of the Bristol Myers Squibb’s royalty obligation under the BMS Agreement. Bristol Myers Squibb’s royalty obligation continues on a licensed-product by licensed-product basis until the later of (i) the expiration of the last claim of the licensed patents covering the licensed products in the country, (ii) the twelfth anniversary of the first commercial sale of a licensed product in a country, or (iii) the expiration of any applicable regulatory, pediatric, orphan drug or data exclusivity with respect to such product. The Company elected the practical expedient related to contract modifications upon adoption of ASC 606 and combined the original agreement and Amendment 1. The Company determined that the exclusive research, development and commercialization license, the related research services and expertise related to the development of product candidates should be combined with the participation in the joint research committee as one combined performance obligation for each collaboration target. The Company also concluded that, at the inception of the agreement, Bristol Myers Squibb’s options for the third and fourth targets were material rights and performance obligations. As such, the material rights were accounted for as part of the initial transaction price. The Company received an upfront payment of $ 50.0 million from Bristol Myers Squibb in July 2014. In January and December 2016, Bristol Myers Squibb exercised the option to select the third and fourth targets, and paid the Company $ 10.0 million and $ 15.0 million, respectively, pursuant to the terms of the BMS Agreement. In December 2016, Bristol Myers Squibb selected a clinical candidate pursuant to the BMS Agreement, which triggered a $ 2.0 million pre-clinical milestone payment to the Company. In November 2017, the Company recognized a $ 10.0 million milestone payment from Bristol Myers Squibb upon approval of the investigational new drug application for the CTLA-4-directed Probody therapeutic. The initial transaction price for the BMS Agreement and Amendment 1, collectively, was $ 304.7 million consisting of the upfront fees of $ 250.0 million, target selection fees for the third and fourth targets of $ 25.0 million, estimated research and development service fees of $ 17.7 million and milestone payments received up to January 1, 2018, of $ 12.0 million . The Company determined that the remaining potential milestone payments were probable of significant revenue reversal as their achievement was highly dependent on factors outside the Company’s control. Therefore, these payments were fully constrained and were not included in the transaction price upon the adoption of ASC 606 on January 1, 2018. The initial transaction price for the combined obligation for each collaboration target is recognized using an input measure. In applying the input method of revenue recognition, the Company uses actual FTE hours incurred relative to estimated total FTE hours expected to be incurred for each combined performance obligation over the estimated research service period of each collaboration target. During the first quarter of 2019, Bristol Myers Squibb terminated pre-clinical activities on three of the first four collaboration targets selected under the original 2014 BMS Agreement. The Company determined that upon the termination of pre-clinical activities on the three collaboration targets, it has no further obligations related to such targets. The Company accounted for the termination of the three targets as a modification and the related remaining unrecognized transaction price was reallocated to the remaining performance obligations. The Company continues to be obligated to perform research work under Amendment 1 executed in March 2017. In February 2020, Bristol Myers Squibb dosed the first patient in the Part 2 cohort expansion portion of its ongoing BMS-986249 clinical study for the CTLA-4 program, which triggered a $ 10.0 million milestone payment to the Company pursuant to the terms of the BMS Agreement. The $ 10.0 million milestone payment was recognized as revenue in the first quarter of 2020 as the Company had completed its performance obligation related to this collaboration target. In February 2021, the Company and Bristol Myers Squibb entered into Amendment Number 2 to amend the Collaboration and License Agreement (“Amendment 2”), as amended by Amendment 1. Subsequent to Amendment 2, in addition to Bristol Myers Squibb’s ongoing development of the CTLA-4 program, Bristol Myers Squibb also had the exclusive worldwide rights to develop and commercialize Probody therapeutics for up to five oncology targets. Under the terms of Amendment 2, the period for target selection was extended and the Company will continue to collaborate with Bristol Myers Squibb to discover and conduct preclinical development of Probody therapeutics against targets selected by Bristol Myers Squibb over the estimated research period, which is projected to end in April 2025. Pursuant to Amendment 2, the Company was eligible to receive contingent payments for development, regulatory and sales milestones. It is also entitled to tiered mid-single to low double-digit percentage of royalties from potential future sales. The Company accounted for Amendment 2 as a modification and reallocated the remaining unrecognized transaction price to the remaining performance obligations. The Company reevaluated the remaining potential milestone payments and determined that significant revenue reversal was still probable as the achievement of such milestones was highly dependent on factors outside the Company’s control. As a result, these payments continued to be fully constrained and were not included in the transaction price on December 31, 2021. As of December 31, 2021, the Company has received in aggregate $ 297.0 million in upfront and milestone payments under the agreement. As of December 31, 2021, the Company is eligible for up to approximately $ 2.1 billion in contingent payments for development, regulatory and sales milestones based on the ongoing collaboration projects, including the CTLA-4 program, with BMS. As of December 31, 2021 and 2020, deferred revenue relating to the BMS Agreement was $ 178.3 million and $ 178.3 million, respectively. ImmunoGen, Inc. In January 2014, the Company and ImmunoGen, Inc. (“ImmunoGen”) entered into the Research Collaboration Agreement (the “ImmunoGen Research Agreement”). The ImmunoGen Research Agreement provided the Company with the right to use ImmunoGen’s Antibody Drug Conjugate (“ADC”) technology in combination with the Company’s Probody therapeutic technology to create a conditionally activated ADC directed at one specified target under a research license, and to subsequently obtain an exclusive, worldwide development and commercialization license to use ImmunoGen’s ADC technology to develop and commercialize such conditionally activated ADCs. The Company made no upfront cash payment in |
License Agreement
License Agreement | 12 Months Ended |
Dec. 31, 2021 | |
Research and Development [Abstract] | |
License Agreement | 10. License Agreement UCSB The Company has an exclusive, worldwide license agreement with UCSB (the “UCSB Agreement”), relating to the use of certain patents and technology relating to its core technology, including its therapeutic antibodies, and to certain patent rights the Company co-owns with UCSB covering Probody antibodies and other pro-proteins. Pursuant to the UCSB Agreement, the Company is obligated to (i) make royalty payments to UCSB on net sales of its products covered under the agreement, subject to annual minimum amounts, (ii) make milestone payments to UCSB upon the occurrence of certain events, (iii) make a milestone payment to UCSB upon occurrence of an IPO or change of control, and (iv) reimburse UCSB for prosecution and maintenance of the licensed patents. If the Company sublicenses its rights under the UCSB Agreement, it is obligated to pay UCSB a percentage of the total sublicense revenue received, which total amount would be first reduced by the aggregate amount of certain research and development related expenses incurred by the Company and other permitted deductions. As part of the UCSB Agreement, the Company has annual minimum royalty obligations of $ 0.2 million under the terms of certain exclusive licensed patent rights. The royalty obligations are cancellable any time by giving notice to the licensor, with the termination being effective 60 days after giving notice. In April 2019, the Company entered into Amendment No.3 to the UCSB Agreement to adjust and clarify certain sublicense terms (“Amendment No.3”). In connection with the amendment, the Company issued to UCSB 150,000 shares of CytomX common stock with a fair value of $ 10.68 per share. Under the terms of Amendment No.3, the Company and UCSB agreed to modify the determination of sublicense revenues payable by the Company to UCSB on certain existing collaboration agreements and on collaboration agreements executed subsequent to Amendment No.3. In exchange, the Company agreed to make an upfront payment of $ 1.0 million as well as additional annual license maintenance fees of $ 0.8 million through 2031 . In the event that the Company terminates the agreement due to material concern of the safety or efficacy of the related technology, 50 % of all remaining maintenance fees will become due immediately. Otherwise, all remaining maintenance fees will become due immediately upon early termination of the agreement unless there is a material breach by UCSB. Pursuant to Amendment No.3, the Company recorded in research and development expense a charge of $ 3.4 million relating to sublicense and maintenance fees representing the 150,000 shares issued with a fair value of $ 1.6 million, the upfront payment of $ 1.0 million and the additional annual maintenance fee of $ 0.8 million during the second quarter of 2019. In June 2019, the Company incurred an additional $ 0.8 million of sublicense fees related to the $ 10.0 million milestone payment for the second target selected by AbbVie under the Discovery Agreement. In February 2020, the Company recorded $ 0.8 million of sublicense fees triggered by the $ 10.0 million milestone payment from Bristol Myers Squibb’s dosing of the first patient in the Part 2 cohort expansion portion of its ongoing BMS-986249 clinical study for the CTLA-4 program. In March 2020, the Company incurred additional sublicense fees of $ 6.0 million related to the $ 80.0 million upfront fee received pursuant to the Astellas Agreement entered into in March 2020, and $ 1.4 million related to the $ 40.0 million milestone payment from AbbVie for satisfying the CD71 dose escalation success criteria under the CD71 Agreement in March 2020. During the years ended December 31, 2021, 2020, and 2019, the Company incurred sublicense expenses of $ 1.0 million, $ 9.1 million, and $ 4.3 million, respectively, under the provisions of the UCSB Agreement. ImmunoGen In December 2019, the Company entered into a License Agreement (the “ImmunoGen 2019 License”) with ImmunoGen, Inc. to obtain an exclusive license with respect to epithelial cell adhesion molecule (“EPCAM”). Under the ImmunoGen 2019 License, ImmunoGen agreed to transfer its know-how, patents, intellectual property rights, and technology transfer materials and information related to its EpCAM program. The license gives the Company the sole ability to develop, manufacture, use and commercialize any licensed product that incorporates, is comprised of, or otherwise derived from a Probody that targets EpCAM in any human therapeutic field on a worldwide basis. In exchange, the Company agreed to make non-refundable and non-creditable payments including an upfront license payment of $ 7.5 million and certain clinical development, approval and commercialization milestone payments, if achieved and royalties on product sales. The upfront license fee of $ 7.5 million was recorded as research and development expense in December 2019. |
Commitments and Contingencies
Commitments and Contingencies | 12 Months Ended |
Dec. 31, 2021 | |
Commitments and Contingencies Disclosure [Abstract] | |
Commitments and Contingencies | 11. Commitments and Contingencies Legal Proceedings On March 4, 2020 , Vytacera Bio, LLC filed a patent infringement lawsuit against the Company in the U.S. District Court for the District of Delaware. The lawsuit alleges that the Company's use, offers to sell, and/or sales of the Probody® technology platform for basic research applications constitutes infringement. The complaint seeks unspecified monetary damages. The Company filed an Answer, Affirmative Defenses, and Counterclaims on May 26, 2020 . Vytacera Bio, LLC filed its Answer to CytomX Therapeutics Inc.’s Counterclaims on June 5, 2020 . On October 13, 2021, the Court granted the parties’ stipulation to stay all pending case deadlines except for certain matters. All case deadlines are stayed until the Court resolves the parties’ claim construction disputes. The Company believes that the lawsuit is without merit and intends to vigorously defend itself , and has no t recorded any amount for claims associated with this lawsuit as of December 31, 2021. Indemnifications In the ordinary course of business, the Company enters into agreements that may include indemnification provisions. Pursuant to such agreements, the Company may indemnify, hold harmless and defend an indemnified party for losses suffered or incurred by the indemnified party. Some of the provisions will limit losses to those arising from third party actions. In some cases, the indemnification will continue after the termination of the agreement. The maximum potential amount of future payments the Company could be required to make under these provisions is not determinable. The Company has never incurred material costs to defend lawsuits or settle claims related to these indemnification provisions. The Company has also entered into indemnification agreements with its directors and officers that may require the Company to indemnify its directors and officers against liabilities that may arise by reason of their status or service as directors or officers to the fullest extent permitted by Delaware corporate law. The Company currently has directors’ and officers’ insurance. |
Leases
Leases | 12 Months Ended |
Dec. 31, 2021 | |
Leases [Abstract] | |
Leases | 12. Leases Operating Lease In December 2015, the Company entered into a lease (the “2016 Lease”) of office and laboratory space located in South San Francisco, California for the Company’s corporate headquarters. The 2016 Lease has an initial term of ten years through 2026 and the Company has an option to extend the initial term for an additional five years at the then fair rental value as determined pursuant to the 2016 Lease. In addition, the Company obtained a standby letter of credit (the “Letter of Credit”) in an amount of approximately $ 0.9 million, which may be drawn by the Landlord to be applied for certain purposes upon the Company’s breach of any provisions under the 2016 Lease. The Company has recorded the $ 0.9 million of cash securing the Letter of Credit as non-current restricted cash on its balance sheet as of December 31, 2021 and 2020. Rent expense during the years ended December 31, 2021, 2020, and 2019 was $ 5.1 million, $ 5.1 million and $ 4.8 million, respectively. Supplemental information related to leases are as follows: Year Ended December 31, 2021 December 31, 2020 (in thousands) Cash paid for amounts included in the measurement of lease liabilities Operating cash flows from operating leases $ 5,129 $ 4,990 December 31, 2021 December 31, 2020 (in thousands) Supplemental balance sheet information related to leases: Operating lease right-of-use assets $ 19,362 $ 22,495 Current operating lease liabilities 3,618 3,195 Non-current operating lease liabilities 18,056 21,675 Total operating lease liabilities $ 21,674 $ 24,870 Weighted-average remaining lease term (in years) Operating lease 4.75 5.75 Weighted-average discount rate Operating lease 8.25 % 8.25 % December 31, 2021 (in thousands) Maturity of operating lease liabilities 2022 5,273 2023 5,420 2024 5,572 2025 5,729 2026 and beyond 4,387 Total lease payments 26,381 Less imputed interest ( 4,707 ) Present value of lease liabilities $ 21,674 |
Common Stock
Common Stock | 12 Months Ended |
Dec. 31, 2021 | |
Equity [Abstract] | |
Common Stock | 13. Common Stock In February 2020, the Company entered into an Open Market Sale Agreement (the “Sales Agreement”) with Jefferies LLC (“Jefferies”), to sell shares of the Company’s common stock, par value $ 0.00001 per share, with aggregate gross sales proceeds of up to $ 75,000,000 , from time to time upon the Company’s request, through an at the market offering under which Jefferies will act as sales agent. Pursuant to the Sales Agreement, Jefferies as the sales agent will receive a commission of 3.0 % of the gross sales price for shares of common stock sold under the Sales Agreement. During December 2020, the Company sold 1,535,217 shares at an average price of $ 7.62 per shares and received net proceeds of approximately $ 11.3 million after deducting the 3.0 % sales commission and related issuance cost. In January 2021, the Company completed an underwritten public offering of 14,285,714 shares of common stock at a price of $ 7.00 per share. The aggregate net proceeds received by the Company from the offering were approximately $ 93.6 million, after deducting underwriting discounts and commissions and offering expenses of $ 6.4 million. The Company also granted the underwriters the option for 30 days to purchase up to 2,142,857 additional shares of common stock at the public offering price, less the underwriting discounts and commissions. In February 2021, the underwriters exercised the option in full which resulted in additional net proceeds of $ 14.1 million to the Company, after deducting the underwriting discounts and commissions of $ 0.9 million. |
Stock-based Compensation
Stock-based Compensation | 12 Months Ended |
Dec. 31, 2021 | |
Share-Based Payment Arrangement [Abstract] | |
Stock-based Compensation | 14. Stock-based Compensation The 2010 Plan and 2011 Plan In 2010, the Company adopted its 2010 Stock Incentive Plan (the “2010 Plan”) which provided for the granting of stock options to employees, directors and consultants of the Company. Options granted under the 2010 Plan were either incentive stock options (“ISOs”) or nonqualified stock options (“NSOs”). In February 2012, the Company adopted its 2011 Stock Incentive Plan (the “2011 Plan”). The 2011 Plan is divided into two separate equity programs, an option and stock appreciation rights grant program and a stock award program. In conjunction with adopting the 2011 Plan, the Company discontinued the 2010 Plan and released the shares reserved and still available under that plan. In connection with the consummation of the IPO in October 2015, the board of directors adopted the Company’s 2015 Equity Incentive Plan (the “2015 Plan” and collectively with the 2010 Plan and 2011 Plan, the “Plans”). In conjunction with adopting the 2015 Plan, the Company discontinued the 2011 Plan with respect to new equity awards. The 2015 Plan The 2015 Plan authorized the board of directors to grant incentive stock options, non-statutory stock options and RSUs to employees, directors, non-employee directors and consultants of the Company. Sto ck options under the 2015 Plan may be granted for periods of up to ten years . All stock options issued to date have had a 10 -year life. Under the terms of the 2015 Plan, stock options may be granted at an exercise price not less than the estimated fair value of the Company’s common stock on the date of grant, as determined by the Company’s board of directors. For employees holding more than 10 % of the voting rights of all classes of stock, the exercise price of ISOs and NSOs may not be less than 110 % of the estimated fair value of the shares on the date of grant, as determined by the board of directors. To date, stock options granted under the 2015 Plan generally vest over four years and vest at a rate of 25 % upon the first anniversary of the issuance date and 1/48 th per month thereafter. The initial number of shares of common stock available for future issuance under the 2015 Plan was 2,444,735 . Beginning on January 1, 2016 and continuing until the expiration of the 2015 Plan, the total number of shares of common stock available for issuance under the 2015 Plan will automatically increase annually on January 1 by 4 % of the total number of issued and outstanding shares of common stock as of January 1 of the same year. As of December 31, 2021 and 2020, 2,276,341 shares and 2,698,798 shares of common stock, respectively, were available for future issuance under the 2015 Plan. The 2019 Plan In September 2019, the Board of Directors adopted the 2019 Employment Inducement Incentive Plan (the “2019 Plan”) which provides for the grant of stock options and other equity awards to any employee who has not previously been an employee or director of the Company or who is commencing employment with the Company following a bona fide period of nonemployment by the Company. Awards granted under the 2019 Plan are intended to constitute “employment inducement awards” under Nasdaq Listing Rule 5635(c)(4). Options granted under the 2019 Plan are nonqualified stock options (“NSOs”) which may be exercisable for periods of up to ten years and the options shall be granted at an exercise price of not less than 100 % of the fair market value of the Company’s common stock on the date of grant. The initial number of shares of common stock available for future issuance under the 2019 Plan was 1,815,000 . During 2021, t he total number of shares of common stock available for issuance under the 2019 Plan has increased by 1,000,000 shares. As of December 31, 2021 and 2020, 486,234 shares and 204,600 shares, respectively, of common stock were available for future issuance under the 2019 Plan. Activity under the Company’s stock option plans is set forth below: Options Outstanding Number of Weighted- Weighted- Aggregate (in thousands) Balances at December 31, 2020 10,929,530 $ 10.77 Options granted 5,178,897 7.10 Options exercised ( 528,503 ) 2.70 Options cancelled ( 3,387,708 ) 11.26 Balances at December 31, 2021 12,192,216 9.42 7.5 $ 1,182 Options Exercisable—December 31, 2021 6,054,635 11.46 6.1 $ 1,155 The aggregate intrinsic values of options outstanding, exercisable, vested and expected to vest were calculated as the difference between the exercise price of the options and the quoted market price of the underlying common stock as of December 31, 2021. The aggregate intrinsic value of stock options exercised in the years ended December 31, 2021, 2020, and 2019 was $ 2.2 million, $ 4.4 million, and $ 0.9 million, respectively. The options granted in the years ended December 31, 2021, 2020, and 2019 had weighted-average per share grant-date fair values of $ 3.97 , $ 3.94 , and $ 7.03 respectively. As of December 31, 2021, the unrecognized compensation expense with respect to options granted was $ 23.6 million and is expected to be recognized over 2.9 years. Early Exercise of Employee Options Certain stock options granted under the Plans provide option holders the right to elect to exercise unvested options in exchange for restricted common stock. Such unvested restricted shares are subject to a repurchase right held by the Company at the original issuance price in the event the optionee’s service to the Company is terminated either voluntarily or involuntarily. The right usually lapses 25 % on the first anniversary of the vesting start date and in 36 equal monthly amounts thereafter. These repurchase terms are considered to be a forfeiture provision. The cash or full recourse notes received from employees for exercise of unvested options is treated as a refundable deposit and is classified as a liability on the balance sheets. Time-based RSUs ("TRSU") and Performance-based RSUs ("PSU") In October 2021, the Company granted 439,000 TRSUs as recognition awards to certain employees with an aggregated grant fair value of $ 2.3 million. 50% of the RSUs granted will vest at the end of the first year of the grant date and the remaining 50% will vest at the end of the second year provided the grantee continues to provide services to the Company. The Company recorded $ 0.2 million of stock-based compensation expense related to the TRSUs for the year end December 31, 2021. In conjunction with the TRSU grants, the Company also granted 435,000 performance-based RSUs (“PSUs”) as recognition awards to executive employees with an aggregated grant date fair value of $ 2.3 million. 50% of the PSUs granted will vest within one year of the grant date upon achievement of certain specific milestones and the remaining 50% will vest within two years of the grant date upon achievement of additional company objectives. As of December 31, 2021, the Company determined that it is not probable that the performance conditions will be satisfied and hence recorded no compensation cost for these awards as of and for the year ended December 31, 2021. As of December 31, 2021, the unrecognized compensation expense with respect to the TRSUs was $ 2.1 million which is expected to be recognized over 1.6 years. The fair value of RSUs, including time-based RSUs and performance-based RSUs is based on the market price of the Company's shares on the date of grant. The following table summarizes the Company's RSU activities: Number of Weighted- Aggregate Weighted Average Grant Date Fair Value (in thousands) Balances at December 31, 2020 — $ - RSU's awarded 874,000 5.34 RSU's vested — - RSU's cancelled ( 5,750 ) 5.34 Balances at December 31, 2021 868,250 1.31 $ 3,760 5.34 Ending Exercisable—December 31, 2021 - - $ - $ - Employee Stock Purchase Plan Concurrent with the completion of the IPO in October 2015, the Company’s Employee Stock Purchase Plan (“ESPP”) became effective. The ESPP allows eligible employees to purchase shares of the Company’s common stock at a discount through payroll deductions of up to 15 % of their eligible compensation, subject to any plan limitations. The ESPP generally provides for six-month offering periods, and at the end of each offering period, employees are able to purchase shares at 85 % of the lower of the fair market value of the Company’s common stock on the first trading day of the offering period or on the last trading day of the offering period. The Company issued 183,865 shares and 128,684 shares of common stock under the ESPP in 2021 and 2020, respectively. Shares available for future purchase under the ESPP were 1,751,818 shares and 1,935,683 shares at December 31, 2021 and 2020, respectively. The compensation expense related to the ESPP was $ 0.4 million, $ 0.4 million, and $ 0.6 million for the years ended December 31, 2021, 2020 and 2019, respectively. As of December 31, 2021, there was $ 0.2 million of unrecognized compensation cost related to the ESPP, which the Company expects to recognize over 5 months. Stock Based Compensation Total stock-based compensation recorded related to options granted to employees and non-employees and employee stock purchase plan was as follows (in thousands): Year Ended December 31, 2021 2020 2019 Research and development $ 5,797 $ 6,825 $ 9,226 General and administrative 7,370 7,961 9,874 Total stock-based compensation expense $ 13,167 $ 14,786 $ 19,100 Stock-based compensation expense for employees was $ 13.1 million, $ 14.7 million, and $ 18.9 million for the years ended December 31, 2021, 2020, and 2019, respectively. Stock-based compensation expense for non-employees was $ 0.1 million, $ 0.1 million, and $ 0.2 million for the years ended December 31, 2021, 2020, and 2019, respectively. The Company estimated the fair value of employee stock options and ESPP using the Black-Scholes valuation model based on the date of grant with the following assumptions: Options ESPP Year Ended December 31, Year Ended December 31, 2021 2020 2019 2021 2020 2019 Expected volatility 69.6 % - 74.8 % 64.4 % - 73.3 % 64.4 % - 68.6 % 46.87 % - 69.58 % 47.3 % - 122.1 % 60.8 % - 71.9 % Risk-free interest rate 0.5 % - 1.3 % 0.2 % - 1.3 % 1.4 % - 2.5 % 0.04 % - 0.10 % 0.1 % - 0.2 % 1.6 % - 2.4 % Dividend yield — % — % — % — % — % — % Expected term 4.5 - 4.8 4.7 - 4.9 4.9 - 5.0 0.5 0.5 0.5 Expected term. The expected term of stock options represents the period that the stock options are expected to remain outstanding and is based on vesting terms, exercise term and contractual lives of the options. The expected term of the ESPP shares is equal to the six-month look-back period. Expected volatility. The expected stock price volatility for the Company’s stock options is based on the historical stock price volatility which is commensurate with the estimated expected term of the stock awards. Volatility for ESPP shares is equal to the Company’s historical volatility over a six-month offering period. Risk-free interest rate. The risk-free interest rate is based on the U.S. Treasury yield with a maturity equal to the expected term of the stock options in effect at the time of grant. Dividend yield. The expected dividend is assumed to be zero as the Company has never paid dividends and has no current plan to pay any dividends on its common stock. |
Income Taxes
Income Taxes | 12 Months Ended |
Dec. 31, 2021 | |
Income Tax Disclosure [Abstract] | |
Income Taxes | 15. Inco me Taxes The Company derives its income only from the United States. The components of the benefit from income taxes are as follows (in thousands): Years Ended December 31, 2021 2020 2019 Current: Federal $ — $ ( 13,912 ) $ ( 390 ) State — 1 — Total current — ( 13,911 ) ( 390 ) Deferred: Federal — — ( 37 ) State — — — Total deferred — — ( 37 ) Benefit from income taxes $ — $ ( 13,911 ) $ ( 427 ) A reconciliation of the Company’s effective tax rate to the statutory U.S. federal rate is as follows: Years Ended December 31, 2021 2020 2019 U.S. federal taxes at statutory rate 21.0 % 21.0 % 21.0 % State tax, net of federal benefit 1.5 % 2.0 % 1.0 % Stock compensation ( 3.1 )% ( 1.3 )% ( 1.0 )% Tax credits 2.0 % 6.6 % 1.9 % Change in valuation allowance ( 21.4 )% ( 27.1 )% ( 22.3 )% Net operating loss carryback 0.0 % 16.6 % 0.0 % Return to provision adjustment 0.0 % 0.0 % ( 0.2 )% Other 0.0 % ( 0.1 )% ( 0.1 )% Total ( 0.0 )% 17.7 % 0.3 % The types of temporary differences that give rise to significant portions of the Company’s deferred income tax assets and liabilities are set out below (in thousands): Year Ended December 31, 2021 2020 Net operating loss carryforwards $ 49,070 $ 38,485 Research and development credits 20,809 16,803 Lease liability 4,555 5,223 Intangible assets 3,804 3,923 Deferred revenue 60,285 49,537 Accrued liabilities 1,933 1,512 Stock-based compensation 7,480 8,578 Other 29 20 Total gross deferred income tax assets 147,965 124,081 Less: valuation allowance ( 143,355 ) ( 118,539 ) Deferred tax assets, net of valuation allowance 4,610 5,542 Fixed assets ( 253 ) ( 433 ) Right-of-use assets ( 4,069 ) ( 4,724 ) Prepaid expenses ( 288 ) ( 385 ) Deferred tax liabilities ( 4,610 ) ( 5,542 ) Net deferred income tax liabilities $ — $ — On March 27, 2020, the Coronavirus Aid, Relief, and Economic Security Act (“CARES Act”) was enacted in response to the COVID-19 pandemic. The tax relief measures under the CARES Act for businesses include a five-year net operating loss carryback, suspension of annual deduction limitation of 80 % of taxable income from net operating losses generated in a tax year beginning after December 31, 2017, changes in the deductibility of interest, acceleration of alternative minimum tax credit refunds, payroll tax relief, and a technical correction to allow accelerated deductions for qualified improvement property. The Company recognized income tax benefit of $ 13.9 million for the year ended December 31, 2020, through the net operating loss carryback under the CARES Act which generated a refund of income taxes paid for 2018. The Company has established a valuation allowance against all of its net deferred tax assets. Management considered all available evidence, both positive and negative, including but not limited to our historical operating results, income or loss in recent periods, cumulative losses in recent years, forecasted earnings, future taxable income, and significant risk and uncertainty related to forecasts, and concluded the deferred tax assets are not more likely than not to be realized. The net change in the total valuation allowance for the years ended December 31, 2021, 2020 and 2019 was an increas e of 24.8 million, $ 3.9 million, a nd $ 29.1 million, respectively. The Company had net operating loss carryforwards for federal and state income tax purposes of approximately $ 225.5 million and $ 24.2 million, respectively, as of December 31, 2021, available to reduce future taxable income. Of the federal net operating loss carryforwards, $ 65.6 million will begin to expire in 2034 , if not utilized and $ 159.9 million will carryforward indefinitely. The state net operating loss carryforwards will begin to expire in 2032 , if not utilized. The Company also has federal and state research and development tax credits carryforwards of $ 19.1 million and $ 11.2 million, respectively, as of December 31, 2021 available to reduce future income taxes. The federal research and development tax credits will begin to expire in 2031 if not utilized. The state research and development tax credits have no expiration date. Internal Revenue Code section 382 (“IRC Section 382”) places a limitation (the “Section 382 Limitation”) on the amount of taxable income that can be offset by net operating loss (“NOL”) carryforwards after a change in control (generally greater than 50 % change in ownership) of a loss corporation. California has similar rules. The Company has performed an IRC Section 382 analysis and determined there was an ownership change in 2017 that resulted in 382 limitations. When an ownership change occurs, IRC Section 382 limits the use of NOLs and credits in subsequent periods based on the annual 382 limitations. The annual 382 limitations may limit the full use of available tax attributes in one year but the identified ownership changes may not result in expiration of tax attributes for use prior to expiration of their respective carryforward periods. Accordingly, none of the tax attributes have been reduced but limited the full use in 2018. The Company has determined that, while an ownership change has occurred, the applicable limits would not impair the value or anticipated use of the Company’s federal and state net operating losses. Although realization is not assured, management believes it is more likely than not that any limitation under IRC Section 382 will not impair the realizability of the deferred income tax assets related to federal and state net operating loss carryforwards. The Company reviewed its stock ownership for the year ended December 31, 2021 and concluded no ownership changes occurred in current year which would result in a reduction of its net operating loss or in its research and development credits expiring unused. If additional ownership change occurs, the utilization of net operating loss and credit carryforwards could be significantly reduced. A reconciliation of the beginning and ending unrecognized tax benefit amount is as follows (in thousands): Year Ended December 31, 2021 2020 2019 Balance at the beginning of the year $ 6,454 $ 5,249 $ 3,756 Additions based on tax positions related to current year 1,326 1,205 1,403 Adjustment based on tax positions related to prior years — — 90 Balance at end of the year $ 7,780 $ 6,454 $ 5,249 Of the unrecognized tax benefits as of December 31, 2021, 2020 and 2019, approximately $ 0 , $ 0 , and $ 0.9 million, respectively, would affect the Company’s effective tax rate if recognized. The Company recognizes interest and penalties related to uncertain tax positions in income tax expense. To the extent accrued interest and penalties do not ultimately become payable, amounts accrued will be reduced and reflected as a reduction of the provision for income taxes in the period that such determination is made. Interest and penalties have no t been accrued for 2021, 2020 and 2019. The Company files income tax returns in the U.S. federal and state jurisdictions. The tax years 2010 to 2020 remains open to U.S. federal and state examination to the extent of the utilization of net operating loss and credit carryovers. As of December 31, 2021, the Company is under examination by the State of California. |
Defined Contribution Plan
Defined Contribution Plan | 12 Months Ended |
Dec. 31, 2021 | |
Retirement Benefits [Abstract] | |
Defined Contribution Plan | 16. Defined Contribution Plan The Company sponsors a defined contribution plan under Section 401(k) of the Internal Revenue Code covering substantially all full-time U.S. employees. Employee contributions are voluntary and are determined on an individual basis subject to the maximum allowable under federal tax regulations. During the years ended December 31, 2021, 2020 and 2019, the Company made contributions to the plan of $ 0.9 million, $ 0.8 million, and $ 0.8 million, respectively. |
Selected Quarterly Financial Da
Selected Quarterly Financial Data (Unaudited) | 12 Months Ended |
Dec. 31, 2021 | |
Selected Quarterly Financial Information [Abstract] | |
Selected Quarterly Financial Data (Unaudited) | 17. Selected Quarterly Financial Data (Unaudited) The following tables present selected quarterly financial data for 2021 and 2020 (in thousands, except share and per share data): March 31, 2021 As Reported Restatement Adjustment As Restated Condensed Balance Sheets Deferred revenue, current portion $ 76,636 $ ( 33,119 ) $ 43,517 Total current liabilities 98,049 ( 33,119 ) 64,930 Deferred revenue, net of current portion 169,280 98,470 267,750 Total liabilities 288,136 65,351 353,487 Accumulated deficit ( 465,669 ) ( 65,351 ) ( 531,020 ) Total stockholders' equity (deficit) 146,022 ( 65,351 ) 80,671 Total liabilities and stockholders' equity (deficit) 434,158 - 434,158 Three Months Ended March 31, 2021 Three Months Ended March 31, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 1,228 $ 258 $ 1,486 $ 30,096 $ 4,262 $ 34,358 Amgen 2,582 ( 36 ) 2,546 1,695 74 1,769 Astellas 4,756 ( 591 ) 4,165 387 ( 338 ) 49 BMS 7,405 ( 7,405 ) - 17,415 ( 6,696 ) 10,719 Total revenue $ 15,971 $ ( 7,774 ) $ 8,197 $ 49,593 $ ( 2,698 ) $ 46,895 Three Months Ended March 31, 2021 Three Months Ended March 31, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 15,971 $ ( 7,774 ) $ 8,197 $ 49,593 $ ( 2,698 ) $ 46,895 Operating expenses: Research and development 22,371 - 22,371 42,814 - 42,814 General and administrative 9,227 - 9,227 9,572 - 9,572 Total operating expenses 31,598 - 31,598 52,386 - 52,386 Loss from operations ( 15,627 ) ( 7,774 ) ( 23,401 ) ( 2,793 ) ( 2,698 ) ( 5,491 ) Interest income 68 - 68 1,075 - 1,075 Other income (expense) 5 - 5 12 - 12 Loss before income taxes ( 15,554 ) ( 7,774 ) ( 23,328 ) ( 1,706 ) ( 2,698 ) ( 4,404 ) Loss/(Benefit) from income taxes - - - ( 13,911 ) - ( 13,911 ) Net income (loss) ( 15,554 ) ( 7,774 ) ( 23,328 ) 12,205 ( 2,698 ) 9,507 Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax 4 - 4 279 - 279 Comprehensive income (loss) $ ( 15,550 ) $ ( 7,774 ) $ ( 23,324 ) $ 12,484 $ ( 2,698 ) $ 9,786 Net income (loss) per share Basic $ ( 0.26 ) $ ( 0.38 ) $ 0.27 $ 0.21 Diluted $ ( 0.26 ) $ ( 0.38 ) $ 0.26 $ 0.20 Shares used to compute net loss per share Basic 60,968,111 60,968,111 45,723,955 45,723,955 Diluted 60,968,111 60,968,111 47,044,774 47,044,774 Three Months Ended March 31, 2021 Three Months Ended March 31, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Cash Flow Net loss $ ( 15,554 ) $ ( 7,774 ) $ ( 23,328 ) $ 12,205 $ ( 2,698 ) $ 9,507 Changes in operating assets and liabilities: Deferred revenue ( 15,214 ) 7,774 ( 7,440 ) 80,416 2,698 83,114 Net cash used in operating activities ( 29,940 ) - ( 29,940 ) ( 49,737 ) - ( 49,737 ) June 30, 2021 As Reported Restatement Adjustment As Restated Condensed Balance Sheets Deferred revenue, current portion $ 72,369 $ ( 33,055 ) $ 39,314 Total current liabilities 93,377 ( 33,055 ) 60,322 Deferred revenue, net of current portion 158,189 105,899 264,088 Total liabilities 271,487 72,844 344,331 Accumulated deficit ( 484,912 ) ( 72,844 ) ( 557,756 ) Total stockholders' equity (deficit) 130,953 ( 72,844 ) 58,109 Total liabilities and stockholders' equity (deficit) 402,440 - 402,440 Three Months Ended June 30, 2021 Three Months Ended June 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 2,078 $ 656 $ 2,734 $ 1,319 $ ( 966 ) $ 353 Amgen 1,874 ( 159 ) 1,715 3,678 ( 57 ) 3,621 Astellas 4,931 ( 585 ) 4,346 4,204 ( 3,181 ) 1,023 BMS 7,405 ( 7,405 ) - 7,407 ( 5,416 ) 1,991 Total revenue $ 16,288 $ ( 7,493 ) $ 8,795 $ 16,608 $ ( 9,620 ) $ 6,988 Three Months Ended June 30, 2021 Three Months Ended June 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 16,288 $ ( 7,493 ) $ 8,795 $ 16,608 $ ( 9,620 ) $ 6,988 Operating expenses: Research and development 26,100 - 26,100 24,066 - 24,066 General and administrative 9,393 - 9,393 8,680 - 8,680 Total operating expenses 35,493 - 35,493 32,746 - 32,746 Loss from operations ( 19,205 ) ( 7,493 ) ( 26,698 ) ( 16,138 ) ( 9,620 ) ( 25,758 ) Interest income 44 - 44 454 - 454 Other income (expense) ( 82 ) - ( 82 ) 5 - 5 Loss before income taxes ( 19,243 ) ( 7,493 ) ( 26,736 ) ( 15,679 ) ( 9,620 ) ( 25,299 ) Loss/(Benefit) from income taxes - - - - - - Net loss ( 19,243 ) ( 7,493 ) ( 26,736 ) ( 15,679 ) ( 9,620 ) ( 25,299 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax 58 - 58 ( 320 ) - ( 320 ) Comprehensive income (loss) $ ( 19,185 ) $ ( 7,493 ) $ ( 26,678 ) $ ( 15,999 ) $ ( 9,620 ) $ ( 25,619 ) Net loss per share, basic and diluted $ ( 0.30 ) $ ( 0.41 ) $ ( 0.34 ) $ ( 0.55 ) Shares used to compute net loss per share, basic and diluted 65,055,998 65,055,998 46,057,063 46,057,063 Six Months Ended June 30, 2021 Six Months Ended June 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 3,306 $ 914 $ 4,220 $ 31,415 $ 3,296 $ 34,711 Amgen 4,456 ( 195 ) 4,261 5,373 17 5,390 Astellas 9,687 ( 1,176 ) 8,511 4,591 ( 3,519 ) 1,072 BMS 14,810 ( 14,810 ) - 24,822 ( 12,112 ) 12,710 Total revenue $ 32,259 $ ( 15,267 ) $ 16,992 $ 66,201 $ ( 12,318 ) $ 53,883 Six Months Ended June 30, 2021 Six Months Ended June 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 32,259 $ ( 15,267 ) $ 16,992 $ 66,201 $ ( 12,318 ) $ 53,883 Operating expenses: Research and development 48,471 - 48,471 66,880 - 66,880 General and administrative 18,620 - 18,620 18,252 - 18,252 Total operating expenses 67,091 - 67,091 85,132 - 85,132 Loss from operations ( 34,832 ) ( 15,267 ) ( 50,099 ) ( 18,931 ) ( 12,318 ) ( 31,249 ) Interest income 112 - 112 1,529 - 1,529 Other income (expense) ( 77 ) - ( 77 ) 17 - 17 Loss before income taxes ( 34,797 ) ( 15,267 ) ( 50,064 ) ( 17,385 ) ( 12,318 ) ( 29,703 ) Loss/(Benefit) from income taxes - - - ( 13,911 ) - ( 13,911 ) Net loss ( 34,797 ) ( 15,267 ) ( 50,064 ) ( 3,474 ) ( 12,318 ) ( 15,792 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax 62 - 62 ( 41 ) - ( 41 ) Comprehensive income (loss) $ ( 34,735 ) $ ( 15,267 ) $ ( 50,002 ) $ ( 3,515 ) $ ( 12,318 ) $ ( 15,833 ) Net loss per share, basic and diluted $ ( 0.55 ) $ ( 0.79 ) $ ( 0.08 ) $ ( 0.34 ) Shares used to compute net loss per share, basic and diluted 63,023,349 63,023,349 45,890,510 45,890,510 Six Months Ended June 30, 2021 Six Months Ended June 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Cash Flow Net loss $ ( 34,797 ) $ ( 15,267 ) $ ( 50,064 ) $ ( 3,474 ) $ ( 12,318 ) $ ( 15,792 ) Changes in operating assets and liabilities: Deferred revenue ( 30,572 ) 15,267 ( 15,305 ) 64,014 12,318 76,332 Net cash used in operating activities ( 58,139 ) - ( 58,139 ) 47,364 - 47,364 September 30, 2021 As Reported Restatement Adjustment As Restated Condensed Balance Sheets Deferred revenue, current portion $ 73,089 $ ( 32,245 ) $ 40,844 Total current liabilities 99,772 ( 32,245 ) 67,527 Deferred revenue, net of current portion 140,770 113,487 254,257 Total liabilities 259,559 81,242 340,801 Accumulated deficit ( 507,496 ) ( 81,242 ) ( 588,738 ) Total stockholders' equity (deficit) 111,674 ( 81,242 ) 30,432 Total liabilities and stockholders' equity (deficit) 371,233 - 371,233 Three Months Ended September 30, 2021 Three Months Ended September 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 2,867 $ ( 590 ) $ 2,277 $ 4,209 $ ( 966 ) $ 3,243 Amgen 2,428 ( 76 ) 2,352 1,633 ( 85 ) 1,548 Astellas 4,887 ( 327 ) 4,560 4,543 ( 1,868 ) 2,675 BMS 7,405 ( 7,405 ) - 7,403 ( 7,403 ) - Total revenue $ 17,587 $ ( 8,398 ) $ 9,189 $ 17,788 $ ( 10,322 ) $ 7,466 Three Months Ended September 30, 2021 Three Months Ended September 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 17,587 $ ( 8,398 ) $ 9,189 $ 17,788 $ ( 10,322 ) $ 7,466 Operating expenses: Research and development 29,143 - 29,143 24,049 - 24,049 General and administrative 11,085 - 11,085 8,634 - 8,634 Total operating expenses 40,228 - 40,228 32,683 - 32,683 Loss from operations ( 22,641 ) ( 8,398 ) ( 31,039 ) ( 14,895 ) ( 10,322 ) ( 25,217 ) Interest income 70 - 70 200 - 200 Other income (expense) ( 13 ) - ( 13 ) ( 15 ) - ( 15 ) Loss before income taxes ( 22,584 ) ( 8,398 ) ( 30,982 ) ( 14,710 ) ( 10,322 ) ( 25,032 ) Loss/(Benefit) from income taxes - - - - - - Net loss ( 22,584 ) ( 8,398 ) ( 30,982 ) ( 14,710 ) ( 10,322 ) ( 25,032 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax 37 - 37 ( 63 ) - ( 63 ) Comprehensive income (loss) $ ( 22,547 ) $ ( 8,398 ) $ ( 30,945 ) $ ( 14,773 ) $ ( 10,322 ) $ ( 25,095 ) Net loss per share, basic and diluted $ ( 0.35 ) $ ( 0.48 ) $ ( 0.32 ) $ ( 0.54 ) Shares used to compute net loss per share, basic and diluted 65,208,066 65,208,066 46,195,121 46,195,121 Nine Months Ended September 30, 2021 Nine Months Ended September 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 6,173 $ 324 $ 6,497 $ 35,624 $ 2,330 $ 37,954 Amgen 6,884 ( 271 ) 6,613 7,006 ( 68 ) 6,938 Astellas 14,574 ( 1,503 ) 13,071 9,134 ( 5,387 ) 3,747 BMS 22,215 ( 22,215 ) - 32,225 ( 19,515 ) 12,710 Total revenue $ 49,846 $ ( 23,665 ) $ 26,181 $ 83,989 $ ( 22,640 ) $ 61,349 Nine Months Ended September 30, 2021 Nine Months Ended September 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 49,846 $ ( 23,665 ) $ 26,181 $ 83,989 $ ( 22,640 ) $ 61,349 Operating expenses: Research and development 77,614 - 77,614 90,929 - 90,929 General and administrative 29,705 - 29,705 26,886 - 26,886 Total operating expenses 107,319 - 107,319 117,815 - 117,815 Loss from operations ( 57,473 ) ( 23,665 ) ( 81,138 ) ( 33,826 ) ( 22,640 ) ( 56,466 ) Interest income 182 - 182 1,729 - 1,729 Other income (expense) ( 90 ) - ( 90 ) 2 - 2 Loss before income taxes ( 57,381 ) ( 23,665 ) ( 81,046 ) ( 32,095 ) ( 22,640 ) ( 54,735 ) Loss/(Benefit) from income taxes - - - ( 13,911 ) - ( 13,911 ) Net loss ( 57,381 ) ( 23,665 ) ( 81,046 ) ( 18,184 ) ( 22,640 ) ( 40,824 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax 99 - 99 ( 104 ) - ( 104 ) Comprehensive income (loss) $ ( 57,282 ) $ ( 23,665 ) $ ( 80,947 ) $ ( 18,288 ) $ ( 22,640 ) $ ( 40,928 ) Net loss per share, basic and diluted $ ( 0.90 ) $ ( 1.27 ) $ ( 0.40 ) $ ( 0.89 ) Shares used to compute net loss per share, basic and diluted 63,759,585 63,759,585 45,992,786 45,992,786 Nine Months Ended September 30, 2021 Nine Months Ended September 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Cash Flow Net loss $ ( 57,381 ) $ ( 23,665 ) $ ( 81,046 ) $ ( 18,184 ) $ ( 22,640 ) $ ( 40,824 ) Changes in operating assets and liabilities: Deferred revenue ( 47,271 ) 23,665 ( 23,606 ) 46,766 22,640 69,406 Net cash used in operating activities ( 87,839 ) - ( 87,839 ) 22,686 - 22,686 Three Months Ended December 31, 2021 Three Months Ended December 31, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 5,672 $ ( 621 ) $ 5,051 $ 2,568 $ ( 659 ) $ 1,909 Amgen 1,860 16 1,876 1,602 ( 18 ) 1,584 Astellas 4,791 ( 586 ) 4,205 4,798 ( 1,213 ) 3,585 BMS 7,404 ( 7,404 ) - 7,405 ( 7,405 ) ( 0 ) Total revenue $ 19,727 $ ( 8,595 ) $ 11,132 $ 16,373 $ ( 9,295 ) $ 7,078 Three Months Ended December 31, 2021 Three Months Ended December 31, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 19,727 $ ( 8,595 ) $ 11,132 $ 16,373 $ ( 9,295 ) $ 7,078 Operating expenses: Research and development 36,580 - 36,580 22,007 - 22,007 General and administrative 9,455 - 9,455 9,145 - 9,145 Total operating expenses 46,035 - 46,035 31,152 - 31,152 Loss from operations ( 26,308 ) ( 8,595 ) ( 34,903 ) ( 14,779 ) ( 9,295 ) ( 24,074 ) Interest income 73 - 73 107 - 107 Other income (expense) 7 - 7 ( 29 ) - ( 29 ) Loss before income taxes ( 26,228 ) ( 8,595 ) ( 34,823 ) ( 14,701 ) ( 9,295 ) ( 23,996 ) Loss/(Benefit) from income taxes - - - - - - Net loss ( 26,228 ) ( 8,595 ) ( 34,823 ) ( 14,701 ) ( 9,295 ) ( 23,996 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax ( 294 ) - ( 294 ) - - - Comprehensive income (loss) $ ( 26,522 ) $ ( 8,595 ) $ ( 35,117 ) $ ( 14,701 ) $ ( 9,295 ) $ ( 23,996 ) Net loss per share, basic and diluted $ ( 0.40 ) $ ( 0.53 ) $ ( 0.32 ) $ ( 0.51 ) Shares used to compute net loss per share, basic and diluted 65,295,995 65,295,995 46,600,605 46,600,605 |
Basis of Presentation and Sum_2
Basis of Presentation and Summary of Significant Accounting Policies (Policies) | 12 Months Ended |
Dec. 31, 2021 | |
Accounting Policies [Abstract] | |
Basis of Presentation | Basis of Presentation The accompanying financial statements have been prepared in conformity with accounting principles generally accepted in the United States of America (“U.S. GAAP”). |
Use of Estimates | Use of Estimates The preparation of the financial statements in conformity with U.S. GAAP requires management to make estimates and assumptions that affect the reported amounts of assets and liabilities, disclosure of contingent assets and liabilities at the date of the financial statements and reported amounts of revenues and expenses during the reporting periods. Actual results could differ from those estimates. |
Concentration of Credit Risk and Other Risks and Uncertainties | Concentration of Credit Risk and Other Risks and Uncertainties The Company is subject to a number of risks similar to other biopharmaceutical companies in the early stage, including, but not limited to, the need to obtain adequate additional funding, possible failure of preclinical testing or clinical trials, the need to obtain marketing approval for its product candidates, competitors developing new technological innovations, the need to successfully commercialize and gain market acceptance of the Company’s products, and protection of proprietary technology. If the Company does not successfully obtain regulatory approval, commercialize or partner any of its product candidates, it will be unable to generate revenue from product sales or achieve profitability. Financial instruments that potentially subject the Company to a concentration of credit risk consist of cash and cash equivalents, short-term investments and accounts receivable. Substantially all the Company’s cash is held by one financial institution. Such deposits may, at times, exceed federally insured limits. The Company invests its cash equivalents in highly rated money market funds and its short-term investments in U.S. Government Bonds. Customers and collaboration partners who represent 10% or more of the Company’s total revenue during each period presented or accounts receivable balance at each respective balance sheet date are as follows: Revenue Accounts Receivable, net Year Ended December 31, December 31, 2021 2020 2019 2021 2020 (As Restated) (As Restated) (As Restated) AbbVie Ireland Unlimited Company $ 11,546 $ 39,863 $ 5,305 $ — $ — Amgen, Inc. 8,488 8,522 4,087 — — Astellas Pharma Inc. 17,278 7,332 — 790 798 Bristol Myers Squibb Company — 12,710 17,510 — — Total revenue from customers who represent 10% or more $ 37,312 $ 68,427 $ 26,902 $ 790 $ 798 The Company’s customers are located in the United States of America, Ireland and Japan. |
Segments | Segments Management has determined that it has one business activity and operates as one operating segment as it only reports financial information on an aggregate basis to its chief executive officer and chief financial officer, who are the Company’s chief operating decision makers. All long-lived assets are maintained in the United States of America. |
Cash and Cash Equivalents | Cash and Cash Equivalents The Company considers all highly liquid investments purchased with original maturities of three months or less at the date of purchase to be cash equivalents. |
Restricted Cash | Restricted Cash Restricted cash represents a standby letter of credit issued pursuant to an office lease. The following table provides a reconciliation of cash, cash equivalents, and restricted cash reported within the balance sheets that sum to the total of the amounts shown in the statement of cash flows: December 31 2021 2020 2019 (in thousands) Cash and cash equivalents $ 205,530 $ 191,859 $ 188,425 Restricted cash - non-current assets 917 917 917 Total $ 206,447 $ 192,776 $ 189,342 |
Investments | Investments All investments have been classified as available-for-sale (“AFS”) and are carried at fair value as determined based upon quoted market prices or pricing models for similar securities at period end. Investments that are required for use in current operations and that mature in less than 12 months are classified as short-term investments in the accompanying balance sheets. The amortized cost of securities is adjusted for amortization of premiums and accretion of discounts to maturity. Dividend and interest income are recognized when earned. Realized gains and losses are included in earnings and are derived using the specific identification method for determining the cost of securities sold. The Company assesses impairment of its AFS debt securities investments at each reporting period. Unrealized gains resulting from the excess of the fair value over the amortized cost basis of an investment are reported as a component of accumulated other comprehensive income (loss), net of tax. Unrealized losses or impairments resulting from the fair value of the AFS debt security being below the amortized cost basis are evaluated, using the discounted cash flow model, for identification of credit losses and non-credit related losses. Any credit losses are charged to earnings against the allowance for credit losses of the security, limited to the difference between the fair value and the amortized cost basis of the security. Any difference between the fair value of the security and the amortized cost basis, less the allowance for credit losses, are reported in other comprehensive income (loss). Expected cash inflows due to improvements in credit are recognized through a reversal of the allowance for credit losses subject to the total allowance previously recognized. In the event of impairment of any security, if management (i) has the intent to sell such security or (ii) will more-likely-than-not be required to sell such security before recovery of its amortized cost basis, such AFS debt security’s amortized cost basis will be written down to its fair value through earnings along with any existing allowance for credit losses. |
Property and Equipment, net | Property and Equipment, net Property and equipment are recorded at cost net of accumulated depreciation and amortization. Depreciation is provided using the straight-line method over the estimated useful lives of the respective assets. The useful lives of property and equipment are as follows: Machinery and equipment 5 years Computer equipment and software 3 years Furniture and fixtures 3 years Leasehold improvements Shorter of remaining lease term or estimated life of the assets Maintenance and repairs that do not extend the life or improve the asset are expensed when incurred. |
Goodwill and Intangible Assets | Goodwill and Intangible Asset s Goodwill represents the excess of the purchase price paid over the fair value of tangible and identifiable intangible assets acquired in business combinations. Goodwill and other intangible assets with indefinite lives are not amortized, but are assigned to reporting units and tested for impairment annually, or whenever there is an impairment indicator. Intangible assets are comprised of in-process research and development. The Company assesses impairment indicators annually as of December 31 or more frequently, if a change in circumstances or the occurrence of events suggests the remaining value may not be recoverable. Intangible assets that are not deemed to have an indefinite life are amortized over their estimated useful lives. There was no impairment of goodwill or intangible assets identified during the years ended December 31, 2021, 2020 and 2019. |
Impairment of Long-Lived Assets | Impairment of Long-Lived Assets Long-lived assets are reviewed for impairment whenever events or changes in circumstances indicate that the carrying amount of an asset (or asset group) may not be recoverable and prior to any goodwill impairment test. An impairment loss is recognized when the total of estimated undiscounted future cash flows expected to result from the use of the asset (or asset group) and its eventual disposition is less than its carrying amount. Impairment, if any, would be assessed using discounted cash flows or other appropriate measures of fair value. There was no impairment of long-lived assets during the years ended December 31, 2021, 2020 and 2019. |
Revenue Recognition | Revenue Recognition The Company’s revenues are primarily derived through its license, research, development and commercialization agreements. The terms of these types of agreements may include (i) licenses for the Company’s technology or programs, (ii) research and development services, and (iii) services or obligations in connection with participation in research or steering committees. Payments to the Company under these arrangements typically include one or more of the following: nonrefundable upfront and license fees, research funding, milestone and other contingent payments to the Company for the achievement of defined collaboration objectives and certain preclinical, clinical, regulatory and sales-based events, as well as royalties on sales of any commercialized products. The Company assesses whether the promises in its arrangements with customers are distinct performance obligations that should be accounted for separately. Judgment is required to determine whether the license to the Company’s intellectual property is distinct from the research and development services or participation on steering committees. The Company’s collaboration and license agreements may include contingent payments related to specified research, development and regulatory milestones. Such milestone payments are typically payable under the collaborations when the collaboration partner claims or selects a target, or initiates or advances a covered product candidate in preclinical or clinical development, upon submission for marketing approval of a covered product with regulatory authorities, or upon receipt of actual marketing approvals of a covered product or for additional indications. Milestone payments that are not within the control of the Company or the licensee, such as regulatory approvals, are not considered probable of being achieved until those approvals are received. At each reporting date, the Company re-evaluates whether the milestones are considered probable of being achieved and estimates the amount to be included in the transaction price by using the most likely amount method. If it is probable that a significant revenue reversal would not occur, the associated milestone value is included in the transaction price in such period of determination. The Company’s collaboration and license agreements may also include contingent payments related to sales-based milestones. Sales-based milestones are typically payable when annual sales of a covered product reach specified levels. Sales-based milestones are recognized at the later of when the associated performance obligation has been satisfied or when the sales occur. Unlike other contingency payments, such as regulatory milestones, sales-based milestones are not included in the transaction price based on estimates at the inception of the contract; instead, are included when the sales or usage occur. The transaction price in each arrangement is allocated to the identified performance obligations based on the relative standalone selling price (“SSP”) of each distinct performance obligation, which requires judgment. In instances where SSP is not directly observable, such as when a license or service is not sold separately, SSP is determined using information that may include market conditions and other observable inputs. Due to the early stage of the Company’s licensed technology, the license of such technology is typically combined with research and development services and steering committee participation as one performance obligation. In the event that the Company receives non-cash consideration such as consideration in the form of a research license and research support services from the counterparty, the transaction price of a non-monetary exchange that has commercial substance is estimated based on the fair value of the non-cash consideration received, which may be determined through a valuation analysis. In certain cases, the Company’s performance creates an asset that does not have an alternative use to the customer and the Company has an enforceable right to payment at all times for performance completed to date. In these cases, the Company utilizes judgment to assess the nature of the combined performance obligation to determine whether the combined performance obligation is satisfied over time or at a point in time and, if over time, the appropriate method of measuring progress for purposes of recognizing revenue. The Company evaluates the measure of progress each reporting period and, if necessary, adjusts the measure of performance and related revenue recognition. Any consideration payable to the Company’s customers is treated as a reduction to the transaction price and revenue, unless the payment to the customer is in exchange for distinct good and services. |
Comprehensive Income (Loss) | Comprehensive Income (Loss ) Comprehensive income (loss) represents all changes in stockholders’ equity (deficit) except those resulting from distributions to stockholders. The Company’s non-credit related unrealized gains and losses on investments and impact of adoption of new accounting pronouncements during the period represent the components of other comprehensive income (loss) that is excluded from the reported net loss. |
Contract Balances | Contract Balances Customer payments are recorded as deferred revenue upon receipt or when due and may require deferral of revenue recognition to a future period until the Company satisfies its performance obligations under these arrangements. Amounts payable to the Company are recorded as accounts receivable when the Company’s right to consideration is unconditional. |
Research and Development Expenses | Research and Development Expenses The Company records accrued liabilities for estimated costs of research and development activities conducted by third-party service providers, which include the conduct of preclinical and clinical studies, and contract manufacturing activities. The Company records the estimated costs of research and development activities based upon the estimated amount of services provided but not yet invoiced, and includes these costs in accrued liabilities in the balance sheets and within research and development expense in the statements of operations. These costs are a significant component of the Company’s research and development expenses. The Company accrues for these costs based on factors such as estimates of the work completed and in accordance with agreements established with its third-party service providers under the service agreements. The Company makes significant judgments and estimates in determining the accrued liabilities balance in each reporting period. As actual costs become known, the Company adjusts its accrued liabilities. The Company has not experienced any material differences between accrued costs and actual costs incurred. However, the status and timing of actual services performed may vary from the Company’s estimates, resulting in adjustments to expense in future periods. Changes in these estimates that result in material changes to the Company’s accruals could materially affect the Company’s results of operations. Research and development expenses include costs directly attributable to the conduct of research and development programs, including the cost of salaries, payroll taxes, employee benefits, materials, supplies, depreciation on and maintenance of research equipment, the cost of services provided by outside contractors, and the allocated portions of facility costs, such as rent, utilities, insurance, repairs and maintenance, depreciation, and general support services. All costs associated with research and development are expensed as incurred. In January 2019, the Company acquired certain technology know-how that is complementary to the Company’s proprietary Probody technology from a third party for $ 5.0 million. The Company plans to use this technology in certain of the Company’s discovery stage projects, and has concluded that the technology acquired does not have an alternative future use. Accordingly, the $ 5.0 million has been recorded as research and development expense for 2019. |
Stock-Based Compensation | Stock-based Compensation The Company measures compensation expense for all stock-based payment awards, including employee stock options, restricted stock units ("RSUs"), and employee stock purchases related to Employee Stock Purchase Plan ("ESPP") based on estimated fair values of the award at the grant date, and recognizes compensation expense over the requisite service vesting period. Stock options forfeitures are accounted for in the period in which they occur. To determine the fair value of a stock option award on the grant date, the Company uses the Black-Scholes option pricing model which consist of estimating variables such as: expected life, volatility, and risk-free interest rate. Expected life and volatility are estimated primarily from the Company's historical records, and the risk-free rate is based on the U.S. Treasury yield curve in effect at the time of grant commensurate with the expected life assumption. These estimates involve inherent uncertainties and the application of judgment. The Company measures its restricted stock unit awards based on the market price of the Company’s common shares on the date of grant. Share-based compensation expense for performance-based awards is recognized when it becomes probable that the performance condition will be met. The Company reassesses the estimated probability at each reporting period, and if it is determined at a future date that a performance condition is probable of being achieved, the Company will recognize a cumulative catch-up adjustment and record the remaining expense ratably over the remaining requisite service period. |
Income Taxes | Income Taxes The Company accounts for income taxes using an asset and liability approach. Deferred tax assets and liabilities reflect the net tax effects of temporary differences between the financial statement carrying amounts of existing assets and liabilities and their respective tax bases. Deferred tax assets and liabilities are measured using enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. The Company records a valuation allowance to reduce its deferred tax assets to reflect the net amount that it believes as more likely than not to be realized. Realization of the deferred tax assets is dependent on the generation of future taxable income, the amount and timing of which are uncertain. The valuation allowance requires an assessment of both positive and negative evidence when determining whether it is more likely than not that deferred tax assets are recoverable. Based upon the weight of available evidence at December 31, 2021, the Company continues to maintain a full valuation allowance against all of its deferred tax assets after management considered all available evidence, both positive and negative, including but not limited to its historical operating results, income or loss in recent periods, cumulative income in recent years, forecasted earnings, future taxable income, and significant risk and uncertainty related to forecasts. The Company recognizes the tax effects of an uncertain tax position only if it is more likely than not that it will be sustained based solely on its technical merits as of the reporting date and only in an amount more likely than not that it will be sustained upon review by the tax authorities. The Company evaluates uncertain tax positions on a quarterly basis and adjust the liability for changes in facts and circumstances, such as new regulations or interpretations by the taxing authorities, new information obtained during a tax examination, significant amendment to an existing tax law, or resolution of an examination. To the extent that the final tax outcome of these matters is different than the amounts recorded, such differences will impact the income tax provision in the period in which such determination is made. The resolution of its uncertain income tax positions is dependent on uncontrollable factors such as law changes, new case law, and the willingness of the income tax authorities to settle, including the timing thereof and other factors. Although the Company does not anticipate significant changes to its uncertain income tax positions in the next twelve months, items outside of its control could cause its uncertain income tax positions to change in the future, which would be recorded in its statements of operations. Interest and/or penalties related to income tax matters are recognized as a component of income tax expense. |
Leases | Leases The Company determines if an arrangement is or contains a lease at inception. Operating leases are recorded as operating lease right-of-use (“ROU”) assets and operating lease liabilities in the Company’s balance sheet. ROU assets represent the Company’s right to use an underlying asset for the lease term and lease liabilities represent its obligation to make lease payments arising from the lease. Operating lease ROU assets and liabilities are recognized at commencement date based on the present value of lease payments over the lease term. The Company uses an implicit rate when readily available, or its incremental borrowing rate based on the information available at lease commencement date in determining the present value of lease payments. The operating lease ROU assets also include any lease prepayments made and reduced by lease incentives. The Company’s lease terms may include options to extend the lease when it is reasonably certain that such option will be exercised. Lease expenses are recognized on a straight-line basis over the lease term. The Company elected the short-term lease recognition exemption. The Company’s operating lease arrangement includes lease and non-lease components which are generally accounted for separately. |
Adopted Accounting Pronouncements | In December 2019, the FASB issued ASU 2019-12, Income Taxes (Topic 740): Simplifying the Accounting for Income Taxes. The amendments in this ASU simplify the accounting for income taxes by removing certain exceptions to the general principles of ASC 740 in order to reduce cost and complexity of its application. The ASU removes the exception related to the incremental approach for intra-period tax allocation as well as two exceptions related to accounting for outside basis differences of equity method investments and foreign subsidiaries. The ASU also amends the scope of ASC 740 related to a franchise tax (or similar tax) that is partially based on income; clarifies when a step-up in the tax basis of goodwill should be considered part of the business combination in which the book goodwill was originally recognized and when it should be considered a separate transaction; specifies that an entity is not required to allocate income tax expense to a legal entity that is both not subject to tax and disregarded by the taxing authority; and clarifies that all tax effects, both deferred and current, should be accounted for in the interim period that includes the enactment date. The Company adopted this ASU on January 1, 2021 , and there was no material impact on the financial statements upon adoption of this ASU. |
Basis of Presentation and Sum_3
Basis of Presentation and Summary of Significant Accounting Policies (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Accounting Policies [Abstract] | |
Schedule of Customers and Collaboration Partners who Represent 10% or More of Total Revenue During Each Period Presented or Net Accounts Receivable Balance | Customers and collaboration partners who represent 10% or more of the Company’s total revenue during each period presented or accounts receivable balance at each respective balance sheet date are as follows: Revenue Accounts Receivable, net Year Ended December 31, December 31, 2021 2020 2019 2021 2020 (As Restated) (As Restated) (As Restated) AbbVie Ireland Unlimited Company $ 11,546 $ 39,863 $ 5,305 $ — $ — Amgen, Inc. 8,488 8,522 4,087 — — Astellas Pharma Inc. 17,278 7,332 — 790 798 Bristol Myers Squibb Company — 12,710 17,510 — — Total revenue from customers who represent 10% or more $ 37,312 $ 68,427 $ 26,902 $ 790 $ 798 |
Schedule of Cash, Cash Equivalents, and Restricted Cash | The following table provides a reconciliation of cash, cash equivalents, and restricted cash reported within the balance sheets that sum to the total of the amounts shown in the statement of cash flows: December 31 2021 2020 2019 (in thousands) Cash and cash equivalents $ 205,530 $ 191,859 $ 188,425 Restricted cash - non-current assets 917 917 917 Total $ 206,447 $ 192,776 $ 189,342 |
Schedule of Useful Lives of Property and Equipment | The useful lives of property and equipment are as follows: Machinery and equipment 5 years Computer equipment and software 3 years Furniture and fixtures 3 years Leasehold improvements Shorter of remaining lease term or estimated life of the assets |
Restatement of Financial Statem
Restatement of Financial Statements (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Accounting Changes and Error Corrections [Abstract] | |
Schedule of Restatement of Financial Statements | December 31, 2021 December 31, 2020 As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated Balance Sheets Deferred revenue, current portion $ 69,262 $ ( 28,446 ) $ 40,816 $ 74,869 $ ( 32,813 ) $ 42,056 Total current liabilities 106,316 ( 28,446 ) 77,870 100,924 ( 32,813 ) 68,111 Deferred revenue, net of current portion 125,660 118,284 243,944 186,261 90,390 276,651 Total liabilities 250,032 89,838 339,870 308,860 57,577 366,437 Accumulated deficit ( 533,724 ) ( 89,838 ) ( 623,562 ) ( 450,115 ) ( 57,577 ) ( 507,692 ) Total stockholders' equity (deficit) 89,379 ( 89,838 ) ( 459 ) 49,803 ( 57,577 ) ( 7,774 ) Total liabilities and stockholders' equity (deficit) 339,411 — 339,411 358,663 — 358,663 Year Ended December 31, 2021 Year Ended December 31, 2020 Year Ended December 31, 2019 As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated Statements of Operations Revenue $ 69,573 $ ( 32,261 ) $ 37,312 $ 100,362 $ ( 31,935 ) $ 68,427 $ 57,489 $ ( 30,587 ) $ 26,902 Operating expenses: Research and development 114,194 — 114,194 112,936 — 112,936 131,619 — 131,619 General and administrative 39,160 — 39,160 36,031 — 36,031 36,765 — 36,765 Total operating expenses 153,354 — 153,354 148,967 — 148,967 168,384 — 168,384 Loss from operations ( 83,781 ) ( 32,261 ) ( 116,042 ) ( 48,605 ) ( 31,935 ) ( 80,540 ) ( 110,895 ) ( 30,587 ) ( 141,482 ) Interest income 255 — 255 1,836 — 1,836 8,365 — 8,365 Other income (expense) ( 83 ) — ( 83 ) ( 27 ) — ( 27 ) ( 135 ) — ( 135 ) Loss before income taxes ( 83,609 ) ( 32,261 ) ( 115,870 ) ( 46,796 ) ( 31,935 ) ( 78,731 ) ( 102,665 ) ( 30,587 ) ( 133,252 ) Loss/(Benefit) from income taxes — — - ( 13,911 ) — ( 13,911 ) ( 427 ) ( 427 ) Net loss ( 83,609 ) ( 32,261 ) ( 115,870 ) ( 32,885 ) ( 31,935 ) ( 64,820 ) ( 102,238 ) ( 30,587 ) ( 132,825 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax ( 195 ) — ( 195 ) ( 104 ) — ( 104 ) 139 — 139 Impact of adoption of new accounting pronouncement - — — — — — 11 — 11 Comprehensive income (loss) $ ( 83,804 ) $ ( 32,261 ) $ ( 116,065 ) $ ( 32,989 ) ( 31,935 ) $ - $ ( 64,924 ) $ ( 102,088 ) $ ( 30,587 ) $ ( 132,675 ) Net loss per share, basic and diluted $ ( 1.30 ) $ ( 1.81 ) $ ( 0.71 ) $ ( 1.40 ) $ ( 2.26 ) $ ( 2.93 ) Shares used to compute net loss per share, basic and diluted 64,146,848 64,146,848 46,145,563 46,145,563 45,335,927 45,335,927 Year Ended December 31, 2021 Year Ended December 31, 2020 Year Ended December 31, 2019 As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated Statements of Stockholders' Equity (Deficit) Net loss ( 83,609 ) ( 32,261 ) ( 115,870 ) ( 32,885 ) ( 31,935 ) ( 64,820 ) ( 102,238 ) ( 30,587 ) ( 132,825 ) Accumulated deficit ( 533,724 ) ( 89,838 ) ( 623,562 ) ( 450,115 ) ( 57,577 ) ( 507,692 ) ( 417,230 ) ( 25,642 ) ( 442,872 ) Total stockholders' equity (deficit) 89,379 ( 89,838 ) ( 459 ) 49,803 ( 57,577 ) ( 7,774 ) 51,113 ( 25,642 ) 25,471 Year Ended December 31, 2021 Year Ended December 31, 2020 Year Ended December 31, 2019 As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated As previously Reported Restatement Adjustment As Restated Statements of Cash Flow Net loss $ ( 83,609 ) $ ( 32,261 ) $ ( 115,870 ) $ ( 32,885 ) $ ( 31,935 ) $ ( 64,820 ) $ ( 102,238 ) $ ( 30,587 ) $ ( 132,825 ) Changes in operating assets and liabilities: Deferred revenue ( 66,209 ) 32,261 ( 33,948 ) 30,891 31,935 62,826 ( 47,741 ) 30,587 ( 17,154 ) Net cash used in operating activities ( 119,031 ) — ( 119,031 ) 5,259 — 5,259 ( 140,480 ) — ( 140,480 ) |
Net Loss Per Share (Tables)
Net Loss Per Share (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Earnings Per Share [Abstract] | |
Summary of Potentially Dilutive Securities Excluded from Computation of Diluted Net Loss Per Share | The following weighted-average outstanding shares of potentially dilutive securities are excluded from the computation of diluted net loss per share for the periods presented, because including them would have been anti-dilutive: Year Ended December 31, 2021 2020 2019 Options, RSUs and ESPP to purchase common stock 11,987,362 11,388,691 9,687,844 |
Fair Value Measurements and I_2
Fair Value Measurements and Investments (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Fair Value Disclosures [Abstract] | |
Schedule of Investments Subject to Fair Value Measurements on a Recurring Basis | The following tables set forth the fair value of the Company’s investments subject to fair value measurements on a recurring basis and the level of inputs used in such measurements: December 31, 2021 Valuation Amortized Allowance for Credit Losses Gross Gross Aggregate (in thousands) Assets Money market funds Level I 165,736 $ — $ — $ — $ 165,736 Restricted cash (money market funds) Level I 917 — — — 917 U.S. Government bonds Level I 99,938 — — ( 242 ) 99,696 Total Securities 266,591 $ — $ — $ ( 242 ) $ 266,349 December 31, 2020 Valuation Amortized Allowance Gross Gross Aggregate (in thousands) Assets Money market funds Level I $ 131,121 $ — $ — $ — $ 131,121 Restricted cash (money market funds) Level I 917 — — — 917 U.S. Government bonds Level I 124,254 — 6 — 124,260 Total securities $ 256,292 $ — $ 6 $ — $ 256,298 |
Property and Equipment (Tables)
Property and Equipment (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Property, Plant and Equipment [Abstract] | |
Summary of Property and Equipment, Net | Property and equipment, net consisted of the following: December 31 2021 2020 (in thousands) Machinery and equipment $ 15,086 $ 13,772 Computer equipment and software 1,608 1,600 Furniture and fixtures 1,054 1,024 Leasehold improvements 1,736 1,728 Construction in progress 308 252 19,792 18,376 Less: accumulated depreciation and amortization ( 13,832 ) ( 11,426 ) $ 5,960 $ 6,950 |
Intangible Assets (Tables)
Intangible Assets (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Goodwill and Intangible Assets Disclosure [Abstract] | |
Schedule of Intangible Assets | December 31, 2021 2020 (in thousands) Probody platform intangible asset $ 1,750 $ 1,750 Less accumulated amortization ( 729 ) ( 583 ) $ 1,021 $ 1,167 |
Accrued Liabilities (Tables)
Accrued Liabilities (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Accrued Liabilities, Current [Abstract] | |
Schedule of Accrued Liabilities | Accrued liabilities consisted of the following: December 31, 2021 2020 (in thousands) Research and clinical expenses $ 18,861 $ 10,092 Payroll and related expenses 9,576 8,362 Legal and professional expenses 1,468 815 Operating lease liabilities - short term 3,618 3,195 Other accrued expenses 713 595 Total $ 34,236 $ 23,059 |
Collaboration and License Agr_2
Collaboration and License Agreements (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Organization, Consolidation and Presentation of Financial Statements [Abstract] | |
Schedule of Revenue by Collaboration Partners | The following table summarizes the revenue by collaboration partners (in thousands): Year Ended December 31, 2021 2020 2019 (As Restated) (As Restated) (As Restated) AbbVie $ 11,546 $ 39,863 $ 5,305 Amgen 8,488 8,522 4,087 Astellas 17,278 7,332 — Bristol Myers Squibb — 12,710 17,510 Total revenue $ 37,312 $ 68,427 $ 26,902 |
Summary of Contract Liabilities | The following table presents changes in the Company’s total contract liabilities for the years ended December 31, 2021 and 2020 (in thousands): Balance at Additions Deductions Balance at (As Restated) (As Restated) (As Restated) (As Restated) Deferred revenue $ 273,035 $ 10,000 $ ( 27,154 ) $ 255,881 Balance at Additions Deductions Balance at (As Restated) (As Restated) (As Restated) (As Restated) Deferred revenue $ 255,881 $ 121,635 $ ( 58,809 ) $ 318,707 Balance at Additions Deductions Balance at (As Restated) (As Restated) (As Restated) (As Restated) Deferred revenue $ 318,707 $ 3,834 $ ( 37,781 ) $ 284,760 |
Leases (Tables)
Leases (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Leases [Abstract] | |
Summary of Supplemental Information Related to Leases | Supplemental information related to leases are as follows: Year Ended December 31, 2021 December 31, 2020 (in thousands) Cash paid for amounts included in the measurement of lease liabilities Operating cash flows from operating leases $ 5,129 $ 4,990 December 31, 2021 December 31, 2020 (in thousands) Supplemental balance sheet information related to leases: Operating lease right-of-use assets $ 19,362 $ 22,495 Current operating lease liabilities 3,618 3,195 Non-current operating lease liabilities 18,056 21,675 Total operating lease liabilities $ 21,674 $ 24,870 Weighted-average remaining lease term (in years) Operating lease 4.75 5.75 Weighted-average discount rate Operating lease 8.25 % 8.25 % |
Schedule of Maturity of Operating Lease Liabilities | December 31, 2021 (in thousands) Maturity of operating lease liabilities 2022 5,273 2023 5,420 2024 5,572 2025 5,729 2026 and beyond 4,387 Total lease payments 26,381 Less imputed interest ( 4,707 ) Present value of lease liabilities $ 21,674 |
Stock-based Compensation (Table
Stock-based Compensation (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |
Schedule of Activity Under Company's Stock Option Plans | Activity under the Company’s stock option plans is set forth below: Options Outstanding Number of Weighted- Weighted- Aggregate (in thousands) Balances at December 31, 2020 10,929,530 $ 10.77 Options granted 5,178,897 7.10 Options exercised ( 528,503 ) 2.70 Options cancelled ( 3,387,708 ) 11.26 Balances at December 31, 2021 12,192,216 9.42 7.5 $ 1,182 Options Exercisable—December 31, 2021 6,054,635 11.46 6.1 $ 1,155 |
Total Stock-based Compensation Recognized | Total stock-based compensation recorded related to options granted to employees and non-employees and employee stock purchase plan was as follows (in thousands): Year Ended December 31, 2021 2020 2019 Research and development $ 5,797 $ 6,825 $ 9,226 General and administrative 7,370 7,961 9,874 Total stock-based compensation expense $ 13,167 $ 14,786 $ 19,100 |
Schedule of Estimated Fair Value of Employee Stock Options and ESPP Using Black-Scholes Valuation Model | The Company estimated the fair value of employee stock options and ESPP using the Black-Scholes valuation model based on the date of grant with the following assumptions: Options ESPP Year Ended December 31, Year Ended December 31, 2021 2020 2019 2021 2020 2019 Expected volatility 69.6 % - 74.8 % 64.4 % - 73.3 % 64.4 % - 68.6 % 46.87 % - 69.58 % 47.3 % - 122.1 % 60.8 % - 71.9 % Risk-free interest rate 0.5 % - 1.3 % 0.2 % - 1.3 % 1.4 % - 2.5 % 0.04 % - 0.10 % 0.1 % - 0.2 % 1.6 % - 2.4 % Dividend yield — % — % — % — % — % — % Expected term 4.5 - 4.8 4.7 - 4.9 4.9 - 5.0 0.5 0.5 0.5 |
RSU's | |
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |
Schedule of Company's TRSU Activities | The following table summarizes the Company's RSU activities: Number of Weighted- Aggregate Weighted Average Grant Date Fair Value (in thousands) Balances at December 31, 2020 — $ - RSU's awarded 874,000 5.34 RSU's vested — - RSU's cancelled ( 5,750 ) 5.34 Balances at December 31, 2021 868,250 1.31 $ 3,760 5.34 Ending Exercisable—December 31, 2021 - - $ - $ - |
Income Taxes (Tables)
Income Taxes (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Income Tax Disclosure [Abstract] | |
Schedule of Components of Benefit from Income Taxes | The Company derives its income only from the United States. The components of the benefit from income taxes are as follows (in thousands): Years Ended December 31, 2021 2020 2019 Current: Federal $ — $ ( 13,912 ) $ ( 390 ) State — 1 — Total current — ( 13,911 ) ( 390 ) Deferred: Federal — — ( 37 ) State — — — Total deferred — — ( 37 ) Benefit from income taxes $ — $ ( 13,911 ) $ ( 427 ) |
Schedule of Effective Tax Rate Reconciliation | A reconciliation of the Company’s effective tax rate to the statutory U.S. federal rate is as follows: Years Ended December 31, 2021 2020 2019 U.S. federal taxes at statutory rate 21.0 % 21.0 % 21.0 % State tax, net of federal benefit 1.5 % 2.0 % 1.0 % Stock compensation ( 3.1 )% ( 1.3 )% ( 1.0 )% Tax credits 2.0 % 6.6 % 1.9 % Change in valuation allowance ( 21.4 )% ( 27.1 )% ( 22.3 )% Net operating loss carryback 0.0 % 16.6 % 0.0 % Return to provision adjustment 0.0 % 0.0 % ( 0.2 )% Other 0.0 % ( 0.1 )% ( 0.1 )% Total ( 0.0 )% 17.7 % 0.3 % |
Schedule of Deferred Income Tax Assets and Liabilities | The types of temporary differences that give rise to significant portions of the Company’s deferred income tax assets and liabilities are set out below (in thousands): Year Ended December 31, 2021 2020 Net operating loss carryforwards $ 49,070 $ 38,485 Research and development credits 20,809 16,803 Lease liability 4,555 5,223 Intangible assets 3,804 3,923 Deferred revenue 60,285 49,537 Accrued liabilities 1,933 1,512 Stock-based compensation 7,480 8,578 Other 29 20 Total gross deferred income tax assets 147,965 124,081 Less: valuation allowance ( 143,355 ) ( 118,539 ) Deferred tax assets, net of valuation allowance 4,610 5,542 Fixed assets ( 253 ) ( 433 ) Right-of-use assets ( 4,069 ) ( 4,724 ) Prepaid expenses ( 288 ) ( 385 ) Deferred tax liabilities ( 4,610 ) ( 5,542 ) Net deferred income tax liabilities $ — $ — |
Schedule of Reconciliation of Unrecognized Tax Benefits | A reconciliation of the beginning and ending unrecognized tax benefit amount is as follows (in thousands): Year Ended December 31, 2021 2020 2019 Balance at the beginning of the year $ 6,454 $ 5,249 $ 3,756 Additions based on tax positions related to current year 1,326 1,205 1,403 Adjustment based on tax positions related to prior years — — 90 Balance at end of the year $ 7,780 $ 6,454 $ 5,249 |
Selected Quarterly Financial _2
Selected Quarterly Financial Data (Unaudited) (Tables) | 12 Months Ended |
Dec. 31, 2021 | |
Selected Quarterly Financial Information [Abstract] | |
Schedule of selected quarterly financial data | The following tables present selected quarterly financial data for 2021 and 2020 (in thousands, except share and per share data): March 31, 2021 As Reported Restatement Adjustment As Restated Condensed Balance Sheets Deferred revenue, current portion $ 76,636 $ ( 33,119 ) $ 43,517 Total current liabilities 98,049 ( 33,119 ) 64,930 Deferred revenue, net of current portion 169,280 98,470 267,750 Total liabilities 288,136 65,351 353,487 Accumulated deficit ( 465,669 ) ( 65,351 ) ( 531,020 ) Total stockholders' equity (deficit) 146,022 ( 65,351 ) 80,671 Total liabilities and stockholders' equity (deficit) 434,158 - 434,158 Three Months Ended March 31, 2021 Three Months Ended March 31, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 1,228 $ 258 $ 1,486 $ 30,096 $ 4,262 $ 34,358 Amgen 2,582 ( 36 ) 2,546 1,695 74 1,769 Astellas 4,756 ( 591 ) 4,165 387 ( 338 ) 49 BMS 7,405 ( 7,405 ) - 17,415 ( 6,696 ) 10,719 Total revenue $ 15,971 $ ( 7,774 ) $ 8,197 $ 49,593 $ ( 2,698 ) $ 46,895 Three Months Ended March 31, 2021 Three Months Ended March 31, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 15,971 $ ( 7,774 ) $ 8,197 $ 49,593 $ ( 2,698 ) $ 46,895 Operating expenses: Research and development 22,371 - 22,371 42,814 - 42,814 General and administrative 9,227 - 9,227 9,572 - 9,572 Total operating expenses 31,598 - 31,598 52,386 - 52,386 Loss from operations ( 15,627 ) ( 7,774 ) ( 23,401 ) ( 2,793 ) ( 2,698 ) ( 5,491 ) Interest income 68 - 68 1,075 - 1,075 Other income (expense) 5 - 5 12 - 12 Loss before income taxes ( 15,554 ) ( 7,774 ) ( 23,328 ) ( 1,706 ) ( 2,698 ) ( 4,404 ) Loss/(Benefit) from income taxes - - - ( 13,911 ) - ( 13,911 ) Net income (loss) ( 15,554 ) ( 7,774 ) ( 23,328 ) 12,205 ( 2,698 ) 9,507 Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax 4 - 4 279 - 279 Comprehensive income (loss) $ ( 15,550 ) $ ( 7,774 ) $ ( 23,324 ) $ 12,484 $ ( 2,698 ) $ 9,786 Net income (loss) per share Basic $ ( 0.26 ) $ ( 0.38 ) $ 0.27 $ 0.21 Diluted $ ( 0.26 ) $ ( 0.38 ) $ 0.26 $ 0.20 Shares used to compute net loss per share Basic 60,968,111 60,968,111 45,723,955 45,723,955 Diluted 60,968,111 60,968,111 47,044,774 47,044,774 Three Months Ended March 31, 2021 Three Months Ended March 31, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Cash Flow Net loss $ ( 15,554 ) $ ( 7,774 ) $ ( 23,328 ) $ 12,205 $ ( 2,698 ) $ 9,507 Changes in operating assets and liabilities: Deferred revenue ( 15,214 ) 7,774 ( 7,440 ) 80,416 2,698 83,114 Net cash used in operating activities ( 29,940 ) - ( 29,940 ) ( 49,737 ) - ( 49,737 ) June 30, 2021 As Reported Restatement Adjustment As Restated Condensed Balance Sheets Deferred revenue, current portion $ 72,369 $ ( 33,055 ) $ 39,314 Total current liabilities 93,377 ( 33,055 ) 60,322 Deferred revenue, net of current portion 158,189 105,899 264,088 Total liabilities 271,487 72,844 344,331 Accumulated deficit ( 484,912 ) ( 72,844 ) ( 557,756 ) Total stockholders' equity (deficit) 130,953 ( 72,844 ) 58,109 Total liabilities and stockholders' equity (deficit) 402,440 - 402,440 Three Months Ended June 30, 2021 Three Months Ended June 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 2,078 $ 656 $ 2,734 $ 1,319 $ ( 966 ) $ 353 Amgen 1,874 ( 159 ) 1,715 3,678 ( 57 ) 3,621 Astellas 4,931 ( 585 ) 4,346 4,204 ( 3,181 ) 1,023 BMS 7,405 ( 7,405 ) - 7,407 ( 5,416 ) 1,991 Total revenue $ 16,288 $ ( 7,493 ) $ 8,795 $ 16,608 $ ( 9,620 ) $ 6,988 Three Months Ended June 30, 2021 Three Months Ended June 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 16,288 $ ( 7,493 ) $ 8,795 $ 16,608 $ ( 9,620 ) $ 6,988 Operating expenses: Research and development 26,100 - 26,100 24,066 - 24,066 General and administrative 9,393 - 9,393 8,680 - 8,680 Total operating expenses 35,493 - 35,493 32,746 - 32,746 Loss from operations ( 19,205 ) ( 7,493 ) ( 26,698 ) ( 16,138 ) ( 9,620 ) ( 25,758 ) Interest income 44 - 44 454 - 454 Other income (expense) ( 82 ) - ( 82 ) 5 - 5 Loss before income taxes ( 19,243 ) ( 7,493 ) ( 26,736 ) ( 15,679 ) ( 9,620 ) ( 25,299 ) Loss/(Benefit) from income taxes - - - - - - Net loss ( 19,243 ) ( 7,493 ) ( 26,736 ) ( 15,679 ) ( 9,620 ) ( 25,299 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax 58 - 58 ( 320 ) - ( 320 ) Comprehensive income (loss) $ ( 19,185 ) $ ( 7,493 ) $ ( 26,678 ) $ ( 15,999 ) $ ( 9,620 ) $ ( 25,619 ) Net loss per share, basic and diluted $ ( 0.30 ) $ ( 0.41 ) $ ( 0.34 ) $ ( 0.55 ) Shares used to compute net loss per share, basic and diluted 65,055,998 65,055,998 46,057,063 46,057,063 Six Months Ended June 30, 2021 Six Months Ended June 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 3,306 $ 914 $ 4,220 $ 31,415 $ 3,296 $ 34,711 Amgen 4,456 ( 195 ) 4,261 5,373 17 5,390 Astellas 9,687 ( 1,176 ) 8,511 4,591 ( 3,519 ) 1,072 BMS 14,810 ( 14,810 ) - 24,822 ( 12,112 ) 12,710 Total revenue $ 32,259 $ ( 15,267 ) $ 16,992 $ 66,201 $ ( 12,318 ) $ 53,883 Six Months Ended June 30, 2021 Six Months Ended June 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 32,259 $ ( 15,267 ) $ 16,992 $ 66,201 $ ( 12,318 ) $ 53,883 Operating expenses: Research and development 48,471 - 48,471 66,880 - 66,880 General and administrative 18,620 - 18,620 18,252 - 18,252 Total operating expenses 67,091 - 67,091 85,132 - 85,132 Loss from operations ( 34,832 ) ( 15,267 ) ( 50,099 ) ( 18,931 ) ( 12,318 ) ( 31,249 ) Interest income 112 - 112 1,529 - 1,529 Other income (expense) ( 77 ) - ( 77 ) 17 - 17 Loss before income taxes ( 34,797 ) ( 15,267 ) ( 50,064 ) ( 17,385 ) ( 12,318 ) ( 29,703 ) Loss/(Benefit) from income taxes - - - ( 13,911 ) - ( 13,911 ) Net loss ( 34,797 ) ( 15,267 ) ( 50,064 ) ( 3,474 ) ( 12,318 ) ( 15,792 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax 62 - 62 ( 41 ) - ( 41 ) Comprehensive income (loss) $ ( 34,735 ) $ ( 15,267 ) $ ( 50,002 ) $ ( 3,515 ) $ ( 12,318 ) $ ( 15,833 ) Net loss per share, basic and diluted $ ( 0.55 ) $ ( 0.79 ) $ ( 0.08 ) $ ( 0.34 ) Shares used to compute net loss per share, basic and diluted 63,023,349 63,023,349 45,890,510 45,890,510 Six Months Ended June 30, 2021 Six Months Ended June 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Cash Flow Net loss $ ( 34,797 ) $ ( 15,267 ) $ ( 50,064 ) $ ( 3,474 ) $ ( 12,318 ) $ ( 15,792 ) Changes in operating assets and liabilities: Deferred revenue ( 30,572 ) 15,267 ( 15,305 ) 64,014 12,318 76,332 Net cash used in operating activities ( 58,139 ) - ( 58,139 ) 47,364 - 47,364 September 30, 2021 As Reported Restatement Adjustment As Restated Condensed Balance Sheets Deferred revenue, current portion $ 73,089 $ ( 32,245 ) $ 40,844 Total current liabilities 99,772 ( 32,245 ) 67,527 Deferred revenue, net of current portion 140,770 113,487 254,257 Total liabilities 259,559 81,242 340,801 Accumulated deficit ( 507,496 ) ( 81,242 ) ( 588,738 ) Total stockholders' equity (deficit) 111,674 ( 81,242 ) 30,432 Total liabilities and stockholders' equity (deficit) 371,233 - 371,233 Three Months Ended September 30, 2021 Three Months Ended September 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 2,867 $ ( 590 ) $ 2,277 $ 4,209 $ ( 966 ) $ 3,243 Amgen 2,428 ( 76 ) 2,352 1,633 ( 85 ) 1,548 Astellas 4,887 ( 327 ) 4,560 4,543 ( 1,868 ) 2,675 BMS 7,405 ( 7,405 ) - 7,403 ( 7,403 ) - Total revenue $ 17,587 $ ( 8,398 ) $ 9,189 $ 17,788 $ ( 10,322 ) $ 7,466 Three Months Ended September 30, 2021 Three Months Ended September 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 17,587 $ ( 8,398 ) $ 9,189 $ 17,788 $ ( 10,322 ) $ 7,466 Operating expenses: Research and development 29,143 - 29,143 24,049 - 24,049 General and administrative 11,085 - 11,085 8,634 - 8,634 Total operating expenses 40,228 - 40,228 32,683 - 32,683 Loss from operations ( 22,641 ) ( 8,398 ) ( 31,039 ) ( 14,895 ) ( 10,322 ) ( 25,217 ) Interest income 70 - 70 200 - 200 Other income (expense) ( 13 ) - ( 13 ) ( 15 ) - ( 15 ) Loss before income taxes ( 22,584 ) ( 8,398 ) ( 30,982 ) ( 14,710 ) ( 10,322 ) ( 25,032 ) Loss/(Benefit) from income taxes - - - - - - Net loss ( 22,584 ) ( 8,398 ) ( 30,982 ) ( 14,710 ) ( 10,322 ) ( 25,032 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax 37 - 37 ( 63 ) - ( 63 ) Comprehensive income (loss) $ ( 22,547 ) $ ( 8,398 ) $ ( 30,945 ) $ ( 14,773 ) $ ( 10,322 ) $ ( 25,095 ) Net loss per share, basic and diluted $ ( 0.35 ) $ ( 0.48 ) $ ( 0.32 ) $ ( 0.54 ) Shares used to compute net loss per share, basic and diluted 65,208,066 65,208,066 46,195,121 46,195,121 Nine Months Ended September 30, 2021 Nine Months Ended September 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 6,173 $ 324 $ 6,497 $ 35,624 $ 2,330 $ 37,954 Amgen 6,884 ( 271 ) 6,613 7,006 ( 68 ) 6,938 Astellas 14,574 ( 1,503 ) 13,071 9,134 ( 5,387 ) 3,747 BMS 22,215 ( 22,215 ) - 32,225 ( 19,515 ) 12,710 Total revenue $ 49,846 $ ( 23,665 ) $ 26,181 $ 83,989 $ ( 22,640 ) $ 61,349 Nine Months Ended September 30, 2021 Nine Months Ended September 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 49,846 $ ( 23,665 ) $ 26,181 $ 83,989 $ ( 22,640 ) $ 61,349 Operating expenses: Research and development 77,614 - 77,614 90,929 - 90,929 General and administrative 29,705 - 29,705 26,886 - 26,886 Total operating expenses 107,319 - 107,319 117,815 - 117,815 Loss from operations ( 57,473 ) ( 23,665 ) ( 81,138 ) ( 33,826 ) ( 22,640 ) ( 56,466 ) Interest income 182 - 182 1,729 - 1,729 Other income (expense) ( 90 ) - ( 90 ) 2 - 2 Loss before income taxes ( 57,381 ) ( 23,665 ) ( 81,046 ) ( 32,095 ) ( 22,640 ) ( 54,735 ) Loss/(Benefit) from income taxes - - - ( 13,911 ) - ( 13,911 ) Net loss ( 57,381 ) ( 23,665 ) ( 81,046 ) ( 18,184 ) ( 22,640 ) ( 40,824 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax 99 - 99 ( 104 ) - ( 104 ) Comprehensive income (loss) $ ( 57,282 ) $ ( 23,665 ) $ ( 80,947 ) $ ( 18,288 ) $ ( 22,640 ) $ ( 40,928 ) Net loss per share, basic and diluted $ ( 0.90 ) $ ( 1.27 ) $ ( 0.40 ) $ ( 0.89 ) Shares used to compute net loss per share, basic and diluted 63,759,585 63,759,585 45,992,786 45,992,786 Nine Months Ended September 30, 2021 Nine Months Ended September 30, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Cash Flow Net loss $ ( 57,381 ) $ ( 23,665 ) $ ( 81,046 ) $ ( 18,184 ) $ ( 22,640 ) $ ( 40,824 ) Changes in operating assets and liabilities: Deferred revenue ( 47,271 ) 23,665 ( 23,606 ) 46,766 22,640 69,406 Net cash used in operating activities ( 87,839 ) - ( 87,839 ) 22,686 - 22,686 Three Months Ended December 31, 2021 Three Months Ended December 31, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Revenue AbbVie $ 5,672 $ ( 621 ) $ 5,051 $ 2,568 $ ( 659 ) $ 1,909 Amgen 1,860 16 1,876 1,602 ( 18 ) 1,584 Astellas 4,791 ( 586 ) 4,205 4,798 ( 1,213 ) 3,585 BMS 7,404 ( 7,404 ) - 7,405 ( 7,405 ) ( 0 ) Total revenue $ 19,727 $ ( 8,595 ) $ 11,132 $ 16,373 $ ( 9,295 ) $ 7,078 Three Months Ended December 31, 2021 Three Months Ended December 31, 2020 As Reported Restatement Adjustment As Restated As Reported Restatement Adjustment As Restated Condensed Statements of Operations Revenue $ 19,727 $ ( 8,595 ) $ 11,132 $ 16,373 $ ( 9,295 ) $ 7,078 Operating expenses: Research and development 36,580 - 36,580 22,007 - 22,007 General and administrative 9,455 - 9,455 9,145 - 9,145 Total operating expenses 46,035 - 46,035 31,152 - 31,152 Loss from operations ( 26,308 ) ( 8,595 ) ( 34,903 ) ( 14,779 ) ( 9,295 ) ( 24,074 ) Interest income 73 - 73 107 - 107 Other income (expense) 7 - 7 ( 29 ) - ( 29 ) Loss before income taxes ( 26,228 ) ( 8,595 ) ( 34,823 ) ( 14,701 ) ( 9,295 ) ( 23,996 ) Loss/(Benefit) from income taxes - - - - - - Net loss ( 26,228 ) ( 8,595 ) ( 34,823 ) ( 14,701 ) ( 9,295 ) ( 23,996 ) Other comprehensive income (loss): Unrealized gain / (loss) on investments, net of tax ( 294 ) - ( 294 ) - - - Comprehensive income (loss) $ ( 26,522 ) $ ( 8,595 ) $ ( 35,117 ) $ ( 14,701 ) $ ( 9,295 ) $ ( 23,996 ) Net loss per share, basic and diluted $ ( 0.40 ) $ ( 0.53 ) $ ( 0.32 ) $ ( 0.51 ) Shares used to compute net loss per share, basic and diluted 65,295,995 65,295,995 46,600,605 46,600,605 |
Basis of Presentation and Sum_4
Basis of Presentation and Summary of Significant Accounting Policies - Schedule of Customers and Collaboration Partners who Represent 10% or More of Total Revenue During Each Period Presented or Net Accounts Receivable Balance (Details) - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||||||||
Dec. 31, 2021 | Sep. 30, 2021 | Jun. 30, 2021 | Mar. 31, 2021 | Dec. 31, 2020 | Sep. 30, 2020 | Jun. 30, 2020 | Mar. 31, 2020 | Jun. 30, 2021 | Jun. 30, 2020 | Sep. 30, 2021 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Concentration Risk [Line Items] | |||||||||||||||
Revenues | $ 11,132 | $ 9,189 | $ 8,795 | $ 8,197 | $ 7,078 | $ 7,466 | $ 6,988 | $ 46,895 | $ 16,992 | $ 53,883 | $ 26,181 | $ 61,349 | $ 37,312 | $ 68,427 | $ 26,902 |
Accounts receivable | 790 | 798 | 790 | 798 | |||||||||||
AbbVie Ireland Unlimited Company | |||||||||||||||
Concentration Risk [Line Items] | |||||||||||||||
Revenues | 5,051 | 2,277 | 2,734 | 1,486 | 1,909 | 3,243 | 353 | 34,358 | 4,220 | 34,711 | 6,497 | 37,954 | |||
Amgen Inc | |||||||||||||||
Concentration Risk [Line Items] | |||||||||||||||
Revenues | 1,876 | 2,352 | 1,715 | 2,546 | 1,584 | 1,548 | 3,621 | 1,769 | 4,261 | 5,390 | 6,613 | 6,938 | |||
Astellas Pharma Inc. | |||||||||||||||
Concentration Risk [Line Items] | |||||||||||||||
Revenues | 4,205 | 4,560 | 4,346 | 4,165 | 3,585 | 2,675 | 1,023 | 49 | 8,511 | 1,072 | 13,071 | 3,747 | |||
Bristol Myers Squibb Company | |||||||||||||||
Concentration Risk [Line Items] | |||||||||||||||
Revenues | $ 0 | $ 0 | 0 | $ 1,991 | $ 10,719 | $ 0 | $ 12,710 | $ 12,710 | |||||||
Major Customer | |||||||||||||||
Concentration Risk [Line Items] | |||||||||||||||
Revenues | 37,312 | 68,427 | 26,902 | ||||||||||||
Accounts receivable | 790 | 798 | 790 | 798 | |||||||||||
Major Customer | AbbVie Ireland Unlimited Company | |||||||||||||||
Concentration Risk [Line Items] | |||||||||||||||
Revenues | 11,546 | 39,863 | 5,305 | ||||||||||||
Accounts receivable | 0 | 0 | 0 | 0 | |||||||||||
Major Customer | Amgen Inc | |||||||||||||||
Concentration Risk [Line Items] | |||||||||||||||
Revenues | 8,488 | 8,522 | 4,087 | ||||||||||||
Accounts receivable | 0 | 0 | 0 | 0 | |||||||||||
Major Customer | Astellas Pharma Inc. | |||||||||||||||
Concentration Risk [Line Items] | |||||||||||||||
Revenues | 17,278 | 7,332 | 0 | ||||||||||||
Accounts receivable | 790 | 798 | 790 | 798 | |||||||||||
Major Customer | Bristol Myers Squibb Company | |||||||||||||||
Concentration Risk [Line Items] | |||||||||||||||
Revenues | 0 | 12,710 | $ 17,510 | ||||||||||||
Accounts receivable | $ 0 | $ 0 | $ 0 | $ 0 |
Basis of Presentation and Sum_5
Basis of Presentation and Summary of Significant Accounting Policies - Additional Information (Details) | 1 Months Ended | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||||||||
Jan. 31, 2019 USD ($) | Dec. 31, 2021 USD ($) | Sep. 30, 2021 USD ($) | Jun. 30, 2021 USD ($) | Mar. 31, 2021 USD ($) | Dec. 31, 2020 USD ($) | Sep. 30, 2020 USD ($) | Jun. 30, 2020 USD ($) | Mar. 31, 2020 USD ($) | Jun. 30, 2021 USD ($) | Jun. 30, 2020 USD ($) | Sep. 30, 2021 USD ($) | Sep. 30, 2020 USD ($) | Dec. 31, 2021 USD ($) Activity Segment | Dec. 31, 2020 USD ($) | Dec. 31, 2019 USD ($) | |
Summary Of Significant Accounting Policies [Line Items] | ||||||||||||||||
Number of business activities | Activity | 1 | |||||||||||||||
Number of operating segments | Segment | 1 | |||||||||||||||
Impairment of goodwill | $ 0 | $ 0 | ||||||||||||||
Impairment of intangible assets | $ 0 | 0 | 0 | |||||||||||||
Impairment of long-lived assets | 0 | 0 | 0 | |||||||||||||
Increase in accumulated deficit balance | $ (623,562,000) | $ (588,738,000) | $ (557,756,000) | $ (531,020,000) | $ (507,692,000) | $ (557,756,000) | $ (588,738,000) | (623,562,000) | (507,692,000) | (442,872,000) | ||||||
Research and development expense | 36,580,000 | $ 29,143,000 | $ 26,100,000 | $ 22,371,000 | 22,007,000 | $ 24,049,000 | $ 24,066,000 | $ 42,814,000 | $ 48,471,000 | $ 66,880,000 | $ 77,614,000 | $ 90,929,000 | 114,194,000 | 112,936,000 | $ 131,619,000 | |
Operating Lease, Right-of-Use Asset | 19,362,000 | 22,495,000 | 19,362,000 | 22,495,000 | ||||||||||||
Operating Lease, Liability | $ 21,674,000 | $ 24,870,000 | 21,674,000 | $ 24,870,000 | ||||||||||||
Probody technology | ||||||||||||||||
Summary Of Significant Accounting Policies [Line Items] | ||||||||||||||||
Acquired, technology know-how | $ 5,000,000 | |||||||||||||||
Research and development expense | $ 5,000,000 |
Basis of Presentation and Sum_6
Basis of Presentation and Summary of Significant Accounting Policies - Summary of Reconciliation of Cash, Cash Equivalents, and Restricted Cash (Details) - USD ($) $ in Thousands | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | Dec. 31, 2018 |
Cash and Cash Equivalents [Abstract] | ||||
Cash and cash equivalents | $ 205,530 | $ 191,859 | $ 188,425 | |
Restricted cash - non-current assets | 917 | 917 | 917 | |
Cash, cash equivalents, and restricted cash | $ 206,447 | $ 192,776 | $ 189,342 | $ 248,494 |
Basis of Presentation and Sum_7
Basis of Presentation and Summary of Significant Accounting Policies - Schedule of Useful Lives of Property and Equipment (Details) | 12 Months Ended |
Dec. 31, 2021 | |
Machinery and equipment | |
Property Plant And Equipment [Line Items] | |
Estimated useful life of property and equipment | 5 years |
Computer equipment and software | |
Property Plant And Equipment [Line Items] | |
Estimated useful life of property and equipment | 3 years |
Furniture and fixtures | |
Property Plant And Equipment [Line Items] | |
Estimated useful life of property and equipment | 3 years |
Leasehold improvements | |
Property Plant And Equipment [Line Items] | |
Estimated useful life of leasehold improvements, description | Shorter of remaining lease term or estimated life of the assets |
Restatement of Financial Stat_2
Restatement of Financial Statements (Additional Information) (Details) - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||||||||
Dec. 31, 2021 | Sep. 30, 2021 | Jun. 30, 2021 | Mar. 31, 2021 | Dec. 31, 2020 | Sep. 30, 2020 | Jun. 30, 2020 | Mar. 31, 2020 | Jun. 30, 2021 | Jun. 30, 2020 | Sep. 30, 2021 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Summary Of Significant Accounting Policies [Line Items] | |||||||||||||||
Revenue | $ 11,132 | $ 9,189 | $ 8,795 | $ 8,197 | $ 7,078 | $ 7,466 | $ 6,988 | $ 46,895 | $ 16,992 | $ 53,883 | $ 26,181 | $ 61,349 | $ 37,312 | $ 68,427 | $ 26,902 |
Restatement Adjustment | |||||||||||||||
Summary Of Significant Accounting Policies [Line Items] | |||||||||||||||
Revenue | (8,595) | $ (8,398) | $ (7,493) | $ (7,774) | (9,295) | $ (10,322) | $ (9,620) | $ (2,698) | $ (15,267) | $ (12,318) | $ (23,665) | $ (22,640) | (32,261) | (31,935) | $ (30,587) |
Cumulative increase in deferred revenue | $ 89,800 | $ 57,600 | $ 89,800 | $ 57,600 |
Restatement of Financial Stat_3
Restatement of Financial Statements - Statement of Financial Position (Details) - USD ($) $ in Thousands | Dec. 31, 2021 | Sep. 30, 2021 | Jun. 30, 2021 | Mar. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | Dec. 31, 2018 |
Deferred revenues, current portion | $ 40,816 | $ 40,844 | $ 39,314 | $ 43,517 | $ 42,056 | ||
Total current liabilities | 77,870 | 67,527 | 60,322 | 64,930 | 68,111 | ||
Deferred revenue, net of current portion | 243,944 | 254,257 | 264,088 | 267,750 | 276,651 | ||
Total liabilities | 339,870 | 340,801 | 344,331 | 353,487 | 366,437 | ||
Accumulated deficit | (623,562) | (588,738) | (557,756) | (531,020) | (507,692) | $ (442,872) | |
Total stockholders' equity (deficit) | (459) | 30,432 | 58,109 | 80,671 | (7,774) | 25,471 | $ 135,828 |
Total liabilities and stockholders' equity (deficit) | 339,411 | 371,233 | 402,440 | 434,158 | 358,663 | ||
Previously Reported | |||||||
Deferred revenues, current portion | 69,262 | 73,089 | 72,369 | 76,636 | 74,869 | ||
Total current liabilities | 106,316 | 99,772 | 93,377 | 98,049 | 100,924 | ||
Deferred revenue, net of current portion | 125,660 | 140,770 | 158,189 | 169,280 | 186,261 | ||
Total liabilities | 250,032 | 259,559 | 271,487 | 288,136 | 308,860 | ||
Accumulated deficit | (533,724) | (507,496) | (484,912) | (465,669) | (450,115) | (417,230) | |
Total stockholders' equity (deficit) | 89,379 | 111,674 | 130,953 | 146,022 | 49,803 | 51,113 | |
Total liabilities and stockholders' equity (deficit) | 339,411 | 371,233 | 402,440 | 434,158 | 358,663 | ||
Restatement Adjustment | |||||||
Deferred revenues, current portion | (28,446) | (32,245) | (33,055) | (33,119) | (32,813) | ||
Total current liabilities | (28,446) | (32,245) | (33,055) | (33,119) | (32,813) | ||
Deferred revenue, net of current portion | 118,284 | 113,487 | 105,899 | 98,470 | 90,390 | ||
Total liabilities | 89,838 | 81,242 | 72,844 | 65,351 | 57,577 | ||
Accumulated deficit | (89,838) | (81,242) | (72,844) | (65,351) | (57,577) | (25,642) | |
Total stockholders' equity (deficit) | (89,838) | (81,242) | (72,844) | (65,351) | (57,577) | $ (25,642) | |
Total liabilities and stockholders' equity (deficit) | $ 0 | $ 0 | $ 0 | $ 0 | $ 0 |
Restatement of Financial Stat_4
Restatement of Financial Statements - Statement of Operations and Comprehensive Loss (Details) - USD ($) | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||||||||
Dec. 31, 2021 | Sep. 30, 2021 | Jun. 30, 2021 | Mar. 31, 2021 | Dec. 31, 2020 | Sep. 30, 2020 | Jun. 30, 2020 | Mar. 31, 2020 | Jun. 30, 2021 | Jun. 30, 2020 | Sep. 30, 2021 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Revenue | $ 11,132,000 | $ 9,189,000 | $ 8,795,000 | $ 8,197,000 | $ 7,078,000 | $ 7,466,000 | $ 6,988,000 | $ 46,895,000 | $ 16,992,000 | $ 53,883,000 | $ 26,181,000 | $ 61,349,000 | $ 37,312,000 | $ 68,427,000 | $ 26,902,000 |
Research and development | 36,580,000 | 29,143,000 | 26,100,000 | 22,371,000 | 22,007,000 | 24,049,000 | 24,066,000 | 42,814,000 | 48,471,000 | 66,880,000 | 77,614,000 | 90,929,000 | 114,194,000 | 112,936,000 | 131,619,000 |
General and administrative | 9,455,000 | 11,085,000 | 9,393,000 | 9,227,000 | 9,145,000 | 8,634,000 | 8,680,000 | 9,572,000 | 18,620,000 | 18,252,000 | 29,705,000 | 26,886,000 | 39,160,000 | 36,031,000 | 36,765,000 |
Total operating expenses | 46,035,000 | 40,228,000 | 35,493,000 | 31,598,000 | 31,152,000 | 32,683,000 | 32,746,000 | 52,386,000 | 67,091,000 | 85,132,000 | 107,319,000 | 117,815,000 | 153,354,000 | 148,967,000 | 168,384,000 |
Loss from operations | (34,903,000) | (31,039,000) | (26,698,000) | (23,401,000) | (24,074,000) | (25,217,000) | (25,758,000) | (5,491,000) | (50,099,000) | (31,249,000) | (81,138,000) | (56,466,000) | (116,042,000) | (80,540,000) | (141,482,000) |
Interest income | 73,000 | 70,000 | 44,000 | 68,000 | 107,000 | 200,000 | 454,000 | 1,075,000 | 112,000 | 1,529,000 | 182,000 | 1,729,000 | 255,000 | 1,836,000 | 8,365,000 |
Other income (expense) | 7,000 | (13,000) | (82,000) | 5,000 | (29,000) | (15,000) | 5,000 | 12,000 | (77,000) | 17,000 | (90,000) | 2,000 | (83,000) | (27,000) | (135,000) |
Loss before income taxes | (34,823,000) | (30,982,000) | (26,736,000) | (23,328,000) | (23,996,000) | (25,032,000) | (25,299,000) | (4,404,000) | (50,064,000) | (29,703,000) | (81,046,000) | (54,735,000) | (115,870,000) | (78,731,000) | (133,252,000) |
Loss/(Benefit) from income taxes | (13,911,000) | (13,911,000) | (13,911,000) | 0 | (13,911,000) | (427,000) | |||||||||
Net loss (As Restated) | (34,823,000) | (30,982,000) | (26,736,000) | (23,328,000) | (23,996,000) | (25,032,000) | (25,299,000) | 9,507,000 | (50,064,000) | (15,792,000) | (81,046,000) | (40,824,000) | (115,870,000) | (64,820,000) | (132,825,000) |
Unrealized gain / (loss) on investments, net of tax | (294,000) | 37,000 | 58,000 | 4,000 | (63,000) | (320,000) | 279,000 | 62,000 | (41,000) | 99,000 | (104,000) | (195,000) | (104,000) | 139,000 | |
Impact of adoption of new accounting pronouncement | 0 | 0 | 11,000 | ||||||||||||
Comprehensive income (loss) | $ (35,117,000) | $ (30,945,000) | $ (26,678,000) | $ (23,324,000) | $ (23,996,000) | $ (25,095,000) | $ (25,619,000) | $ 9,786,000 | $ (50,002,000) | $ (15,833,000) | $ (80,947,000) | $ (40,928,000) | $ (116,065,000) | $ (64,924,000) | $ (132,675,000) |
Net loss per share, basic | $ (0.53) | $ (0.48) | $ (0.41) | $ (0.38) | $ (0.51) | $ (0.54) | $ (0.55) | $ 0.21 | $ (0.79) | $ (0.34) | $ (1.27) | $ (0.89) | $ (1.81) | $ (1.40) | $ (2.93) |
Net loss per share, diluted | $ (0.53) | $ (0.48) | $ (0.41) | $ (0.38) | $ (0.51) | $ (0.54) | $ (0.55) | $ 0.20 | $ (0.79) | $ (0.34) | $ (1.27) | $ (0.89) | $ (1.81) | $ (1.40) | $ (2.93) |
Shares used to compute net loss per share, basic | 65,295,995 | 65,208,066 | 65,055,998 | 60,968,111 | 46,600,605 | 46,195,121 | 46,057,063 | 45,723,955 | 63,023,349 | 45,890,510 | 63,759,585 | 45,992,786 | 64,146,848 | 46,145,563 | 45,335,927 |
Shares used to compute net loss per share, diluted | 65,295,995 | 65,208,066 | 65,055,998 | 60,968,111 | 46,600,605 | 46,195,121 | 46,057,063 | 47,044,774 | 63,023,349 | 45,890,510 | 63,759,585 | 45,992,786 | 64,146,848 | 46,145,563 | 45,335,927 |
Previously Reported | |||||||||||||||
Revenue | $ 19,727,000 | $ 17,587,000 | $ 16,288,000 | $ 15,971,000 | $ 16,373,000 | $ 17,788,000 | $ 16,608,000 | $ 49,593,000 | $ 32,259,000 | $ 66,201,000 | $ 49,846,000 | $ 83,989,000 | $ 69,573,000 | $ 100,362,000 | $ 57,489,000 |
Research and development | 36,580,000 | 29,143,000 | 26,100,000 | 22,371,000 | 22,007,000 | 24,049,000 | 24,066,000 | 42,814,000 | 48,471,000 | 66,880,000 | 77,614,000 | 90,929,000 | 114,194,000 | 112,936,000 | 131,619,000 |
General and administrative | 9,455,000 | 11,085,000 | 9,393,000 | 9,227,000 | 9,145,000 | 8,634,000 | 8,680,000 | 9,572,000 | 18,620,000 | 18,252,000 | 29,705,000 | 26,886,000 | 39,160,000 | 36,031,000 | 36,765,000 |
Total operating expenses | 46,035,000 | 40,228,000 | 35,493,000 | 31,598,000 | 31,152,000 | 32,683,000 | 32,746,000 | 52,386,000 | 67,091,000 | 85,132,000 | 107,319,000 | 117,815,000 | 153,354,000 | 148,967,000 | 168,384,000 |
Loss from operations | (26,308,000) | (22,641,000) | (19,205,000) | (15,627,000) | (14,779,000) | (14,895,000) | (16,138,000) | (2,793,000) | (34,832,000) | (18,931,000) | (57,473,000) | (33,826,000) | (83,781,000) | (48,605,000) | (110,895,000) |
Interest income | 73,000 | 70,000 | 44,000 | 68,000 | 107,000 | 200,000 | 454,000 | 1,075,000 | 112,000 | 1,529,000 | 182,000 | 1,729,000 | 255,000 | 1,836,000 | 8,365,000 |
Other income (expense) | 7,000 | (13,000) | (82,000) | 5,000 | (29,000) | (15,000) | 5,000 | 12,000 | (77,000) | 17,000 | (90,000) | 2,000 | (83,000) | (27,000) | (135,000) |
Loss before income taxes | (26,228,000) | (22,584,000) | (19,243,000) | (15,554,000) | (14,701,000) | (14,710,000) | (15,679,000) | (1,706,000) | (34,797,000) | (17,385,000) | (57,381,000) | (32,095,000) | (83,609,000) | (46,796,000) | (102,665,000) |
Loss/(Benefit) from income taxes | (13,911,000) | (13,911,000) | (13,911,000) | 0 | (13,911,000) | (427,000) | |||||||||
Net loss (As Restated) | (26,228,000) | (22,584,000) | (19,243,000) | (15,554,000) | (14,701,000) | (14,710,000) | (15,679,000) | 12,205,000 | (34,797,000) | (3,474,000) | (57,381,000) | (18,184,000) | (83,609,000) | (32,885,000) | (102,238,000) |
Unrealized gain / (loss) on investments, net of tax | (294,000) | 37,000 | 58,000 | 4,000 | (63,000) | (320,000) | 279,000 | 62,000 | (41,000) | 99,000 | (104,000) | (195,000) | (104,000) | 139,000 | |
Impact of adoption of new accounting pronouncement | 0 | 0 | 11,000 | ||||||||||||
Comprehensive income (loss) | $ (26,522,000) | $ (22,547,000) | $ (19,185,000) | $ (15,550,000) | $ (14,701,000) | $ (14,773,000) | $ (15,999,000) | $ 12,484,000 | $ (34,735,000) | $ (3,515,000) | $ (57,282,000) | $ (18,288,000) | $ (83,804,000) | $ (32,989,000) | $ (102,088,000) |
Net loss per share, basic | $ (0.40) | $ (0.35) | $ (0.30) | $ (0.26) | $ (0.32) | $ (0.32) | $ (0.34) | $ 0.27 | $ (0.55) | $ (0.08) | $ (0.90) | $ (0.40) | $ (1.30) | $ (0.71) | $ (2.26) |
Net loss per share, diluted | $ (0.40) | $ (0.35) | $ (0.30) | $ (0.26) | $ (0.32) | $ (0.32) | $ (0.34) | $ 0.26 | $ (0.55) | $ (0.08) | $ (0.90) | $ (0.40) | $ (1.30) | $ (0.71) | $ (2.26) |
Shares used to compute net loss per share, basic | 65,295,995 | 65,208,066 | 65,055,998 | 60,968,111 | 46,600,605 | 46,195,121 | 46,057,063 | 45,723,955 | 63,023,349 | 45,890,510 | 63,759,585 | 45,992,786 | 64,146,848 | 46,145,563 | 45,335,927 |
Shares used to compute net loss per share, diluted | 65,295,995 | 65,208,066 | 65,055,998 | 60,968,111 | 46,600,605 | 46,195,121 | 46,057,063 | 47,044,774 | 63,023,349 | 45,890,510 | 63,759,585 | 45,992,786 | 64,146,848 | 46,145,563 | 45,335,927 |
Restatement Adjustment | |||||||||||||||
Revenue | $ (8,595,000) | $ (8,398,000) | $ (7,493,000) | $ (7,774,000) | $ (9,295,000) | $ (10,322,000) | $ (9,620,000) | $ (2,698,000) | $ (15,267,000) | $ (12,318,000) | $ (23,665,000) | $ (22,640,000) | $ (32,261,000) | $ (31,935,000) | $ (30,587,000) |
Research and development | 0 | ||||||||||||||
General and administrative | 0 | ||||||||||||||
Total operating expenses | 0 | 0 | 0 | 0 | |||||||||||
Loss from operations | (8,595,000) | (8,398,000) | (7,493,000) | (7,774,000) | (9,295,000) | (10,322,000) | (9,620,000) | (2,698,000) | (15,267,000) | (12,318,000) | (23,665,000) | (22,640,000) | (32,261,000) | (31,935,000) | (30,587,000) |
Interest income | |||||||||||||||
Other income (expense) | |||||||||||||||
Loss before income taxes | (8,595,000) | (8,398,000) | (7,493,000) | (7,774,000) | (9,295,000) | (10,322,000) | (9,620,000) | (2,698,000) | (15,267,000) | (12,318,000) | (23,665,000) | (22,640,000) | (32,261,000) | (31,935,000) | (30,587,000) |
Net loss (As Restated) | (8,595,000) | (8,398,000) | (7,493,000) | (7,774,000) | (9,295,000) | (10,322,000) | (9,620,000) | (2,698,000) | (15,267,000) | (12,318,000) | (23,665,000) | (22,640,000) | (32,261,000) | (31,935,000) | (30,587,000) |
Unrealized gain / (loss) on investments, net of tax | |||||||||||||||
Comprehensive income (loss) | $ (8,595,000) | $ (8,398,000) | $ (7,493,000) | $ (7,774,000) | $ (9,295,000) | $ (10,322,000) | $ (9,620,000) | $ (2,698,000) | $ (15,267,000) | $ (12,318,000) | $ (23,665,000) | $ (22,640,000) | $ (32,261,000) | $ (31,935,000) | $ (30,587,000) |
Restatement of Financial Stat_5
Restatement of Financial Statements - Statements of Stockholders' Equity (Deficit) (Details) - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | ||||||||||||
Dec. 31, 2021 | Sep. 30, 2021 | Jun. 30, 2021 | Mar. 31, 2021 | Dec. 31, 2020 | Sep. 30, 2020 | Jun. 30, 2020 | Mar. 31, 2020 | Jun. 30, 2021 | Jun. 30, 2020 | Sep. 30, 2021 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | Dec. 31, 2018 | |
Net loss | $ (34,823) | $ (30,982) | $ (26,736) | $ (23,328) | $ (23,996) | $ (25,032) | $ (25,299) | $ 9,507 | $ (50,064) | $ (15,792) | $ (81,046) | $ (40,824) | $ (115,870) | $ (64,820) | $ (132,825) | |
Accumulated deficit | (623,562) | (588,738) | (557,756) | (531,020) | (507,692) | (557,756) | (588,738) | (623,562) | (507,692) | (442,872) | ||||||
Total stockholders' equity (deficit) | (459) | 30,432 | 58,109 | 80,671 | (7,774) | 58,109 | 30,432 | (459) | (7,774) | 25,471 | $ 135,828 | |||||
Previously Reported | ||||||||||||||||
Net loss | (26,228) | (22,584) | (19,243) | (15,554) | (14,701) | (14,710) | (15,679) | 12,205 | (34,797) | (3,474) | (57,381) | (18,184) | (83,609) | (32,885) | (102,238) | |
Accumulated deficit | (533,724) | (507,496) | (484,912) | (465,669) | (450,115) | (484,912) | (507,496) | (533,724) | (450,115) | (417,230) | ||||||
Total stockholders' equity (deficit) | 89,379 | 111,674 | 130,953 | 146,022 | 49,803 | 130,953 | 111,674 | 89,379 | 49,803 | 51,113 | ||||||
Restatement Adjustment | ||||||||||||||||
Net loss | (8,595) | (8,398) | (7,493) | (7,774) | (9,295) | $ (10,322) | $ (9,620) | $ (2,698) | (15,267) | $ (12,318) | (23,665) | $ (22,640) | (32,261) | (31,935) | (30,587) | |
Accumulated deficit | (89,838) | (81,242) | (72,844) | (65,351) | (57,577) | (72,844) | (81,242) | (89,838) | (57,577) | (25,642) | ||||||
Total stockholders' equity (deficit) | $ (89,838) | $ (81,242) | $ (72,844) | $ (65,351) | $ (57,577) | $ (72,844) | $ (81,242) | $ (89,838) | $ (57,577) | $ (25,642) |
Restatement of Financial Stat_6
Restatement of Financial Statements - Statement Of Cash Flows (Details) - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||
Mar. 31, 2021 | Mar. 31, 2020 | Jun. 30, 2021 | Jun. 30, 2020 | Sep. 30, 2021 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Net loss | $ (23,328) | $ 9,507 | $ (50,064) | $ (15,792) | $ (81,046) | $ (40,824) | $ (115,870) | $ (64,820) | $ (132,825) |
Deferred revenue | (7,440) | 83,114 | (15,305) | 76,332 | (23,606) | 69,406 | (33,948) | 62,826 | (17,154) |
Net cash used in operating activities | (29,940) | (49,737) | (58,139) | 47,364 | (87,839) | 22,686 | (119,031) | 5,259 | (140,480) |
Cash, cash equivalents and restricted cash, beginning of year | 192,776 | 189,342 | 192,776 | 189,342 | 192,776 | 189,342 | 192,776 | 189,342 | 248,494 |
Cash, cash equivalents and restricted cash, end of year | 206,447 | 192,776 | 189,342 | ||||||
Previously Reported | |||||||||
Net loss | (15,554) | 12,205 | (34,797) | (3,474) | (57,381) | (18,184) | (83,609) | (32,885) | (102,238) |
Deferred revenue | (15,214) | 80,416 | (30,572) | 64,014 | (47,271) | 46,766 | (66,209) | 30,891 | (47,741) |
Net cash used in operating activities | (29,940) | (49,737) | (58,139) | 47,364 | (87,839) | 22,686 | (119,031) | 5,259 | (140,480) |
Restatement Adjustment | |||||||||
Net loss | (7,774) | (2,698) | (15,267) | (12,318) | (23,665) | (22,640) | (32,261) | (31,935) | (30,587) |
Deferred revenue | $ 7,774 | $ 2,698 | $ 15,267 | $ 12,318 | $ 23,665 | $ 22,640 | 32,261 | 31,935 | 30,587 |
Net cash used in operating activities | $ 0 | $ 0 | $ 0 |
Adopted Accounting Pronouncem_2
Adopted Accounting Pronouncements - Additional Information (Details) | Dec. 31, 2021 |
Summary Of Significant Accounting Policies [Line Items] | |
Change in accounting principle, accounting standards update, adopted [true false] | false |
ASU 2019-12 | |
Summary Of Significant Accounting Policies [Line Items] | |
Change in accounting principle, accounting standards update, adoption date | Jan. 01, 2021 |
Change in accounting principle, accounting standards update, immaterial effect [true false] | true |
Net Loss Per Share - Summary of
Net Loss Per Share - Summary of Potentially Dilutive Securities Excluded from Computation of Diluted Net Loss Per Share (Details) - shares | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Options, RSUs and ESPP to purchase common stock | |||
Antidilutive Securities Excluded From Computation Of Earnings Per Share [Line Items] | |||
Anti-dilutive securities excluded from computation of diluted net loss per share | 11,987,362 | 11,388,691 | 9,687,844 |
Fair Value Measurements and I_3
Fair Value Measurements and Investments - Schedule of Investments Subject to Fair Value Measurements on a Recurring Basis (Details) - USD ($) $ in Thousands | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 |
Fair Value Assets And Liabilities Measured On Recurring And Nonrecurring Basis [Line Items] | |||
Amortized Cost | $ 266,591 | $ 256,292 | |
Gross Unrealized Holding Gains | 0 | 6 | |
Gross Unrealized Holding Losses | 242 | ||
Aggregate Fair Value | 266,349 | 256,298 | |
Cash and cash equivalents | 205,530 | 191,859 | $ 188,425 |
Level I | Money market funds | |||
Fair Value Assets And Liabilities Measured On Recurring And Nonrecurring Basis [Line Items] | |||
Cash and cash equivalents | 165,736 | 131,121 | |
Level I | Restricted cash (money market funds) | |||
Fair Value Assets And Liabilities Measured On Recurring And Nonrecurring Basis [Line Items] | |||
Restricted cash | 917 | 917 | |
Level I | U.S. Government bonds | |||
Fair Value Assets And Liabilities Measured On Recurring And Nonrecurring Basis [Line Items] | |||
Short-term Investments, Amortized Cost | 99,938 | 124,254 | |
Short-term Investments, Gross Unrealized Holding Gains | 0 | 6 | |
Short-term Investments, Gross Unrealized Holding Losses | (242) | ||
Aggregate Fair Value | $ 99,696 | $ 124,260 |
Fair Value Measurements and I_4
Fair Value Measurements and Investments - Additional Information (Details) | 12 Months Ended |
Dec. 31, 2021 | |
U.S. Government bonds | |
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] | |
Debt securities, available for sale, maturity period | 12 months |
Property and Equipment - Summar
Property and Equipment - Summary of Property and Equipment, Net (Details) - USD ($) $ in Thousands | Dec. 31, 2021 | Dec. 31, 2020 |
Property, Plant and Equipment [Abstract] | ||
Machinery and equipment | $ 15,086 | $ 13,772 |
Computer equipment and software | 1,608 | 1,600 |
Furniture and fixtures | 1,054 | 1,024 |
Leasehold improvements | 1,736 | 1,728 |
Construction in progress | 308 | 252 |
Total property and equipment | 19,792 | 18,376 |
Less: accumulated depreciation and amortization | (13,832) | (11,426) |
Property and equipment, net | $ 5,960 | $ 6,950 |
Property and Equipment - Additi
Property and Equipment - Additional Information (Details) - USD ($) $ in Millions | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Property, Plant and Equipment [Abstract] | |||
Depreciation and amortization | $ 2.6 | $ 2.4 | $ 2.5 |
Intangible Assets - Additional
Intangible Assets - Additional Information (Details) - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Finite Lived Intangible Assets [Line Items] | |||
Amortization expense of intangible assets | $ 146 | $ 146 | $ 146 |
Probody Platform Intangible Asset | |||
Finite Lived Intangible Assets [Line Items] | |||
Average estimated lives of patents | 12 years | ||
Amortization expense of intangible assets | $ 100 | $ 100 | $ 100 |
Intangible Assets - Schedule of
Intangible Assets - Schedule of Intangible Assets (Details) - USD ($) $ in Thousands | Dec. 31, 2021 | Dec. 31, 2020 |
Goodwill | ||
Goodwill | $ 949 | $ 949 |
Probody Platform Intangible Asset | ||
Intangible assets | ||
Intangible assets, gross | 1,750 | 1,750 |
Less accumulated amortization | 729 | 583 |
Intangible assets, net | $ 1,021 | $ 1,167 |
Accrued Liabilities - Summary o
Accrued Liabilities - Summary of Accrued Liabilities (Details) - USD ($) $ in Thousands | Dec. 31, 2021 | Dec. 31, 2020 |
Accrued Liabilities, Current [Abstract] | ||
Research and clinical expenses | $ 18,861 | $ 10,092 |
Payroll and related expenses | 9,576 | 8,362 |
Legal and professional expenses | 1,468 | 815 |
Operating lease liabilities - short term | 3,618 | 3,195 |
Other accrued expenses | 713 | 595 |
Total | $ 34,236 | $ 23,059 |
Collaboration and License Agr_3
Collaboration and License Agreements - Schedule of Revenue by Collaboration Partners (Details) - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | |||
Revenue | $ 37,312 | $ 68,427 | $ 26,902 |
AbbVie | |||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | |||
Revenue | 11,546 | 39,863 | 5,305 |
Amgen | |||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | |||
Revenue | 8,488 | 8,522 | 4,087 |
Bristol Myers Squibb | |||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | |||
Revenue | 0 | 12,710 | 17,510 |
Astellas | |||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | |||
Revenue | $ 17,278 | $ 7,332 | $ 0 |
Collaboration and License Agr_4
Collaboration and License Agreements - AbbVie Ireland Unlimited Company - Additional Information (Details) $ in Thousands | 1 Months Ended | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||||||||||||||||
May 31, 2020 USD ($) | Mar. 31, 2020 USD ($) | Jun. 30, 2019 USD ($) | May 31, 2018 USD ($) | Jul. 31, 2017 USD ($) | Apr. 30, 2016 USD ($) Target Agreement AccountingUnit | Dec. 31, 2021 USD ($) | Sep. 30, 2021 USD ($) | Jun. 30, 2021 USD ($) | Mar. 31, 2021 USD ($) | Dec. 31, 2020 USD ($) | Sep. 30, 2020 USD ($) | Jun. 30, 2020 USD ($) | Mar. 31, 2020 USD ($) | Jun. 30, 2018 USD ($) | Jun. 30, 2021 USD ($) | Jun. 30, 2020 USD ($) | Sep. 30, 2021 USD ($) | Sep. 30, 2020 USD ($) | Dec. 31, 2021 USD ($) | Dec. 31, 2020 USD ($) | Dec. 31, 2019 USD ($) | Dec. 31, 2018 USD ($) | Mar. 31, 2017 USD ($) Target | |
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Revenue | $ 11,132 | $ 9,189 | $ 8,795 | $ 8,197 | $ 7,078 | $ 7,466 | $ 6,988 | $ 46,895 | $ 16,992 | $ 53,883 | $ 26,181 | $ 61,349 | $ 37,312 | $ 68,427 | $ 26,902 | |||||||||
Type of Revenue [Extensible List] | us-gaap:LicenseAndServiceMember | us-gaap:LicenseAndServiceMember | us-gaap:LicenseAndServiceMember | |||||||||||||||||||||
Deferred revenue | 284,760 | 318,707 | $ 284,760 | $ 318,707 | $ 255,881 | $ 273,035 | ||||||||||||||||||
Second target in exchange | $ 10,000 | |||||||||||||||||||||||
CD71 Agreement | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Revenue | $ 9,900 | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Revenue | 5,051 | $ 2,277 | $ 2,734 | $ 1,486 | 1,909 | $ 3,243 | $ 353 | 34,358 | $ 4,220 | $ 34,711 | $ 6,497 | $ 37,954 | ||||||||||||
AbbVie Ireland Unlimited Company | ASC 606 | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Upfront payment received | $ 30,000 | |||||||||||||||||||||||
Milestone payment received | 14,000 | |||||||||||||||||||||||
Total transaction price | 39,800 | |||||||||||||||||||||||
Estimated sublicense fees | $ 4,200 | |||||||||||||||||||||||
Number of accounting units | AccountingUnit | 2 | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | Collaborative Arrangement | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Number of collaboration agreements | Agreement | 2 | |||||||||||||||||||||||
Percentage of net profits or net losses related to development and commercialization costs | 35% | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | CD71 Agreement | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Upfront payment received | $ 20,000 | 100,000 | ||||||||||||||||||||||
Milestone payment received | $ 40,000 | $ 40,000 | 100,000 | |||||||||||||||||||||
Sublicense fees paid | $ 4,000 | $ 1,000 | ||||||||||||||||||||||
Milestone payments received | $ 40,000 | $ 21,000 | $ 14,000 | |||||||||||||||||||||
Revenue | $ 26,600 | |||||||||||||||||||||||
Deferred revenue | 16,100 | 25,200 | 16,100 | 25,200 | ||||||||||||||||||||
AbbVie Ireland Unlimited Company | CD71 Agreement | Transferred over Time | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Type of Revenue [Extensible List] | us-gaap:LicenseAndServiceMember | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | CD71 Agreement | ASC 606 | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Upfront payment received | 20,000 | |||||||||||||||||||||||
Total transaction price | 29,800 | |||||||||||||||||||||||
Estimated sublicense fees | 4,200 | |||||||||||||||||||||||
Milestone payment received | $ 14,000 | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | CD71 Agreement | U.S | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Profit split on U.S. sales | 35% | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | CD71 Agreement | Maximum | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Contingent payments receivable upon achieving development, regulatory and commercial milestones | $ 470,000 | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | Seattle Genetics Agreement | ASC 606 | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Sublicense fees paid | 1,000 | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | Discovery Agreement | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Upfront payment received | 10,000 | |||||||||||||||||||||||
Number of targets selected | Target | 1 | |||||||||||||||||||||||
Deferred revenue | $ 6,500 | $ 8,900 | $ 6,500 | $ 8,900 | ||||||||||||||||||||
AbbVie Ireland Unlimited Company | Discovery Agreement | ASC 606 | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Upfront payment received | 10,000 | |||||||||||||||||||||||
Total transaction price | $ 10,000 | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | Discovery Agreement | Second Target | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Milestone payments received | $ 10,000 | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | Discovery Agreement | Second Target | ASC 606 | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Total transaction price | $ 10,000 | |||||||||||||||||||||||
Estimated research service period | 5 years | |||||||||||||||||||||||
Cost based input method | $ 10,000 | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | Discovery Agreement | Maximum | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Number of targets | Target | 2 | |||||||||||||||||||||||
AbbVie Ireland Unlimited Company | Discovery Agreement | Maximum | Development, Regulatory and Commercial Milestone Payments | ||||||||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||||||||
Contingent milestone payments receivable | $ 265,000 |
Collaboration and License Agr_5
Collaboration and License Agreements - Amgen, Inc - Additional Information (Details) $ / shares in Units, $ in Thousands | 1 Months Ended | 3 Months Ended | 12 Months Ended | |||||
Sep. 29, 2017 USD ($) Target | Oct. 31, 2017 USD ($) $ / shares shares | Jun. 30, 2020 | Jun. 30, 2019 | Dec. 31, 2021 USD ($) | Dec. 31, 2020 USD ($) | Dec. 31, 2019 USD ($) | Dec. 31, 2018 USD ($) | |
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||
Common stock, value of shares issued in connection with agreement | $ 107,712 | $ 11,288 | $ 0 | |||||
Accrued liabilities | 34,236 | 23,059 | ||||||
Deferred revenue | 284,760 | 318,707 | $ 255,881 | $ 273,035 | ||||
Amgen | EGFR Products | ||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||
Deferred revenue | 21,800 | |||||||
Amgen | Amgen Other Products | ||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||
Deferred revenue | 1,800 | |||||||
Collaboration and License Agreement | Amgen | ||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||
Upfront payment received | $ 40,000 | $ 40,000 | ||||||
Common stock, shares issuable under agreement | shares | 1,156,069 | |||||||
Common stock, shares issuable under agreement, price per share | $ / shares | $ 17.30 | |||||||
Common stock, value of shares issued in connection with agreement | $ 20,000 | |||||||
Number of targets selected | Target | 1 | |||||||
Number of additional collaboration target | Target | 2 | |||||||
Total transaction price | $ 51,200 | |||||||
Portion of transaction price allocated to premium on sale of common stock | 500 | |||||||
Estimated fair value of products | 10,700 | |||||||
Collaboration and License Agreement | Amgen | Maximum | ||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||
Contingent payments payable | 203,000 | |||||||
Collaboration and License Agreement | Amgen | EGFR Products | ||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||
Total transaction price | 46,400 | |||||||
Estimated research service period | 8 years | 7 years | ||||||
Deferred revenue | 21,800 | 29,800 | ||||||
Collaboration and License Agreement | Amgen | EGFR Products | Maximum | ||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||
Contingent milestone payments receivable | $ 460,000 | |||||||
Percentage share of profit and losses | 50% | |||||||
Collaboration and License Agreement | Amgen | Amgen Products | Maximum | ||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||
Contingent milestone payments receivable | $ 950,000 | |||||||
Number of targets | Target | 3 | |||||||
Collaboration and License Agreement | Amgen | Amgen Other Products | ||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||
Total transaction price | $ 4,800 | |||||||
Estimated research service period | 6 years | |||||||
Revenue recognition upon performance obligation | $ 4,800 | |||||||
Deferred revenue | $ 1,800 | $ 2,300 | ||||||
Sublicense Agreement | Amgen | Maximum | UC Regents | ||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||
Sublicense payment percentage | 7.50% |
Collaboration and License Agr_6
Collaboration and License Agreements - Astellas Pharma Inc - Additional Information (Details) $ in Thousands | 1 Months Ended | |||||
Mar. 23, 2020 USD ($) Target | Mar. 31, 2020 USD ($) | Dec. 31, 2021 USD ($) | Dec. 31, 2020 USD ($) | Dec. 31, 2019 USD ($) | Dec. 31, 2018 USD ($) | |
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||
Deferred revenue | $ 284,760 | $ 318,707 | $ 255,881 | $ 273,035 | ||
Astellas Pharma Inc. | ||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||
Deferred revenue | 60,300 | |||||
Collaboration and License Agreement | Astellas Pharma Inc. | ||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||
Number of targets selected | Target | 1 | |||||
Number of additional collaboration target | Target | 3 | |||||
Upfront payment received | $ 80,000 | $ 80,000 | ||||
Total transaction price | 103,200 | |||||
Research and development service fees | 23,200 | |||||
Deferred revenue | 60,300 | 74,200 | ||||
Amount due from customer | $ 800 | $ 800 | ||||
Collaboration and License Agreement | Astellas Pharma Inc. | Additional Contingent Payments | ||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||
Contingent milestone payments receivable | $ 900,000 | |||||
Collaboration and License Agreement | Astellas Pharma Inc. | Maximum | ||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||
Number of targets | Target | 4 | |||||
Right to expand the number of additional collaboration target | Target | 5 | |||||
Contingent milestone payments receivable | $ 1,600,000 | |||||
Collaboration and License Agreement | Astellas Pharma Inc. | Minimum | ||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||
Right to expand the number of additional collaboration target | Target | 3 |
Collaboration and License Agr_7
Collaboration and License Agreements - Bristol-Myers Squibb Company - Additional Information (Details) $ in Thousands | 1 Months Ended | 3 Months Ended | 12 Months Ended | |||||||||||
Jan. 01, 2018 USD ($) | Apr. 25, 2017 USD ($) Target | Jul. 07, 2014 USD ($) Term Target | Jul. 31, 2014 USD ($) | Mar. 31, 2020 USD ($) | Dec. 31, 2021 USD ($) | Dec. 31, 2020 USD ($) | Feb. 29, 2020 USD ($) | Dec. 31, 2019 USD ($) | Dec. 31, 2018 USD ($) | Nov. 30, 2017 USD ($) | Mar. 17, 2017 Target | Dec. 31, 2016 USD ($) | Jan. 31, 2016 USD ($) | |
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||
Number of research targets selected | Target | 8 | |||||||||||||
Deferred revenue | $ 284,760 | $ 318,707 | $ 255,881 | $ 273,035 | ||||||||||
Bristol Myers Squibb Company | ||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||
Upfront payment received | 297,000 | |||||||||||||
Milestone payment received | 297,000 | |||||||||||||
Deferred revenue | $ 178,300 | $ 178,300 | ||||||||||||
Collaborative Arrangement | Bristol Myers Squibb Company | ||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||
Collaboration target research term | 2 years | |||||||||||||
Number of additional collaboration target | Target | 2 | |||||||||||||
Research terms | Each collaboration target had a two-year research term and the two additional targets had to be nominated by Bristol Myers Squibb within five years of the effective date of the BMS Agreement. The research term for each collaboration target could be extended in one year increments up to three times. | |||||||||||||
Extension of research term for each collaboration target | 1 year | |||||||||||||
Upfront payment received | $ 200,000 | $ 50,000 | $ 50,000 | |||||||||||
Contingent milestone payments receivable | $ 10,000 | $ 15,000 | $ 10,000 | |||||||||||
Total transaction price | 304,700 | |||||||||||||
Upfront payment received | 250,000 | |||||||||||||
Research and development service fees | 17,700 | |||||||||||||
Milestone payment received | $ 12,000 | $ 10,000 | ||||||||||||
Deferred revenue | $ 178,300 | |||||||||||||
Target selection fees | $ 25,000 | |||||||||||||
Collaborative Arrangement | Bristol Myers Squibb Company | Pre Clinical Candidate | ||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||
Contingent milestone payments receivable | $ 2,000 | |||||||||||||
Collaborative Arrangement | Bristol Myers Squibb Company | New Drug Application for CTLA-4 | ||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||
Contingent milestone payments receivable | $ 10,000 | |||||||||||||
Collaborative Arrangement | Maximum | Bristol Myers Squibb Company | ||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||
Number of oncology target | Target | 4 | |||||||||||||
Number of collaboration target | Target | 2 | |||||||||||||
Period of nomination of additional target from effective date | 5 years | |||||||||||||
Times of increments for extended collaboration target research time | Term | 3 | |||||||||||||
Collaborative Arrangement | Maximum | Bristol Myers Squibb Company | Each Of Two Additional Targets | ||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||
Contingent milestone payments receivable | $ 25,000 | |||||||||||||
Collaboration and License Agreement | Maximum | Bristol Myers Squibb Company | ||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||
Number of additional collaboration target | Target | 8 | |||||||||||||
Contingent milestone payments receivable | $ 2,100,000 |
Collaboration and License Agr_8
Collaboration and License Agreements - ImmunoGen, Inc - Additional Information (Details) | 1 Months Ended | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||||||||||
Jan. 31, 2014 USD ($) Target | Dec. 31, 2021 USD ($) | Sep. 30, 2021 USD ($) | Jun. 30, 2021 USD ($) | Mar. 31, 2021 USD ($) | Dec. 31, 2020 USD ($) | Sep. 30, 2020 USD ($) | Jun. 30, 2020 USD ($) | Mar. 31, 2020 USD ($) | Jun. 30, 2021 USD ($) | Jun. 30, 2020 USD ($) | Sep. 30, 2021 USD ($) | Sep. 30, 2020 USD ($) | Dec. 31, 2021 USD ($) | Dec. 31, 2020 USD ($) | Dec. 31, 2019 USD ($) | Feb. 29, 2020 USD ($) | Apr. 25, 2017 Target | |
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||
Number of research targets selected | Target | 8 | |||||||||||||||||
Research and development expense | $ 36,580,000 | $ 29,143,000 | $ 26,100,000 | $ 22,371,000 | $ 22,007,000 | $ 24,049,000 | $ 24,066,000 | $ 42,814,000 | $ 48,471,000 | $ 66,880,000 | $ 77,614,000 | $ 90,929,000 | $ 114,194,000 | $ 112,936,000 | $ 131,619,000 | |||
Collaborative Arrangement | Immuno Gen Inc | ||||||||||||||||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||||||||||||||||
Upfront cash payment | $ 0 | |||||||||||||||||
Number of research targets selected | Target | 2 | |||||||||||||||||
Milestone payments payable | $ 3,000,000 | |||||||||||||||||
Research and development expense | $ 3,000,000 |
Collaboration and License Agr_9
Collaboration and License Agreements - Summary of Contract Liabilities (Details) - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Revenue from Contract with Customer [Abstract] | |||
Balance at Beginning of Period | $ 318,707 | $ 255,881 | $ 273,035 |
Additions | 3,834 | 121,635 | 10,000 |
Deductions | (37,781) | (58,809) | (27,154) |
Balance at End of Period | $ 284,760 | $ 318,707 | $ 255,881 |
Collaboration and License Ag_10
Collaboration and License Agreements - Contract Liabilities - Additional Information (Details) - USD ($) $ in Thousands | 12 Months Ended | |||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | Dec. 31, 2018 | |
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||
Deferred revenue | $ 284,760 | $ 318,707 | $ 255,881 | $ 273,035 |
AbbVie Ireland Unlimited Company | CD71 Agreement | ||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||
Deferred revenue | $ 16,100 | 25,200 | ||
Deferred Revenue Recognition Maturity Year | 2023 | |||
AbbVie Ireland Unlimited Company | First Target under Discovery Agreement | ||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||
Deferred revenue | $ 6,500 | |||
Deferred Revenue Recognition Maturity Year | 2022 | |||
Astellas Pharma Inc. | ||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||
Deferred revenue | $ 60,300 | |||
Deferred Revenue Recognition Maturity Year | 2026 | |||
Amgen Inc | EGFR Products | ||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||
Deferred revenue | $ 21,800 | |||
Deferred Revenue Recognition Maturity Year | 2024 | |||
Amgen Inc | Amgen Other Products | ||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||
Deferred revenue | $ 1,800 | |||
Deferred Revenue Recognition Maturity Year | 2023 | |||
Bristol Myers Squibb Company | ||||
Collaborative Arrangements And Noncollaborative Arrangement Transactions [Line Items] | ||||
Deferred revenue | $ 178,300 | $ 178,300 | ||
Deferred Revenue Recognition Maturity Year | 2025 |
License Agreement - Additional
License Agreement - Additional Information (Details) - USD ($) $ / shares in Units, $ in Thousands | 1 Months Ended | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||||||||||||||||||
Mar. 23, 2020 | Jan. 01, 2018 | Apr. 25, 2017 | Jul. 07, 2014 | Mar. 31, 2020 | Feb. 29, 2020 | Jun. 30, 2019 | Apr. 30, 2019 | Apr. 30, 2016 | Jul. 31, 2014 | Dec. 31, 2021 | Sep. 30, 2021 | Jun. 30, 2021 | Mar. 31, 2021 | Dec. 31, 2020 | Sep. 30, 2020 | Jun. 30, 2020 | Mar. 31, 2020 | Jun. 30, 2019 | Jun. 30, 2021 | Jun. 30, 2020 | Sep. 30, 2021 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
License Agreement [Line Items] | ||||||||||||||||||||||||||
Annual minimum royalty obligations | $ 200 | $ 200 | ||||||||||||||||||||||||
License termination period | 60 days | |||||||||||||||||||||||||
Common stock, shares issued | 65,392,758 | 48,251,819 | 65,392,758 | 48,251,819 | ||||||||||||||||||||||
Research and development | $ 36,580 | $ 29,143 | $ 26,100 | $ 22,371 | $ 22,007 | $ 24,049 | $ 24,066 | $ 42,814 | $ 48,471 | $ 66,880 | $ 77,614 | $ 90,929 | $ 114,194 | $ 112,936 | $ 131,619 | |||||||||||
Accrued Liabilities, Current | $ 34,236 | $ 23,059 | 34,236 | 23,059 | ||||||||||||||||||||||
AbbVie | Discovery Agreement | Second Target | ||||||||||||||||||||||||||
License Agreement [Line Items] | ||||||||||||||||||||||||||
Additional sublicense fees | $ 800 | |||||||||||||||||||||||||
Milestone payment receivable | $ 10,000 | |||||||||||||||||||||||||
Bristol Myers Squibb Company | ||||||||||||||||||||||||||
License Agreement [Line Items] | ||||||||||||||||||||||||||
Upfront payment received | 297,000 | |||||||||||||||||||||||||
Milestone payment received | 297,000 | |||||||||||||||||||||||||
Bristol Myers Squibb Company | Collaboration and License Agreement | ||||||||||||||||||||||||||
License Agreement [Line Items] | ||||||||||||||||||||||||||
Milestone payment receivable | $ 10,000 | |||||||||||||||||||||||||
Sublicense fees | $ 800 | |||||||||||||||||||||||||
Bristol Myers Squibb Company | Collaborative Arrangement | ||||||||||||||||||||||||||
License Agreement [Line Items] | ||||||||||||||||||||||||||
Upfront payment received | $ 200,000 | $ 50,000 | $ 50,000 | |||||||||||||||||||||||
Milestone payment received | $ 12,000 | 10,000 | ||||||||||||||||||||||||
Astellas Pharma Inc. | Collaboration and License Agreement | ||||||||||||||||||||||||||
License Agreement [Line Items] | ||||||||||||||||||||||||||
Additional sublicense fees | $ 6,000 | |||||||||||||||||||||||||
Upfront payment received | $ 80,000 | 80,000 | ||||||||||||||||||||||||
AbbVie Ireland Unlimited Company | Discovery Agreement | ||||||||||||||||||||||||||
License Agreement [Line Items] | ||||||||||||||||||||||||||
Upfront payment received | $ 10,000 | |||||||||||||||||||||||||
AbbVie Ireland Unlimited Company | CD71 Agreement | ||||||||||||||||||||||||||
License Agreement [Line Items] | ||||||||||||||||||||||||||
Additional sublicense fees | 1,400 | |||||||||||||||||||||||||
Upfront payment received | $ 20,000 | 100,000 | ||||||||||||||||||||||||
Milestone payment received | $ 40,000 | 40,000 | 100,000 | |||||||||||||||||||||||
Immuno Gen Inc | Collaborative Arrangement | ||||||||||||||||||||||||||
License Agreement [Line Items] | ||||||||||||||||||||||||||
Research and development | $ 3,000 | |||||||||||||||||||||||||
Upfront license payment | 7,500 | |||||||||||||||||||||||||
UCSB | ||||||||||||||||||||||||||
License Agreement [Line Items] | ||||||||||||||||||||||||||
Common stock, shares issued | 150,000 | |||||||||||||||||||||||||
Fair value of common stock price per share | $ 10.68 | |||||||||||||||||||||||||
Payment of upfront fees | $ 1,000 | $ 1,000 | ||||||||||||||||||||||||
Annual license maintenance fees | $ 800 | $ 800 | ||||||||||||||||||||||||
License payment term | 2031 | |||||||||||||||||||||||||
Percentage of remaining maintenance fees outstanding | 50% | |||||||||||||||||||||||||
Fair value of common stock issued | $ 1,600 | |||||||||||||||||||||||||
Sublicense fees | $ 1,000 | $ 9,100 | $ 4,300 | |||||||||||||||||||||||
UCSB | Sublicense and Maintenance Fees | ||||||||||||||||||||||||||
License Agreement [Line Items] | ||||||||||||||||||||||||||
Research and development | $ 3,400 |
Commitments and Contingencies -
Commitments and Contingencies - Additional Information (Details) - Patent Infringement Lawsuit - USD ($) | 12 Months Ended | |
Mar. 04, 2020 | Dec. 31, 2021 | |
Loss Contingencies [Line Items] | ||
Lawsuit filed date | March 4, 2020 | |
Name of plaintiff | Vytacera Bio, LLC | |
Loss contingency, answer, affirmative defenses and counterclaims filing date | May 26, 2020 | |
Loss contingency, answer and counterclaims by plaintiff filing date | Jun. 05, 2020 | |
Loss contingency claim amount | $ 0 |
Leases - Additional Information
Leases - Additional Information (Details) - USD ($) $ in Thousands | 12 Months Ended | |||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | Dec. 31, 2015 | |
Operating Leased Assets [Line Items] | ||||
Restricted cash | $ 917 | $ 917 | $ 917 | |
Rent expense | 5,100 | 5,100 | $ 4,800 | |
Letter of Credit | ||||
Operating Leased Assets [Line Items] | ||||
Letter of credit outstanding, amount | 900 | |||
Restricted cash | $ 900 | $ 900 | ||
New Lease Agreement | ||||
Operating Leased Assets [Line Items] | ||||
Lease term description | The 2016 Lease has an initial term of ten years through 2026 and the Company has an option to extend the initial term for an additional five years at the then fair rental value as determined pursuant to the 2016 Lease. | |||
Initial lease term | 10 years | |||
Extended lease term | 5 years |
Leases - Summary of Supplementa
Leases - Summary of Supplemental Information Related to Leases (Details) - USD ($) $ in Thousands | 12 Months Ended | |
Dec. 31, 2021 | Dec. 31, 2020 | |
Cash paid for amounts included in the measurement of lease liabilities | ||
Operating cash flows from operating leases | $ 5,129 | $ 4,990 |
Supplemental balance sheet information related to leases: | ||
Operating lease right-of-use asset | 19,362 | 22,495 |
Current operating lease liabilities | $ 3,618 | $ 3,195 |
Operating Lease, Liability, Current, Statement of Financial Position [Extensible List] | Total current liabilities | Total current liabilities |
Non-current operating lease liabilities | $ 18,056 | $ 21,675 |
Total operating lease liabilities | $ 21,674 | $ 24,870 |
Weighted-average remaining lease term (in years) | ||
Operating lease | 4 years 9 months | 5 years 9 months |
Weighted-average discount rate | ||
Operating lease | 8.25% | 8.25% |
Leases - Schedule of Maturity o
Leases - Schedule of Maturity of Operating Lease Liabilities (Details) - USD ($) $ in Thousands | Dec. 31, 2021 | Dec. 31, 2020 |
Maturity of operating lease liabilities | ||
2022 | $ 5,273 | |
2023 | 5,420 | |
2024 | 5,572 | |
2025 | 5,729 | |
2026 and beyond | 4,387 | |
Total lease payments | 26,381 | |
Less imputed interest | (4,707) | |
Present value of lease liabilities | $ 21,674 | $ 24,870 |
Common Stock - Additional Infor
Common Stock - Additional Information (Details) - USD ($) | 1 Months Ended | 12 Months Ended | |||||
Feb. 28, 2021 | Jan. 31, 2021 | Dec. 31, 2020 | Feb. 29, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Class Of Stock [Line Items] | |||||||
Common stock, shares authorized | 150,000,000 | 150,000,000 | 150,000,000 | ||||
Common stock, par value | $ 0.00001 | $ 0.00001 | $ 0.00001 | ||||
Proceeds from issuance of common stock, net of issuance costs | $ 107,712,000 | $ 11,288,000 | $ 0 | ||||
Jefferies LLC | |||||||
Class Of Stock [Line Items] | |||||||
Common stock, par value | $ 0.00001 | ||||||
Issuance of common stock in follow-on offering, net of issuance costs, shares | 1,535,217 | ||||||
Proceeds from issuance of common stock, net of issuance costs | $ 11,300,000 | ||||||
Percentage of sales commission | 3% | ||||||
Average price | $ 7.62 | ||||||
Percentage of sales commission and issuance cost | 3% | 3% | |||||
Jefferies LLC | Maximum | |||||||
Class Of Stock [Line Items] | |||||||
Proceeds from issuance of common stock, net of issuance costs | $ 75,000,000 | ||||||
Underwritten Public Offering | |||||||
Class Of Stock [Line Items] | |||||||
Proceeds from issuance of common stock, net of issuance costs | $ 93,600,000 | ||||||
Underwriters | |||||||
Class Of Stock [Line Items] | |||||||
Proceeds from issuance of common stock, net of issuance costs | $ 14,100,000 | ||||||
Common Stock | |||||||
Class Of Stock [Line Items] | |||||||
Issuance of common stock in follow-on offering, net of issuance costs, shares | 16,428,571 | 1,535,217 | 150,000 | ||||
Common Stock | Underwritten Public Offering | |||||||
Class Of Stock [Line Items] | |||||||
Issuance of common stock in follow-on offering, net of issuance costs, shares | 14,285,714 | ||||||
Common stock price, per share | $ 7 | ||||||
Underwriting discounts and commissions and offering expenses | $ 900,000 | $ 6,400,000 | |||||
Common Stock | Underwriters | |||||||
Class Of Stock [Line Items] | |||||||
Issuance of common stock in follow-on offering, net of issuance costs, shares | 2,142,857 | ||||||
Period granted to underwriters to purchase additional shares | 30 days |
Stock-based Compensation - Addi
Stock-based Compensation - Additional Information (Details) - USD ($) $ / shares in Units, $ in Thousands | 1 Months Ended | 12 Months Ended | |||||
Jan. 01, 2016 | Oct. 31, 2021 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | Sep. 30, 2019 | Dec. 31, 2015 | |
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Stock option expiration period | 10 years | ||||||
Options granted generally vest period | 36 months | ||||||
Options granted generally vest percent | 2.08% | ||||||
Aggregate intrinsic value of stock options exercised | $ 2,200 | $ 4,400 | $ 900 | ||||
Weighted average grant date fair value, options granted | $ 3.97 | $ 3.94 | $ 7.03 | ||||
Unrecognized compensation expense, options granted | $ 23,600 | ||||||
Number of shares issued during period | 183,865 | 128,684 | |||||
Stock-based compensation expense | $ 13,167 | $ 14,786 | $ 19,100 | ||||
Share-based Payment Arrangement, Option [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Unrecognized stock-based compensation cost, period for recognition | 2 years 10 months 24 days | ||||||
Stock-based compensation expense | $ 13,100 | $ 14,700 | 18,900 | ||||
Employee Stock Purchase Plan [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Estimated fair value of the shares on the date of grant | 85% | ||||||
Common stock, capital shares reserved for future issuance | 1,751,818 | 1,935,683 | |||||
Unrecognized stock-based compensation cost, period for recognition | 5 months | ||||||
Plan maximum percentage of eligible compensation to purchase shares | 15% | ||||||
Stock-based compensation expense | $ 400 | $ 400 | 600 | ||||
Unrecognized stock-based compensation cost | 200 | ||||||
Non Employees [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Stock-based compensation expense | 100 | $ 100 | $ 200 | ||||
RSU's | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Unrecognized compensation expense, options granted | $ 2,100 | ||||||
Unrecognized stock-based compensation cost, period for recognition | 1 year 7 months 6 days | ||||||
Stock-based compensation expense | $ 200 | ||||||
RSU's Awarded | 439,000 | 874,000 | |||||
RSU's Awarded, Grant date fair value | $ 2,300 | $ 3,760 | |||||
Vesting rights, description | 50% of the RSUs granted will vest at the end of the first year of the grant date and the remaining 50% will vest at the end of the second year provided the grantee continues to provide services to the Company. | ||||||
PSU's | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
RSU's Awarded | 435,000 | ||||||
RSU's Awarded, Grant date fair value | $ 2,300 | ||||||
Vesting rights, description | 50% of the PSUs granted will vest within one year of the grant date upon achievement of certain specific milestones and the remaining 50% will vest within two years of the grant date upon achievement of additional company objectives. | ||||||
Share-based Payment Arrangement, Tranche Two [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Options granted generally vest percent | 2.08% | ||||||
Two Thousand Fifteen Stock Incentive Plan [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Stock option expiration period | 10 years | ||||||
Employees holding voting rights of all classes of stock, percentage | 10% | ||||||
Common stock, capital shares reserved for future issuance | 2,276,341 | 2,698,798 | 2,444,735 | ||||
Increase in number of shares available for issuance, as proportion of issued and outstanding shares of common stock, percentage | 4% | ||||||
Two Thousand Fifteen Stock Incentive Plan [Member] | Share-based Payment Arrangement, Tranche One [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Options granted generally vest period | 4 years | ||||||
Options granted generally vest percent | 25% | ||||||
Two Thousand Nineteen Stock Incentive Plan [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Common stock, capital shares reserved for future issuance | 486,234 | 204,600 | 1,815,000 | ||||
Increase in Common Stock Capital Shares Reserved For Future Issuance | 1,000,000 | ||||||
Early Exercise Of Employee Options [Member] | Share-based Payment Arrangement, Tranche One [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Options granted generally vest percent | 25% | ||||||
Minimum [Member] | Two Thousand Fifteen Stock Incentive Plan [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Estimated fair value of the shares on the date of grant | 110% | ||||||
Minimum [Member] | Two Thousand Nineteen Stock Incentive Plan [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Estimated fair value of the shares on the date of grant | 100% | ||||||
Maximum [Member] | Two Thousand Nineteen Stock Incentive Plan [Member] | |||||||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||||||
Stock option expiration period | 10 years |
Stock-based Compensation - Sche
Stock-based Compensation - Schedule of Activity Under Company's Stock Option Plans (Details) - USD ($) $ / shares in Units, $ in Thousands | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Number of Options | |||
Balances, beginning of the period | 10,929,530 | ||
Options granted | 5,178,897 | ||
Options exercised | (528,503) | ||
Options cancelled | (3,387,708) | ||
Balances, end of the period | 12,192,216 | 10,929,530 | |
Options Exercisable, end of the period | 6,054,635 | ||
Options Outstanding, Weighted-Average Exercise Price Per Share | |||
Balances, beginning of the period | $ 10.77 | ||
Options granted | 7.10 | ||
Options exercised | 2.70 | ||
Options cancelled | 11.26 | ||
Balances, end of the period | 9.42 | $ 10.77 | |
Options Exercisable, end of the period | $ 11.46 | ||
Options Outstanding, Weighted- Average Remaining Contractual Life (years) | |||
Balances, end of the period | 7 years 6 months | ||
Options Exercisable, end of the period | 6 years 1 month 6 days | ||
Aggregate Intrinsic Value | |||
Options exercised | $ 2,200 | $ 4,400 | $ 900 |
Balances at December 31, 2020 | 1,182 | ||
Options Exercisable—December 31, 2020 | $ 1,155 |
Stock-based Compensation - Sc_2
Stock-based Compensation - Schedule of Company's RSU Activities (Details) - RSU's - USD ($) $ / shares in Units, $ in Thousands | 1 Months Ended | 12 Months Ended |
Oct. 31, 2021 | Dec. 31, 2021 | |
Share-Based Compensation Arrangement by Share-Based Payment Award, Equity Instruments Other than Options, Nonvested, Number of Shares [Roll Forward] | ||
Balances, beginning of the period | 0 | |
RSU's Awarded | 439,000 | 874,000 |
RSU's Vested | 0 | |
RSU's Cancelled | (5,750) | |
Balances, end of the period | 868,250 | |
Weighted Average Remaining Contractual Life (years) | ||
Balances, end of the period | 1 year 3 months 21 days | |
Aggregate Intrinsic Value | ||
Balances, end of the period | $ 2,300 | $ 3,760 |
Weighted Average Grant Date Fair Value | ||
RSU's Awarded | $ 5.34 | |
RSU's Cancelled | 5.34 | |
Balances, end of the period | $ 5.34 |
Stock-based Compensation - Tota
Stock-based Compensation - Total Stock-based Compensation Recognized (Details) - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Stock-based compensation expense: | |||
Stock-based compensation expense | $ 13,167 | $ 14,786 | $ 19,100 |
Research and Development Expense [Member] | |||
Stock-based compensation expense: | |||
Stock-based compensation expense | 5,797 | 6,825 | 9,226 |
General and Administrative Expense [Member] | |||
Stock-based compensation expense: | |||
Stock-based compensation expense | $ 7,370 | $ 7,961 | $ 9,874 |
Stock-based Compensation - Sc_3
Stock-based Compensation - Schedule of Estimated Fair Value of Employee Stock Options and ESPP Using Black-Scholes Valuation Model (Details) | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Employee Stock Option | |||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||
Expected volatility, minimum | 69.60% | 64.40% | 64.40% |
Expected volatility, maximum | 74.80% | 73.30% | 68.60% |
Risk-free interest rate, minimum | 0.50% | 0.20% | 1.40% |
Risk-free interest rate, maximum | 1.30% | 1.30% | 2.50% |
Employee Stock Option | Minimum [Member] | |||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||
Dividend yield | 0% | 0% | 0% |
Expected term (in years) | 4 years 6 months | 4 years 8 months 12 days | 4 years 10 months 24 days |
Employee Stock Option | Maximum [Member] | |||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||
Expected term (in years) | 4 years 9 months 18 days | 4 years 10 months 24 days | 5 years |
Employee Stock Purchase Plan [Member] | |||
Share Based Compensation Arrangement By Share Based Payment Award [Line Items] | |||
Expected volatility, minimum | 46.87% | 47.30% | 60.80% |
Expected volatility, maximum | 69.58% | 122.10% | 71.90% |
Risk-free interest rate, minimum | 0.04% | 0.10% | 1.60% |
Risk-free interest rate, maximum | 0.10% | 0.20% | 2.40% |
Expected term (in years) | 6 months | 6 months | 6 months |
Income Taxes - Additional Infor
Income Taxes - Additional Information (Details) - USD ($) | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | ||||
Mar. 27, 2020 | Mar. 31, 2020 | Jun. 30, 2020 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | Dec. 31, 2017 | |
Income Tax Contingency [Line Items] | ||||||||
Net operating loss carryback | 5 years | |||||||
Percentage of taxable income from net operating losses for suspension of annual deduction limitation | 80% | |||||||
Deferred tax asset, net change in total valuation allowance increase during period | $ 24,800 | $ 3,900,000 | $ 29,100,000 | |||||
Unrecognized tax benefits would affect company's effective tax rate | 0 | 0 | 900,000 | |||||
Income tax expense (benefit) | $ 13,911,000 | $ 13,911,000 | $ 13,911,000 | 0 | 13,911,000 | 427,000 | ||
Interest and penalties accrued | 0 | $ 0 | $ 0 | |||||
Minimum | ||||||||
Income Tax Contingency [Line Items] | ||||||||
Percentage of change in ownership | 50% | |||||||
Federal | ||||||||
Income Tax Contingency [Line Items] | ||||||||
Net operating loss carryforwards | $ 225,500,000 | |||||||
Operating loss carryforwards expiration year | 2034 | |||||||
Operating loss carryforwards to expire if not utilized | $ 65,600,000 | |||||||
Operating loss carryforwards not subject to expiration | $ 159,900,000 | |||||||
Open tax year | 2010 2011 2012 2013 2014 2015 2016 2017 2018 | |||||||
Federal | Research and Development Tax Credits | ||||||||
Income Tax Contingency [Line Items] | ||||||||
Tax credit carry forwards | $ 19,100,000 | |||||||
Tax credit carryforward, expiration | 2031 | |||||||
State | ||||||||
Income Tax Contingency [Line Items] | ||||||||
Net operating loss carryforwards | $ 24,200,000 | |||||||
Operating loss carryforwards expiration year | 2032 | |||||||
Open tax year | 2010 2011 2012 2013 2014 2015 2016 2017 2018 | |||||||
State | Research and Development Tax Credits | ||||||||
Income Tax Contingency [Line Items] | ||||||||
Tax credit carry forwards | $ 11,200,000 |
Income Taxes - Schedule of Comp
Income Taxes - Schedule of Components of Benefit from Income Taxes (Details) - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | ||
Mar. 31, 2020 | Jun. 30, 2020 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Current: | ||||||
Federal | $ 0 | $ (13,912) | $ (390) | |||
State | 0 | 1 | ||||
Total current | 0 | (13,911) | (390) | |||
Deferred: | ||||||
Federal | 0 | (37) | ||||
State | 0 | |||||
Total deferred | 0 | (37) | ||||
Benefit from income taxes | $ (13,911) | $ (13,911) | $ (13,911) | $ 0 | $ (13,911) | $ (427) |
Income Taxes - Schedule of Effe
Income Taxes - Schedule of Effective Tax Rate Reconciliation (Details) | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Effective Income Tax Rate Reconciliation, Percent [Abstract] | |||
U.S. federal taxes at statutory rate | 21% | 21% | 21% |
State tax, net of federal benefit | 1.50% | 2% | 1% |
Stock compensation | (3.10%) | (1.30%) | (1.00%) |
Tax credits | 2% | 6.60% | 1.90% |
Change in valuation allowance | (21.40%) | (27.10%) | (22.30%) |
Net operating loss carryback | 0% | 16.60% | 0% |
Return to provision adjustment | 0% | 0% | (0.20%) |
Other | 0% | (0.10%) | (0.10%) |
Total | 0% | 17.70% | 0.30% |
Income Taxes - Schedule of Defe
Income Taxes - Schedule of Deferred Income Tax Assets and Liabilities (Details) - USD ($) $ in Thousands | Dec. 31, 2021 | Dec. 31, 2020 |
Components of Deferred Tax Assets and Liabilities [Abstract] | ||
Net operating loss carryforwards | $ 49,070 | $ 38,485 |
Research and development credits | 20,809 | 16,803 |
Lease liability | 4,555 | 5,223 |
Intangible assets | 3,804 | 3,923 |
Deferred revenue | 60,285 | 49,537 |
Accrued liabilities | 1,933 | 1,512 |
Stock-based compensation | 7,480 | 8,578 |
Other | 29 | 20 |
Total gross deferred income tax assets | 147,965 | 124,081 |
Less: valuation allowance | (143,355) | (118,539) |
Deferred tax assets, net of valuation allowance | 4,610 | 5,542 |
Fixed assets | (253) | (433) |
Right-of-use assets | (4,069) | (4,724) |
Prepaid expenses | (288) | (385) |
Deferred tax liabilities | (4,610) | (5,542) |
Net deferred income tax liabilities | $ 0 | $ 0 |
Income Taxes- Schedule of Recon
Income Taxes- Schedule of Reconciliation of Unrecognized Tax Benefits (Details) - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Reconciliation of Unrecognized Tax Benefits, Excluding Amounts Pertaining to Examined Tax Returns [Roll Forward] | |||
Balance at the beginning of the year | $ 6,454 | $ 5,249 | $ 3,756 |
Additions based on tax positions related to current year | 1,326 | 1,205 | 1,403 |
Adjustment based on tax positions related to prior years | 0 | 90 | |
Balance at end of the year | $ 7,780 | $ 6,454 | $ 5,249 |
Defined Contribution Plan - Add
Defined Contribution Plan - Additional Information (Details) - USD ($) $ in Millions | 12 Months Ended | ||
Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Retirement Benefits [Abstract] | |||
Company contributions to defined contribution plan | $ 0.9 | $ 0.8 | $ 0.8 |
Selected Quarterly Financial _3
Selected Quarterly Financial Data (Unaudited) Condensed Balance Sheets (Details) - USD ($) $ in Thousands | Dec. 31, 2021 | Sep. 30, 2021 | Jun. 30, 2021 | Mar. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | Dec. 31, 2018 |
Deferred revenues, current portion | $ 40,816 | $ 40,844 | $ 39,314 | $ 43,517 | $ 42,056 | ||
Total current liabilities | 77,870 | 67,527 | 60,322 | 64,930 | 68,111 | ||
Deferred revenue, net of current portion | 243,944 | 254,257 | 264,088 | 267,750 | 276,651 | ||
Total liabilities | 339,870 | 340,801 | 344,331 | 353,487 | 366,437 | ||
Accumulated deficit | (623,562) | (588,738) | (557,756) | (531,020) | (507,692) | $ (442,872) | |
Total stockholders' equity (deficit) | (459) | 30,432 | 58,109 | 80,671 | (7,774) | 25,471 | $ 135,828 |
Total liabilities and stockholders' equity (deficit) | 339,411 | 371,233 | 402,440 | 434,158 | 358,663 | ||
Previously Reported | |||||||
Deferred revenues, current portion | 69,262 | 73,089 | 72,369 | 76,636 | 74,869 | ||
Total current liabilities | 106,316 | 99,772 | 93,377 | 98,049 | 100,924 | ||
Deferred revenue, net of current portion | 125,660 | 140,770 | 158,189 | 169,280 | 186,261 | ||
Total liabilities | 250,032 | 259,559 | 271,487 | 288,136 | 308,860 | ||
Accumulated deficit | (533,724) | (507,496) | (484,912) | (465,669) | (450,115) | (417,230) | |
Total stockholders' equity (deficit) | 89,379 | 111,674 | 130,953 | 146,022 | 49,803 | 51,113 | |
Total liabilities and stockholders' equity (deficit) | 339,411 | 371,233 | 402,440 | 434,158 | 358,663 | ||
Restatement Adjustment | |||||||
Deferred revenues, current portion | (28,446) | (32,245) | (33,055) | (33,119) | (32,813) | ||
Total current liabilities | (28,446) | (32,245) | (33,055) | (33,119) | (32,813) | ||
Deferred revenue, net of current portion | 118,284 | 113,487 | 105,899 | 98,470 | 90,390 | ||
Total liabilities | 89,838 | 81,242 | 72,844 | 65,351 | 57,577 | ||
Accumulated deficit | (89,838) | (81,242) | (72,844) | (65,351) | (57,577) | (25,642) | |
Total stockholders' equity (deficit) | (89,838) | (81,242) | (72,844) | (65,351) | (57,577) | $ (25,642) | |
Total liabilities and stockholders' equity (deficit) | $ 0 | $ 0 | $ 0 | $ 0 | $ 0 |
Selected Quarterly Financial _4
Selected Quarterly Financial Data (Unaudited) Condensed Statements of Operations (Details) - USD ($) $ / shares in Units, $ in Thousands | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||||||||
Dec. 31, 2021 | Sep. 30, 2021 | Jun. 30, 2021 | Mar. 31, 2021 | Dec. 31, 2020 | Sep. 30, 2020 | Jun. 30, 2020 | Mar. 31, 2020 | Jun. 30, 2021 | Jun. 30, 2020 | Sep. 30, 2021 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Revenue | $ 11,132 | $ 9,189 | $ 8,795 | $ 8,197 | $ 7,078 | $ 7,466 | $ 6,988 | $ 46,895 | $ 16,992 | $ 53,883 | $ 26,181 | $ 61,349 | $ 37,312 | $ 68,427 | $ 26,902 |
Operating expenses: | |||||||||||||||
Research and development | 36,580 | 29,143 | 26,100 | 22,371 | 22,007 | 24,049 | 24,066 | 42,814 | 48,471 | 66,880 | 77,614 | 90,929 | 114,194 | 112,936 | 131,619 |
General and administrative | 9,455 | 11,085 | 9,393 | 9,227 | 9,145 | 8,634 | 8,680 | 9,572 | 18,620 | 18,252 | 29,705 | 26,886 | 39,160 | 36,031 | 36,765 |
Total operating expenses | 46,035 | 40,228 | 35,493 | 31,598 | 31,152 | 32,683 | 32,746 | 52,386 | 67,091 | 85,132 | 107,319 | 117,815 | 153,354 | 148,967 | 168,384 |
Loss from operations | (34,903) | (31,039) | (26,698) | (23,401) | (24,074) | (25,217) | (25,758) | (5,491) | (50,099) | (31,249) | (81,138) | (56,466) | (116,042) | (80,540) | (141,482) |
Interest income | 73 | 70 | 44 | 68 | 107 | 200 | 454 | 1,075 | 112 | 1,529 | 182 | 1,729 | 255 | 1,836 | 8,365 |
Other income (expense) | 7 | (13) | (82) | 5 | (29) | (15) | 5 | 12 | (77) | 17 | (90) | 2 | (83) | (27) | (135) |
Loss before income taxes | (34,823) | (30,982) | (26,736) | (23,328) | (23,996) | (25,032) | (25,299) | (4,404) | (50,064) | (29,703) | (81,046) | (54,735) | (115,870) | (78,731) | (133,252) |
Loss/(Benefit) from income taxes | (13,911) | (13,911) | (13,911) | 0 | (13,911) | (427) | |||||||||
Net income (loss) | (34,823) | (30,982) | (26,736) | (23,328) | (23,996) | (25,032) | (25,299) | 9,507 | (50,064) | (15,792) | (81,046) | (40,824) | (115,870) | (64,820) | (132,825) |
Other comprehensive income (loss): | |||||||||||||||
Unrealized gain / (loss) on investments, net of tax | (294) | 37 | 58 | 4 | (63) | (320) | 279 | 62 | (41) | 99 | (104) | (195) | (104) | 139 | |
Comprehensive income (loss) | $ (35,117) | $ (30,945) | $ (26,678) | $ (23,324) | $ (23,996) | $ (25,095) | $ (25,619) | $ 9,786 | $ (50,002) | $ (15,833) | $ (80,947) | $ (40,928) | $ (116,065) | $ (64,924) | $ (132,675) |
Net income (loss) per share | |||||||||||||||
Basic | $ (0.53) | $ (0.48) | $ (0.41) | $ (0.38) | $ (0.51) | $ (0.54) | $ (0.55) | $ 0.21 | $ (0.79) | $ (0.34) | $ (1.27) | $ (0.89) | $ (1.81) | $ (1.40) | $ (2.93) |
Diluted | $ (0.53) | $ (0.48) | $ (0.41) | $ (0.38) | $ (0.51) | $ (0.54) | $ (0.55) | $ 0.20 | $ (0.79) | $ (0.34) | $ (1.27) | $ (0.89) | $ (1.81) | $ (1.40) | $ (2.93) |
Shares used to compute net loss per share | |||||||||||||||
Basic | 65,295,995 | 65,208,066 | 65,055,998 | 60,968,111 | 46,600,605 | 46,195,121 | 46,057,063 | 45,723,955 | 63,023,349 | 45,890,510 | 63,759,585 | 45,992,786 | 64,146,848 | 46,145,563 | 45,335,927 |
Diluted | 65,295,995 | 65,208,066 | 65,055,998 | 60,968,111 | 46,600,605 | 46,195,121 | 46,057,063 | 47,044,774 | 63,023,349 | 45,890,510 | 63,759,585 | 45,992,786 | 64,146,848 | 46,145,563 | 45,335,927 |
AbbVie | |||||||||||||||
Revenue | $ 5,051 | $ 2,277 | $ 2,734 | $ 1,486 | $ 1,909 | $ 3,243 | $ 353 | $ 34,358 | $ 4,220 | $ 34,711 | $ 6,497 | $ 37,954 | |||
Amgen | |||||||||||||||
Revenue | 1,876 | 2,352 | 1,715 | 2,546 | 1,584 | 1,548 | 3,621 | 1,769 | 4,261 | 5,390 | 6,613 | 6,938 | |||
Astellas | |||||||||||||||
Revenue | 4,205 | 4,560 | 4,346 | 4,165 | 3,585 | 2,675 | 1,023 | 49 | 8,511 | 1,072 | 13,071 | 3,747 | |||
Bristol Myers Squibb Company [Member] | |||||||||||||||
Revenue | 0 | 0 | 0 | 1,991 | 10,719 | 0 | 12,710 | 12,710 | |||||||
Previously Reported | |||||||||||||||
Revenue | 19,727 | 17,587 | 16,288 | 15,971 | 16,373 | 17,788 | 16,608 | 49,593 | 32,259 | 66,201 | 49,846 | 83,989 | $ 69,573 | $ 100,362 | $ 57,489 |
Operating expenses: | |||||||||||||||
Research and development | 36,580 | 29,143 | 26,100 | 22,371 | 22,007 | 24,049 | 24,066 | 42,814 | 48,471 | 66,880 | 77,614 | 90,929 | 114,194 | 112,936 | 131,619 |
General and administrative | 9,455 | 11,085 | 9,393 | 9,227 | 9,145 | 8,634 | 8,680 | 9,572 | 18,620 | 18,252 | 29,705 | 26,886 | 39,160 | 36,031 | 36,765 |
Total operating expenses | 46,035 | 40,228 | 35,493 | 31,598 | 31,152 | 32,683 | 32,746 | 52,386 | 67,091 | 85,132 | 107,319 | 117,815 | 153,354 | 148,967 | 168,384 |
Loss from operations | (26,308) | (22,641) | (19,205) | (15,627) | (14,779) | (14,895) | (16,138) | (2,793) | (34,832) | (18,931) | (57,473) | (33,826) | (83,781) | (48,605) | (110,895) |
Interest income | 73 | 70 | 44 | 68 | 107 | 200 | 454 | 1,075 | 112 | 1,529 | 182 | 1,729 | 255 | 1,836 | 8,365 |
Other income (expense) | 7 | (13) | (82) | 5 | (29) | (15) | 5 | 12 | (77) | 17 | (90) | 2 | (83) | (27) | (135) |
Loss before income taxes | (26,228) | (22,584) | (19,243) | (15,554) | (14,701) | (14,710) | (15,679) | (1,706) | (34,797) | (17,385) | (57,381) | (32,095) | (83,609) | (46,796) | (102,665) |
Loss/(Benefit) from income taxes | (13,911) | (13,911) | (13,911) | 0 | (13,911) | (427) | |||||||||
Net income (loss) | (26,228) | (22,584) | (19,243) | (15,554) | (14,701) | (14,710) | (15,679) | 12,205 | (34,797) | (3,474) | (57,381) | (18,184) | (83,609) | (32,885) | (102,238) |
Other comprehensive income (loss): | |||||||||||||||
Unrealized gain / (loss) on investments, net of tax | (294) | 37 | 58 | 4 | (63) | (320) | 279 | 62 | (41) | 99 | (104) | (195) | (104) | 139 | |
Comprehensive income (loss) | $ (26,522) | $ (22,547) | $ (19,185) | $ (15,550) | $ (14,701) | $ (14,773) | $ (15,999) | $ 12,484 | $ (34,735) | $ (3,515) | $ (57,282) | $ (18,288) | $ (83,804) | $ (32,989) | $ (102,088) |
Net income (loss) per share | |||||||||||||||
Basic | $ (0.40) | $ (0.35) | $ (0.30) | $ (0.26) | $ (0.32) | $ (0.32) | $ (0.34) | $ 0.27 | $ (0.55) | $ (0.08) | $ (0.90) | $ (0.40) | $ (1.30) | $ (0.71) | $ (2.26) |
Diluted | $ (0.40) | $ (0.35) | $ (0.30) | $ (0.26) | $ (0.32) | $ (0.32) | $ (0.34) | $ 0.26 | $ (0.55) | $ (0.08) | $ (0.90) | $ (0.40) | $ (1.30) | $ (0.71) | $ (2.26) |
Shares used to compute net loss per share | |||||||||||||||
Basic | 65,295,995 | 65,208,066 | 65,055,998 | 60,968,111 | 46,600,605 | 46,195,121 | 46,057,063 | 45,723,955 | 63,023,349 | 45,890,510 | 63,759,585 | 45,992,786 | 64,146,848 | 46,145,563 | 45,335,927 |
Diluted | 65,295,995 | 65,208,066 | 65,055,998 | 60,968,111 | 46,600,605 | 46,195,121 | 46,057,063 | 47,044,774 | 63,023,349 | 45,890,510 | 63,759,585 | 45,992,786 | 64,146,848 | 46,145,563 | 45,335,927 |
Previously Reported | AbbVie | |||||||||||||||
Revenue | $ 5,672 | $ 2,867 | $ 2,078 | $ 1,228 | $ 2,568 | $ 4,209 | $ 1,319 | $ 30,096 | $ 3,306 | $ 31,415 | $ 6,173 | $ 35,624 | |||
Previously Reported | Amgen | |||||||||||||||
Revenue | 1,860 | 2,428 | 1,874 | 2,582 | 1,602 | 1,633 | 3,678 | 1,695 | 4,456 | 5,373 | 6,884 | 7,006 | |||
Previously Reported | Astellas | |||||||||||||||
Revenue | 4,791 | 4,887 | 4,931 | 4,756 | 4,798 | 4,543 | 4,204 | 387 | 9,687 | 4,591 | 14,574 | 9,134 | |||
Previously Reported | Bristol Myers Squibb Company [Member] | |||||||||||||||
Revenue | 7,404 | 7,405 | 7,405 | 7,405 | 7,405 | 7,403 | 7,407 | 17,415 | 14,810 | 24,822 | 22,215 | 32,225 | |||
Restatement Adjustment | |||||||||||||||
Revenue | (8,595) | (8,398) | (7,493) | (7,774) | (9,295) | (10,322) | (9,620) | (2,698) | (15,267) | (12,318) | (23,665) | (22,640) | $ (32,261) | $ (31,935) | $ (30,587) |
Operating expenses: | |||||||||||||||
Research and development | 0 | ||||||||||||||
General and administrative | 0 | ||||||||||||||
Total operating expenses | 0 | 0 | 0 | 0 | |||||||||||
Loss from operations | (8,595) | (8,398) | (7,493) | (7,774) | (9,295) | (10,322) | (9,620) | (2,698) | (15,267) | (12,318) | (23,665) | (22,640) | (32,261) | (31,935) | (30,587) |
Interest income | |||||||||||||||
Other income (expense) | |||||||||||||||
Loss before income taxes | (8,595) | (8,398) | (7,493) | (7,774) | (9,295) | (10,322) | (9,620) | (2,698) | (15,267) | (12,318) | (23,665) | (22,640) | (32,261) | (31,935) | (30,587) |
Net income (loss) | (8,595) | (8,398) | (7,493) | (7,774) | (9,295) | (10,322) | (9,620) | (2,698) | (15,267) | (12,318) | (23,665) | (22,640) | (32,261) | (31,935) | (30,587) |
Other comprehensive income (loss): | |||||||||||||||
Unrealized gain / (loss) on investments, net of tax | |||||||||||||||
Comprehensive income (loss) | (8,595) | (8,398) | (7,493) | (7,774) | (9,295) | (10,322) | (9,620) | (2,698) | (15,267) | (12,318) | (23,665) | (22,640) | $ (32,261) | $ (31,935) | $ (30,587) |
Restatement Adjustment | AbbVie | |||||||||||||||
Revenue | (621) | (590) | 656 | 258 | (659) | (966) | (966) | 4,262 | 914 | 3,296 | 324 | 2,330 | |||
Restatement Adjustment | Amgen | |||||||||||||||
Revenue | 16 | (76) | (159) | (36) | (18) | (85) | (57) | 74 | (195) | 17 | (271) | (68) | |||
Restatement Adjustment | Astellas | |||||||||||||||
Revenue | (586) | (327) | (585) | (591) | (1,213) | (1,868) | (3,181) | (338) | (1,176) | (3,519) | (1,503) | (5,387) | |||
Restatement Adjustment | Bristol Myers Squibb Company [Member] | |||||||||||||||
Revenue | $ (7,404) | $ (7,405) | $ (7,405) | $ (7,405) | $ (7,405) | $ (7,403) | $ (5,416) | $ (6,696) | $ (14,810) | $ (12,112) | $ (22,215) | $ (19,515) |
Selected Quarterly Financial _5
Selected Quarterly Financial Data (Unaudited) Condensed Statements of Cash Flow (Details) - USD ($) $ in Thousands | 3 Months Ended | 6 Months Ended | 9 Months Ended | 12 Months Ended | |||||
Mar. 31, 2021 | Mar. 31, 2020 | Jun. 30, 2021 | Jun. 30, 2020 | Sep. 30, 2021 | Sep. 30, 2020 | Dec. 31, 2021 | Dec. 31, 2020 | Dec. 31, 2019 | |
Net loss | $ (23,328) | $ 9,507 | $ (50,064) | $ (15,792) | $ (81,046) | $ (40,824) | $ (115,870) | $ (64,820) | $ (132,825) |
Deferred revenue | (7,440) | 83,114 | (15,305) | 76,332 | (23,606) | 69,406 | (33,948) | 62,826 | (17,154) |
Net cash used in operating activities | (29,940) | (49,737) | (58,139) | 47,364 | (87,839) | 22,686 | (119,031) | 5,259 | (140,480) |
Previously Reported | |||||||||
Net loss | (15,554) | 12,205 | (34,797) | (3,474) | (57,381) | (18,184) | (83,609) | (32,885) | (102,238) |
Deferred revenue | (15,214) | 80,416 | (30,572) | 64,014 | (47,271) | 46,766 | (66,209) | 30,891 | (47,741) |
Net cash used in operating activities | (29,940) | (49,737) | (58,139) | 47,364 | (87,839) | 22,686 | (119,031) | 5,259 | (140,480) |
Restatement Adjustment | |||||||||
Net loss | (7,774) | (2,698) | (15,267) | (12,318) | (23,665) | (22,640) | (32,261) | (31,935) | (30,587) |
Deferred revenue | $ 7,774 | $ 2,698 | $ 15,267 | $ 12,318 | $ 23,665 | $ 22,640 | 32,261 | 31,935 | 30,587 |
Net cash used in operating activities | $ 0 | $ 0 | $ 0 |