Document and Entity Information
Document and Entity Information - shares | 3 Months Ended | |
Mar. 31, 2018 | Apr. 30, 2018 | |
Document And Entity Information [Abstract] | ||
Entity Registrant Name | AGIOS PHARMACEUTICALS INC | |
Trading Symbol | AGIO | |
Entity Central Index Key | 1,439,222 | |
Current Fiscal Year End Date | --12-31 | |
Entity Filer Category | Large Accelerated Filer | |
Document Type | 10-Q | |
Document Period End Date | Mar. 31, 2018 | |
Document Fiscal Year Focus | 2,018 | |
Document Fiscal Period Focus | Q1 | |
Amendment Flag | false | |
Entity Common Stock, Shares Outstanding | 57,605,621 |
Condensed Consolidated Balance
Condensed Consolidated Balance Sheets - USD ($) $ in Thousands | Mar. 31, 2018 | Dec. 31, 2017 |
Current assets: | ||
Cash and cash equivalents | $ 364,469 | $ 102,724 |
Marketable securities | 417,981 | 321,212 |
Collaboration receivable – related party | 3,512 | 2,448 |
Royalty receivable – related party | 1,417 | 1,222 |
Prepaid expenses and other current assets | 15,614 | 17,655 |
Total current assets | 802,993 | 445,261 |
Marketable securities | 212,297 | 143,814 |
Property and equipment, net | 23,732 | 24,431 |
Other non-current assets | 1,104 | 891 |
Total assets | 1,040,126 | 614,397 |
Current liabilities: | ||
Accounts payable | 17,932 | 22,767 |
Accrued expenses | 17,005 | 34,031 |
Deferred revenue – related party | 39,212 | 37,842 |
Deferred rent | 550 | 301 |
Total current liabilities | 74,699 | 94,941 |
Deferred revenue, net of current portion – related party | 81,831 | 125,798 |
Deferred rent, net of current portion | 18,002 | 18,155 |
Total liabilities | 174,532 | 238,894 |
Stockholders’ equity: | ||
Preferred stock, $0.001 par value; 25,000,000 shares authorized; no shares issued or outstanding at March 31, 2018 and December 31, 2017 | 0 | 0 |
Common stock, $0.001 par value; 125,000,000 shares authorized; 57,541,613 and 48,826,153 shares issued and outstanding at March 31, 2018 and December 31, 2017, respectively | 58 | 49 |
Additional paid-in capital | 1,717,609 | 1,174,904 |
Accumulated other comprehensive loss | (2,643) | (1,389) |
Accumulated deficit | (849,430) | (798,061) |
Total stockholders’ equity | 865,594 | 375,503 |
Total liabilities and stockholders’ equity | $ 1,040,126 | $ 614,397 |
Condensed Consolidated Balance3
Condensed Consolidated Balance Sheets (Parenthetical) - $ / shares | Mar. 31, 2018 | Dec. 31, 2017 |
Statement of Financial Position [Abstract] | ||
Preferred stock, par value (in usd per share) | $ 0.001 | $ 0.001 |
Preferred stock, shares authorized (in shares) | 25,000,000 | 25,000,000 |
Preferred stock, shares issued (in shares) | 0 | 0 |
Preferred stock, shares outstanding (in shares) | 0 | 0 |
Common stock, par value (in usd per share) | $ 0.001 | $ 0.001 |
Common stock, shares authorized (in shares) | 125,000,000 | 125,000,000 |
Common stock, shares issued (in shares) | 57,541,613 | 48,826,153 |
Common stock, shares outstanding (in shares) | 57,541,613 | 48,826,153 |
Condensed Consolidated Statemen
Condensed Consolidated Statements of Operations - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Income Statement [Abstract] | ||
Collaboration revenue – related party | $ 7,345 | $ 10,508 |
Royalty revenue – related party | 1,417 | 0 |
Total revenue | 8,762 | 10,508 |
Operating expenses: | ||
Research and development (net of $2,776 and $8,794 of cost reimbursement from related party for the three months ended March 31, 2017 and 2016, respectively) | 78,224 | 62,732 |
General and administrative | 24,550 | 14,823 |
Total operating expenses | 102,774 | 77,555 |
Loss from operations | (94,012) | (67,047) |
Interest income | 3,187 | 881 |
Net loss | $ (90,825) | $ (66,166) |
Net loss per share – basic and diluted (usd per share) | $ (1.63) | $ (1.56) |
Weighted-average number of common shares used in computing net loss per share – basic and diluted (in shares) | 55,694,603 | 42,280,525 |
Condensed Consolidated Stateme5
Condensed Consolidated Statements of Operations (Parenthetical) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Income Statement [Abstract] | ||
Reduction of research and development expenses | $ 0 | $ 2,776 |
Condensed Consolidated Stateme6
Condensed Consolidated Statements of Comprehensive Loss - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Statement of Comprehensive Income [Abstract] | ||
Net loss | $ (90,825) | $ (66,166) |
Other comprehensive (loss) income | ||
Unrealized (loss) gain on available-for-sale securities | (1,254) | 101 |
Comprehensive loss | $ (92,079) | $ (66,065) |
Condensed Consolidated Stateme7
Condensed Consolidated Statements of Cash Flows - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Operating activities | ||
Net loss | $ (90,825) | $ (66,166) |
Adjustments to reconcile net loss to net cash used in operating activities: | ||
Depreciation | 1,725 | 1,591 |
Stock-based compensation expense | 14,522 | 10,734 |
Net amortization of premium and discounts on investments | (406) | 163 |
Loss on disposal of property and equipment | 0 | 40 |
Changes in operating assets and liabilities: | ||
Collaboration receivable – related party | (1,064) | (6,379) |
Royalty receivable – related party | (195) | 0 |
Tenant improvement and other receivables | 0 | (24) |
Prepaid expenses and other current and non-current assets | 1,901 | (3,425) |
Accounts payable | (4,469) | (994) |
Accrued expenses | (17,144) | (6,889) |
Deferred revenue – related party | (3,141) | (1,924) |
Deferred rent | 96 | (801) |
Net cash used in operating activities | (99,000) | (74,074) |
Investing activities | ||
Purchases of marketable securities | (330,971) | (26,740) |
Proceeds from maturities and sales of marketable securities | 164,871 | 136,585 |
Purchases of property and equipment | (1,432) | (293) |
Net cash (used in) provided by investing activities | (167,532) | 109,552 |
Financing activities | ||
Payment of public offering costs, net of reimbursements | (188) | (100) |
Proceeds from public offering of common stock, net of commissions | 516,206 | 0 |
Net proceeds from stock option exercises and employee stock purchase plan | 12,259 | 4,146 |
Net cash provided by financing activities | 528,277 | 4,046 |
Net change in cash and cash equivalents | 261,745 | 39,524 |
Cash and cash equivalents at beginning of the period | 102,724 | 160,754 |
Cash and cash equivalents at end of the period | 364,469 | 200,278 |
Supplemental disclosure of non-cash investing and financing transactions | ||
Additions to property and equipment in accounts payable and accrued expenses | 605 | 213 |
Proceeds from stock option exercises in other current assets | 73 | 6 |
Public offering costs in accounts payable and accrued expenses | 0 | 329 |
Public offering costs in accounts payable and accrued expenses | $ 158 | $ 0 |
Overview and Basis of Presentat
Overview and Basis of Presentation | 3 Months Ended |
Mar. 31, 2018 | |
Organization, Consolidation and Presentation of Financial Statements [Abstract] | |
Overview and Basis of Presentation | Overview and Basis of Presentation References to Agios Throughout this Quarterly Report on Form 10-Q, “we,” “us,” and “our,” and similar expressions, except where the context requires otherwise, refer to Agios Pharmaceuticals, Inc. and its consolidated subsidiaries, and “our Board of Directors” refers to the board of directors of Agios Pharmaceuticals, Inc. Overview We are a biopharmaceutical company committed to the fundamental transformation of patients’ lives through scientific leadership in the field of cellular metabolism, with the goal of making transformative, first- or best-in-class medicines. Our therapeutic areas of focus are cancer and rare genetic diseases, or RGDs, which are diseases that are directly caused by changes in genes or chromosomes, often passed from one generation to the next. Most RGDs are often associated with severe or life-threatening features. The incidence of a single RGD can vary widely but is generally very infrequent, usually equal to or less than one per 100,000 births. In both areas of cancer and RGDs, we are seeking to unlock the biology of cellular metabolism as a platform to create transformative therapies. We are located in Cambridge, Massachusetts. Basis of presentation The condensed consolidated balance sheet as of March 31, 2018 , and the condensed consolidated statements of operations, comprehensive loss, and cash flows for the three months ended March 31, 2018 and 2017 are unaudited. The unaudited condensed consolidated financial statements have been prepared on the same basis as the annual financial statements and, in the opinion of our management, reflect all adjustments, which include only normal recurring adjustments, necessary to fairly state our financial position as of March 31, 2018 , and our results of operations and cash flows for the three months ended March 31, 2018 and 2017 . The financial data and the other financial information disclosed in these notes to the condensed consolidated financial statements related to the three -month period are also unaudited. The results of operations for the three months ended March 31, 2018 are not necessarily indicative of the results to be expected for the year ending December 31, 2018 or for any other future annual or interim period. The year-end condensed consolidated balance sheet data was derived from our audited financial statements, but does not include all disclosures required by U.S. generally accepted accounting principles, or U.S. GAAP. Accordingly, the condensed consolidated interim financial statements should be read in conjunction with the audited consolidated financial statements and notes thereto included in our Annual Report on Form 10-K for the year ended December 31, 2017 that was filed with the Securities and Exchange Commission, or the SEC, on February 14, 2018 . Our consolidated financial statements include our accounts and the accounts of our wholly owned subsidiaries, Agios Securities Corporation, Agios International Sarl, and Agios Limited. All intercompany transactions have been eliminated in consolidation. The consolidated financial statements have been prepared in conformity with U.S. GAAP. Liquidity In January 2018 , we completed a public offering of 7,089,553 shares of common stock at an offering price of $67.00 per share. We received net proceeds from this offering of $448.9 million , after deducting underwriting discounts and commissions paid by us. In addition, we granted the underwriters the right to purchase up to an additional 1,063,433 shares of common stock, which was exercised in January 2018 , resulting in additional net proceeds to us of $67.3 million , after underwriting discounts and commissions. After giving effect to the full exercise of the over-allotment option, the number of shares sold by us in the public offering totaled 8,152,986 shares, and net proceeds to us totaled $516.2 million , after underwriting discounts and commissions. As of March 31, 2018 , we had cash, cash equivalents and marketable securities of $994.7 million . Although we have incurred recurring losses and expect to continue to incur losses for the foreseeable future, we expect our cash, cash equivalents and marketable securities will be sufficient to fund current operations for at least the next twelve months from the issuance date of these financial statements. |
Summary of Significant Accounti
Summary of Significant Accounting Policies and Recent Accounting Pronouncements | 3 Months Ended |
Mar. 31, 2018 | |
Accounting Policies [Abstract] | |
Summary of Significant Accounting Policies and Recent Accounting Pronouncements | Summary of Significant Accounting Policies and Recent Accounting Pronouncements Significant accounting policies Revenue from Contracts with Customers In May 2014, the Financial Accounting Standards Board, or FASB, issued ASU No. 2014-09, Revenue from Contracts with Customers (Topic 606) , or ASU 2014-09. ASU 2014-09 was codified as Accounting Standards Codification, or ASC, 606, Revenue from Contracts with Customers , or ASC 606. Subsequently, the FASB issued ASU 2015-14, Revenue from Contracts with Customers (Topic 606) , which adjusted the effective date of ASU 2014-09; ASU No. 2016-08, Revenue from Contracts with Customers (Topic 606): Principal versus Agent Considerations (Reporting Revenue Gross versus Net) , which amends the principal-versus-agent implementation guidance and illustrations in ASU 2014-09; ASU No. 2016-10, Revenue from Contracts with Customers (Topic 606): Identifying Performance Obligations and Licensing, which clarifies identifying performance obligations and licensing implementation guidance and illustrations in ASU 2014-09; ASU No. 2016-12, Revenue from Contracts with Customers (Topic 606): Narrow-Scope Improvements and Practical Expedients , which addresses implementation issues and is intended to reduce the cost and complexity of applying the new revenue standard in ASU 2014-09; ASU No. 2017-13, Revenue Recognition (Topic 605), Revenue from Contracts with Customers (Topic 606), Leases (Topic 840), and Leases (Topic 842): Amendments to SEC Paragraphs Pursuant to the Staff Announcement at the July 20, 2017 EITF Meeting and Rescission of Prior SEC Staff Announcements and Observer Comments (SEC Update) , which codifies recent announcements by the SEC staff; and ASU No. 2017-14, Income Statement—Reporting Comprehensive Income (Topic 220), Revenue Recognition (Topic 605), and Revenue from Contracts with Customers (Topic 606) (SEC Update) , which codifies SEC Release 33-10403, or collectively with ASU 2014-09, the Revenue ASUs. We were required to adopt the Revenue ASUs effective January 1, 2018. The guidance permits two methods of adoption: retrospectively to each prior reporting period presented (the full retrospective method), or retrospectively with the cumulative effect of initially applying the guidance recognized at the date of initial application (the modified retrospective method). We adopted the new standard under the modified retrospective method. In adopting the Revenue ASUs, we applied the practical expedient that permits aggregating the effect of all modifications that occurred prior to January 1, 2018. No other practical expedients were used. Upon finalization of our assessment, which resulted in changes to our estimates as of December 31, 2017, the impact of the cumulative effect of the accounting changes upon the adoption of the standard (in thousands) is as follows: December 31, 2017 Cumulative Effect January 1, 2018 Deferred revenue – related party, current and net of current portions $ 163,640 $ (39,456 ) $ 124,184 Accumulated deficit (798,061 ) 39,456 (758,605 ) The following tables summarize the effects of adopting ASC 606 on our unaudited condensed consolidated financial statements for the three months ended March 31, 2018 (in thousands, except per share data): Condensed Consolidated Balance Sheets March 31, 2018 Under Topic Under Topic Effect of Deferred revenue – related party $ 39,212 $ 35,396 $ 3,816 Deferred revenue, net of current portion – related party 81,831 122,060 (40,229 ) Accumulated deficit (849,430 ) (885,843 ) 36,413 Condensed Consolidated Statements of Operations Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Collaboration revenue – related party $ 7,345 $ 9,977 $ (2,632 ) Research and development expense 78,224 77,813 411 Total operating expenses 102,774 102,363 411 Loss from operations (94,012 ) (90,969 ) (3,043 ) Net loss (90,825 ) (87,782 ) (3,043 ) Net loss per share – basic and diluted (1.63 ) (1.58 ) (0.05 ) Condensed Consolidated Statements of Comprehensive Loss Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Net loss $ (90,825 ) $ (87,782 ) $ (3,043 ) Comprehensive loss (92,079 ) (89,036 ) (3,043 ) Condensed Consolidated Statements of Cash Flows Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Net loss $ (90,825 ) $ (87,782 ) $ (3,043 ) Adjustments to reconcile net loss to net cash used in operating activities: Deferred revenue – related party (3,141 ) (6,184 ) 3,043 Recent accounting pronouncements In February 2016, the FASB issued ASU No. 2016-02, Leases (Topic 842), or ASU 2016-02, which establishes principles that lessees and lessors shall apply to report useful information to users of financial statements about the amount, timing and uncertainty of cash flows arising from a lease. ASU 2016-02 was codified as ASC 842, Leases . Subsequently, the FASB issued ASU 2017-13, Revenue Recognition (Topic 605), Revenue from Contracts with Customers (Topic 606), Leases (Topic 840), and Leases (Topic 842): Amendments to SEC Paragraphs Pursuant to the Staff Announcement at the July 20, 2017 EITF Meeting and Rescission of Prior SEC Staff Announcements and Observer Comments (SEC Update) , which codifies recent announcements by the SEC staff; and ASU 2018-01, Leases (Topic 842): Land Easement Practical Expedient for Transition to Topic 842 , which provides a transition practical expedient for existing or expired land easements, or collectively with ASU 2016-02, the Leases ASUs. We will adopt ASC 842 effective January 1, 2019. We are currently in the process of evaluating the impact of the guidance on our consolidated financial statements. Other accounting standards that have been issued by the FASB or other standards-setting bodies that do not require adoption until a future date are not expected to have a material impact on our financial statements upon adoption. |
Fair Value Measurements
Fair Value Measurements | 3 Months Ended |
Mar. 31, 2018 | |
Fair Value Disclosures [Abstract] | |
Fair Value Measurements | Fair Value Measurements We record cash equivalents and marketable securities at fair value. ASC 820, Fair Value Measurements and Disclosures , establishes a fair value hierarchy for those instruments measured at fair value that distinguishes between assumptions based on market data (observable inputs) and our own assumptions (unobservable inputs). The hierarchy consists of three levels: Level 1 – Unadjusted quoted prices in active markets for identical assets or liabilities. Level 2 – Quoted prices for similar assets and liabilities in active markets, quoted prices in markets that are not active, or inputs which are observable, directly or indirectly, for substantially the full term of the asset or liability. Level 3 – Unobservable inputs that reflect our own assumptions about the assumptions market participants would use in pricing the asset or liability in which there is little, if any, market activity for the asset or liability at the measurement date. The following table summarizes our cash equivalents and marketable securities measured at fair value on a recurring basis as of March 31, 2018 (in thousands): Level 1 Level 2 Level 3 Total Cash equivalents $ 262,897 $ 84,827 $ — $ 347,724 Marketable securities: Certificates of deposit — 5,226 — 5,226 U.S. Treasuries — 179,580 — 179,580 Government securities — 128,968 — 128,968 Corporate debt securities — 316,504 — 316,504 Total cash equivalents and marketable securities $ 262,897 $ 715,105 $ — $ 978,002 Cash equivalents and marketable securities have been initially valued at the transaction price and subsequently valued, at the end of each reporting period, utilizing third-party pricing services or other market observable data. The pricing services utilize industry standard valuation models, including both income and market based approaches, and observable market inputs to determine value. After completing our validation procedures, we did not adjust or override any fair value measurements provided by the pricing services as of March 31, 2018 . There have been no changes to the valuation methods during the three months ended March 31, 2018 . We evaluate transfers between levels at the end of each reporting period. There were no transfers between Level 1 and Level 2 during the three months ended March 31, 2018 . We have no financial assets or liabilities that were classified as Level 3 at any point during the three months ended March 31, 2018 . |
Marketable Securities
Marketable Securities | 3 Months Ended |
Mar. 31, 2018 | |
Investments, Debt and Equity Securities [Abstract] | |
Marketable Securities | Marketable Securities Our marketable securities are classified as available-for-sale pursuant to ASC 320, Investments – Debt and Equity Securities , and are recorded at fair value, with unrealized gains and losses included as a component of accumulated other comprehensive loss in stockholders’ equity and a component of total comprehensive loss in the condensed consolidated statements of comprehensive loss , until realized. Realized gains and losses are included in investment income on a specific-identification basis. There were no realized gains or losses on marketable securities for the three months ended March 31, 2018 and 2017 and, as a result, there were no reclassifications of any amounts out of accumulated other comprehensive loss for those periods. Marketable securities at March 31, 2018 consisted of the following (in thousands): Amortized Unrealized Unrealized Fair Current: Certificates of deposit $ 4,760 $ — $ (8 ) $ 4,752 U.S Treasuries 144,849 — (209 ) 144,640 Government securities 71,773 — (141 ) 71,632 Corporate debt securities 197,334 — (377 ) 196,957 Non-current: Certificates of deposit 480 — (6 ) 474 U.S Treasuries 35,318 — (378 ) 34,940 Government securities 57,646 — (310 ) 57,336 Corporate debt securities 120,752 — (1,205 ) 119,547 Total marketable securities $ 632,912 $ — $ (2,634 ) $ 630,278 Marketable securities at December 31, 2017 consisted of the following (in thousands): Amortized Unrealized Unrealized Fair Current: Certificates of deposit $ 8,081 $ — $ (11 ) $ 8,070 U.S. Treasuries 113,852 — (119 ) 113,733 Government securities 44,421 — (57 ) 44,364 Corporate debt securities 155,222 — (177 ) 155,045 Non-current: Certificates of deposit 960 — (8 ) 952 U.S. Treasuries 36,165 — (311 ) 35,854 Government securities 23,992 — (182 ) 23,810 Corporate debt securities 83,722 — (524 ) 83,198 Total marketable securities $ 466,415 $ — $ (1,389 ) $ 465,026 At March 31, 2018 and December 31, 2017 , we held both current and non-current investments. Investments classified as current have maturities of less than one year . Investments classified as non-current are those that: (i) have a maturity of one to two years , and (ii) we do not intend to liquidate within the next twelve months , although these funds are available for use and therefore classified as available-for-sale. At March 31, 2018 and December 31, 2017 , we held 257 and 240 debt securities that were in an unrealized loss position for less than one year, respectively. The aggregate fair value of debt securities in an unrealized loss position at March 31, 2018 and December 31, 2017 was $572.7 million and $439.4 million , respectively. There were no individual securities that were in a significant unrealized loss position as of March 31, 2018 and December 31, 2017 . Given our intent and ability to hold such securities until recovery, and the lack of material of change in the credit risk of these investments, we do not consider these marketable securities to be other-than-temporarily impaired as of March 31, 2018 and December 31, 2017 . |
Collaboration Agreements
Collaboration Agreements | 3 Months Ended |
Mar. 31, 2018 | |
Revenue Recognition and Deferred Revenue [Abstract] | |
Collaboration Agreements | Collaboration Agreements Celgene Corporation To date, our revenue has primarily been generated from our collaboration agreements with Celgene, or collectively, the Collaboration Agreements. Celgene is a related party through ownership of our common stock. In April 2010, we entered into a discovery and development collaboration and license agreement focused on cancer metabolism, or the 2010 Agreement. The 2010 Agreement was amended in October 2011 and July 2014. In April 2015, we entered into a joint worldwide development and profit share collaboration and license agreement with Celgene, and our wholly owned subsidiary, Agios International Sarl, entered into a collaboration and license agreement with Celgene International II Sarl, or collectively, the AG-881 Agreements, to establish a worldwide collaboration focused on the development and commercialization of AG-881 products. In May 2016, we entered into a master research and collaboration agreement with Celgene, or the 2016 Agreement. 2016 Agreement In May 2016, we entered into the 2016 Agreement focused on metabolic immuno-oncology, or MIO, a developing field which aims to modulate the activity of relevant immune cells by targeting critical metabolic nodes, thereby, enhancing the immune mediated anti-tumor response. In addition to new programs identified under the 2016 Agreement, both parties also agreed that all future development and commercialization of two remaining cancer metabolism programs discovered under the 2010 Agreement, including AG-270, an inhibitor of methionine adenosyltransferase 2a, will now be governed by the 2016 Agreement. During the research term of the 2016 Agreement, we plan to conduct research programs focused on discovering compounds that are active against metabolic targets in the immuno-oncology, or IO, field. The initial four-year research term will expire on May 17, 2020, and may be extended for up to two, or in specified cases, up to four additional one-year terms. For each program under the 2016 Agreement, we may nominate compounds that meet specified criteria as development candidates and, in limited circumstances, Celgene may also nominate compounds as development candidates for each such program. Celgene may designate the applicable program for further development following any such nomination, after which we may conduct, at our expense, additional preclinical and clinical development for such program through the completion of an initial phase 1 dose escalation study. At the end of the research term, Celgene may designate for continued development up to three research programs for which development candidates have yet to be nominated, which are referred to as continuation programs. We may conduct further research and preclinical and clinical development activities on any continuation program, at our expense, through the completion of an initial phase 1 dose escalation study. We granted Celgene the right to obtain exclusive options for development and commercialization rights for each program that Celgene has designated for further development, and for each continuation program. Celgene may exercise each such option beginning on the designation of a development candidate for such program (or on the designation of such program as a continuation program) and ending on the earlier of: (i) the end of a specified period after we have furnished Celgene with specified information about the initial phase 1 dose escalation study for such program, or (ii) January 1, 2030. Research programs that have applications in the inflammation or autoimmune, or I&I, field that may result from the 2016 Agreement will also be subject to the exclusive options described above. We will retain rights to any program that Celgene does not designate for further development or as to which it does not exercise its option. Under the terms of the 2016 Agreement, following Celgene’s exercise of its option with respect to a program, the parties will enter into either a co-development and co-commercialization agreement if such program is in the IO field, or a license agreement if such program is in the I&I field. Under each co-development and co-commercialization agreement, the two parties will co-develop and co-commercialize licensed products worldwide. Either we or Celgene will lead development and commercialization of licensed products for the United States, and Celgene will lead development and commercialization of licensed products outside of the United States. Depending on the country, the parties will each have the right to provide a portion of field-based marketing activities. Under each license agreement, Celgene will have the sole right to develop and commercialize licensed products worldwide. Co-development and co-commercialization agreements Under each co-development and co-commercialization agreement entered into under the 2016 Agreement, the parties will split all post-option exercise worldwide development costs, subject to specified exceptions, as well as any profits from any net sales of, or commercialization losses related to, licensed products in the IO field. Celgene has the option to designate one program in the IO field as the 65/35 program, for which Celgene will be the lead party for the United States and will have a 65% profit or loss share. For programs in the IO field other than the 65/35 program, we and Celgene will alternate, on a program-by-program basis, being the lead party for the United States, with us having the right to be the lead party for the first such program, and each party will have a 50% profit or loss share. The lead party for the United States will book commercial sales of licensed products, if any, in the United States, and Celgene will book commercial sales of licensed products, if any, outside of the United States. License agreements Under each license agreement under the 2016 Agreement, Celgene will be responsible for all post-option exercise worldwide development and associated costs, subject to specified exceptions, as well as worldwide commercialization and associated costs, for licensed products in the I&I field. Financial terms Under the terms of the 2016 Agreement, we received an initial upfront payment in the amount of $200.0 million . The 2016 Agreement provides specified rights to extend the research term for up to two , or in specified cases, up to four , additional years by paying a $40.0 million per-year extension fee. Celgene will pay an $8.0 million designation fee for each program that Celgene designates for further development and for each continuation program. During the three months ended March 31, 2017, we received $8.0 million from Celgene upon the designation of AG-270 as a development candidate. For each program as to which Celgene exercises its option to develop and commercialize, subject to antitrust clearance, Celgene will pay an option exercise fee of at least $30.0 million for any designated development program and at least $35.0 million for any continuation programs. In certain cases, Celgene may exercise its option to develop and commercialize two early-stage I&I programs, prior to Celgene designating the program for further development, by paying an option exercise fee of $10.0 million . We are eligible to receive the following milestone-based payments associated with the 2016 Agreement: Program Milestone Amount 65/35 program in IO field Specified clinical development event $25.0 million 65/35 program in IO field Specified regulatory milestone events Up to $183.8 million 50/50 program in IO field Specified clinical development event $20.0 million 50/50 program in IO field Specified regulatory milestone events Up to $148.8 million I&I field Specified clinical development event $25.0 million I&I field Specified regulatory milestone events Up to $236.3 million I&I field Specified commercial milestone events Up to $125.0 million Additionally, for each licensed program in the I&I field, we are eligible to receive royalties at tiered, low double-digit percentage rates on Celgene’s net sales, if any. Opt-out right Under the 2016 Agreement, we may elect to opt out of the cost and profit share under any co-development and co-commercialization agreement, subject to specified exceptions. Upon opting out, Celgene will have the sole right to develop, manufacture and commercialize the applicable licensed products throughout the world, at its cost, and we will undertake transitional activities reasonably necessary to transfer the development, manufacture and commercialization of such licensed products to Celgene, at our expense. Further, in lieu of the profit or loss sharing described above, we would be eligible to receive royalties at tiered, low double-digit percentage rates on Celgene’s net sales, if any, of the applicable licensed products. However, we would continue to be eligible to receive the developmental and regulatory milestone-based payments described above. Term The term of the 2016 Agreement commenced on May 17, 2016 and, if not terminated earlier, will expire upon the later of the last-to-expire of the research term and all option exercise periods, or, if an option is exercised by Celgene for one or more programs in the collaboration, upon the termination or expiration of the last-to-exist co-development and co-commercialization agreement or license agreement, as applicable, for any such program. Termination Subject to specified exceptions, Celgene may terminate the 2016 Agreement in its entirety for any reason by providing us with prior written notice if there are no active co-development and co-commercialization agreements or license agreements in place or on a program-by-program basis if there are no active co-development and co-commercialization agreements or license agreements in place for the terminated program(s). Either party may terminate the 2016 Agreement for the insolvency of the other party. On a program-by-program basis, prior to the exercise of an option, either party may terminate the 2016 Agreement either in its entirety or with respect to one or more programs on prior written notice to the other party in the case of an uncured material breach by the other party that frustrates the fundamental purpose of the 2016 Agreement. Following the exercise of an option for a program, either party may terminate the 2016 Agreement with respect to such program if such party terminates the co-development and co-commercialization agreement or license agreement for such program for an uncured material breach by the other party that frustrates the fundamental purpose of such agreement. Either party may terminate a co-development and co-commercialization agreement or a license agreement upon the bankruptcy or insolvency of the other party. Either party also has the right to terminate the co-development and co-commercialization agreement or license agreement if the other party or any of its affiliates challenges the validity, scope or enforceability of or otherwise opposes, any patent included within the intellectual property rights licensed to the other party under such agreement. Exclusivity While any of Celgene’s options remain available under the 2016 Agreement, subject to specified exceptions, we may not directly or indirectly develop, manufacture or commercialize, outside of the 2016 Agreement, any therapeutic modality in the IO or I&I field with specified activity against a metabolic target. During the term of each co-development and co-commercialization agreement and license agreement, subject to specified exceptions, neither we nor Celgene may directly or indirectly develop, manufacture or commercialize outside of such agreement any therapeutic modality in any field with specified activity against the metabolic target that is the focus of the program licensed under such agreement. TIBSOVO® (ivosidenib) Letter Agreement In May 2016, we entered into a letter agreement with Celgene regarding TIBSOVO® (ivosidenib), or the TIBSOVO® (ivosidenib) Letter Agreement. Under the TIBSOVO® (ivosidenib) Letter Agreement, the parties agreed to terminate the 2010 Agreement, effective as of August 15, 2016, as to the program directed to the isocitrate dehydrogenase 1, or IDH1, target, for which TIBSOVO® (ivosidenib) is the lead development candidate. Under the 2010 Agreement, Celgene had held development and commercialization rights to the IDH1 program outside of the United States, and we held such rights inside the United States. As a result of the termination, we obtained global rights to TIBSOVO® (ivosidenib) and the IDH1 program. Neither party will have any further financial obligation, including royalties or milestone payments, to the other concerning TIBSOVO® (ivosidenib) or the IDH1 program. Under the terms of the termination, the parties also agreed to conduct specified transitional activities in connection with the termination. In addition, pursuant to the TIBSOVO® (ivosidenib) Letter Agreement, the parties are released from their exclusivity obligations under the 2010 Agreement with respect to the IDH1 program. The termination does not affect the AG-881 Agreements , which are directed to both the IDH1 target and the isocitrate dehydrogenase 2, or IDH2, target. AG-881 Agreements In April 2015, we entered into the AG-881 Agreements. The AG-881 Agreements establish a joint worldwide collaboration focused on the development and commercialization of AG-881 products. Under the terms of the AG-881 Agreements, we received an initial upfront payment of $10.0 million in May 2015 and are eligible to receive milestone-based payments described below. The parties will split all worldwide development costs equally, subject to specified exceptions, as well as any profits from any net sales of, or commercialization losses related to, licensed AG-881 products. Either party may, at its own expense and with the other party's permission, undertake additional development activities outside of the scope of the development plan agreed upon with the other party. We are eligible to receive up to $70.0 million in potential milestone payments under the AG-881 Agreements. The potential milestone payments are comprised of: (i) a $15.0 million milestone payment for filing of a first new drug application, or NDA, in a major market, and (ii) up to $55.0 million in milestone payments upon achievement of specified regulatory milestone events. We may also receive royalties at tiered, low-double digit to mid-teen percentage rates on net sales if we elect not to participate in the development and commercialization of AG-881. Termination Celgene may terminate the AG-881 Agreements in their entirety for any reason upon ninety days written notice to us. Either party may terminate the AG-881 Agreements for the insolvency of the other party. Either party may terminate the AG-881 Agreements in their entirety or with respect to one of the agreements upon prior written notice to the other party in the case of an uncured material breach by the other party that frustrates the fundamental purpose of the AG-881 Agreements. If one of the AG-881 Agreements terminates, the other will terminate automatically. 2010 Agreement In April 2010, we entered into the 2010 Agreement, which was amended in October 2011 and July 2014. The goal of the collaboration was to discover, develop and commercialize disease-altering therapies in oncology based on our cancer metabolism research platform. We initially led discovery, preclinical and early clinical development for all cancer metabolism programs under the collaboration. The discovery phase of the 2010 Agreement expired in April 2016. Upon agreement to terminate the 2010 Agreement, effective as of August 15, 2016, as to the program directed to the IDH1 target, for which TIBSOVO® (ivosidenib) is the lead development candidate, the sole program remaining under the 2010 Agreement is IDHIFA®, a co-commercialized licensed program for which Celgene leads and funds global development and commercialization activities. We have exercised our right to participate in a portion of commercialization activities in the United States for IDHIFA® in accordance with the applicable commercialization plan. On August 1, 2017, the U.S. Food and Drug Administration, or FDA, granted Celgene approval of IDHIFA® for the treatment of adult patients with relapsed or refractory acute myeloid leukemia, or R/R AML, with an IDH2 mutation as detected by an FDA-approved test. Under the remaining terms of the 2010 Agreement, we are eligible to receive up to $95.0 million in potential milestone payments for the IDHIFA® program. The potential milestone payments are comprised of: (i) up to $70.0 million in milestone payments upon achievement of specified ex-U.S. regulatory milestone events, and (ii) a $25.0 million milestone payment upon achievement of a specified ex-U.S. commercial milestone event. Under the 2010 Agreement, we may also receive royalties at tiered, low-double digit to mid-teen percentage rates on net sales of IDHIFA®. Assuming all other revenue recognition criteria are met, royalty payments will be recognized as revenue in the period in which they are earned. During the three months ended March 31, 2018 , we earned $1.4 million in royalty revenue under the 2010 Agreement. Unless terminated earlier by either party, the term of the 2010 Agreement will continue until the expiration of all royalty terms with respect to IDHIFA®. Celgene may terminate this agreement for convenience in its entirety upon ninety days written notice to us. If either party is in material breach and fails to cure such breach within the specified cure period, the other party may terminate the 2010 Agreement in its entirety. Either party may terminate the agreement in the event of specified insolvency events involving the other party. Accounting analysis and revenue recognition – collaboration revenue On January 1, 2018 we adopted ASC 606 under the modified retrospective method. Prior to January 1, 2018 we accounted for the Collaboration Agreements under ASC 605-25, Multiple Element Arrangements. Accounting under ASC 606 In adopting ASC 606, we applied the practical expedient that permits aggregating the effect of all modifications that occurred prior to January 1, 2018. No other practical expedients were used. Similar to the accounting under ASC 605-25, the 2016 Agreement was determined to be a modification of the 2010 Agreement and the AG-881 Agreements. In determining the appropriate amount of revenue to be recognized under ASC 606, we performed the following steps: (i) identified the promised goods or services in the contract; (ii) determined whether the promised goods or services are performance obligations including whether they are distinct in the context of the contract; (iii) measured the transaction price, including the constraint on variable consideration; (iv) allocated the transaction price to the performance obligations; and (v) recognized revenue when (or as) we satisfy each performance obligation. As part of the accounting for these arrangements, we must develop assumptions that require judgment to determine the stand-alone selling price, or SSP, for each performance obligation identified in the contract. We use key assumptions to determine the SSP, which include forecast of revenues, development timelines, reimbursement rates for personnel costs, discount rates and probabilities of technical and regulatory success. The satisfied and unsatisfied performance obligations at the time of the ASC 606 adoption, each of which are considered by us to be distinct within the context of the contract, their SSP, the method of recognizing the allocated consideration, and the period through which they are expected to be recognized are as follows: Performance Obligations SSP No. of Performance Obligation(s) Recognition Method Fully satisfied at time of adoption Licenses (1) $ 86.7 million 4 Fully satisfied; recognized upon adoption of ASC 606 Research and development services (2) (3) $ 350.7 million 10 Fully satisfied; recognized upon adoption of ASC 606 Partially satisfied at time of adoption Research and development services (2) (3) $ 266.6 million 6 Proportionally as services are delivered over the performance period, expected to be through September 2022 (4) (1) The SSP was developed by probability weighting multiple cash flow scenarios using the income approach. Our management estimates within the models include the expected, probability-weighted net profits from estimated future sales, an estimate of the direct cost incurred to generate future cash flows, a discount rate and other business forecast factors. There are significant judgments and estimates inherent in the determination of the SSP of these units of accounting. These judgments and estimates include assumptions regarding future operating performance, the timelines of the clinical trials and regulatory approvals, and other factors. If different reasonable assumptions are utilized, the SSP and revenue recognized would vary. (2) The SSP was developed using our management’s best estimate of the cost of obtaining these services at arm’s length from a third-party provider. (3) The SSP was developed using internal full time equivalent costs to support the development services. (4) We determined that recognizing revenue on a proportional basis using the ratio of effort incurred to date compared to the total estimated effort required to complete the performance obligation best depicts the satisfaction of our obligations under the Collaboration Agreements. During the three months ended March 31, 2018 , we recognized the following as collaboration revenue (in thousands): Three Months Ended March 31, 2018 Performance Obligation Under Topic Under Topic Effect of Collaboration revenue - related party Research and development services $ 6,364 $ 8,953 $ (2,589 ) Committee participations — 43 (43 ) Reduction of research and development expenses Development services — 411 (411 ) During the three months ended March 31, 2017 , we recognized as collaboration revenue the following non-contingent consideration allocated to each undelivered element (in thousands): Undelivered Element Revenue Recognized On-going research and development services $ 10,387 Committee participations 42 Total collaboration revenue - related party $ 10,429 During the three months ended March 31, 2017 , we recognized $2.8 million as a reduction of research and development expenses. During the three months ended March 31, 2018 , we did not recognize any reductions to research and development expenses. Development and commercialization expenses that were not contemplated as of the modification dates due to the high level of uncertainty are recognized as collaboration revenue or a reduction of research and development expenses in the period in which they are earned. There was no impact from the adoption of ASC 606 on these obligations. For the three months ended March 31, 2018 and 2017 , we recognized the following collaboration revenue and reduction of research and development expenses related to such expenses (in thousands): Three Months Ended March 31, 2018 2017 Collaboration revenue - related party Commercialization activities $ 981 $ 79 Reduction of research and development expenses Research and development activities — 14 For the three months ended March 31, 2018 and 2017 , we recognized the following totals of collaboration revenue and reduction of research and development expenses (in thousands): Three Months Ended March 31, 2018 2017 Collaboration revenue - related party $ 7,345 $ 10,508 Reduction of research and development expenses — 2,776 The following table presents changes in our contract assets and liabilities during the three months ended March 31, 2018 (in thousands): December 31, 2017 Additions Deductions March 31, 2018 Contract assets (1) Collaboration receivable – related party $ 2,448 $ 3,512 $ (2,448 ) $ 3,512 Royalty receivable – related party 1,222 1,417 (1,222 ) 1,417 Contract liabilities (2) Deferred revenue – related party, current and net of current portions 163,640 4,204 (46,801 ) 121,043 (1) Additions to contract assets relate to amounts billed to Celgene for reimbursable costs incurred by us during the reporting period. Deductions to contract assets relate to collection of receivables during the reporting period. (2) Additions to contract liabilities relate to consideration from Celgene during the reporting period. Deductions to contract liabilities relate to deferred revenue recognized as revenue during the reporting period and cumulative catch-up adjustment recognized upon adoption of ASC 606 on January 1, 2018. During the three months ended March 31, 2018 , we recognized the following as revenue due to changes in the contract asset and the contract liability balances (in thousands): Amounts included in the contract liability at the beginning of the period $ 5,984 Performance obligations satisfied in previous periods 323 As of March 31, 2018 , the aggregate amount of the transaction price allocated to performance obligations that are partially unsatisfied was $132.6 million . We consider the total consideration expected to be earned in the next twelve months for services to be performed as current deferred revenue, and consideration that is expected to be earned subsequent to twelve months from the balance sheet date as noncurrent deferred revenue. Accounting analysis and revenue recognition – milestone revenue At each reporting period we evaluate whether milestones are considered probable of being reached and, to the extent that a significant reversal would not occur in future periods, estimate the amount to be included in the transaction price using the most likely amount method. Milestone payments that are not within our control, such as regulatory approvals, are not considered probable of being achieved and are excluded from the transaction price until those approvals are received. No milestones were earned during the three months ended March 31, 2018 and 2017 . The next potential milestone expected to be achieved under our collaboration agreements with Celgene is the filing of a first new drug application equivalent in an ex-U.S. country. Achievement of this event will result in milestone payments of $15.0 million under the 2010 Agreement. Aurigene Discovery Technologies Limited In April 2017, we entered into a new global license agreement with Aurigene Discovery Technologies Limited, or Aurigene, to research, develop and commercialize small molecule inhibitors for dihydroorotate dehydrogenase, or DHODH, or the Aurigene Agreement. Under the terms of the Aurigene Agreement, Aurigene will provide to us exclusive rights to its portfolio of novel small molecules for DHODH. Financial terms of the Aurigene Agreement include a $3.0 million upfront payment and potential future milestone payments of up to $17.0 million if we achieve certain development and regulatory milestones. The next potential milestone expected to be achieved under our collaboration agreements with Aurigene is the initiation of the first phase 1 clinical trial for AG-636, our DHODH inhibitor. Achievement of this event will result in milestone payments owed to Aurigene of $2.0 million . Aurigene is also eligible to receive low single-digit royalties on net product sales, if any. We will conduct preclinical studies and, if successful, fund further global research and development, as well as regulatory and commercial activities. The term of the Aurigene Agreement will continue until the earlier of: (a) termination for convenience at our sole discretion upon 90 days prior written notice, (b) termination by either party for material breach, or (c) the expiration of the last-to-expire of all payment obligations hereunder with respect to all licensed products under the Aurigene Agreement. Accounting analysis The $3.0 million upfront payment was incurred in May 2017 and recorded as research and development expense. Costs incurred and milestone payments due to Aurigene prior to regulatory approval are recognized as expenses in the period incurred. Payments due to Aurigene upon or subsequent to regulatory approval will be capitalized and amortized over the shorter of the remaining license or product patent life. |
Accrued Expenses
Accrued Expenses | 3 Months Ended |
Mar. 31, 2018 | |
Payables and Accruals [Abstract] | |
Accrued Expenses | Accrued Expenses Accrued expenses consist of the following (in thousands): March 31, December 31, Accrued compensation $ 4,966 $ 15,693 Accrued research and development costs 9,951 14,849 Accrued professional fees 1,853 3,140 Accrued other 235 349 Total accrued expenses $ 17,005 $ 34,031 |
Share-Based Payments
Share-Based Payments | 3 Months Ended |
Mar. 31, 2018 | |
Disclosure of Compensation Related Costs, Share-based Payments [Abstract] | |
Share-Based Payments | Share-Based Payments 2013 Stock Incentive Plan In June 2013, our Board of Directors adopted and, in July 2013 our stockholders approved, the 2013 Stock Incentive Plan, or the 2013 Plan. The 2013 Plan became effective upon the closing of our initial public offering and provides for the grant of incentive stock options, non-qualified stock options, stock appreciation rights, restricted stock awards, restricted stock units, or RSUs, performance-based stock units, or PSUs, and other stock-based awards. Following the adoption of the 2013 Plan, we granted no further stock options or other awards under the 2007 Stock Incentive Plan, or the 2007 Plan. Any options or awards outstanding under the 2007 Plan at the time of adoption of the 2013 Plan remained outstanding and effective. As of March 31, 2018 , the total number of shares reserved under the 2007 Plan and the 2013 Plan are 8,624,887 , and we had 1,938,247 shares available for future issuance under the 2013 Plan. Stock options The following table presents stock option activity for the three months ended March 31, 2018 : Number of Stock Options Weighted- Average Exercise Price Outstanding at December 31, 2017 5,577,562 $ 49.58 Granted 1,107,220 77.22 Exercised (477,847 ) 22.81 Forfeited/Expired (102,127 ) 88.78 Outstanding at March 31, 2018 6,104,808 $ 56.03 Exercisable at March 31, 2018 2,863,417 $ 48.14 Vested and expected to vest at March 31, 2018 6,104,808 $ 56.03 At March 31, 2018 , the total unrecognized compensation expense related to unvested stock option awards was $130.0 million , which we expect to recognize over a weighted-average period of approximately 3.0 years . Restricted stock units The following table presents RSU activity for the three months ended March 31, 2018 : Number of Stock Units Weighted-Average Grant Date Fair Value Unvested shares at December 31, 2017 125,584 $ 47.46 Granted 338,093 77.54 Vested (57,250 ) 41.76 Forfeited (781 ) 77.70 Unvested shares at March 31, 2018 405,646 $ 73.28 As of March 31, 2018 , there was approximately $26.7 million of total unrecognized compensation expense related to RSUs, which we expect to be recognized over a weighted-average period of approximately 2.6 years . Performance-based stock units The following table presents PSU activity for the three months ended March 31, 2018 : Number of Stock Units Weighted-Average Grant Date Fair Value Unvested shares at December 31, 2017 176,186 $ 52.98 Granted — — Vested — — Forfeited — — Unvested shares at March 31, 2018 176,186 $ 52.98 Stock-based compensation expense associated with these PSUs is recognized if the underlying performance condition is considered probable of achievement using our management’s best estimates. Performance-based vesting criteria primarily relate to milestone events specific to our corporate goals, specifically regulatory milestones related to our product candidates. As of March 31, 2018 , there was approximately $9.3 million of total unrecognized compensation expense related to PSUs with performance-based vesting criteria that are not considered probable of achievement. 2013 Employee Stock Purchase Plan In June 2013, our Board of Directors adopted, and in July 2013 our stockholders approved, the 2013 Employee Stock Purchase Plan, or the 2013 ESPP. We issued 27,377 shares and 33,521 shares during the three months ended March 31, 2018 and 2017 , respectively, under the 2013 ESPP. The 2013 ESPP provides participating employees with the opportunity to purchase up to an aggregate of 327,272 shares of our common stock. As of March 31, 2018 , we had 186,414 shares available for future issuance under the 2013 ESPP. Stock-based compensation expense Stock-based compensation expense by award type included within the condensed consolidated statements of operations is as follows (in thousands): Three Months Ended March 31, 2018 2017 Stock options $ 12,472 $ 9,902 Restricted stock units 1,797 595 Employee Stock Purchase Plan 253 237 Total stock-based compensation expense $ 14,522 $ 10,734 Expenses related to equity-based awards were allocated as follows in the condensed consolidated statements of operations (in thousands): Three Months Ended March 31, 2018 2017 Research and development expense $ 8,640 $ 7,025 General and administrative expense 5,882 3,709 Total stock-based compensation expense $ 14,522 $ 10,734 |
Loss per Share
Loss per Share | 3 Months Ended |
Mar. 31, 2018 | |
Earnings Per Share [Abstract] | |
Loss per Share | Loss per Share Basic net loss per share is calculated by dividing net loss by the weighted average shares outstanding during the period, without consideration for common stock equivalents. Diluted net loss per share is calculated by adjusting the weighted average shares outstanding for the dilutive effect of common stock equivalents outstanding for the period, determined using the treasury stock method. For purposes of the dilutive net loss per share calculation, stock options, RSUs and ESPP options are considered to be common stock equivalents, while PSUs with vesting conditions that were not met as of March 31, 2018 are not considered to be common stock equivalents. Since we had a net loss for all periods presented, the effect of all potentially dilutive securities is anti-dilutive. Accordingly, basic and diluted net loss per share was the same for all periods presented. The following common stock equivalents were excluded from the calculation of diluted net loss per share applicable to common stockholders for the periods indicated because including them would have had an anti-dilutive effect: Three Months Ended March 31, 2018 2017 Stock options 6,104,808 6,129,794 Restricted stock units 405,646 126,850 Employee Stock Purchase Plan options 5,289 5,533 Total common stock equivalents 6,515,743 6,262,177 |
Summary of Significant Accoun16
Summary of Significant Accounting Policies and Recent Accounting Pronouncements (Policies) | 3 Months Ended |
Mar. 31, 2018 | |
Accounting Policies [Abstract] | |
Basis of presentation | Basis of presentation The condensed consolidated balance sheet as of March 31, 2018 , and the condensed consolidated statements of operations, comprehensive loss, and cash flows for the three months ended March 31, 2018 and 2017 are unaudited. The unaudited condensed consolidated financial statements have been prepared on the same basis as the annual financial statements and, in the opinion of our management, reflect all adjustments, which include only normal recurring adjustments, necessary to fairly state our financial position as of March 31, 2018 , and our results of operations and cash flows for the three months ended March 31, 2018 and 2017 . The financial data and the other financial information disclosed in these notes to the condensed consolidated financial statements related to the three -month period are also unaudited. The results of operations for the three months ended March 31, 2018 are not necessarily indicative of the results to be expected for the year ending December 31, 2018 or for any other future annual or interim period. The year-end condensed consolidated balance sheet data was derived from our audited financial statements, but does not include all disclosures required by U.S. generally accepted accounting principles, or U.S. GAAP. Accordingly, the condensed consolidated interim financial statements should be read in conjunction with the audited consolidated financial statements and notes thereto included in our Annual Report on Form 10-K for the year ended December 31, 2017 that was filed with the Securities and Exchange Commission, or the SEC, on February 14, 2018 . Our consolidated financial statements include our accounts and the accounts of our wholly owned subsidiaries, Agios Securities Corporation, Agios International Sarl, and Agios Limited. All intercompany transactions have been eliminated in consolidation. The consolidated financial statements have been prepared in conformity with U.S. GAAP. |
Significant accounting policies and Recent accounting pronouncements | Significant accounting policies Revenue from Contracts with Customers In May 2014, the Financial Accounting Standards Board, or FASB, issued ASU No. 2014-09, Revenue from Contracts with Customers (Topic 606) , or ASU 2014-09. ASU 2014-09 was codified as Accounting Standards Codification, or ASC, 606, Revenue from Contracts with Customers , or ASC 606. Subsequently, the FASB issued ASU 2015-14, Revenue from Contracts with Customers (Topic 606) , which adjusted the effective date of ASU 2014-09; ASU No. 2016-08, Revenue from Contracts with Customers (Topic 606): Principal versus Agent Considerations (Reporting Revenue Gross versus Net) , which amends the principal-versus-agent implementation guidance and illustrations in ASU 2014-09; ASU No. 2016-10, Revenue from Contracts with Customers (Topic 606): Identifying Performance Obligations and Licensing, which clarifies identifying performance obligations and licensing implementation guidance and illustrations in ASU 2014-09; ASU No. 2016-12, Revenue from Contracts with Customers (Topic 606): Narrow-Scope Improvements and Practical Expedients , which addresses implementation issues and is intended to reduce the cost and complexity of applying the new revenue standard in ASU 2014-09; ASU No. 2017-13, Revenue Recognition (Topic 605), Revenue from Contracts with Customers (Topic 606), Leases (Topic 840), and Leases (Topic 842): Amendments to SEC Paragraphs Pursuant to the Staff Announcement at the July 20, 2017 EITF Meeting and Rescission of Prior SEC Staff Announcements and Observer Comments (SEC Update) , which codifies recent announcements by the SEC staff; and ASU No. 2017-14, Income Statement—Reporting Comprehensive Income (Topic 220), Revenue Recognition (Topic 605), and Revenue from Contracts with Customers (Topic 606) (SEC Update) , which codifies SEC Release 33-10403, or collectively with ASU 2014-09, the Revenue ASUs. We were required to adopt the Revenue ASUs effective January 1, 2018. The guidance permits two methods of adoption: retrospectively to each prior reporting period presented (the full retrospective method), or retrospectively with the cumulative effect of initially applying the guidance recognized at the date of initial application (the modified retrospective method). We adopted the new standard under the modified retrospective method. In adopting the Revenue ASUs, we applied the practical expedient that permits aggregating the effect of all modifications that occurred prior to January 1, 2018. No other practical expedients were used. Upon finalization of our assessment, which resulted in changes to our estimates as of December 31, 2017, the impact of the cumulative effect of the accounting changes upon the adoption of the standard (in thousands) is as follows: December 31, 2017 Cumulative Effect January 1, 2018 Deferred revenue – related party, current and net of current portions $ 163,640 $ (39,456 ) $ 124,184 Accumulated deficit (798,061 ) 39,456 (758,605 ) The following tables summarize the effects of adopting ASC 606 on our unaudited condensed consolidated financial statements for the three months ended March 31, 2018 (in thousands, except per share data): Condensed Consolidated Balance Sheets March 31, 2018 Under Topic Under Topic Effect of Deferred revenue – related party $ 39,212 $ 35,396 $ 3,816 Deferred revenue, net of current portion – related party 81,831 122,060 (40,229 ) Accumulated deficit (849,430 ) (885,843 ) 36,413 Condensed Consolidated Statements of Operations Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Collaboration revenue – related party $ 7,345 $ 9,977 $ (2,632 ) Research and development expense 78,224 77,813 411 Total operating expenses 102,774 102,363 411 Loss from operations (94,012 ) (90,969 ) (3,043 ) Net loss (90,825 ) (87,782 ) (3,043 ) Net loss per share – basic and diluted (1.63 ) (1.58 ) (0.05 ) Condensed Consolidated Statements of Comprehensive Loss Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Net loss $ (90,825 ) $ (87,782 ) $ (3,043 ) Comprehensive loss (92,079 ) (89,036 ) (3,043 ) Condensed Consolidated Statements of Cash Flows Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Net loss $ (90,825 ) $ (87,782 ) $ (3,043 ) Adjustments to reconcile net loss to net cash used in operating activities: Deferred revenue – related party (3,141 ) (6,184 ) 3,043 Recent accounting pronouncements In February 2016, the FASB issued ASU No. 2016-02, Leases (Topic 842), or ASU 2016-02, which establishes principles that lessees and lessors shall apply to report useful information to users of financial statements about the amount, timing and uncertainty of cash flows arising from a lease. ASU 2016-02 was codified as ASC 842, Leases . Subsequently, the FASB issued ASU 2017-13, Revenue Recognition (Topic 605), Revenue from Contracts with Customers (Topic 606), Leases (Topic 840), and Leases (Topic 842): Amendments to SEC Paragraphs Pursuant to the Staff Announcement at the July 20, 2017 EITF Meeting and Rescission of Prior SEC Staff Announcements and Observer Comments (SEC Update) , which codifies recent announcements by the SEC staff; and ASU 2018-01, Leases (Topic 842): Land Easement Practical Expedient for Transition to Topic 842 , which provides a transition practical expedient for existing or expired land easements, or collectively with ASU 2016-02, the Leases ASUs. We will adopt ASC 842 effective January 1, 2019. We are currently in the process of evaluating the impact of the guidance on our consolidated financial statements. Other accounting standards that have been issued by the FASB or other standards-setting bodies that do not require adoption until a future date are not expected to have a material impact on our financial statements upon adoption. |
Fair Value Measurements | We record cash equivalents and marketable securities at fair value. ASC 820, Fair Value Measurements and Disclosures , establishes a fair value hierarchy for those instruments measured at fair value that distinguishes between assumptions based on market data (observable inputs) and our own assumptions (unobservable inputs). The hierarchy consists of three levels: Level 1 – Unadjusted quoted prices in active markets for identical assets or liabilities. Level 2 – Quoted prices for similar assets and liabilities in active markets, quoted prices in markets that are not active, or inputs which are observable, directly or indirectly, for substantially the full term of the asset or liability. Level 3 – Unobservable inputs that reflect our own assumptions about the assumptions market participants would use in pricing the asset or liability in which there is little, if any, market activity for the asset or liability at the measurement date. |
Marketable Securities | Our marketable securities are classified as available-for-sale pursuant to ASC 320, Investments – Debt and Equity Securities , and are recorded at fair value, with unrealized gains and losses included as a component of accumulated other comprehensive loss in stockholders’ equity and a component of total comprehensive loss in the condensed consolidated statements of comprehensive loss , until realized. Realized gains and losses are included in investment income on a specific-identification basis. At March 31, 2018 and December 31, 2017 , we held both current and non-current investments. Investments classified as current have maturities of less than one year . Investments classified as non-current are those that: (i) have a maturity of one to two years , and (ii) we do not intend to liquidate within the next twelve months , although these funds are available for use and therefore classified as available-for-sale. |
Collaboration Revenue | On January 1, 2018 we adopted ASC 606 under the modified retrospective method. Prior to January 1, 2018 we accounted for the Collaboration Agreements under ASC 605-25, Multiple Element Arrangements. Accounting under ASC 606 In adopting ASC 606, we applied the practical expedient that permits aggregating the effect of all modifications that occurred prior to January 1, 2018. No other practical expedients were used. Similar to the accounting under ASC 605-25, the 2016 Agreement was determined to be a modification of the 2010 Agreement and the AG-881 Agreements. In determining the appropriate amount of revenue to be recognized under ASC 606, we performed the following steps: (i) identified the promised goods or services in the contract; (ii) determined whether the promised goods or services are performance obligations including whether they are distinct in the context of the contract; (iii) measured the transaction price, including the constraint on variable consideration; (iv) allocated the transaction price to the performance obligations; and (v) recognized revenue when (or as) we satisfy each performance obligation. As part of the accounting for these arrangements, we must develop assumptions that require judgment to determine the stand-alone selling price, or SSP, for each performance obligation identified in the contract. We use key assumptions to determine the SSP, which include forecast of revenues, development timelines, reimbursement rates for personnel costs, discount rates and probabilities of technical and regulatory success. |
Loss per Share | Basic net loss per share is calculated by dividing net loss by the weighted average shares outstanding during the period, without consideration for common stock equivalents. Diluted net loss per share is calculated by adjusting the weighted average shares outstanding for the dilutive effect of common stock equivalents outstanding for the period, determined using the treasury stock method. For purposes of the dilutive net loss per share calculation, stock options, RSUs and ESPP options are considered to be common stock equivalents, while PSUs with vesting conditions that were not met as of March 31, 2018 are not considered to be common stock equivalents. Since we had a net loss for all periods presented, the effect of all potentially dilutive securities is anti-dilutive. Accordingly, basic and diluted net loss per share was the same for all periods presented. |
Summary of Significant Accoun17
Summary of Significant Accounting Policies and Recent Accounting Pronouncements (Tables) | 3 Months Ended |
Mar. 31, 2018 | |
Accounting Policies [Abstract] | |
Schedule of Impact of New Accounting Pronouncements | the impact of the cumulative effect of the accounting changes upon the adoption of the standard (in thousands) is as follows: December 31, 2017 Cumulative Effect January 1, 2018 Deferred revenue – related party, current and net of current portions $ 163,640 $ (39,456 ) $ 124,184 Accumulated deficit (798,061 ) 39,456 (758,605 ) The following tables summarize the effects of adopting ASC 606 on our unaudited condensed consolidated financial statements for the three months ended March 31, 2018 (in thousands, except per share data): Condensed Consolidated Balance Sheets March 31, 2018 Under Topic Under Topic Effect of Deferred revenue – related party $ 39,212 $ 35,396 $ 3,816 Deferred revenue, net of current portion – related party 81,831 122,060 (40,229 ) Accumulated deficit (849,430 ) (885,843 ) 36,413 Condensed Consolidated Statements of Operations Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Collaboration revenue – related party $ 7,345 $ 9,977 $ (2,632 ) Research and development expense 78,224 77,813 411 Total operating expenses 102,774 102,363 411 Loss from operations (94,012 ) (90,969 ) (3,043 ) Net loss (90,825 ) (87,782 ) (3,043 ) Net loss per share – basic and diluted (1.63 ) (1.58 ) (0.05 ) Condensed Consolidated Statements of Comprehensive Loss Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Net loss $ (90,825 ) $ (87,782 ) $ (3,043 ) Comprehensive loss (92,079 ) (89,036 ) (3,043 ) Condensed Consolidated Statements of Cash Flows Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Net loss $ (90,825 ) $ (87,782 ) $ (3,043 ) Adjustments to reconcile net loss to net cash used in operating activities: Deferred revenue – related party (3,141 ) (6,184 ) 3,043 During the three months ended March 31, 2018 , we recognized the following as collaboration revenue (in thousands): Three Months Ended March 31, 2018 Performance Obligation Under Topic Under Topic Effect of Collaboration revenue - related party Research and development services $ 6,364 $ 8,953 $ (2,589 ) Committee participations — 43 (43 ) Reduction of research and development expenses Development services — 411 (411 ) |
Fair Value Measurements (Tables
Fair Value Measurements (Tables) | 3 Months Ended |
Mar. 31, 2018 | |
Fair Value Disclosures [Abstract] | |
Cash Equivalents and Marketable Securities Measured at Fair Value on a Recurring Basis | The following table summarizes our cash equivalents and marketable securities measured at fair value on a recurring basis as of March 31, 2018 (in thousands): Level 1 Level 2 Level 3 Total Cash equivalents $ 262,897 $ 84,827 $ — $ 347,724 Marketable securities: Certificates of deposit — 5,226 — 5,226 U.S. Treasuries — 179,580 — 179,580 Government securities — 128,968 — 128,968 Corporate debt securities — 316,504 — 316,504 Total cash equivalents and marketable securities $ 262,897 $ 715,105 $ — $ 978,002 |
Marketable Securities (Tables)
Marketable Securities (Tables) | 3 Months Ended |
Mar. 31, 2018 | |
Investments, Debt and Equity Securities [Abstract] | |
Marketable Securities | Marketable securities at March 31, 2018 consisted of the following (in thousands): Amortized Unrealized Unrealized Fair Current: Certificates of deposit $ 4,760 $ — $ (8 ) $ 4,752 U.S Treasuries 144,849 — (209 ) 144,640 Government securities 71,773 — (141 ) 71,632 Corporate debt securities 197,334 — (377 ) 196,957 Non-current: Certificates of deposit 480 — (6 ) 474 U.S Treasuries 35,318 — (378 ) 34,940 Government securities 57,646 — (310 ) 57,336 Corporate debt securities 120,752 — (1,205 ) 119,547 Total marketable securities $ 632,912 $ — $ (2,634 ) $ 630,278 Marketable securities at December 31, 2017 consisted of the following (in thousands): Amortized Unrealized Unrealized Fair Current: Certificates of deposit $ 8,081 $ — $ (11 ) $ 8,070 U.S. Treasuries 113,852 — (119 ) 113,733 Government securities 44,421 — (57 ) 44,364 Corporate debt securities 155,222 — (177 ) 155,045 Non-current: Certificates of deposit 960 — (8 ) 952 U.S. Treasuries 36,165 — (311 ) 35,854 Government securities 23,992 — (182 ) 23,810 Corporate debt securities 83,722 — (524 ) 83,198 Total marketable securities $ 466,415 $ — $ (1,389 ) $ 465,026 |
Collaboration Agreements (Table
Collaboration Agreements (Tables) | 3 Months Ended |
Mar. 31, 2018 | |
Revenue Recognition and Deferred Revenue [Abstract] | |
Schedule of Milestone-Based Payments Associated With 2016 Agreement | We are eligible to receive the following milestone-based payments associated with the 2016 Agreement: Program Milestone Amount 65/35 program in IO field Specified clinical development event $25.0 million 65/35 program in IO field Specified regulatory milestone events Up to $183.8 million 50/50 program in IO field Specified clinical development event $20.0 million 50/50 program in IO field Specified regulatory milestone events Up to $148.8 million I&I field Specified clinical development event $25.0 million I&I field Specified regulatory milestone events Up to $236.3 million I&I field Specified commercial milestone events Up to $125.0 million |
Schedule of Satisfied and Unsatisfied Performance Obligations | The satisfied and unsatisfied performance obligations at the time of the ASC 606 adoption, each of which are considered by us to be distinct within the context of the contract, their SSP, the method of recognizing the allocated consideration, and the period through which they are expected to be recognized are as follows: Performance Obligations SSP No. of Performance Obligation(s) Recognition Method Fully satisfied at time of adoption Licenses (1) $ 86.7 million 4 Fully satisfied; recognized upon adoption of ASC 606 Research and development services (2) (3) $ 350.7 million 10 Fully satisfied; recognized upon adoption of ASC 606 Partially satisfied at time of adoption Research and development services (2) (3) $ 266.6 million 6 Proportionally as services are delivered over the performance period, expected to be through September 2022 (4) (1) The SSP was developed by probability weighting multiple cash flow scenarios using the income approach. Our management estimates within the models include the expected, probability-weighted net profits from estimated future sales, an estimate of the direct cost incurred to generate future cash flows, a discount rate and other business forecast factors. There are significant judgments and estimates inherent in the determination of the SSP of these units of accounting. These judgments and estimates include assumptions regarding future operating performance, the timelines of the clinical trials and regulatory approvals, and other factors. If different reasonable assumptions are utilized, the SSP and revenue recognized would vary. (2) The SSP was developed using our management’s best estimate of the cost of obtaining these services at arm’s length from a third-party provider. (3) The SSP was developed using internal full time equivalent costs to support the development services. (4) We determined that recognizing revenue on a proportional basis using the ratio of effort incurred to date compared to the total estimated effort required to complete the performance obligation best depicts the satisfaction of our obligations under the Collaboration Agreements. |
Schedule of Impact of New Accounting Pronouncements | the impact of the cumulative effect of the accounting changes upon the adoption of the standard (in thousands) is as follows: December 31, 2017 Cumulative Effect January 1, 2018 Deferred revenue – related party, current and net of current portions $ 163,640 $ (39,456 ) $ 124,184 Accumulated deficit (798,061 ) 39,456 (758,605 ) The following tables summarize the effects of adopting ASC 606 on our unaudited condensed consolidated financial statements for the three months ended March 31, 2018 (in thousands, except per share data): Condensed Consolidated Balance Sheets March 31, 2018 Under Topic Under Topic Effect of Deferred revenue – related party $ 39,212 $ 35,396 $ 3,816 Deferred revenue, net of current portion – related party 81,831 122,060 (40,229 ) Accumulated deficit (849,430 ) (885,843 ) 36,413 Condensed Consolidated Statements of Operations Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Collaboration revenue – related party $ 7,345 $ 9,977 $ (2,632 ) Research and development expense 78,224 77,813 411 Total operating expenses 102,774 102,363 411 Loss from operations (94,012 ) (90,969 ) (3,043 ) Net loss (90,825 ) (87,782 ) (3,043 ) Net loss per share – basic and diluted (1.63 ) (1.58 ) (0.05 ) Condensed Consolidated Statements of Comprehensive Loss Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Net loss $ (90,825 ) $ (87,782 ) $ (3,043 ) Comprehensive loss (92,079 ) (89,036 ) (3,043 ) Condensed Consolidated Statements of Cash Flows Three Months Ended March 31, 2018 Under Topic Under Topic Effect of Net loss $ (90,825 ) $ (87,782 ) $ (3,043 ) Adjustments to reconcile net loss to net cash used in operating activities: Deferred revenue – related party (3,141 ) (6,184 ) 3,043 During the three months ended March 31, 2018 , we recognized the following as collaboration revenue (in thousands): Three Months Ended March 31, 2018 Performance Obligation Under Topic Under Topic Effect of Collaboration revenue - related party Research and development services $ 6,364 $ 8,953 $ (2,589 ) Committee participations — 43 (43 ) Reduction of research and development expenses Development services — 411 (411 ) |
Summary of Multiple-deliverable Arrangements Revenue | For the three months ended March 31, 2018 and 2017 , we recognized the following collaboration revenue and reduction of research and development expenses related to such expenses (in thousands): Three Months Ended March 31, 2018 2017 Collaboration revenue - related party Commercialization activities $ 981 $ 79 Reduction of research and development expenses Research and development activities — 14 During the three months ended March 31, 2017 , we recognized as collaboration revenue the following non-contingent consideration allocated to each undelivered element (in thousands): Undelivered Element Revenue Recognized On-going research and development services $ 10,387 Committee participations 42 Total collaboration revenue - related party $ 10,429 For the three months ended March 31, 2018 and 2017 , we recognized the following totals of collaboration revenue and reduction of research and development expenses (in thousands): Three Months Ended March 31, 2018 2017 Collaboration revenue - related party $ 7,345 $ 10,508 Reduction of research and development expenses — 2,776 |
Contract with Customer, Asset and Liability | During the three months ended March 31, 2018 , we recognized the following as revenue due to changes in the contract asset and the contract liability balances (in thousands): Amounts included in the contract liability at the beginning of the period $ 5,984 Performance obligations satisfied in previous periods 323 The following table presents changes in our contract assets and liabilities during the three months ended March 31, 2018 (in thousands): December 31, 2017 Additions Deductions March 31, 2018 Contract assets (1) Collaboration receivable – related party $ 2,448 $ 3,512 $ (2,448 ) $ 3,512 Royalty receivable – related party 1,222 1,417 (1,222 ) 1,417 Contract liabilities (2) Deferred revenue – related party, current and net of current portions 163,640 4,204 (46,801 ) 121,043 (1) Additions to contract assets relate to amounts billed to Celgene for reimbursable costs incurred by us during the reporting period. Deductions to contract assets relate to collection of receivables during the reporting period. (2) Additions to contract liabilities relate to consideration from Celgene during the reporting period. Deductions to contract liabilities relate to deferred revenue recognized as revenue during the reporting period and cumulative catch-up adjustment recognized upon adoption of ASC 606 on January 1, 2018. |
Accrued Expenses (Tables)
Accrued Expenses (Tables) | 3 Months Ended |
Mar. 31, 2018 | |
Payables and Accruals [Abstract] | |
Summary of Accrued Expenses | Accrued expenses consist of the following (in thousands): March 31, December 31, Accrued compensation $ 4,966 $ 15,693 Accrued research and development costs 9,951 14,849 Accrued professional fees 1,853 3,140 Accrued other 235 349 Total accrued expenses $ 17,005 $ 34,031 |
Share-Based Payments (Tables)
Share-Based Payments (Tables) | 3 Months Ended |
Mar. 31, 2018 | |
Disclosure of Compensation Related Costs, Share-based Payments [Abstract] | |
Summary of Company's Stock Option Activity | The following table presents stock option activity for the three months ended March 31, 2018 : Number of Stock Options Weighted- Average Exercise Price Outstanding at December 31, 2017 5,577,562 $ 49.58 Granted 1,107,220 77.22 Exercised (477,847 ) 22.81 Forfeited/Expired (102,127 ) 88.78 Outstanding at March 31, 2018 6,104,808 $ 56.03 Exercisable at March 31, 2018 2,863,417 $ 48.14 Vested and expected to vest at March 31, 2018 6,104,808 $ 56.03 |
Unvested Stock Unit Activity | The following table presents RSU activity for the three months ended March 31, 2018 : Number of Stock Units Weighted-Average Grant Date Fair Value Unvested shares at December 31, 2017 125,584 $ 47.46 Granted 338,093 77.54 Vested (57,250 ) 41.76 Forfeited (781 ) 77.70 Unvested shares at March 31, 2018 405,646 $ 73.28 |
Schedule of Performance-Based Units | The following table presents PSU activity for the three months ended March 31, 2018 : Number of Stock Units Weighted-Average Grant Date Fair Value Unvested shares at December 31, 2017 176,186 $ 52.98 Granted — — Vested — — Forfeited — — Unvested shares at March 31, 2018 176,186 $ 52.98 |
Schedule of Stock-Based Compensation Expense by Award Type Included Within the Condensed Consolidated Statements of Operations | Stock-based compensation expense by award type included within the condensed consolidated statements of operations is as follows (in thousands): Three Months Ended March 31, 2018 2017 Stock options $ 12,472 $ 9,902 Restricted stock units 1,797 595 Employee Stock Purchase Plan 253 237 Total stock-based compensation expense $ 14,522 $ 10,734 |
Summary of Allocated Stock-Based Compensation Expense | Expenses related to equity-based awards were allocated as follows in the condensed consolidated statements of operations (in thousands): Three Months Ended March 31, 2018 2017 Research and development expense $ 8,640 $ 7,025 General and administrative expense 5,882 3,709 Total stock-based compensation expense $ 14,522 $ 10,734 |
Loss per Share (Tables)
Loss per Share (Tables) | 3 Months Ended |
Mar. 31, 2018 | |
Earnings Per Share [Abstract] | |
Common Stock Excluded from Calculation of Diluted Earnings Per Share | The following common stock equivalents were excluded from the calculation of diluted net loss per share applicable to common stockholders for the periods indicated because including them would have had an anti-dilutive effect: Three Months Ended March 31, 2018 2017 Stock options 6,104,808 6,129,794 Restricted stock units 405,646 126,850 Employee Stock Purchase Plan options 5,289 5,533 Total common stock equivalents 6,515,743 6,262,177 |
Overview and Basis of Present24
Overview and Basis of Presentation - Additional Information (Details) - USD ($) $ / shares in Units, $ in Thousands | 1 Months Ended | 3 Months Ended | |
Jan. 31, 2018 | Mar. 31, 2018 | Mar. 31, 2017 | |
Subsidiary, Sale of Stock [Line Items] | |||
Number of shares issued from public offering (in shares) | 8,152,986 | ||
Proceeds from public offering of common stock, net of commissions | $ 516,200 | $ 516,206 | $ 0 |
Cash, cash equivalents, and short-term investments | $ 994,700 | ||
Public Offering | |||
Subsidiary, Sale of Stock [Line Items] | |||
Number of shares issued from public offering (in shares) | 7,089,553 | ||
Offer price (in usd per share) | $ 67 | ||
Proceeds from public offering of common stock, net of commissions | $ 448,900 | ||
Over-Allotment Option | |||
Subsidiary, Sale of Stock [Line Items] | |||
Number of shares issued from public offering (in shares) | 1,063,433 | ||
Proceeds from public offering of common stock, net of commissions | $ 67,300 |
Summary of Significant Accoun25
Summary of Significant Accounting Policies and Recent Accounting Pronouncements - Impact of the Cumulative Effect of Accounting Changes Upon Adoption of ASC 606 (Details) - USD ($) $ in Thousands | Mar. 31, 2018 | Jan. 01, 2018 | Dec. 31, 2017 |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |||
Deferred revenue – related party, current and net of current portions | $ 124,184 | ||
Accumulated deficit | $ (849,430) | (758,605) | $ (798,061) |
Before ASC 606 | |||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |||
Deferred revenue – related party, current and net of current portions | 163,640 | ||
Accumulated deficit | (885,843) | $ (798,061) | |
Accounting Standards Update 2014-09 | ASC 606 Adjustments | |||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |||
Deferred revenue – related party, current and net of current portions | (39,456) | ||
Accumulated deficit | $ 36,413 | $ 39,456 |
Summary of Significant Accoun26
Summary of Significant Accounting Policies and Recent Accounting Pronouncements - Schedule of Effects of Adopting ASC 606 on Unaudited Balance Sheet (Details) - USD ($) $ in Thousands | Mar. 31, 2018 | Jan. 01, 2018 | Dec. 31, 2017 |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |||
Deferred revenue – related party | $ 39,212 | $ 37,842 | |
Deferred revenue, net of current portion – related party | 81,831 | 125,798 | |
Accumulated deficit | (849,430) | $ (758,605) | (798,061) |
Before ASC 606 | |||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |||
Deferred revenue – related party | 35,396 | ||
Deferred revenue, net of current portion – related party | 122,060 | ||
Accumulated deficit | (885,843) | $ (798,061) | |
Accounting Standards Update 2014-09 | ASC 606 Adjustments | |||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |||
Deferred revenue – related party | 3,816 | ||
Deferred revenue, net of current portion – related party | (40,229) | ||
Accumulated deficit | $ 36,413 | $ 39,456 |
Summary of Significant Accoun27
Summary of Significant Accounting Policies and Recent Accounting Pronouncements - Schedule of Effects of Adopting ASC 606 on Unaudited Statements of Operations (Details) - USD ($) $ / shares in Units, $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | $ 7,345 | $ 10,508 |
Research and development expense | 78,224 | 62,732 |
Total operating expenses | 102,774 | 77,555 |
Loss from operations | (94,012) | (67,047) |
Net loss | $ (90,825) | $ (66,166) |
Net loss per share – basic and diluted (usd per share) | $ (1.63) | $ (1.56) |
Before ASC 606 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | $ 9,977 | |
Research and development expense | 77,813 | |
Total operating expenses | 102,363 | |
Loss from operations | (90,969) | |
Net loss | $ (87,782) | |
Net loss per share – basic and diluted (usd per share) | $ (1.58) | |
Accounting Standards Update 2014-09 | ASC 606 Adjustments | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | $ (2,632) | |
Research and development expense | 411 | |
Total operating expenses | 411 | |
Loss from operations | (3,043) | |
Net loss | $ (3,043) | |
Net loss per share – basic and diluted (usd per share) | $ (0.05) |
Summary of Significant Accoun28
Summary of Significant Accounting Policies and Recent Accounting Pronouncements - Schedule of Effects of Adopting ASC 606 on Unaudited Statements of Comprehensive Loss (Details) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Net loss | $ (90,825) | $ (66,166) |
Comprehensive loss | (92,079) | $ (66,065) |
Before ASC 606 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Net loss | (87,782) | |
Comprehensive loss | (89,036) | |
Accounting Standards Update 2014-09 | ASC 606 Adjustments | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Net loss | (3,043) | |
Comprehensive loss | $ (3,043) |
Summary of Significant Accoun29
Summary of Significant Accounting Policies and Recent Accounting Pronouncements - Schedule of Effects of Adopting ASC 606 on Unaudited Statements of Cash Flows (Details) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Net loss | $ (90,825) | $ (66,166) |
Adjustments to reconcile net loss to net cash used in operating activities: | ||
Deferred revenue – related party | (3,141) | $ (1,924) |
Before ASC 606 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Net loss | (87,782) | |
Adjustments to reconcile net loss to net cash used in operating activities: | ||
Deferred revenue – related party | (6,184) | |
Accounting Standards Update 2014-09 | ASC 606 Adjustments | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Net loss | (3,043) | |
Adjustments to reconcile net loss to net cash used in operating activities: | ||
Deferred revenue – related party | $ 3,043 |
Fair Value Measurements - Cash
Fair Value Measurements - Cash Equivalents and Marketable Securities Measured at Fair Value on a Recurring Basis (Details) - Fair Value, Measurements, Recurring $ in Thousands | Mar. 31, 2018USD ($) |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Cash equivalents | $ 347,724 |
Total cash equivalents and marketable securities | 978,002 |
Certificates of deposit | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 5,226 |
U.S. Treasuries | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 179,580 |
Government securities | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 128,968 |
Corporate debt securities | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 316,504 |
Level 1 | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Cash equivalents | 262,897 |
Total cash equivalents and marketable securities | 262,897 |
Level 1 | Certificates of deposit | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 0 |
Level 1 | U.S. Treasuries | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 0 |
Level 1 | Government securities | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 0 |
Level 1 | Corporate debt securities | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 0 |
Level 2 | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Cash equivalents | 84,827 |
Total cash equivalents and marketable securities | 715,105 |
Level 2 | Certificates of deposit | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 5,226 |
Level 2 | U.S. Treasuries | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 179,580 |
Level 2 | Government securities | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 128,968 |
Level 2 | Corporate debt securities | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 316,504 |
Level 3 | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Cash equivalents | 0 |
Total cash equivalents and marketable securities | 0 |
Level 3 | Certificates of deposit | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 0 |
Level 3 | U.S. Treasuries | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 0 |
Level 3 | Government securities | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | 0 |
Level 3 | Corporate debt securities | |
Fair Value, Balance Sheet Grouping, Financial Statement Captions [Line Items] | |
Marketable securities | $ 0 |
Fair Value Measurements - Addit
Fair Value Measurements - Additional Information (Details) | Mar. 31, 2018USD ($) |
Level 3 | |
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items] | |
Fair value of assets (liabilities) | $ 0 |
Marketable Securities - Additio
Marketable Securities - Additional Information (Details) | 3 Months Ended | ||
Mar. 31, 2018USD ($)security | Mar. 31, 2017USD ($) | Dec. 31, 2017USD ($)security | |
Schedule of Available-for-sale Securities [Line Items] | |||
Realized gain (loss) on marketable securities | $ 0 | $ 0 | |
Reclassifications out of accumulated other comprehensive income | $ 0 | $ 0 | |
Established time period for liquidation | 12 months | ||
Debt securities in an unrealized loss position | security | 257 | 240 | |
Aggregate fair value of debt securities in an unrealized loss position | $ 572,700,000 | $ 439,400,000 | |
Maximum | |||
Schedule of Available-for-sale Securities [Line Items] | |||
Minimum maturity (in years) | 1 year | ||
Maximum maturity (in years) | 2 years | ||
Minimum | |||
Schedule of Available-for-sale Securities [Line Items] | |||
Minimum maturity (in years) | 1 year |
Marketable Securities - Summary
Marketable Securities - Summary of Marketable Securities (Details) - USD ($) $ in Thousands | Mar. 31, 2018 | Dec. 31, 2017 |
Schedule of Available-for-sale Securities [Line Items] | ||
Amortized Cost | $ 632,912 | $ 466,415 |
Unrealized Gains | 0 | 0 |
Unrealized Losses | (2,634) | (1,389) |
Fair Value | 630,278 | 465,026 |
Current: | Certificates of deposit | ||
Schedule of Available-for-sale Securities [Line Items] | ||
Amortized Cost | 4,760 | 8,081 |
Unrealized Gains | 0 | 0 |
Unrealized Losses | (8) | (11) |
Fair Value | 4,752 | 8,070 |
Current: | U.S. Treasuries | ||
Schedule of Available-for-sale Securities [Line Items] | ||
Amortized Cost | 144,849 | 113,852 |
Unrealized Gains | 0 | 0 |
Unrealized Losses | (209) | (119) |
Fair Value | 144,640 | 113,733 |
Current: | Government securities | ||
Schedule of Available-for-sale Securities [Line Items] | ||
Amortized Cost | 71,773 | 44,421 |
Unrealized Gains | 0 | 0 |
Unrealized Losses | (141) | (57) |
Fair Value | 71,632 | 44,364 |
Current: | Corporate debt securities | ||
Schedule of Available-for-sale Securities [Line Items] | ||
Amortized Cost | 197,334 | 155,222 |
Unrealized Gains | 0 | 0 |
Unrealized Losses | (377) | (177) |
Fair Value | 196,957 | 155,045 |
Non-current: | Certificates of deposit | ||
Schedule of Available-for-sale Securities [Line Items] | ||
Amortized Cost | 480 | 960 |
Unrealized Gains | 0 | 0 |
Unrealized Losses | (6) | (8) |
Fair Value | 474 | 952 |
Non-current: | U.S. Treasuries | ||
Schedule of Available-for-sale Securities [Line Items] | ||
Amortized Cost | 35,318 | 36,165 |
Unrealized Gains | 0 | 0 |
Unrealized Losses | (378) | (311) |
Fair Value | 34,940 | 35,854 |
Non-current: | Government securities | ||
Schedule of Available-for-sale Securities [Line Items] | ||
Amortized Cost | 57,646 | 23,992 |
Unrealized Gains | 0 | 0 |
Unrealized Losses | (310) | (182) |
Fair Value | 57,336 | 23,810 |
Non-current: | Corporate debt securities | ||
Schedule of Available-for-sale Securities [Line Items] | ||
Amortized Cost | 120,752 | 83,722 |
Unrealized Gains | 0 | 0 |
Unrealized Losses | (1,205) | (524) |
Fair Value | $ 119,547 | $ 83,198 |
Collaboration Agreements - 2016
Collaboration Agreements - 2016 Agreement (Details) - 2016 Agreement | 1 Months Ended |
May 31, 2016extensionprogram | |
Celgene | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | |
Number of research programs that can be designated for continued development after the research term | program | 3 |
Celgene | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | |
Remaining cancer metabolism programs | program | 2 |
Term of agreements | 4 years |
Extension period | extension | 2 |
Number of allowable special case extensions | extension | 4 |
Special case extension term | 1 year |
Collaboration Agreements - Co-D
Collaboration Agreements - Co-Development and Co-Commercialization Agreements (Details) - Co-Development and Co-Commercialization Agreements - Celgene | 1 Months Ended |
May 31, 2016 | |
65/35 Program | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | |
Profit or loss share percentage | 65.00% |
Other Than 65/35 Program | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | |
Profit or loss share percentage | 50.00% |
Collaboration Agreements - Fina
Collaboration Agreements - Financial Terms (Details) - Celgene - 2016 Agreement | May 17, 2016USD ($) | May 31, 2016USD ($)extension | Mar. 31, 2017USD ($) |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | |||
Initial payment received | $ 8,000,000 | $ 200,000,000 | $ 8,000,000 |
Extension period | extension | 2 | ||
Number of allowable special case extensions | extension | 4 | ||
Upfront payment agreement extension fee receivable | $ 40,000,000 | ||
Option exercise fee receivable | 30,000,000 | ||
Additional option exercise fee for further development | 10,000,000 | ||
Minimum | |||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | |||
Minimum option exercise fee receivable for continuation program | $ 35,000,000 |
Collaboration Agreements - Summ
Collaboration Agreements - Summary of Milestone-based Receivable Payments (Details) - Celgene $ in Millions | May 31, 2016USD ($) |
Specified clinical development event | Co Commercial Agreement | |
Revenue Recognition, Milestone Method [Line Items] | |
Milestone-based receivable payments, eligible to be received | $ 25 |
Specified clinical development event | 65/35 Program | Co-Development and Co-Commercialization Agreements | |
Revenue Recognition, Milestone Method [Line Items] | |
Milestone-based receivable payments, eligible to be received | 25 |
Specified clinical development event | Other Than 65/35 Program | Co-Development and Co-Commercialization Agreements | |
Revenue Recognition, Milestone Method [Line Items] | |
Milestone-based receivable payments, eligible to be received | 20 |
Specified regulatory milestone events | Maximum | Co Commercial Agreement | |
Revenue Recognition, Milestone Method [Line Items] | |
Milestone-based receivable payments, eligible to be received | 236.3 |
Specified regulatory milestone events | Maximum | 65/35 Program | Co-Development and Co-Commercialization Agreements | |
Revenue Recognition, Milestone Method [Line Items] | |
Milestone-based receivable payments, eligible to be received | 183.8 |
Specified regulatory milestone events | Maximum | Other Than 65/35 Program | Co-Development and Co-Commercialization Agreements | |
Revenue Recognition, Milestone Method [Line Items] | |
Milestone-based receivable payments, eligible to be received | 148.8 |
Specified commercial milestone events | Maximum | Co Commercial Agreement | |
Revenue Recognition, Milestone Method [Line Items] | |
Milestone-based receivable payments, eligible to be received | $ 125 |
Collaboration Agreements - AG-8
Collaboration Agreements - AG-881 Agreements (Details) - AG-881 program licenses - USD ($) | 1 Months Ended | ||
May 31, 2015 | Mar. 31, 2018 | Apr. 27, 2015 | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | |||
Initial payment received | $ 10,000,000 | ||
Milestone-based receivable payments, eligible to be received | $ 70,000,000 | ||
Milestone payment for filing of first NDA | $ 15,000,000 | 15,000,000 | |
Milestone payments upon achievement of specified regulatory milestone events | $ 55,000,000 |
Collaboration Agreements - 2010
Collaboration Agreements - 2010 Agreement (Details) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Royalty revenue | $ 1,417 | $ 0 |
2010 Agreement | ||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Milestone-based receivable payments, eligible to be received | 95,000 | |
Milestone payments upon achievement of specified regulatory milestone events | 70,000 | |
Milestone payment upon achievement of a specified commercial milestone event | $ 25,000 |
Collaboration Agreements - Sche
Collaboration Agreements - Schedule of Satisfied and Unsatisfied Performance Obligations (Details) $ in Millions | 3 Months Ended |
Mar. 31, 2018USD ($)performance_obligation | |
Licenses | Transferred at Point in Time | |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |
Stand-alone selling price | $ | $ 86.7 |
No. of Performance Obligation(s) | performance_obligation | 4 |
Research services | Transferred at Point in Time | |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |
Stand-alone selling price | $ | $ 350.7 |
No. of Performance Obligation(s) | performance_obligation | 10 |
Research services | Transferred over Time | |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |
Stand-alone selling price | $ | $ 266.6 |
No. of Performance Obligation(s) | performance_obligation | 6 |
Collaboration Agreements - Sc41
Collaboration Agreements - Schedule of Effect of Adopting ASC 606 by Performance Obligation (Details) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | $ 7,345 | $ 10,508 |
Reduction of research and development expenses | 0 | 2,776 |
Before ASC 606 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | 9,977 | |
ASC 606 Adjustments | Accounting Standards Update 2014-09 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | (2,632) | |
Research services | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | 6,364 | |
Research services | Before ASC 606 | Accounting Standards Update 2014-09 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | 8,953 | |
Research services | ASC 606 Adjustments | Accounting Standards Update 2014-09 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | (2,589) | |
Development services | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Reduction of research and development expenses | 0 | $ 2,800 |
Development services | Before ASC 606 | Accounting Standards Update 2014-09 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Reduction of research and development expenses | 411 | |
Development services | ASC 606 Adjustments | Accounting Standards Update 2014-09 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Reduction of research and development expenses | (411) | |
Committee participations | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | 0 | |
Committee participations | Before ASC 606 | Accounting Standards Update 2014-09 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | 43 | |
Committee participations | ASC 606 Adjustments | Accounting Standards Update 2014-09 | ||
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | ||
Collaboration revenue – related party | $ (43) |
Collaboration Agreements - Su42
Collaboration Agreements - Summary of Collaboration Revenue (Details) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Collaboration revenue – related party | $ 8,762 | $ 10,508 |
Collaborative arrangement, product | ||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Collaboration revenue – related party | 10,429 | |
Collaborative arrangement, product | Development services | ||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Collaboration revenue – related party | 10,387 | |
Collaborative arrangement, product | Committee participations | ||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Collaboration revenue – related party | $ 42 |
Collaboration Agreements - Rema
Collaboration Agreements - Remaining Unsatisfied Performance Obligations (Details) $ in Millions | 3 Months Ended |
Mar. 31, 2018USD ($) | |
Revenue, Remaining Performance Obligation, Expected Timing of Satisfaction, Start Date [Axis]: 2018-04-01 | |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |
Remaining performance obligation, expected timing of satisfaction | 9 months |
Revenue, Remaining Performance Obligation, Expected Timing of Satisfaction, Start Date [Axis]: (nil) | |
Revenue, Initial Application Period Cumulative Effect Transition [Line Items] | |
Remaining unsatisfied performance obligation | $ 132.6 |
Collaboration Agreements - Su44
Collaboration Agreements - Summary of Revenue Recognized as a Reduction of Research and Development Expenses (Details) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Reduction of research and development expenses | $ 0 | $ 2,776 |
Development services | ||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Reduction of research and development expenses | $ 0 | $ 2,800 |
Collaboration Agreements - Deve
Collaboration Agreements - Development and Commercialization Expense Not Contemplated As Part Of Modifications (Details) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Collaboration revenue – related party | $ 7,345 | $ 10,508 |
Reduction of research and development expenses | 0 | 2,776 |
Collaborative arrangement, product | Not Included In Modification Due To High Level Of Uncertainty | Commercialization activities | ||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Collaboration revenue – related party | 981 | 79 |
Collaborative arrangement, product | Not Included In Modification Due To High Level Of Uncertainty | Research and development activities | ||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||
Reduction of research and development expenses | $ 0 | $ 14 |
Collaboration Agreements - Coll
Collaboration Agreements - Collaboration Revenue and Research and Development Expense (Details) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Revenue Recognition and Deferred Revenue [Abstract] | ||
Collaboration revenue - related party | $ 7,345 | $ 10,508 |
Reduction of research and development expenses | $ 0 | $ 2,776 |
Collaboration Agreements - Sc47
Collaboration Agreements - Schedule of Changes in Contract Assets and Liabilities (Details) $ in Thousands | 3 Months Ended |
Mar. 31, 2018USD ($) | |
Contract liabilities | |
Additions | $ 5,984 |
Collaboration receivable – related party | |
Contract assets | |
Contract assets, beginning balance | 2,448 |
Additions | 3,512 |
Deductions | (2,448) |
Contract assets, ending balance | 3,512 |
Royalty receivable – related party | |
Contract assets | |
Contract assets, beginning balance | 1,222 |
Additions | 1,417 |
Deductions | (1,222) |
Contract assets, ending balance | 1,417 |
Deferred revenue – related party, current and net of current portions | |
Contract liabilities | |
Contract liabilities, beginning balance | 163,640 |
Additions | 4,204 |
Deductions | (46,801) |
Contract liabilities, ending balance | $ 121,043 |
Collaboration Agreements - Sc48
Collaboration Agreements - Schedule of Revenues as a Result of Changes in Contract Asset and Contract Liabilities (Details) $ in Thousands | 3 Months Ended |
Mar. 31, 2018USD ($) | |
Revenue Recognition and Deferred Revenue [Abstract] | |
Amounts included in the contract liability at the beginning of the period | $ 5,984 |
Performance obligations satisfied in previous periods | $ 323 |
Collaboration Agreements - Acco
Collaboration Agreements - Accounting Analysis And Revenue Recognition - Milestone (Details) - USD ($) | 3 Months Ended | ||
Mar. 31, 2018 | Mar. 31, 2017 | Apr. 27, 2015 | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | |||
Milestones achieved | $ 0 | $ 0 | |
AG-881 program licenses | |||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | |||
Milestone payment for filing of first NDA | $ 15,000,000 | $ 15,000,000 |
Collaboration Agreements - Auri
Collaboration Agreements - Aurigene Discovery Technologies Limited (Details) - USD ($) $ in Thousands | 1 Months Ended | 3 Months Ended | ||
May 31, 2017 | Mar. 31, 2018 | Mar. 31, 2017 | Apr. 30, 2017 | |
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||||
Upfront payment | $ 78,224 | $ 62,732 | ||
Aurigene Discovery Technologies Limited | ||||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||||
Upfront payment | $ 3,000 | |||
Potential future milestone payments | $ 17,000 | |||
DHODH Phase One Clinical Trial | Aurigene Discovery Technologies Limited | ||||
Collaborative Arrangements and Non-collaborative Arrangement Transactions [Line Items] | ||||
Potential future milestone payments | $ 2,000 |
Accrued Expenses - Summary of A
Accrued Expenses - Summary of Accrued Expenses (Details) - USD ($) $ in Thousands | Mar. 31, 2018 | Dec. 31, 2017 |
Payables and Accruals [Abstract] | ||
Accrued compensation | $ 4,966 | $ 15,693 |
Accrued research and development costs | 9,951 | 14,849 |
Accrued professional fees | 1,853 | 3,140 |
Accrued other | 235 | 349 |
Total accrued expenses | $ 17,005 | $ 34,031 |
Share-Based Payments - Addition
Share-Based Payments - Additional Information (Details) - USD ($) $ in Millions | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Restricted stock units | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total unrecognized compensation expense related to stock option | $ 26.7 | |
Weighted-average period to recognize compensation expense (in years) | 2 years 6 months 26 days | |
2007 Plan and 2013 Plan | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Common stock reserved for issuance (in shares) | 8,624,887 | |
Shares available for future issuance (in shares) | 1,938,247 | |
2013 Stock Incentive Plan | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total unrecognized compensation expense related to stock option | $ 130 | |
Weighted-average period to recognize compensation expense (in years) | 2 years 11 months 16 days | |
2013 Stock Incentive Plan | Performance-Based Stock Units (PSUs) | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total unrecognized compensation expense related to stock option | $ 9.3 | |
2013 Employee Stock Purchase Plan | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Shares available for future issuance (in shares) | 186,414 | |
Shares issued under 2013 ESPP (in shares) | 27,377 | 33,521 |
Opportunity to purchase of common stock (in shares) | 327,272 |
Share-Based Payments - Summary
Share-Based Payments - Summary of Company's Stock Option Activity (Details) | 3 Months Ended |
Mar. 31, 2018$ / sharesshares | |
Share-based Compensation Arrangement by Share-based Payment Award, Options, Outstanding [Roll Forward] | |
Number of Stock Options, Outstanding, Beginning balance (in shares) | shares | 5,577,562 |
Number of Stock Options, Granted (in shares) | shares | 1,107,220 |
Number of Stock Options, Exercised (in shares) | shares | (477,847) |
Number of Stock Options, Forfeited/Expired (in shares) | shares | (102,127) |
Number of Stock Options, Outstanding, Ending balance (in shares) | shares | 6,104,808 |
Number of Stock Options, Exercisable (in shares) | shares | 2,863,417 |
Number of Stock Options, Vested and expected to vest (in shares) | shares | 6,104,808 |
Share-based Compensation Arrangement by Share-based Payment Award, Options, Outstanding, Weighted Average Exercise Price [Abstract] | |
Weighted-Average Exercise Price, Outstanding, Beginning balance (in usd per share) | $ / shares | $ 49.58 |
Weighted-Average Exercise Price, Granted (in usd per share) | $ / shares | 77.22 |
Weighted-Average Exercise Price, Exercised (in usd per share) | $ / shares | 22.81 |
Weighted-Average Exercise Price, Forfeited/Expired (in usd per share) | $ / shares | 88.78 |
Weighted-Average Exercise Price, Outstanding, Ending balance (in usd per share) | $ / shares | 56.03 |
Weighted-Average Exercise Price, Exercisable (in usd per share) | $ / shares | 48.14 |
Weighted-Average Exercise Price, Vested and expected to vest (in usd per share) | $ / shares | $ 56.03 |
Share-Based Payments - Summar54
Share-Based Payments - Summary of Unvested RSUs Activity (Details) - Restricted stock units | 3 Months Ended |
Mar. 31, 2018$ / sharesshares | |
Share-based Compensation Arrangement by Share-based Payment Award, Equity Instruments Other than Options, Nonvested, Number of Shares [Roll Forward] | |
Unvested shares beginning of period (in shares) | shares | 125,584 |
Granted (in shares) | shares | 338,093 |
Vested (in shares) | shares | (57,250) |
Forfeited/expired (in shares) | shares | (781) |
Unvested shares end of period (in shares) | shares | 405,646 |
Share-based Compensation Arrangement by Share-based Payment Award, Equity Instruments Other than Options, Nonvested, Weighted Average Grant Date Fair Value [Abstract] | |
Weighted-average grant date fair value, Unvested shares beginning of period (in usd per share) | $ / shares | $ 47.46 |
Weighted-average grant date fair value, Granted (in usd per share) | $ / shares | 77.54 |
Weighted-average grant date fair value, Vested (in usd per share) | $ / shares | 41.76 |
Weighted-average grant date fair value, Forfeited/expired (in usd per share) | $ / shares | 77.70 |
Weighted-average grant date fair value, Unvested shares end of period (in usd per share) | $ / shares | $ 73.28 |
Share-Based Payments - Schedule
Share-Based Payments - Schedule of Performance-Based Units (Details) - Performance-Based Stock Units (PSUs) | 3 Months Ended |
Mar. 31, 2018$ / sharesshares | |
Share-based Compensation Arrangement by Share-based Payment Award, Equity Instruments Other than Options, Nonvested, Number of Shares [Roll Forward] | |
Unvested shares beginning of period (in shares) | shares | 176,186 |
Granted (in shares) | shares | 0 |
Vested (in shares) | shares | 0 |
Forfeited/expired (in shares) | shares | 0 |
Unvested shares end of period (in shares) | shares | 176,186 |
Share-based Compensation Arrangement by Share-based Payment Award, Equity Instruments Other than Options, Nonvested, Weighted Average Grant Date Fair Value [Abstract] | |
Weighted-average grant date fair value, Unvested shares beginning of period (in usd per share) | $ / shares | $ 52.98 |
Weighted-average grant date fair value, Granted (in usd per share) | $ / shares | 0 |
Weighted-average grant date fair value, Vested (in usd per share) | $ / shares | 0 |
Weighted-average grant date fair value, Forfeited/expired (in usd per share) | $ / shares | 0 |
Weighted-average grant date fair value, Unvested shares end of period (in usd per share) | $ / shares | $ 52.98 |
Share-Based Payments - Schedu56
Share-Based Payments - Schedule of Stock-Based Compensation Expense by Award Type Included Within the Condensed Consolidated Statements of Operations (Details) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total stock-based compensation expense | $ 14,522 | $ 10,734 |
Stock options | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total stock-based compensation expense | 12,472 | 9,902 |
Restricted stock units | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total stock-based compensation expense | 1,797 | 595 |
Employee Stock Purchase Plan | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total stock-based compensation expense | $ 253 | $ 237 |
Share-Based Payments - Stock-Ba
Share-Based Payments - Stock-Based Compensation Expense for Employee and Non-Employee Stock Options, Restricted Stock Units, Performance-Based Stock Options, Performance-Based Stock Units and Employee Stock Purchase Plan Shares (Details) - USD ($) $ in Thousands | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total stock-based compensation expense | $ 14,522 | $ 10,734 |
Research and development expense | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total stock-based compensation expense | 8,640 | 7,025 |
General and administrative expense | ||
Share-based Compensation Arrangement by Share-based Payment Award [Line Items] | ||
Total stock-based compensation expense | $ 5,882 | $ 3,709 |
Loss per Share - Common Stock E
Loss per Share - Common Stock Excluded from Calculation of Diluted Net Loss Per Share (Details) - shares | 3 Months Ended | |
Mar. 31, 2018 | Mar. 31, 2017 | |
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items] | ||
Antidilutive securities excluded from computation of earnings per share (in shares) | 6,515,743 | 6,262,177 |
Stock options | ||
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items] | ||
Antidilutive securities excluded from computation of earnings per share (in shares) | 6,104,808 | 6,129,794 |
Restricted stock units | ||
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items] | ||
Antidilutive securities excluded from computation of earnings per share (in shares) | 405,646 | 126,850 |
Employee Stock Purchase Plan options | ||
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items] | ||
Antidilutive securities excluded from computation of earnings per share (in shares) | 5,289 | 5,533 |