Document and Entity Information
Document and Entity Information - USD ($) | 12 Months Ended | ||
Dec. 31, 2015 | Feb. 16, 2016 | Jun. 30, 2015 | |
Document and Entity Information | |||
Entity Registrant Name | Innoviva, Inc. | ||
Entity Central Index Key | 1,080,014 | ||
Document Type | 10-K | ||
Document Period End Date | Dec. 31, 2015 | ||
Amendment Flag | false | ||
Current Fiscal Year End Date | --12-31 | ||
Entity Well-known Seasoned Issuer | Yes | ||
Entity Voluntary Filers | No | ||
Entity Current Reporting Status | Yes | ||
Entity Filer Category | Large Accelerated Filer | ||
Entity Public Float | $ 636,988,750 | ||
Entity Common Stock, Shares Outstanding | 114,117,517 | ||
Document Fiscal Year Focus | 2,015 | ||
Document Fiscal Period Focus | FY |
CONSOLIDATED BALANCE SHEETS
CONSOLIDATED BALANCE SHEETS - USD ($) $ in Thousands | Dec. 31, 2015 | Dec. 31, 2014 |
Current assets: | ||
Cash and cash equivalents | $ 159,180 | $ 96,800 |
Short-term marketable securities | 28,103 | 143,698 |
Related party receivables from collaborative arrangements | 26,228 | 10,550 |
Prepaid expenses and other current assets | 814 | 1,134 |
Total current assets | 214,325 | 252,182 |
Marketable securities | 0 | 42,856 |
Property and equipment, net | 221 | 324 |
Capitalized fees paid to a related party, net | 194,368 | 208,191 |
Other assets | 15,158 | 18,101 |
Total assets | 424,072 | 521,654 |
Current liabilities: | ||
Accounts payable | 818 | 0 |
Payable to Theravance Biopharma, Inc. | 0 | 1,056 |
Accrued personnel-related expenses | 1,659 | 1,959 |
Accrued interest payable | 7,911 | 7,551 |
Other accrued liabilities | 2,218 | 2,108 |
Deferred revenue | 885 | 1,082 |
Total current liabilities | 13,491 | 13,756 |
Convertible subordinated notes, due 2023 | 255,109 | 255,109 |
Non-recourse notes, due 2029 | 493,162 | 470,527 |
Other long-term liabilities | 1,856 | 1,823 |
Deferred revenue | $ 3,099 | $ 3,788 |
Commitments and contingencies (Notes 3, 6 and 9) | ||
Stockholders' deficit: | ||
Preferred stock: $0.01 par value, 230 shares authorized, no shares issued and outstanding | ||
Common stock: $0.01 par value, 200,000 shares authorized, 114,933 and 116,445 shares issued as of December 31, 2015 and 2014, respectively | $ 1,149 | $ 1,164 |
Treasury stock: 150 shares as of December 31, 2015 and 2014 | (3,263) | (3,263) |
Additional paid-in capital | 1,351,898 | 1,452,504 |
Accumulated other comprehensive loss | (2) | (87) |
Accumulated deficit | (1,692,427) | (1,673,667) |
Total stockholders' deficit | (342,645) | (223,349) |
Total liabilities and stockholders' deficit | $ 424,072 | $ 521,654 |
CONSOLIDATED BALANCE SHEETS (Pa
CONSOLIDATED BALANCE SHEETS (Parenthetical) - $ / shares shares in Thousands | Dec. 31, 2015 | Dec. 31, 2014 |
CONDENSED CONSOLIDATED BALANCE SHEETS | ||
Preferred stock, par value (in dollars per share) | $ 0.01 | $ 0.01 |
Preferred stock, shares authorized | 230 | 230 |
Preferred stock, shares issued | 0 | 0 |
Preferred stock, shares outstanding | 0 | 0 |
Common stock, par value (in dollars per share) | $ 0.01 | $ 0.01 |
Common stock, shares authorized | 200,000 | 200,000 |
Common stock, shares issued | 114,933 | 116,445 |
Treasury Stock, Shares | 150 | 150 |
CONSOLIDATED STATEMENTS OF OPER
CONSOLIDATED STATEMENTS OF OPERATIONS - USD ($) shares in Thousands, $ in Thousands | 12 Months Ended | ||
Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
Revenue: | |||
Royalty revenue from a related party, net of amortization for capitalized fees paid to a related party of $13,823, $11,066 and $743 in the year ended December 31, 2015, 2014 and 2013 | $ 53,064 | $ 7,351 | $ 1,202 |
Revenue from collaborative arrangements from a related party, net | 885 | 1,082 | 3,330 |
Total net revenue | 53,949 | 8,433 | 4,532 |
Operating expenses: | |||
Research and development | 2,619 | 7,498 | 9,038 |
General and administrative | 19,750 | 34,864 | 24,289 |
Total operating expenses | 22,369 | 42,362 | 33,327 |
Income (loss) from operations | 31,580 | (33,929) | (28,795) |
Other income (expense), net | 1,120 | (3,272) | 6,732 |
Interest income | 343 | 563 | 778 |
Interest expense | (51,803) | (36,892) | (9,348) |
Loss from continuing operations before income taxes | (18,760) | (73,530) | (30,633) |
Income tax expense (benefit) | 0 | 0 | 0 |
Loss from continuing operations, net of tax | (18,760) | (73,530) | (30,633) |
Loss from discontinued operations (Notes 1 and 12) | 0 | (94,934) | (140,068) |
Net loss | $ (18,760) | $ (168,464) | $ (170,701) |
Basic and diluted net loss per share: | |||
Continuing operations, net of tax (in dollars per share) | $ (0.16) | $ (0.66) | $ (0.30) |
Discontinued operations (in dollars per share) | 0 | (0.84) | (1.37) |
Basic and diluted net loss per share (in dollars per share) | (0.16) | (1.50) | (1.67) |
Cash dividend declared per common share (in dollars per share) | $ 0.75 | $ 0.50 | $ 0 |
Shares used to compute basic and diluted net loss per share | 115,372 | 112,059 | 102,425 |
CONSOLIDATED STATEMENTS OF OPE5
CONSOLIDATED STATEMENTS OF OPERATIONS (Parenthetical) - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS | |||
Amortization of capitalized fees paid to a related party | $ 13,823 | $ 11,066 | $ 743 |
CONSOLIDATED STATEMENTS OF COMP
CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE LOSS | |||
Net loss | $ (18,760) | $ (168,464) | $ (170,701) |
Other comprehensive income: | |||
Unrealized gain (loss) on marketable securities, net | 1,305 | (4,001) | 63 |
Less: Realized gain on marketable securities, net | (1,220) | 0 | 0 |
Add: Reclassification adjustments for other-than temporary impairment loss included in net loss | 0 | 3,752 | 0 |
Comprehensive loss | $ (18,675) | $ (168,713) | $ (170,638) |
CONSOLIDATED STATEMENTS OF STOC
CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY (DEFICIT) - USD ($) shares in Thousands, $ in Thousands | Common Stock | Additional Paid-In Capital | Accumulated Other Comprehensive Income (Loss) | Accumulated Deficit | Treasury Stock | Total |
Balance at Dec. 31, 2012 | $ 984 | $ 1,488,447 | $ 99 | $ (1,334,502) | $ 155,028 | |
Balance (in shares) at Dec. 31, 2012 | 98,379 | |||||
Increase (Decrease) in Stockholders' Equity | ||||||
Exercise of stock options, and issuance of common stock units, stock awards and purchase plan | $ 29 | 26,962 | 26,991 | |||
Exercise of stock options, and issuance of common stock units, stock awards and purchase plan (in shares) | 2,964 | |||||
Issuance of common stock in private placement to a related party | $ 35 | 125,995 | 126,030 | |||
Issuance of common stock in private placement to a related party (in shares) | 3,505 | |||||
Stock based compensation | 25,858 | 25,858 | ||||
Conversion of convertible subordinated notes | $ 67 | 171,164 | 171,231 | |||
Conversion of convertible subordinated notes (in shares) | 6,668 | |||||
Capped call options associated with convertible subordinated notes due 2023 | (35,378) | (35,378) | ||||
Net loss | (170,701) | (170,701) | ||||
Other comprehensive income (loss) | 63 | 63 | ||||
Balance at Dec. 31, 2013 | $ 1,115 | 1,803,048 | 162 | (1,505,203) | 299,122 | |
Balance (in shares) at Dec. 31, 2013 | 111,516 | |||||
Increase (Decrease) in Stockholders' Equity | ||||||
Exercise of stock options, and issuance of common stock units, stock awards and purchase plan | $ 17 | 10,813 | 10,830 | |||
Exercise of stock options, and issuance of common stock units, stock awards and purchase plan (in shares) | 1,744 | |||||
Issuance of common stock in private placement to a related party | $ 17 | 38,078 | 38,095 | |||
Issuance of common stock in private placement to a related party (in shares) | 1,665 | |||||
Stock based compensation | 27,485 | 27,485 | ||||
Conversion of convertible subordinated notes | $ 15 | 31,756 | 31,771 | |||
Conversion of convertible subordinated notes (in shares) | 1,520 | |||||
Repurchase of common stock | 3,263 | $ (3,263) | ||||
Repurchase of common stock (in shares) | (150) | |||||
Guarantee issued in connection with distribution to Theravance Biopharma, Inc. related to lease agreements | (1,300) | (1,300) | ||||
Distribution to Theravance Biopharma, Inc. | (402,787) | (402,787) | ||||
Cash dividends declared, $0.50 and $0.75 per common share | (57,852) | (57,852) | ||||
Net loss | (168,464) | (168,464) | ||||
Other comprehensive income (loss) | (249) | (249) | ||||
Balance at Dec. 31, 2014 | $ 1,164 | 1,452,504 | (87) | (1,673,667) | $ (3,263) | (223,349) |
Balance (in shares) at Dec. 31, 2014 | 116,445 | (150) | ||||
Increase (Decrease) in Stockholders' Equity | ||||||
Exercise of stock options, and issuance of common stock units, stock awards and purchase plan | $ 8 | (488) | (480) | |||
Exercise of stock options, and issuance of common stock units, stock awards and purchase plan (in shares) | 740 | |||||
Issuance of common stock in private placement to a related party | $ 4 | 6,524 | 6,528 | |||
Issuance of common stock in private placement to a related party (in shares) | 424 | |||||
Stock based compensation | 6,873 | 6,873 | ||||
Repurchase of common stock | $ (27) | (25,609) | (25,636) | |||
Repurchase of common stock (in shares) | (2,676) | |||||
Cash dividends declared, $0.50 and $0.75 per common share | (87,906) | (87,906) | ||||
Net loss | (18,760) | (18,760) | ||||
Other comprehensive income (loss) | 85 | 85 | ||||
Balance at Dec. 31, 2015 | $ 1,149 | $ 1,351,898 | $ (2) | $ (1,692,427) | $ (3,263) | $ (342,645) |
Balance (in shares) at Dec. 31, 2015 | 114,933 | (150) |
CONSOLIDATED STATEMENTS OF STO8
CONSOLIDATED STATEMENTS OF STOCKHOLDERS' EQUITY (DEFICIT) (Parenthetical) - $ / shares | Jul. 24, 2015 | Apr. 24, 2015 | Feb. 20, 2015 | Oct. 16, 2014 | Jul. 25, 2014 | Dec. 31, 2015 | Sep. 30, 2015 | Jun. 30, 2015 | Mar. 31, 2015 | Dec. 31, 2014 | Sep. 30, 2014 | Jun. 30, 2014 | Mar. 31, 2014 | Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 |
Consolidated Statements of Stockholders' Equity (Deficit) | ||||||||||||||||
Cash dividend declared per common share (in dollars per share) | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0 | $ 0 | $ 0.75 | $ 0.50 | $ 0 |
CONSOLIDATED STATEMENTS OF CASH
CONSOLIDATED STATEMENTS OF CASH FLOWS - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
Cash flows from operating activities | |||
Net loss | $ (18,760) | $ (168,464) | $ (170,701) |
Adjustments to reconcile net loss to net cash provided by (used in) operating activities: | |||
Depreciation and amortization | 13,933 | 12,175 | 3,458 |
Stock-based compensation | 6,873 | 27,390 | 25,687 |
Amortization of premium on investments | 583 | 1,742 | 3,794 |
Interest added to the principal balance of the non-recourse term notes due 2029 | 22,635 | 20,527 | 0 |
Realized gain on sale of marketable securities, net | (1,220) | 0 | 0 |
Amortization of debt issuance costs | 2,943 | 2,408 | 951 |
Other-than-temporary impairment loss on marketable securities | 0 | 3,752 | 0 |
Change in fair value of capped-call derivative assets | 0 | 0 | 1,422 |
Other non-cash items | (3) | (2) | 17 |
Changes in operating assets and liabilities: | |||
Accounts receivable | 0 | 74 | 702 |
Receivables from collaborative arrangements | (15,678) | (7,371) | (2,117) |
Prepaid expenses and other current assets | 320 | (338) | 36 |
Inventories | 0 | (1,908) | (3,100) |
Other assets | 0 | 1,549 | (578) |
Accounts payable | 818 | (7,695) | 1,613 |
Payable to Theravance Biopharma, Inc., net | (1,056) | (15,916) | 0 |
Accrued personnel-related expenses, accrued clinical and development expenses, and other accrued liabilities | (725) | (491) | 5,850 |
Accrued interest payable | 360 | 4,751 | 428 |
Other long-term liabilities | (7) | 275 | (299) |
Deferred revenue | (885) | (3,181) | 3,235 |
Net cash provided by (used in) operating activities | 10,131 | (130,723) | (129,602) |
Cash flows from investing activities | |||
Purchases of property and equipment | (7) | (689) | (2,734) |
Purchases of marketable securities | (86,523) | (276,914) | (410,407) |
Maturities of marketable securities | 137,621 | 339,359 | 255,861 |
Sales of marketable securities | 108,077 | 7,211 | 22,600 |
Capitalized fees paid to a related party | 0 | (135,000) | (85,000) |
Change in restricted cash | 0 | 833 | 0 |
Payments received on notes receivable | 0 | 140 | 100 |
Net cash provided by (used in) investing activities | 159,168 | (65,060) | (219,580) |
Cash flows from financing activities | |||
Proceeds from issuances of common stock, net | 6,048 | 48,925 | 153,021 |
Payments of cash dividends to stockholders | (87,331) | (56,988) | 0 |
Repurchase of common stock | (25,636) | 0 | 0 |
Cash and cash equivalents contributed to Theravance Biopharma, Inc. | 0 | (277,541) | 0 |
Purchase of capped-call options | 0 | 0 | (36,800) |
Proceeds from issuances of note payable, net of debt issuance costs | 0 | 434,677 | 281,622 |
Net cash (used in) provided by financing activities | (106,919) | 149,073 | 397,843 |
Net increase (decrease) in cash and cash equivalents | 62,380 | (46,710) | 48,661 |
Cash and cash equivalents at beginning of period | 96,800 | 143,510 | 94,849 |
Cash and cash equivalents at end of period | 159,180 | 96,800 | 143,510 |
Supplemental disclosure of cash flow information | |||
Cash paid for interest | 25,863 | 9,208 | 7,970 |
Supplemental disclosure of noncash information | |||
Contribution of net assets, excluding cash and cash equivalents to Theravance Biopharma, Inc. | 0 | 125,337 | 0 |
Conversion of convertible subordinated notes into common stock | $ 0 | $ 32,391 | $ 172,499 |
Description of Operations and S
Description of Operations and Summary of Significant Accounting Policies | 12 Months Ended |
Dec. 31, 2015 | |
Description of Operations and Summary of Significant Accounting Policies | |
Description of Operations and Summary of Significant Accounting Policies | 1. Description of Operations and Summary of Significant Accounting Policies Description of Operations Innoviva, Inc. (formerly known as Theravance, Inc. and referred to as "Innoviva", the "Company", or "we" and other similar pronouns) is focused on bringing compelling new medicines to patients in areas of unmet need by leveraging its significant expertise in the development, commercialization and financial management of bio-pharmaceuticals. Innoviva's portfolio is anchored by the respiratory assets partnered with Glaxo Group Limited ("GSK"), including RELVAR ® /BREO ® ELLIPTA ® (fluticasone furoate/ vilanterol, "FF/VI") and ANORO® ELLIPTA ® (umeclidinium bromide/ vilanterol, "UMEC/VI"). Under the Long-Acting Beta 2 Agonist ("LABA") Collaboration Agreement and the Strategic Alliance Agreement with GSK (referred to herein as the "GSK Agreements"), Innoviva is eligible to receive the associated royalty revenues from RELVAR ® /BREO ® ELLIPTA ® and ANORO® ELLIPTA ® . Innoviva is also entitled to 15% of any future payments made by GSK under its agreements originally entered into with us, and since assigned to Theravance Respiratory Company, LLC ("TRC"), relating to the combination FF/UMEC/VI and the Bifunctional Muscarinic Antagonist- Beta 2 Agonist ("MABA") program, as monotherapy and in combination with other therapeutically active components, such as an inhaled corticosteroid, and any other product or combination of products that may be discovered and developed in the future under the LABA Collaboration Agreement ("LABA Collaboration"), which has been assigned to TRC other than RELVAR ® /BREO ® ELLIPTA ® and ANORO® ELLIPTA ® . Business Separation On June 1, 2014, we separated our biopharmaceutical research and drug development operations from our late-stage partnered respiratory assets by transferring our research and drug development operations into our then wholly- owned subsidiary, Theravance Biopharma, Inc. ("Theravance Biopharma"). We contributed $393.0 million of cash, cash equivalents and marketable securities to Theravance Biopharma and all outstanding shares of Theravance Biopharma were then distributed to Innoviva stockholders as a pro-rata dividend distribution on June 2, 2014 by issuing one ordinary share of Theravance Biopharma for every 3.5 shares held of our common stock to stockholders of record on May 15, 2014 (the "Spin-Off"). The Spin-Off resulted in Theravance Biopharma operating as an independent, publicly traded company. The results of operations for the former research and drug development operations conducted by us and by Theravance Biopharma until June 1, 2014 are included as part of this report as discontinued operations. Refer to Notes 11 and 12, "Spin-Off of Theravance Biopharma, Inc.," and "Discontinued Operations" for further information. Principles of Consolidation The consolidated financial statements include the accounts of Innoviva and its wholly owned subsidiaries. All intercompany balances and transactions have been eliminated in consolidation. Use of Management's Estimates The preparation of consolidated financial statements in conformity with U.S. Generally Accepted Accounting Principles ("GAAP") requires management to make estimates and assumptions that affect the amounts reported in the consolidated financial statements and accompanying notes. Actual results could differ materially from those estimates. Management evaluates its significant accounting policies and estimates on an ongoing basis. We base our estimates on historical experience and other relevant assumptions that we believe to be reasonable under the circumstances. These estimates also form the basis for making judgments about the carrying values of assets and liabilities when these values are not readily apparent from other sources. Certain Risks and Concentrations Our financial instruments that are exposed to concentrations of credit risk consist primarily of cash and cash equivalents and marketable securities. Although we deposit our cash with multiple financial institutions, our deposits, at times, may exceed federally insured limits. Refer to "Segment Reporting" below for concentrations with respect to revenues and geographic locations. Segment Reporting We operate in a single segment, which is to provide capital return to stockholders by maximizing the potential value of our respiratory assets partnered with GSK. Revenues are generated from our collaborative arrangements and royalty payment from GSK, located in Great Britain. Our facilities are located within the United States. Variable Interest Entities We evaluate our ownership, contractual and other interest in entities to determine if they are variable-interest entities ("VIE"), whether we have a variable interest in those entities and the nature and extent of those interests. Based on our evaluations, if we determine we are the primary beneficiary of such VIEs, we consolidate such entities into our financial statements. We consolidate the financial results of TRC, which we have determined to be a VIE, because we have the power to direct the economically significant activities of TRC and the obligation to absorb losses of, or the right to receive benefits from, TRC. The financial position and results of operations of TRC are not material for the periods presented. Cash and Cash Equivalents We consider all highly liquid investments purchased with a maturity of three months or less on the date of purchase to be cash equivalents. Cash equivalents are carried at cost, which approximates fair value. Investments in Marketable Securities We invest in short-term investments and marketable securities, primarily corporate notes, government, government agency, and municipal bonds. We limit the amount of credit exposure with any one issuer, industry or geographic area for investments other than instruments backed by the U.S. federal government. We classify our marketable securities as available-for-sale securities and report them at fair value in cash equivalents, short-term investments or marketable securities on the consolidated balance sheets with related unrealized gains and losses included as a component of stockholders' equity (deficit). The amortized cost of debt securities is adjusted for amortization of premiums and accretion of discounts to maturity, which is included in interest income on the consolidated statements of operations. Realized gains and losses, if any, on available-for-sale securities are included in interest income. The cost of securities sold is based on the specific identification method. Interest and dividends on securities classified as available-for-sale are included in interest income. We regularly review all of our investments for other-than-temporary declines in estimated fair value. Our review includes the consideration of the cause of the impairment, including the creditworthiness of the security issuers, the number of securities in an unrealized loss position, the severity and duration of the unrealized losses, whether we have the intent to sell the securities and whether it is more likely than not that we will be required to sell the securities before the recovery of their amortized cost basis. When we determine that the decline in estimated fair value of an investment is below the amortized cost basis and the decline is other-than-temporary, we reduce the carrying value of the security and record a loss for the amount of such decline to other income (expense), net. Fair Value of Financial Instruments We define fair value as the exchange price that would be received for an asset or paid to transfer a liability (an exit price) in the principal or most advantageous market for the asset or liability in an orderly transaction between market participants on the measurement date. Our valuation techniques are based on observable and unobservable inputs. Observable inputs reflect readily obtainable data from independent sources, while unobservable inputs reflect our market assumptions. We classify these inputs into the following hierarchy: Level 1 —Quoted prices for identical instruments in active markets. Level 2 —Quoted prices for similar instruments in active markets; quoted prices for identical or similar instruments in markets that are not active; and model-derived valuations whose inputs are observable or whose significant value drivers are observable. Level 3 —Unobservable inputs and little, if any, market activity for the assets. Financial instruments include cash equivalents, marketable securities, accounts receivable, receivables from collaborative arrangements, accounts payable, and accrued liabilities. Cash equivalents and marketable securities are carried at estimated fair value. The carrying value of accounts receivable, receivables from collaborative arrangements, accounts payable, and accrued liabilities approximate their estimated fair value due to the relatively short-term nature of these instruments. Property and Equipment All property, equipment and leasehold improvements prior to the Spin-Off were related to our former research and drug development operations and thus, were contributed to Theravance Biopharma in connection with the Spin-Off. Property and equipment as of December 31, 2015 and 2014, which consisted of computer software, amounted to $0.2 million and $0.3 million, respectively. Property, equipment and leasehold improvements are stated at cost and depreciated using the straight-line method as follows: Leasehold improvements Shorter of remaining lease terms or useful life Equipment, furniture and fixtures 5 - 7 years Software and computer equipment 3 years Depreciation expense for the years ended December 31, 2015, 2014 and 2013 was $0.1 million, $1.1 million and $2.7 million. Depreciation expense for property and equipment used by our former research and drug development operations is classified within discontinued operations in the consolidated statements of operations. The change in accumulated depreciation is net of asset retirements. Capitalized Software We capitalize certain costs related to direct material and service costs for software obtained for internal use. Capitalized software costs are depreciated over three years. Capitalized Fees paid to a Related Party We capitalize fees paid to licensors related to agreements for approved products or commercialized products. We capitalize these fees as capitalized fees paid to a related party ("Capitalized Fees") and amortize these Capitalized Fees on a straight-line basis over their estimated useful lives upon the commercial launch of the product, which has been shortly after regulatory approval of such product. The estimated useful lives of these Capitalized Fees are based on a country-by-country and product-by-product basis, as the later of the expiration or termination of the last patent right covering the compound in such product in such country and 15 years from first commercial sale of such product in such country, unless the agreement is terminated earlier. Consistent with our policy for classification of costs under the research and development collaborative arrangements, the amortization of these Capitalized Fees are recognized as a reduction of royalty revenue. We review our Capitalized Fees for impairment when events or changes in circumstances indicate that the carrying amount of such assets may not be recoverable. The recoverability of Capitalized Fees is measured by comparing the asset's carrying amount to the expected undiscounted future cash flows that the asset is expected to generate. The determination of recoverability typically requires various estimates and assumptions, including estimating the useful life over which cash flows will occur, their amount, and the asset's residual value, if any. We derive the required cash flow estimates from near-term forecasted product sales and long-term projected sales in the corresponding market. Revenue Recognition Revenue is recognized when the four basic criteria of revenue recognition are met: (1) persuasive evidence of an arrangement exists; (2) delivery has occurred or services have been rendered; (3) the fee is fixed or determinable; and (4) collectability is reasonably assured. Where the revenue recognition criteria are not met, we defer the recognition of revenue by recording deferred revenue until such time that all criteria are met. Collaborative Arrangements and Multiple-Element Arrangements Revenue from nonrefundable, up-front license or technology access payments under license and collaborative arrangements that are not dependent on any future performance by us is recognized when such amounts are earned. If we have continuing obligations to perform under the arrangement, such fees are recognized over the estimated period of continuing performance obligation. Our arrangements can include multiple elements which may consist of license and development agreements. When multiple-element arrangements exist, we evaluate whether these individual deliverables should be accounted for as separate units of accounting or one single unit of accounting. For new or materially amended multiple element arrangements, we identify the deliverables at the inception of the arrangement and each deliverable within a multiple deliverable revenue arrangement is accounted for as a separate unit of accounting if both of the following criteria are met: (1) the delivered item or items have value to the customer on a standalone basis and (2) for an arrangement that includes a general right of return relative to the delivered item(s), delivery or performance of the undelivered item(s) is considered probable and substantially in our control. We allocate revenue to each non-contingent element based on the relative selling price of each element. When applying the relative selling price method, we determine the selling price for each deliverable using vendor-specific objective evidence ("VSOE") of selling price, if it exists, or third-party evidence ("TPE") of selling price, if it exists. If neither VSOE nor TPE of selling price exist for a deliverable, we use the best estimated selling price for that deliverable. Revenue allocated to each element is then recognized based on when the basic four revenue recognition criteria are met for each element. For multiple-element arrangements entered into prior to January 1, 2011, we determined the delivered items under our collaborative arrangements did not meet the criteria to be considered separate accounting units for the purposes of revenue recognition. As a result, we recognized revenue from non-refundable, upfront fees and development contingent payments in the same manner as the final deliverable, which is ratably over the expected term of our performance of research and development services under the agreements. These upfront or contingent payments received, pending recognition as revenue, are recorded as deferred revenue and are classified as a short-term or long-term liability on the consolidated balance sheets and recognized over the estimated period of performance. We periodically review the estimated performance periods of our contracts based on the progress of our programs. Where a portion of non-refundable upfront fees or other payments received are allocated to continuing performance obligations under the terms of a collaborative arrangement, they are recorded as deferred revenue and recognized as revenue, or as an accrued liability and recognized as a reduction of research and development expenses ratably over the term of our estimated performance period under the agreement. We determine the estimated performance periods, and they are periodically reviewed based on the progress of the related program. The effect of any change made to an estimated performance period and, therefore revenue recognized, would occur on a prospective basis in the period that the change was made. Under certain collaborative arrangements, we have been reimbursed for a portion of our research and development expenses. These reimbursements have been reflected as a reduction of research and development expense in our consolidated statements of operations, as we do not consider performing research and development services to be a part of our ongoing and central operations. Therefore, the reimbursement of research and developmental services and any amounts allocated to our research and development services are recorded as a reduction of research and development expense. Amounts deferred under a collaborative arrangement in which the performance obligations are terminated will result in an immediate recognition of any remaining deferred revenue and accrued liability in the period that termination occurred, provided that there are no remaining performance obligations. We account for contingent payments in accordance with FASB Subtopic ASC 605-28 "Revenue Recognition—Milestone Method." We recognize revenue from milestone payments when (i) the milestone event is substantive and its achievability was not reasonably assured at the inception of the agreement and (ii) we do not have ongoing performance obligations related to the achievement of the milestone. Milestone payments are considered substantive if all of the following conditions are met: the milestone payment (a) is commensurate with either our performance to achieve the milestone or the enhancement of the value of the delivered item or items as a result of a specific outcome resulting from our performance to achieve the milestone, (b) relates solely to past performance, and (c) is reasonable relative to all of the deliverables and payment terms (including other potential milestone consideration) within the arrangement. Under our collaborative arrangements with GSK, royalty revenue earned is reduced by amortization expense resulting from the fees paid to GSK, which were recognized as capitalized fees paid to a related party. When amortization expense exceeds amounts recognized for royalty revenues from GSK, negative revenue would be reported in our consolidated statements of operations. Royalties We recognize royalty revenue on licensee net sales of products with respect to which we have contractual royalty rights in the period in which the royalties are earned and reported to us and collectability is reasonably assured. Royalties are recognized net of amortization of capitalized fees associated with any approval and launch milestone payments made to GSK. Product Revenues We currently have no product revenues following the Spin-Off. Prior to the Spin-Off, we recognized revenues from product sales when there was persuasive evidence that an arrangement existed, title and risk of loss transferred, the price was fixed and determinable, and collectability was reasonably assured. Product sales were recognized net of estimated allowances, discounts, sales returns, chargebacks and rebates. Such amounts are presented within discontinued operations in the consolidated statements of operations. Allowance for Doubtful Accounts We maintain a policy to record allowances for potentially doubtful accounts for estimated losses resulting from the inability of our customers to make required payments. As of December 31, 2015, there were no allowances for doubtful accounts and we have not had any write-offs historically. Research and Development Costs Research and development costs are expensed in the period that services are rendered or goods are received. Research and development costs consist primarily of salaries and benefits. Prior to the Spin-Off, research and development costs also included laboratory supplies and facility costs, and fees paid to third parties that conduct certain research and development activities on behalf of us, net of certain external research and development costs reimbursed under collaborative arrangements, which are classified within discontinued operations in the consolidated statements of operations. Fair Value of Stock-Based Compensation Awards We use the Black-Scholes-Merton option pricing model to estimate the fair value of options granted under our equity incentive plans and rights to acquire stock granted under our employee stock purchase plan ("ESPP"). The Black-Scholes-Merton option valuation model requires the use of assumptions, including the expected term of the award and the expected stock price volatility. We use the "simplified" method as described in Staff Accounting Bulletin No. 107, "Share-Based Payment," for the expected option term because the usage of its historical option exercise data is limited due to post-IPO exercise restrictions. Beginning April 1, 2011, we used our historical volatility to estimate expected stock price volatility. Prior to April 1, 2011, we used peer company price volatility to estimate expected stock price volatility due to our limited historical common stock price volatility since our initial public offering in the year ended December 31, 2004. Restricted Stock Units ("RSUs") and Restricted Stock Awards ("RSAs") are measured based on the fair market values of the underlying stock on the dates of grant. Stock-based compensation expense was calculated based on awards ultimately expected to vest and was reduced for estimated forfeitures at the time of grant and revised, if necessary, in subsequent periods if actual forfeitures differed from those estimates. Our estimated annual forfeiture rates for stock options, RSUs and RSAs are based on our historical forfeiture experience. The estimated fair value of stock options, RSUs and RSAs is expensed on a straight-line basis over the expected term of the grant and the estimated fair value of performance-contingent RSUs and RSAs is expensed using an accelerated method over the term of the award once we have determined that it is probable that performance milestones will be achieved. Compensation expense for RSUs and RSAs that contain performance conditions is based on the grant date fair value of the award. Compensation expense is recorded over the requisite service period based on management's best estimate as to whether it is probable that the shares awarded are expected to vest. We assess the probability of the performance milestones being met on a continuous basis. Compensation expense for purchases under the ESPP is recognized based on the fair value of the common stock on the date of offering, less the purchase discount percentage provided for in the plan. We have not recognized, any income tax benefit related to employee stock-based compensation expense as a result of the full valuation allowance on our deferred tax assets including deferred tax assets related to our net operating loss carryforwards. Amortization of Debt Issuance Costs from Non-recourse Notes Payable, due 2029 In April 2014, we entered into certain note purchase agreements relating to the private placement of $450.0 million aggregate principal amount of non-recourse 9% fixed rate term notes due 2029 (the "2029 Notes") issued by our wholly-owned subsidiary. We incurred approximately $15.3 million in transaction costs in connection with issuance of 2029 Notes, which we amortize to interest expense over the estimated life of the 2029 Notes based on the effective interest method. Since the principal and interest payments on the 2029 Notes are based on royalties from product sales, which will vary from quarter to quarter, the 2029 Notes may be repaid prior to the final maturity date in 2029. We continue to assess, on an ongoing basis, our estimates on royalties from products sales as it relates to its impact on payments of principal and interest on the 2029 Notes. To the extent that the interest or principal payments are greater or less than our initial estimates or the timing of such payments is materially different than our original estimates, we prospectively adjust the amortization of the debt issuance costs. Income Taxes We utilize the asset and liability method of accounting for income taxes. Under this method, deferred tax assets and liabilities are determined based on differences between financial reporting and tax basis of assets and liabilities and are measured using enacted tax rates and laws that will be in effect when the differences are expected to reverse. A valuation allowance is provided when it is more likely than not that some portion or all of a deferred tax asset will not be realized. None of our currently unrecognized tax benefits would affect our effective income tax rate if recognized, due to the valuation allowance that currently offsets our deferred tax assets. We do not anticipate the total amount of unrecognized income tax benefits relating to uncertain tax positions existing as of December 31, 2015 will significantly increase or decrease in the next 12 months. We assess all material positions taken in any income tax return, including all significant uncertain positions, in all tax years that are still subject to assessment or challenge by relevant taxing authorities. Assessing an uncertain tax position begins with the initial determination of the position's sustainability and is measured at the largest amount of benefit that is greater than 50% likely to be realized upon ultimate settlement. As of each balance sheet date, unresolved uncertain tax positions must be reassessed, and we will determine whether: the factors underlying the sustainability assertion have changed and whether the amount of the recognized tax benefit is still appropriate. The recognition and measurement of tax benefits requires significant judgment. Judgments concerning the recognition and measurement of a tax benefit might change as new information becomes available. In November 2015, the FASB issued ASU 2015-17, Balance Sheet Classification of Deferred Taxes , which eliminates the requirement for organizations to present deferred tax liabilities and assets as current and noncurrent in a classified balance sheet. The standard requires us to classify all deferred tax assets and liabilities as noncurrent. We adopted this standard in December 2015. This adoption did not have a material impact on our consolidated financial statements. Comprehensive Loss Comprehensive loss is comprised of net loss and other comprehensive income (loss). Other comprehensive income (loss) consists of changes in unrealized and realized gains and losses on our marketable securities, net of tax. Related Parties GSK owned 27.9% of our outstanding common stock as of December 31, 2015. Transactions with GSK are described in Note 3, "Collaborative Arrangements". Prior to the Spin-Off, Robert V. Gunderson, Jr. was one of our directors. We have engaged Gunderson Dettmer Stough Villeneuve Franklin & Hachigian, LLP, of which Mr. Gunderson is a partner, as our primary legal counsel. Fees incurred in the ordinary course of business were, $1.3 million in the year ended December 31, 2014 and $3.2 million in the year ended December 31, 2013. As Mr. Gunderson was not one of our directors for the year ended December 31, 2015, he is no longer considered a related party. Recently Issued Accounting Pronouncements Not Yet Adopted In January 2016, the Financial Accounting Standards Board ("FASB") issued Accounting Standards Update ("ASU") 2016-01, Recognition and Measurement of Financial Assets and Financial Liabilities , which provides guidance for the recognition, measurement, presentation, and disclosure of financial assets and liabilities. This ASU will be effective for us beginning in January 1, 2018. We are evaluating the effects of the adoption of this ASU to our consolidated financial statements. In April 2015, the FASB issued ASU 2015-03, Interest—Imputation of Interest , to simplify the presentation of debt issuance costs. This standard amends existing guidance to require the presentation of debt issuance costs associated with term loans in the balance sheet as a deduction from the carrying amount of the related debt liability instead of a deferred charge. It will be effective for us on January 1, 2016, with early adoption permitted. We plan to adopt ASU 2015-03 on January 1, 2016. Upon adoption of ASU 2015-03, we will apply the guidance retrospectively to all periods presented and classify our debt issuance costs, which are currently included in other assets in the consolidated financial statements, as a deduction to our long-term debt. In May 2014, the FASB issued ASU 2014-09, Revenue from Contracts with Customers ("ASU 2014-09"), which converges the FASB and the International Accounting Standards Board standards on revenue recognition. Areas of revenue recognition that will be affected include, but are not limited to, transfer of control, variable consideration, allocation of transfer pricing, licenses, time value of money, contract costs and disclosures. This guidance is effective for the fiscal years and interim reporting periods beginning after December 15, 2017 (as amended through ASU 2015-14 issued in August 2015), at which time we may adopt the new standard under the full retrospective method or the modified retrospective method. Early adoption is permitted. We are currently evaluating the impact of adopting ASU 2014-09 on our consolidated financial statements and related disclosures. |
Net Loss per Share
Net Loss per Share | 12 Months Ended |
Dec. 31, 2015 | |
Net Loss per Share | |
Net Loss per Share | 2. Net Loss per Share Basic net loss per share is computed by dividing net loss by the weighted- average number of shares of common stock outstanding, less RSAs subject to forfeiture. Diluted net loss per share is computed by dividing net loss by the weighted-average number of shares of common stock outstanding, less RSAs subject to forfeiture, plus all additional common shares that would have been outstanding, assuming dilutive potential common shares had been issued for other dilutive securities. For the years ended December 31, 2015, 2014 and 2013, diluted and basic net loss per common share was identical since potential common shares were excluded from the calculation, as their effect was anti-dilutive. Anti-dilutive Securities The following common equivalent shares were not included in the computation of diluted net loss per share because their effect was anti-dilutive (in thousands): Year Ended December 31, 2015(1) 2014 2013 Outstanding options and awards granted under equity incentive plan and employee stock purchase plan Unvested RSAs Shares issuable upon conversion of convertible subordinated notes Total (1) Includes 4.1 million options, 0.4 million restricted stock units, and 1.0 million unvested RSAs retained by former employees who were transferred to Theravance Biopharma in connection with the Spin-Off during the year ended December 31, 2015. Subsequent to the Spin-Off, stock-based compensation expense associated with the awards held by Theravance Biopharma employees granted prior to the Spin-Off is recognized by Theravance Biopharma. |
Collaborative Arrangements
Collaborative Arrangements | 12 Months Ended |
Dec. 31, 2015 | |
Collaborative Arrangements | |
Collaborative Arrangements | 3. Collaborative Arrangements Net Revenue from Collaborative Arrangements Net revenue from collaborative arrangements from continuing operations relates to our collaborative arrangement with GSK. Net revenue from other collaborative arrangements is reflected as discontinued operations in the consolidated statements of operations. Refer to Notes 1, 11 and 12, "Description of Operations and Summary of Significant Accounting Policies," "Spin-Off of Theravance Biopharma, Inc." and "Discontinued Operations" for further information. Net revenue recognized under our GSK Agreements was as follows (in thousands): Year Ended December 31, 2015 2014 2013 Royalties from a related party $ $ $ Less: amortization of capitalized fees paid to a related party ) ) ) Royalty revenue LABA collaboration(1) — — Strategic alliance—MABA program Total net revenue from GSK $ $ $ (1) Deferred revenue under this agreement was fully recognized in the year ended December 31, 2013. LABA Collaboration In November 2002, we entered into our LABA Collaboration Agreement with GSK to develop and commercialize once-daily LABA products for the treatment of chronic obstructive pulmonary disease ("COPD") and asthma. As a result of the launch and approval of RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA® in the U.S., Japan and Europe, we paid milestone fees to GSK totaling $220.0 million during the year ended December 31, 2014. Although we have no further milestone payment obligations to GSK pursuant to the LABA Collaboration Agreement, we continue to have ongoing development and commercialization activities under the GSK Agreements that are expected to continue over the life of the agreements. The milestone fees paid to GSK were recognized as capitalized fees paid to a related party, which are being amortized over their estimated useful lives commencing upon the commercial launch of the product. The amortization expense is recorded as a reduction to the royalties from GSK. We are entitled to receive annual royalties from GSK on sales of RELVAR®/BREO® ELLIPTA® as follows: 15% on the first $3.0 billion of annual global net sales and 5% for all annual global net sales above $3.0 billion. Sales of single-agent LABA medicines and combination medicines would be combined for the purposes of this royalty calculation. For other products combined with a LABA from the LABA Collaboration, such as ANORO® ELLIPTA®, royalties are upward tiering and range from 6.5% to 10%. 2004 Strategic Alliance In March 2004, we entered into the Strategic Alliance Agreement with GSK where GSK received an option to license exclusive development and commercialization rights to product candidates from certain of our discovery programs on pre-determined terms and on an exclusive, worldwide basis. In 2005, GSK licensed our MABA program for the treatment of COPD, and in October 2011, we and GSK expanded the MABA program by adding six additional Innoviva-discovered preclinical MABA compounds (the "Additional MABAs"). The development program is fully funded by GSK and is still currently in early stages of Phase II trials. As a result of the transactions effected by the Spin-Off, we are only entitled to receive 15% of any contingent payments and royalties payable by GSK from sales of FF/UMEC/VI (and MABA, and MABA/FF) while Theravance Biopharma receives 85% of those same payments. Purchases of Common Stock under the Company's Governance Agreement and Common Stock Purchase Agreements with GSK In the year ended December 31, 2015, GSK purchased approximately 424,081 shares of our common stock pursuant to its periodic "top-up" rights under our Amended and Restated Governance Agreement, dated as of June 4, 2004, as amended, among us, GSK and certain GSK affiliates, for an aggregate purchase price of approximately $6.5 million. GSK Contingent Payments and Revenue The potential future contingent payments receivable related to the MABA program of $363.0 million are not deemed substantive milestones due to the fact that the achievement of the event underlying the payment predominantly relates to GSK's performance of future development, manufacturing and commercialization activities for product candidates after licensing the program. The Company is entitled to 15% of any milestone payments. Reimbursement of Research and Development Costs Reimbursement of research and development costs from continuing operations is solely related to the GSK Agreements. Under the GSK Agreements, we are entitled to reimbursement of certain research and development costs. For the years ended December 31, 2015, 2014 and 2013, research and development costs reimbursed from GSK was zero, $0.1 million and $0.5 million. Reimbursement of research and development costs from other collaborative arrangements has been reflected as discontinued operations in the consolidated statements of operations. Refer to Notes 1, 11 and 12, "Description of Operations and Summary of Significant Accounting Policies," "Spin-Off of Theravance Biopharma, Inc." and "Discontinued Operations" for further information. |
Available-for-Sale Securities a
Available-for-Sale Securities and Fair Value Measurements | 12 Months Ended |
Dec. 31, 2015 | |
Available-for-Sale Securities and Fair Value Measurements | |
Available-for-Sale Securities and Fair Value Measurements | 4. Available-for-Sale Securities and Fair Value Measurements Available-for Sale Securities The classification of available-for-sale securities in the consolidated balance sheets is as follows (in thousands): December 31, 2015 2014 Cash and cash equivalents $ $ Short-term marketable securities Marketable securities — Total $ $ The estimated fair value of available-for-sale securities is based on quoted market prices for these or similar investments that were based on prices obtained from a commercial pricing service. Available-for-sale securities are summarized below (in thousands): December 31, 2015 Amortized Cost Gross Unrealized Gains Gross Unrealized Losses Other Than Temporary Impairment Loss Estimated Fair Value U.S. government agencies $ $ — $ ) $ — $ U.S. corporate notes — ) — U.S. commercial paper — — — Money market funds — — — Total $ $ — $ ) $ — $ December 31, 2014 Amortized Cost Gross Unrealized Gains Gross Unrealized Losses Other Than Temporary Impairment Loss Estimated Fair Value U.S. government securities $ $ $ — $ — $ U.S. government agencies ) — U.S. corporate notes ) — U.S. commercial paper — — — Ordinary shares of Theravance Biopharma — — ) Money market funds — — — Total $ $ $ ) $ ) $ We determined that the unrealized loss on our Theravance Biopharma equity securities as of December 31, 2014 was other-than-temporary. Therefore, we recognized a loss of $3.8 million on these equity securities, which was charged to other income (expense), net on the consolidated statements of operations. As of December 31, 2015, all of the available-for-sale debt securities had contractual maturities within one year and the average duration of debt securities was approximately one month. We do not intend to sell the investments in debt that are in an unrealized loss position, and it is unlikely that we will be required to sell the investments before recovery of their amortized cost basis, which may be maturity. We have determined that the gross unrealized losses on our available-for-sale debt securities as of December 31, 2015 were temporary in nature. All available-for-sale debt securities with unrealized losses as of December 31, 2015 have been in a loss position for less than twelve months. During the year ended December 31, 2015, we recognized a gain of $1.2 million from the sale of all of the ordinary shares of Theravance Biopharma that we held as of December 31, 2014, which is included in other income (expense), net in the condensed consolidated statement of operations. In addition, we sold other available-for-sale securities totaling $100.4 million, and the related realized gains and losses were not significant during year ended December 31, 2015 During the years ended December 31, 2014 and 2013, we sold marketable securities totaling $7.2 million and $22.6 million, and the related realized gains and losses were not significant in either of these periods. Fair Value Measurements Our available-for-sale securities are measured at fair value on a recurring basis and our debt is carried at the amortized cost basis. The estimated fair values were as follows: Estimated Fair Value Measurements as of December 31, 2015 Using: Quoted Price in Active Markets for Identical Assets Significant Other Observable Inputs Significant Unobservable Inputs Types of Instruments (In thousands) Level 1 Level 2 Level 3 Total Assets U.S. government agencies $ — $ $ — $ Corporate notes — — Commercial paper — — Money market funds — — Total assets measured as of estimated fair value $ $ $ — $ Liabilities Convertible subordinated notes due 2023 $ — $ $ — $ Non-recourse notes due 2029 — — Total fair value of liabilities $ — $ $ — $ Estimated Fair Value Measurements as of December 31, 2014 Using: Quoted Price in Active Markets for Identical Assets Significant Other Observable Inputs Significant Unobservable Inputs Types of Instruments (In thousands) Level 1 Level 2 Level 3 Total Assets U.S. government securities $ $ — $ — $ U.S. government agencies — — Corporate notes — — Commercial paper — — Ordinary shares of Theravance Biopharma — — Money market funds — — Total assets measured as of estimated fair value $ $ $ — $ Liabilities Convertible subordinated notes due 2023 $ — $ $ — $ Non-recourse notes due 2029 — — Total fair value of liabilities $ — $ $ — $ The fair value of our marketable securities classified within Level 2 is based upon observable inputs that may include benchmark yields, reported trades, broker/dealer quotes, issuer spreads, two-sided markets, benchmark securities, bids, offers and reference data including market research publications. The fair value of our convertible subordinated notes due 2023 and non-recourse notes due 2029 is based on actual trading prices of the instruments. |
Capitalized Fees Paid to a Rela
Capitalized Fees Paid to a Related Party | 12 Months Ended |
Dec. 31, 2015 | |
Capitalized Fees Paid to a Related Party | |
Capitalized Fees Paid to a Related Party | 5. Capitalized Fees paid to a Related Party Capitalized fees paid to a related party, which consist of registrational and launch-related milestone fees paid to GSK, were as follows: December 31, 2015 December 31, 2014 (In thousands) Weighted Average Remaining Amortization Period (Years) Gross Carrying Value Accumulated Amortization Net Carrying Value Gross Carrying Value Accumulated Amortization Net Carrying Value Approval and launch related milestone payments under the LABA Collaboration $ $ ) $ $ $ ) $ These milestone fees are being amortized over their estimated useful lives commencing upon the commercial launch of the product in their respective regions with the amortization expense recorded as a reduction in revenue from collaborative arrangements. Additional information regarding these milestone fees is included in Note 3, "Collaborative Arrangements." Amortization expense for the years ended December 31, 2015, 2014 and 2013 were $13.8 million, $11.1 million and $0.7 million. The remaining estimated amortization expense is $13.8 million for each of the years from 2016 to 2020 and $125.3 million thereafter. |
Stock-Based Compensation
Stock-Based Compensation | 12 Months Ended |
Dec. 31, 2015 | |
Stock-Based Compensation | |
Stock-Based Compensation | 6. Stock-Based Compensation Equity Incentive Plans In May 2012, we adopted the 2012 Equity Incentive Plan (the "2012 Plan"). The 2012 Plan provides for the grant of incentive stock options, nonstatutory stock options, restricted stock awards, stock unit awards and SARs to employees, non-employee directors and consultants. As of December 31, 2015, total shares remaining available for issuance under the 2012 Plan were 3,466,041. Employee Stock Purchase Plan Under the 2004 Employee Stock Purchase Plan (the "ESPP"), our employees may purchase common stock through payroll deductions at a price equal to 85% of the lower of the fair market value of the stock at the beginning of the offering period or at the end of each applicable purchase period. The ESPP provides for consecutive and overlapping offering periods of 24 months in duration, with each offering period composed of four consecutive six-month purchase periods. The purchase periods end on either May 15 or November 15. ESPP contributions are limited to a maximum of 15% of an employee's eligible compensation. The maximum number of shares that an employee may purchase in any purchase period is 2,500. An employee may not purchase shares with a value greater than $25,000 in any calendar year. As of December 31, 2015, total shares remaining available for issuance under the ESPP were 265,711. Performance-Contingent RSAs Since 2011, the Compensation Committee of our Board of Directors (the "Compensation Committee") have approved grants of performance-contingent RSAs to senior management and a non-executive officer. Generally, these awards have dual triggers of vesting based upon the achievement of certain performance goals by a pre-specified date, as well as a requirement for continued employment. Recognition of stock-based compensation expense begins when the performance goals are deemed probable of achievement. Included in these performance-contingent RSAs is the grant of 1,290,000 special long-term retention and incentive performance-contingent RSAs to senior management in 2011. The awards have dual triggers of vesting based upon the achievement of certain performance conditions over a six-year timeframe from 2011 through December 31, 2016 and require continued employment. As of March 31, 2014, we determined that the achievement of the requisite performance conditions for vesting of the first tranche of these awards was probable and the total stock-based compensation expense of $7.0 million for the first tranche was fully recognized through May 2014. In connection with the Spin-Off, our Compensation Committee approved the modification of the remaining tranches related to these awards as the performance conditions associated with the remaining portions of these awards were unlikely to be consistent with the new strategies of each company following the Spin-Off. The remaining 63,000 RSAs for which service-based vesting was not triggered at the time of the Spin-Off remain subject to new performance conditions (as well as the original service conditions). In addition, the RSAs for which both the performance and service-based conditions were not achieved prior to the Spin-Off were entitled to the pro rata dividend distribution made by Theravance on June 2, 2014 of one ordinary share of Theravance Biopharma for every 3.5 shares of Theravance common stock subject to their awards, which will also be subject to the same new performance and service conditions as the original RSAs to which they relate. As of December 31, 2015 and 2014, we determined that the achievement of the requisite performance conditions was not probable and, as a result, no compensation cost was recognized for the remaining equity awards. Performance-Contingent RSUs Prior to 2015, the Compensation Committee had approved grants of performance-contingent RSUs to employees. These awards have dual triggers of vesting based upon the successful achievement of certain corporate operating milestones in specified timelines, as well as a requirement for continued employment. When the performance goals are deemed to be probable of achievement for these types of awards, time-based vesting and, as a result, recognition of stock-based compensation expense commences. There were no outstanding shares as of December 31, 2015. Director Compensation Program Our non-employee directors receive compensation for services provided as a director. Each member of our Board of Directors who is not an employee receives an annual cash retainer for services as a director, member of a committee of the Board of Directors, lead independent director and chairman, as applicable. In addition, prior to the Spin-Off, each non-employee director was entitled to a cash fee for each board and committee meeting attended. Each of our independent directors receives periodic automatic grants of equity awards under a program implemented under the 2012 Plan. These grants are non-discretionary. Only our independent directors or affiliates of such directors are eligible to receive automatic grants under the 2012 Plan. Under the program, as amended following the Spin-Off, each individual who first becomes a non-employee director will, on the date such individual joins the Board of Directors, automatically be granted a one-time grant of RSUs covering a number of shares of our common stock calculated as $250,000 divided by our common stock closing share price on the date of grant as reported on The NASDAQ Global Market, rounded down to the nearest whole share (the "Initial RSUs"), plus a one-time grant of RSUs covering a number of shares of our common stock calculated as $250,000 divided by our common stock closing share price on the date of grant as reported on The NASDAQ Global Market, which would be pro-rated for the number of whole months remaining until the anniversary of the prior year's stockholders' meeting, rounded down to the nearest whole share (the "Pro Rata RSUs"). The Initial RSUs vest in two equal annual installments, while Pro-Rata RSUs vest in a single installment at the sooner of the next annual stockholder meeting or the one-year grant anniversary, in each case subject to the non-employee director's continuous service through the applicable vesting date. Annually, upon his or her re-election to the Board at the Annual Meeting of Stockholders, each non-employee director is automatically granted an RSU covering a number of shares of our common stock calculated as $250,000 divided by our common stock closing share price on the date of grant as reported on The NASDAQ Global Market, rounded down to the nearest whole share. Annual RSUs will vest at the sooner of the next annual stockholder meeting or the one-year anniversary of grant, subject to the non-employee director's continuous service through the applicable vesting date. These RSUs will vest in full upon the director's death or the occurrence of a Change in Control before the director's service terminates. All director RSUs will be settled in shares of our common stock on the vesting date. Director RSUs will carry dividend equivalent rights to be credited with an amount equal to all cash dividends paid on the underlying shares of common stock while unvested. Dividend equivalents will be subject to the same terms and conditions, including vesting, as the RSUs to which they attach and will be paid in cash upon vesting. Stock-Based Compensation Expense In connection with the Spin-Off of Theravance Biopharma, all outstanding shares of Theravance Biopharma were distributed to our stockholders as a pro-rata dividend distribution on June 2, 2014 by issuing one ordinary share of Theravance Biopharma for every 3.5 shares held of Innoviva common stock to stockholders of record on May 15, 2014. Outstanding stock options and RSUs that were not eligible for the dividend distribution were adjusted for the Spin-Off of Theravance Biopharma. The number of shares and exercise price for all outstanding stock options were adjusted and the number of shares for all outstanding RSUs was adjusted. All other terms of these grants remain the same; provided, however, that the vesting and expiration of these grants are based on the holder's continuing employment or service with us or Theravance Biopharma, as applicable. Although the anti-dilution adjustments were required pursuant to the terms of each stock plan, the anti-dilution adjustments were calculated using a volume-weighted average stock price, rather than the stock price as of the date of the dividend distribution, which resulted in incremental compensation expense. The accounting impact of the adjustment to the outstanding stock options and RSUs that occurred in connection with the Spin-Off of Theravance Biopharma was measured by comparing of the fair values of the modified stock options and RSUs to our employees and directors immediately before and after the adjustment. As a result, we recognized incremental stock- based compensation expense of $1.2 million in the second quarter of 2014, of which $0.9 million is included in discontinued operations. All remaining unrecognized stock-based compensation expense associated with this adjustment will be recognized by Theravance Biopharma as it pertains to stock options and RSUs held by individuals now employed by Theravance Biopharma or one if its affiliates. Stock-based compensation expense is included in the consolidated statements of operations as follows: Year Ended December 31, (In thousands) 2015 2014 2013 Research and development $ $ $ General and administrative Stock-based compensation from continuing operations Stock-based compensation from discontinued operations — Total stock-based compensation expense $ $ $ Stock-based compensation expense included in the consolidated statements of operations by award type is as follows: Year Ended December 31, (In thousands) 2015 2014 2013 Stock options $ $ $ RSUs RSAs Performance RSUs — Performance RSAs ESPP Total stock-based compensation expense $ $ $ As of December 31, 2015, the unrecognized stock-based compensation cost, net of expected forfeitures for awards expected to vest, including performance- contingent RSAs for which the performance milestones were determined to be probable of achievement, and the estimated weighted-average amortization period, using the straight-line attribution method, was as follows: (In thousands, except amortization period) Unrecognized Compensation Cost Weighted- Average Amortization Period (Years) Stock options $ RSUs RSAs Performance RSAs Total stock-based compensation expense $ Compensation Awards The following table summarizes equity award activity under the 2012 Plan and Prior Plans and related information: (In thousands) Number of Shares Subject to Outstanding Options Weighted- Average Exercise Price of Outstanding Options Number of Shares Subject to Outstanding RSUs Weighted- Average Fair Value per Share at Grant Number of Shares Outstanding Subject to Vesting or Performance Conditions with Vesting Weighted- Average Fair Value per Share at Grant Balance as of December 31, 2014 Granted — — Exercised ) — — — — Released RSUs/RSAs — — ) ) Forfeited ) ) ) Balance as of December 31, 2015 $ $ $ As of December 31, 2015, the aggregate intrinsic value of the options outstanding was $0.1 million and the aggregate intrinsic value of the options exercisable was $0.1 million. The total intrinsic value of the options exercised was $0.5 million in the year ended December 31, 2015, $17.5 million in the year ended December 31, 2014 and $41.4 million in the year ended December 31, 2013. The total estimated fair value of options vested was $10.0 million in the year ended December 31, 2015, $5.7 million in the year ended December 31, 2014 and $3.7 million in the year ended December 31, 2013. Valuation Assumptions We based the range of weighted-average estimated values of employee stock option grants and rights granted under the ESPP, as well as the weighted-average assumptions used in calculating these values, on estimates as of the date of grant, as follows: Year Ended December 31, 2015(1) 2014 2013 Employee stock options Risk-free interest rate — % 1.6% - 2.1% 0.8% - 2.0% Expected term (in years) — 5 - 6 5 - 6 Volatility — % 52% - 60% 58% - 60% Dividend yield — % 3% - 4% — Weighted-average estimated fair value of stock options granted $ — $15.63 $19.96 (1) There were no stock options granted for the year ended December 31, 2015. Year Ended December 31, 2015 2014 2013 Employee stock purchase plan issuances Risk-free interest rate 0.1% - 0.9% 0.1% - 0.5% 0.1% - 0.3% Expected term (in years) 0.5 - 2 0.5 - 2 0.5 - 2 Volatility 44% - 69% 43% - 55% 56% - 61% Dividend yield 0% - 6% 8% — Weighted-average estimated fair value of ESPP shares granted $4.52 $4.49 $16.44 |
Long-Term Debt
Long-Term Debt | 12 Months Ended |
Dec. 31, 2015 | |
Long-Term Debt. | |
Long-Term Debt | 7. Long-Term Debt Our long-term debt consists of: As of December 31, (In thousands) 2015 2014 Convertible Subordinated Notes due 2023 $ $ Non-Recourse Notes Payable due 2029 Total Long-Term Debt $ $ Convertible Subordinated Notes Due 2023 In January 2013, we completed an underwritten public offering of $287.5 million aggregate principal amount of unsecured convertible subordinated notes, which will mature on January 15, 2023 (the "2023 Notes"). The financing raised proceeds, net of issuance costs, of approximately $281.2 million, less $36.8 million to purchase two privately-negotiated capped call option transactions in connection with the issuance of the notes. The 2023 Notes bear interest at the rate of 2.125% per year that is payable semi-annually in arrears in cash on January 15 and July 15 of each year, beginning on July 15, 2013. The 2023 Notes were convertible, at the option of the holder, into shares of our common stock at an initial conversion rate of 35.9903 shares per $1,000 principal amount of the 2023 Notes, subject to adjustment in certain circumstances, which represents an initial conversion price of approximately $27.79 per share. Following the Spin-Off of Theravance Biopharma, a number of adjustments to the initial conversion rate have been made as described below. Holders of the notes will be able to require us to repurchase some or all of their notes upon the occurrence of a fundamental change at 100% of the principal amount of the notes being repurchased plus accrued and unpaid interest. We may not redeem the notes prior to their stated maturity date. In connection with the offering of the 2023 Notes, we entered into two privately-negotiated capped call option transactions with a single counterparty. The capped call option transaction is an integrated instrument consisting of a call option on our common stock purchased by us with a strike price equal to the initial conversion price of $27.79 per share for the underlying number of shares and a cap price of $38.00 per share, both of which are subject to adjustments consistent with the 2023 Notes. The cap component is economically equivalent to a call option sold by us for the underlying number of shares with an initial strike price of $38.00 per share. As an integrated instrument, the settlement of the capped call coincides with the due date of the convertible debt. Upon settlement, we would receive from our hedge counterparty a number of shares of our common shares that would range from zero, if the stock price was below $27.79 per share, to a maximum of 2,779,659 shares, if the stock price is above $38.00 per share. However, if the market price of our common stock, as measured under the terms of the capped call transactions, exceeds $38.00 per share, there is no incremental anti-dilutive benefit from the capped call. In accordance with the agreement for the 2023 Notes, the conversion rate was adjusted as a result of the completion of the Spin-Off of Theravance Biopharma. The conversion rate was adjusted based on the conversion rate immediately prior to the record date for the Spin-Off and the average of the stock dividend distributed to our common stockholders and our stock prices. This resulted in an adjusted conversion rate of 46.9087 shares per $1,000 principal amount of the 2023 Notes, which represents an adjusted conversion price of approximately $21.32 per share. As a result of the conversion rate adjustment, the capped call strike price and cap price were also adjusted accordingly to $21.32 and $29.16, respectively. On July 15, 2014, certain holders of the 2023 Notes converted their notes into 1,519,402 shares of our common stock at the adjusted conversion price of $21.32 per share. In connection with the partial conversion of the 2023 Notes, we received 149,645 shares of our common stock from our capped call option counterparty and the shares of common stock received were recorded as treasury stock. In connection with the payments of the cash dividends during the years ended December 31, 2015 and 2014, which is further discussed in Note 8, "Shareholders' Deficit", the adjusted conversion rate with respect to our 2023 Notes was further adjusted in total from 46.9087 shares of our common stock per $1,000 principal amount of the 2023 Notes to 50.5818 shares of our common stock per $1,000 principal amount of the 2023 Notes, which represents an adjusted conversion price of approximately $19.77 per share. As a result of the conversion rate adjustment, the capped call strike price and cap price were also adjusted accordingly to $19.77 and $27.04. Non-Recourse Notes Due 2029 In April 2014, we entered into certain note purchase agreements relating to the private placement of $450.0 million aggregate principal amount of non-recourse fixed rate term notes due 2029 (the "2029 Notes") issued by our wholly-owned subsidiary. The 2029 Notes are secured by a security interest in a segregated bank account established to receive 40% of royalties due to us under the LABA Collaboration with GSK commencing on April 1, 2014 and ending upon the earlier of full repayment of principal or May 15, 2029. The amounts in the segregated bank account can only be used to make interest and principal payments on the 2029 Notes. As of December 31, 2015 and 2014, the balance of the segregated bank account was not material. The 2029 Notes bear an annual interest rate of 9%, with interest and principal paid quarterly beginning November 15, 2014. The 2029 Notes may be redeemed at any time prior to maturity, in whole or in part, at specified redemption premiums. Prior to May 15, 2016, in the event that the specified portion of royalties received in a quarter is less than the interest accrued for the quarter, the principal amount of the 2029 Notes will increase by the interest shortfall amount for that period, and considered as payment in kind ("PIK"). Since issuance, $43.2 million of interest expense has been added to the principal balance of the 2029 Note, of which $22.7 million and $20.5 million was added during the years ended December 31, 2015 and 2014, respectively. Since the principal and interest payments on the 2029 Notes are based on royalties from product sales recorded by GSK, which will vary from quarter to quarter and are unknown to us, the 2029 Notes may be repaid prior to the final maturity date in 2029. The 2029 Notes can be prepaid subject to a prepayment premium of 5% until April 17, 2016, 2.5% thereafter until April 17, 2017, and without premium afterwards. In connection with the sale of the 2029 Notes, we incurred approximately $15.3 million in debt issuance costs, which are being amortized to interest expense over the estimated life of the 2029 Notes. |
Shareholders' Deficit
Shareholders' Deficit | 12 Months Ended |
Dec. 31, 2015 | |
Shareholders' Deficit | |
Shareholders' Deficit | 8. Shareholders' Deficit Dividends On February 20, 2015, our Board of Directors declared a quarterly dividend of $0.25 per share of common stock to stockholders of record as of the close of business on March 12, 2015. This dividend was paid on March 31, 2015. On April 24, 2015, our Board of Directors declared a quarterly dividend of $0.25 per share of common stock to stockholders of record as of the close of business on June 12, 2015. This dividend was paid on June 30, 2015. On July 24, 2015, our Board of Directors declared a quarterly dividend of $0.25 per share of common stock to stockholders of record as of the close of business on September 10, 2015. This dividend was paid to our stockholders on September 30, 2015. During the year ended December 31, 2015, we paid an aggregate of $87.3 million in dividends. Unvested RSAs and certain unvested RSUs as of the record date are also entitled to dividends, which will only be paid when the RSAs and such RSUs vest and are released. For further information on the impact of the cash dividend payments on the 2023 Notes, refer to Note 7, "Long-Term Debt". On October 16, 2014, our Board of Directors declared a quarterly dividend of $0.25 per share of common stock to stockholders of record as of the close of business on November 25, 2014. This dividend was paid on December 31, 2014. On July 25, 2014, our Board of Directors declared a quarterly dividend of $0.25 per share of common stock to stockholders of record as of the close of business on August 28, 2014. This dividend was paid on September 18, 2014. Share Repurchase Program On October 28, 2015, we announced the acceleration of our capital return plan with a $150 million share repurchase program effective through the end of 2016 approved by our Board of Directors, replacing our quarterly dividend. As a component of the share repurchase plan, on October 30, 2015, we commenced a "modified Dutch auction" tender offer (the "October 2015 TO") to purchase up to $75 million of our common stock, at a price per share of not less than $8.50 and not greater than $9.25, which will be contingent upon satisfaction of customary conditions. The October 2015 TO expired on December 1, 2015. The following table shows the Company's share repurchase activity and related information on the October 2015 TO: Purchase period end date December 2015 Number of shares purchased and retired (in thousands) 2,576 Average repurchase price per share, including associated fees and expenses $9.56 Share repurchase amount (in millions) $24.6 Additionally, as part of its share repurchase program, during December 2015 we repurchased 100,000 shares of our common stock in the open market at an average price of $9.95 per share for a total of $1.0 million, which were also retired upon repurchase. |
Commitments and Contingencies
Commitments and Contingencies | 12 Months Ended |
Dec. 31, 2015 | |
Commitments and Contingencies | |
Commitments and Contingencies | 9. Commitments and Contingencies Operating Lease and Lease Guarantee Upon the Spin-Off, our facility leases in South San Francisco, California were assigned to Theravance Biopharma. However, if Theravance Biopharma were to default on its lease obligations, we have in substance guaranteed the lease payments for these facilities. We would also be responsible for lease-related payments including utilities, property taxes, and common area maintenance, which may be as much as the actual lease payments. As of December 31, 2015, the total remaining lease payments, which run through May 2020, were $27.6 million. The carrying value of this lease guarantee was $1.3 million as of December 31, 2015 and is reflected in other long-term liabilities in our consolidated balance sheet. Following the Spin-Off, we entered into a Sublease Agreement with Theravance Biopharma to sublease 4,847 square feet of office space in South San Francisco, California, which expires in May 2020. We do not own or lease any other properties. Rent expenses associated with our operating leases for the years ended December 31, 2015, 2014 and 2013 were $0.2 million, $3.0 million, and $6.0 million, respectively. Future minimum lease payments under this lease as of December 31, 2015, were as follows: (In thousands) Years Ending December 31: 2016 $ 2017 2018 2019 2020 Thereafter — Total $ Guarantees and Indemnifications We indemnify our officers and directors for certain events or occurrences, subject to certain limits. We believe the fair value of these indemnification agreements is minimal. Accordingly, we have not recognized any liabilities relating to these agreements as of December 31, 2015. |
Income Taxes
Income Taxes | 12 Months Ended |
Dec. 31, 2015 | |
Income Taxes | |
Income Taxes | 10. Income Taxes Due to ongoing operating losses and the inability to recognize any income tax benefit, there is no provision for income taxes for any periods presented. Deferred income taxes reflect the net tax effects of temporary differences between the carrying amounts of assets and liabilities for financial reporting purposes and the amounts used for income tax purposes. Significant components of our deferred tax assets are as follows: As of December 31, (In thousands) 2015 2014 Deferred tax assets: Net operating loss carryforwards $ $ Deferred revenues Research and development tax credit carryforwards Other Total deferred tax assets Valuation allowance ) ) Net deferred tax assets $ — $ — The differences between the U.S. federal statutory income tax rate to our effective tax rate are as follows: Year Ended December 31, 2015 2014 2013 U.S. federal statutory income tax rate % % % Non-deductible executive compensation ) ) ) Stock-based compensation ) ) Federal and state research credits — Effect of Spin-Off Transaction — ) — Other ) ) ) Change in valuation allowance ) ) Effective tax rate )% )% )% Realization of deferred tax assets is dependent on future taxable income, if any, the timing and the amount of which are uncertain. Accordingly, the deferred tax assets have been fully offset by a valuation allowance. The valuation allowance increased by $4.7 million in the year ended December 31, 2015, decreased by $103.8 million in the year ended December 31, 2014, and increased by $70.1 million in the year ended December 31, 2013. The increase in the valuation allowance in the year ended December 31, 2015 was primarily a result of net operating loss carryforwards. The decrease in the valuation allowance in the year ended December 31, 2014 was primarily a result of the tax impacts of the Spin-Off transaction. In the year ended December 31, 2014, the Company recorded a permanent difference related to the tax gain that was recognized in connection with the Spin-Off, which allowed the Company to utilize approximately $252.7 million of its federal net operating losses. Accordingly, the associated valuation allowance, of $88.6 million, was released. Additionally, as discussed in Note 11 in connection with the Spin-Off, approximately $9.2 million of deferred tax assets were transferred to Theravance Biopharma, Inc. Accordingly, the associated valuation allowance was also decreased. As of December 31, 2015, we had federal net operating loss carryforwards of approximately $1,174.7 million, which will expire from 2024 through 2035, and federal research and development tax credit carryforwards of approximately $45.2 million, which will expire from 2018 through 2034. We also had state net operating loss carryforwards of approximately $676.5 million expiring in the years 2016 through 2035 and state research tax credits of approximately $32.3 million, which do not expire. The net operating loss deferred tax asset balances as of December 31, 2015 and 2014 do not include excess tax benefits from stock option exercises. Stockholders' equity will be credited if and when such excess tax benefits are ultimately realized. Utilization of net operating loss and tax credit carryforwards may be subject to a substantial annual limitation due to ownership change limitations provided by the Internal Revenue Code and similar state provisions. Annual limitations may result in expiration of net operating loss and tax credit carryforwards before some or all of such amounts have been utilized. Our policy is to recognize interest and/or penalties related to income tax matters in income tax expense. As of December 31, 2015 and 2014, we had no accrued interest or penalties due to our net operating losses available to offset any tax adjustment. We conducted an analysis through the year ended December 31, 2014 to determine whether an ownership change had occurred since inception. The analysis indicated that two ownership changes occurred in prior years. However, notwithstanding the applicable annual limitations, no portion of the net operating loss or credit carryforwards are expected to expire before becoming available to reduce federal and state income tax liabilities as a result of those identified ownership changes. If we undergo another ownership change, the utilization of the pre-ownership change net operating loss carryforwards or pre-ownership change tax attributes, such as research tax credits, to offset the post-ownership change income may be subject to an annual limitation, pursuant to Section 382 and 383 of the Internal Revenue Code of 1986, as amended. Similar rules may apply under state tax laws. Uncertain Tax Positions A reconciliation of the beginning and ending balances of the total amounts of unrecognized tax benefits are as follows (in thousands): Unrecognized tax benefits as of December 31, 2012 $ Gross decrease for tax positions for prior years ) Gross increase in tax positions for current year Unrecognized tax benefits as of December 31, 2013 Gross decrease for tax positions for prior years ) Gross increase in tax positions for current year Unrecognized tax benefits as of December 31, 2014 Gross increase in tax positions for current year Unrecognized tax benefits as of December 31, 2015 $ In the event that we are able to recognize these uncertain positions, most of the $15.5 million of the unrecognized benefit would reduce our effective tax rate. We currently have a full valuation allowance against our deferred tax assets, which would impact the timing of the effective tax rate benefit, should any of these uncertain positions be favorably settled in the future. We do not believe it is reasonably possible that our unrecognized tax benefits will significantly change within the next twelve months. We are subject to taxation in the U.S. and various state jurisdictions. The tax years 1998 and forward remain open to examination by the federal and most state tax authorities due to net operating loss and overall credit carryforward positions. |
Spin-Off of Theravance Biopharm
Spin-Off of Theravance Biopharma, Inc. | 12 Months Ended |
Dec. 31, 2015 | |
Spin-Off of Theravance Biopharma, Inc. | |
Spin-Off of Theravance Biopharma, Inc. | 11. Spin-Off of Theravance Biopharma, Inc. On June 1, 2014, we separated our late-stage partnered respiratory assets from our biopharmaceutical research and drug development operations. We contributed the assets and certain liabilities from the research and drug development operations and $393.0 million of cash, cash equivalents and marketable securities to Theravance Biopharma. All outstanding shares of Theravance Biopharma were then distributed to our stockholders of record on May 15, 2014 as a pro-rata dividend distribution of one ordinary share of Theravance Biopharma for every 3.5 shares held of our common stock. On June 1, 2014, we entered into a Separation and Distribution Agreement with Theravance Biopharma that set forth the terms and conditions of the separation of Theravance Biopharma from us. The Separation and Distribution Agreement sets forth a framework for the relationship between us and Theravance Biopharma following the separation regarding principal transactions necessary to separate Theravance Biopharma from us. This agreement also sets forth other provisions that govern certain aspects of our relationship with Theravance Biopharma after the completion of the separation from us and provides for the allocation of assets, liabilities and obligations between Theravance Biopharma and us in connection with the Spin-Off. In addition, we entered into other definitive agreements in connection with the Spin-Off, including (1) a Transition Services Agreement pursuant to which Theravance Biopharma and we will provide each other with a variety of administrative services, including financial, tax, accounting, information technology, legal and human resources services, for a period of time of up to 12 months following the Spin-Off, (2) a Tax Matters Agreement that generally governs the parties' respective rights, responsibilities and obligations after the separation with respect to taxes, (3) a Sublease Agreement that provides for the sublease from Theravance Biopharma to us for certain office space to be utilized in our operations and (4) an Employee Matters Agreement that allocates liabilities and responsibilities relating to employee compensation, benefit plans, programs and other related matters in connection with the separation, including the treatment of outstanding incentive awards and certain retirement and welfare benefit obligations. These arrangements contain the provisions related to the Spin-Off and the distribution of Theravance Biopharma's ordinary shares to our stockholders. The total amount of the Theravance Biopharma share dividend of $402.9 million was based on the net book value of the net assets that were contributed to Theravance Biopharma in connection with the Spin-Off, as follows: (In thousands) June 2, 2014 Cash and cash equivalents $ Marketable investment securities Accounts receivable Reimbursement of certain liabilities Prepaid and other current assets Inventories Fixed assets, net Accrued liabilities ) Deferred revenue ) Other liabilities ) Net book value of assets contributed $ Due to the Spin-Off, the leases for the facilities in South San Francisco, California, which formerly served as our headquarters, were assigned to Theravance Biopharma. We would be held liable by the landlord if Theravance Biopharma defaults under its lease obligations, and thus, we have in substance guaranteed the payments under the lease agreements for these facilities. See Note 9, "Commitments and Contingencies" for further information on this lease guarantee. Theravance Biopharma's historical results of operations have been presented as discontinued operations in our consolidated statement of operations for the years ended December 31, 2015 and 2014. See Note 12, "Discontinued Operations," for further information. |
Discontinued Operations
Discontinued Operations | 12 Months Ended |
Dec. 31, 2015 | |
Discontinued Operations. | |
Discontinued Operations | 12. Discontinued Operations On June 1, 2014, we separated our research and drug development businesses from our late-stage partnered respiratory assets. For further information on the Spin-Off, refer to Notes 1 and 11, "Description of Operations and Summary of Significant Accounting Policies" and "Spin-Off of Theravance Biopharma, Inc.". The significant components of the research and drug development operations, which are presented as discontinued operations on the consolidated statements of operations, were as follows: Year Ended December 31, (In thousands) 2015 2014 2013 Net revenues(1) $ — $ $ Income (loss) from discontinued operations(2) — ) ) (1) Net revenues primarily consist of revenue from collaborative arrangements and product sales. Revenue from collaborative arrangements was recognized from our agreement with R-Pharm CJSC, which was transferred to Theravance Biopharma as a part of the Spin-Off. Product sales were generated from sales of VIBATIV in the U.S. through a limited number of distributors, and title and risk of loss transfer upon receipt by these distributors. Healthcare providers ordered VIBATIV through these distributors. Commencing in the first quarter of 2014, revenue on the sale of VIBATIV was recorded on a sell-through basis, once the distributors sold the product to healthcare providers. Product sales were recorded net of estimated government-mandated rebates and chargebacks, distribution fees, estimated product returns and other deductions. (2) Loss from discontinued operations decreased in the year ended December 31, 2014 compared to the year ended December 31, 2013 primarily as there was no impact of discontinued operations after the Spin- Off occurring in June 2014. Included in the loss from discontinued operations for the year ended December 31, 2014 and the year ended December 31, 2013 are external legal and accounting fees in connection with our separation strategy which we started to incur in the year ended December 31, 2013 and the additional stock-based compensation and cash bonus expense recognized due to the achievement of performance conditions under a special long-term retention and incentive equity and cash bonus awarded to certain employees in the year ended December 31, 2011, which we started to incur in the year ended December 31, 2014. There was no impact of the discontinued operations after the Spin-Off to our revenues and expenses for the year ended December 31, 2015. In May 2013, we entered into a royalty participation agreement with Elan Corporation, plc ("Elan"). The closing of the transaction was subject to closing conditions, including the approval of the transaction by Elan's shareholders. Elan's shareholders did not approve the transaction at an Extraordinary General Meeting. Subsequently, we terminated the agreement and, as a result, Elan paid us a $10.0 million termination fee in June 2013, which is reflected in discontinued operations on the consolidated statements of operations. |
Subsequent Events
Subsequent Events | 12 Months Ended |
Dec. 31, 2015 | |
Subsequent Events | |
Subsequent Events | 13. Subsequent Events In January 2016 and through the middle of February 2016, as part of our share repurchase program as discussed in Note 8—"Shareholders' Deficit", we repurchased 1,419,641 shares of our common stock in the open market at an average price of $9.53 per share for a total purchase price of $13.5 million, which were retired upon repurchase. |
SUPPLEMENTARY FINANCIAL DATA (U
SUPPLEMENTARY FINANCIAL DATA (UNAUDITED) | 12 Months Ended |
Dec. 31, 2015 | |
SUPPLEMENTARY FINANCIAL DATA (UNAUDITED) | |
SUPPLEMENTARY FINANCIAL DATA (UNAUDITED) | SUPPLEMENTARY FINANCIAL DATA (UNAUDITED) (In thousands, except per share amounts) The following table presents certain unaudited consolidated quarterly financial information for the eight quarters in the period ended December 31, 2015. This information has been prepared on the same basis as the audited consolidated financial statements and includes all adjustments (consisting only of normal recurring adjustments) necessary to present fairly the unaudited quarterly results of operations set forth herein. For the Quarters Ended(1) March 31 June 30 September 30 December 31 2015 Net revenue $ $ $ $ Total operating expenses(1) ) ) ) ) Income from operations Net income (loss) $ ) $ ) $ ) $ Basic and diluted net income (loss) per share $ ) $ ) $ ) $ Cash dividends declared per common share $ $ $ $ — For the Quarters Ended(1) March 31 June 30 September 30 December 31 2014 Net revenue $ ) $ $ $ Total operating expenses(1) ) ) ) ) Loss from continuing operations ) ) ) ) Loss from discontinued operations(1) ) ) — — Net loss $ ) $ ) $ ) $ ) Basic and diluted net loss per share: Continuing operations, net of tax $ ) $ ) $ ) $ ) Discontinued operations ) ) — — Total $ ) $ ) $ ) $ ) Cash dividends declared per common share $ — $ — $ $ (1) Amounts were computed independently for each quarter, and the sum of the quarters may not total the annual amounts. |
Description of Operations and24
Description of Operations and Summary of Significant Accounting Policies (Policies) | 12 Months Ended |
Dec. 31, 2015 | |
Description of Operations and Summary of Significant Accounting Policies | |
Business Separation | Business Separation On June 1, 2014, we separated our biopharmaceutical research and drug development operations from our late-stage partnered respiratory assets by transferring our research and drug development operations into our then wholly- owned subsidiary, Theravance Biopharma, Inc. ("Theravance Biopharma"). We contributed $393.0 million of cash, cash equivalents and marketable securities to Theravance Biopharma and all outstanding shares of Theravance Biopharma were then distributed to Innoviva stockholders as a pro-rata dividend distribution on June 2, 2014 by issuing one ordinary share of Theravance Biopharma for every 3.5 shares held of our common stock to stockholders of record on May 15, 2014 (the "Spin-Off"). The Spin-Off resulted in Theravance Biopharma operating as an independent, publicly traded company. The results of operations for the former research and drug development operations conducted by us and by Theravance Biopharma until June 1, 2014 are included as part of this report as discontinued operations. Refer to Notes 11 and 12, "Spin-Off of Theravance Biopharma, Inc.," and "Discontinued Operations" for further information. |
Principles of Consolidation | Principles of Consolidation The consolidated financial statements include the accounts of Innoviva and its wholly owned subsidiaries. All intercompany balances and transactions have been eliminated in consolidation. |
Use of Management's Estimates | Use of Management's Estimates The preparation of consolidated financial statements in conformity with U.S. Generally Accepted Accounting Principles ("GAAP") requires management to make estimates and assumptions that affect the amounts reported in the consolidated financial statements and accompanying notes. Actual results could differ materially from those estimates. Management evaluates its significant accounting policies and estimates on an ongoing basis. We base our estimates on historical experience and other relevant assumptions that we believe to be reasonable under the circumstances. These estimates also form the basis for making judgments about the carrying values of assets and liabilities when these values are not readily apparent from other sources. |
Certain Risks and Concentrations | Certain Risks and Concentrations Our financial instruments that are exposed to concentrations of credit risk consist primarily of cash and cash equivalents and marketable securities. Although we deposit our cash with multiple financial institutions, our deposits, at times, may exceed federally insured limits. Refer to "Segment Reporting" below for concentrations with respect to revenues and geographic locations. |
Segment Reporting | Segment Reporting We operate in a single segment, which is to provide capital return to stockholders by maximizing the potential value of our respiratory assets partnered with GSK. Revenues are generated from our collaborative arrangements and royalty payment from GSK, located in Great Britain. Our facilities are located within the United States. |
Variable Interest Entities | Variable Interest Entities We evaluate our ownership, contractual and other interest in entities to determine if they are variable-interest entities ("VIE"), whether we have a variable interest in those entities and the nature and extent of those interests. Based on our evaluations, if we determine we are the primary beneficiary of such VIEs, we consolidate such entities into our financial statements. We consolidate the financial results of TRC, which we have determined to be a VIE, because we have the power to direct the economically significant activities of TRC and the obligation to absorb losses of, or the right to receive benefits from, TRC. The financial position and results of operations of TRC are not material for the periods presented. |
Cash and Cash Equivalents | Cash and Cash Equivalents We consider all highly liquid investments purchased with a maturity of three months or less on the date of purchase to be cash equivalents. Cash equivalents are carried at cost, which approximates fair value. |
Investments in Marketable Securities | Investments in Marketable Securities We invest in short-term investments and marketable securities, primarily corporate notes, government, government agency, and municipal bonds. We limit the amount of credit exposure with any one issuer, industry or geographic area for investments other than instruments backed by the U.S. federal government. We classify our marketable securities as available-for-sale securities and report them at fair value in cash equivalents, short-term investments or marketable securities on the consolidated balance sheets with related unrealized gains and losses included as a component of stockholders' equity (deficit). The amortized cost of debt securities is adjusted for amortization of premiums and accretion of discounts to maturity, which is included in interest income on the consolidated statements of operations. Realized gains and losses, if any, on available-for-sale securities are included in interest income. The cost of securities sold is based on the specific identification method. Interest and dividends on securities classified as available-for-sale are included in interest income. We regularly review all of our investments for other-than-temporary declines in estimated fair value. Our review includes the consideration of the cause of the impairment, including the creditworthiness of the security issuers, the number of securities in an unrealized loss position, the severity and duration of the unrealized losses, whether we have the intent to sell the securities and whether it is more likely than not that we will be required to sell the securities before the recovery of their amortized cost basis. When we determine that the decline in estimated fair value of an investment is below the amortized cost basis and the decline is other-than-temporary, we reduce the carrying value of the security and record a loss for the amount of such decline to other income (expense), net. |
Fair Value of Financial Instruments | Fair Value of Financial Instruments We define fair value as the exchange price that would be received for an asset or paid to transfer a liability (an exit price) in the principal or most advantageous market for the asset or liability in an orderly transaction between market participants on the measurement date. Our valuation techniques are based on observable and unobservable inputs. Observable inputs reflect readily obtainable data from independent sources, while unobservable inputs reflect our market assumptions. We classify these inputs into the following hierarchy: Level 1 —Quoted prices for identical instruments in active markets. Level 2 —Quoted prices for similar instruments in active markets; quoted prices for identical or similar instruments in markets that are not active; and model-derived valuations whose inputs are observable or whose significant value drivers are observable. Level 3 —Unobservable inputs and little, if any, market activity for the assets. Financial instruments include cash equivalents, marketable securities, accounts receivable, receivables from collaborative arrangements, accounts payable, and accrued liabilities. Cash equivalents and marketable securities are carried at estimated fair value. The carrying value of accounts receivable, receivables from collaborative arrangements, accounts payable, and accrued liabilities approximate their estimated fair value due to the relatively short-term nature of these instruments. |
Property and Equipment | Property and Equipment All property, equipment and leasehold improvements prior to the Spin-Off were related to our former research and drug development operations and thus, were contributed to Theravance Biopharma in connection with the Spin-Off. Property and equipment as of December 31, 2015 and 2014, which consisted of computer software, amounted to $0.2 million and $0.3 million, respectively. Property, equipment and leasehold improvements are stated at cost and depreciated using the straight-line method as follows: Leasehold improvements Shorter of remaining lease terms or useful life Equipment, furniture and fixtures 5 - 7 years Software and computer equipment 3 years Depreciation expense for the years ended December 31, 2015, 2014 and 2013 was $0.1 million, $1.1 million and $2.7 million. Depreciation expense for property and equipment used by our former research and drug development operations is classified within discontinued operations in the consolidated statements of operations. The change in accumulated depreciation is net of asset retirements. |
Capitalized Software | Capitalized Software We capitalize certain costs related to direct material and service costs for software obtained for internal use. Capitalized software costs are depreciated over three years. |
Capitalized Fees Paid to a Related Party | Capitalized Fees paid to a Related Party We capitalize fees paid to licensors related to agreements for approved products or commercialized products. We capitalize these fees as capitalized fees paid to a related party ("Capitalized Fees") and amortize these Capitalized Fees on a straight-line basis over their estimated useful lives upon the commercial launch of the product, which has been shortly after regulatory approval of such product. The estimated useful lives of these Capitalized Fees are based on a country-by-country and product-by-product basis, as the later of the expiration or termination of the last patent right covering the compound in such product in such country and 15 years from first commercial sale of such product in such country, unless the agreement is terminated earlier. Consistent with our policy for classification of costs under the research and development collaborative arrangements, the amortization of these Capitalized Fees are recognized as a reduction of royalty revenue. We review our Capitalized Fees for impairment when events or changes in circumstances indicate that the carrying amount of such assets may not be recoverable. The recoverability of Capitalized Fees is measured by comparing the asset's carrying amount to the expected undiscounted future cash flows that the asset is expected to generate. The determination of recoverability typically requires various estimates and assumptions, including estimating the useful life over which cash flows will occur, their amount, and the asset's residual value, if any. We derive the required cash flow estimates from near-term forecasted product sales and long-term projected sales in the corresponding market. |
Revenue Recognition | Revenue Recognition Revenue is recognized when the four basic criteria of revenue recognition are met: (1) persuasive evidence of an arrangement exists; (2) delivery has occurred or services have been rendered; (3) the fee is fixed or determinable; and (4) collectability is reasonably assured. Where the revenue recognition criteria are not met, we defer the recognition of revenue by recording deferred revenue until such time that all criteria are met. Collaborative Arrangements and Multiple-Element Arrangements Revenue from nonrefundable, up-front license or technology access payments under license and collaborative arrangements that are not dependent on any future performance by us is recognized when such amounts are earned. If we have continuing obligations to perform under the arrangement, such fees are recognized over the estimated period of continuing performance obligation. Our arrangements can include multiple elements which may consist of license and development agreements. When multiple-element arrangements exist, we evaluate whether these individual deliverables should be accounted for as separate units of accounting or one single unit of accounting. For new or materially amended multiple element arrangements, we identify the deliverables at the inception of the arrangement and each deliverable within a multiple deliverable revenue arrangement is accounted for as a separate unit of accounting if both of the following criteria are met: (1) the delivered item or items have value to the customer on a standalone basis and (2) for an arrangement that includes a general right of return relative to the delivered item(s), delivery or performance of the undelivered item(s) is considered probable and substantially in our control. We allocate revenue to each non-contingent element based on the relative selling price of each element. When applying the relative selling price method, we determine the selling price for each deliverable using vendor-specific objective evidence ("VSOE") of selling price, if it exists, or third-party evidence ("TPE") of selling price, if it exists. If neither VSOE nor TPE of selling price exist for a deliverable, we use the best estimated selling price for that deliverable. Revenue allocated to each element is then recognized based on when the basic four revenue recognition criteria are met for each element. For multiple-element arrangements entered into prior to January 1, 2011, we determined the delivered items under our collaborative arrangements did not meet the criteria to be considered separate accounting units for the purposes of revenue recognition. As a result, we recognized revenue from non-refundable, upfront fees and development contingent payments in the same manner as the final deliverable, which is ratably over the expected term of our performance of research and development services under the agreements. These upfront or contingent payments received, pending recognition as revenue, are recorded as deferred revenue and are classified as a short-term or long-term liability on the consolidated balance sheets and recognized over the estimated period of performance. We periodically review the estimated performance periods of our contracts based on the progress of our programs. Where a portion of non-refundable upfront fees or other payments received are allocated to continuing performance obligations under the terms of a collaborative arrangement, they are recorded as deferred revenue and recognized as revenue, or as an accrued liability and recognized as a reduction of research and development expenses ratably over the term of our estimated performance period under the agreement. We determine the estimated performance periods, and they are periodically reviewed based on the progress of the related program. The effect of any change made to an estimated performance period and, therefore revenue recognized, would occur on a prospective basis in the period that the change was made. Under certain collaborative arrangements, we have been reimbursed for a portion of our research and development expenses. These reimbursements have been reflected as a reduction of research and development expense in our consolidated statements of operations, as we do not consider performing research and development services to be a part of our ongoing and central operations. Therefore, the reimbursement of research and developmental services and any amounts allocated to our research and development services are recorded as a reduction of research and development expense. Amounts deferred under a collaborative arrangement in which the performance obligations are terminated will result in an immediate recognition of any remaining deferred revenue and accrued liability in the period that termination occurred, provided that there are no remaining performance obligations. We account for contingent payments in accordance with FASB Subtopic ASC 605-28 "Revenue Recognition—Milestone Method." We recognize revenue from milestone payments when (i) the milestone event is substantive and its achievability was not reasonably assured at the inception of the agreement and (ii) we do not have ongoing performance obligations related to the achievement of the milestone. Milestone payments are considered substantive if all of the following conditions are met: the milestone payment (a) is commensurate with either our performance to achieve the milestone or the enhancement of the value of the delivered item or items as a result of a specific outcome resulting from our performance to achieve the milestone, (b) relates solely to past performance, and (c) is reasonable relative to all of the deliverables and payment terms (including other potential milestone consideration) within the arrangement. Under our collaborative arrangements with GSK, royalty revenue earned is reduced by amortization expense resulting from the fees paid to GSK, which were recognized as capitalized fees paid to a related party. When amortization expense exceeds amounts recognized for royalty revenues from GSK, negative revenue would be reported in our consolidated statements of operations. Royalties We recognize royalty revenue on licensee net sales of products with respect to which we have contractual royalty rights in the period in which the royalties are earned and reported to us and collectability is reasonably assured. Royalties are recognized net of amortization of capitalized fees associated with any approval and launch milestone payments made to GSK. Product Revenues We currently have no product revenues following the Spin-Off. Prior to the Spin-Off, we recognized revenues from product sales when there was persuasive evidence that an arrangement existed, title and risk of loss transferred, the price was fixed and determinable, and collectability was reasonably assured. Product sales were recognized net of estimated allowances, discounts, sales returns, chargebacks and rebates. Such amounts are presented within discontinued operations in the consolidated statements of operations. Allowance for Doubtful Accounts We maintain a policy to record allowances for potentially doubtful accounts for estimated losses resulting from the inability of our customers to make required payments. As of December 31, 2015, there were no allowances for doubtful accounts and we have not had any write-offs historically. |
Research and Development Costs | Research and Development Costs Research and development costs are expensed in the period that services are rendered or goods are received. Research and development costs consist primarily of salaries and benefits. Prior to the Spin-Off, research and development costs also included laboratory supplies and facility costs, and fees paid to third parties that conduct certain research and development activities on behalf of us, net of certain external research and development costs reimbursed under collaborative arrangements, which are classified within discontinued operations in the consolidated statements of operations. |
Fair Value of Stock-Based Compensation Awards | Fair Value of Stock-Based Compensation Awards We use the Black-Scholes-Merton option pricing model to estimate the fair value of options granted under our equity incentive plans and rights to acquire stock granted under our employee stock purchase plan ("ESPP"). The Black-Scholes-Merton option valuation model requires the use of assumptions, including the expected term of the award and the expected stock price volatility. We use the "simplified" method as described in Staff Accounting Bulletin No. 107, "Share-Based Payment," for the expected option term because the usage of its historical option exercise data is limited due to post-IPO exercise restrictions. Beginning April 1, 2011, we used our historical volatility to estimate expected stock price volatility. Prior to April 1, 2011, we used peer company price volatility to estimate expected stock price volatility due to our limited historical common stock price volatility since our initial public offering in the year ended December 31, 2004. Restricted Stock Units ("RSUs") and Restricted Stock Awards ("RSAs") are measured based on the fair market values of the underlying stock on the dates of grant. Stock-based compensation expense was calculated based on awards ultimately expected to vest and was reduced for estimated forfeitures at the time of grant and revised, if necessary, in subsequent periods if actual forfeitures differed from those estimates. Our estimated annual forfeiture rates for stock options, RSUs and RSAs are based on our historical forfeiture experience. The estimated fair value of stock options, RSUs and RSAs is expensed on a straight-line basis over the expected term of the grant and the estimated fair value of performance-contingent RSUs and RSAs is expensed using an accelerated method over the term of the award once we have determined that it is probable that performance milestones will be achieved. Compensation expense for RSUs and RSAs that contain performance conditions is based on the grant date fair value of the award. Compensation expense is recorded over the requisite service period based on management's best estimate as to whether it is probable that the shares awarded are expected to vest. We assess the probability of the performance milestones being met on a continuous basis. Compensation expense for purchases under the ESPP is recognized based on the fair value of the common stock on the date of offering, less the purchase discount percentage provided for in the plan. We have not recognized, any income tax benefit related to employee stock-based compensation expense as a result of the full valuation allowance on our deferred tax assets including deferred tax assets related to our net operating loss carryforwards. |
Amortization of Debt Issuance Costs from Non-recourse Notes Payable, due 2029 | Amortization of Debt Issuance Costs from Non-recourse Notes Payable, due 2029 In April 2014, we entered into certain note purchase agreements relating to the private placement of $450.0 million aggregate principal amount of non-recourse 9% fixed rate term notes due 2029 (the "2029 Notes") issued by our wholly-owned subsidiary. We incurred approximately $15.3 million in transaction costs in connection with issuance of 2029 Notes, which we amortize to interest expense over the estimated life of the 2029 Notes based on the effective interest method. Since the principal and interest payments on the 2029 Notes are based on royalties from product sales, which will vary from quarter to quarter, the 2029 Notes may be repaid prior to the final maturity date in 2029. We continue to assess, on an ongoing basis, our estimates on royalties from products sales as it relates to its impact on payments of principal and interest on the 2029 Notes. To the extent that the interest or principal payments are greater or less than our initial estimates or the timing of such payments is materially different than our original estimates, we prospectively adjust the amortization of the debt issuance costs. |
Income Taxes | Income Taxes We utilize the asset and liability method of accounting for income taxes. Under this method, deferred tax assets and liabilities are determined based on differences between financial reporting and tax basis of assets and liabilities and are measured using enacted tax rates and laws that will be in effect when the differences are expected to reverse. A valuation allowance is provided when it is more likely than not that some portion or all of a deferred tax asset will not be realized. None of our currently unrecognized tax benefits would affect our effective income tax rate if recognized, due to the valuation allowance that currently offsets our deferred tax assets. We do not anticipate the total amount of unrecognized income tax benefits relating to uncertain tax positions existing as of December 31, 2015 will significantly increase or decrease in the next 12 months. We assess all material positions taken in any income tax return, including all significant uncertain positions, in all tax years that are still subject to assessment or challenge by relevant taxing authorities. Assessing an uncertain tax position begins with the initial determination of the position's sustainability and is measured at the largest amount of benefit that is greater than 50% likely to be realized upon ultimate settlement. As of each balance sheet date, unresolved uncertain tax positions must be reassessed, and we will determine whether: the factors underlying the sustainability assertion have changed and whether the amount of the recognized tax benefit is still appropriate. The recognition and measurement of tax benefits requires significant judgment. Judgments concerning the recognition and measurement of a tax benefit might change as new information becomes available. In November 2015, the FASB issued ASU 2015-17, Balance Sheet Classification of Deferred Taxes , which eliminates the requirement for organizations to present deferred tax liabilities and assets as current and noncurrent in a classified balance sheet. The standard requires us to classify all deferred tax assets and liabilities as noncurrent. We adopted this standard in December 2015. This adoption did not have a material impact on our consolidated financial statements. |
Comprehensive Loss | Comprehensive Loss Comprehensive loss is comprised of net loss and other comprehensive income (loss). Other comprehensive income (loss) consists of changes in unrealized and realized gains and losses on our marketable securities, net of tax. |
Related Parties | Related Parties GSK owned 27.9% of our outstanding common stock as of December 31, 2015. Transactions with GSK are described in Note 3, "Collaborative Arrangements". Prior to the Spin-Off, Robert V. Gunderson, Jr. was one of our directors. We have engaged Gunderson Dettmer Stough Villeneuve Franklin & Hachigian, LLP, of which Mr. Gunderson is a partner, as our primary legal counsel. Fees incurred in the ordinary course of business were, $1.3 million in the year ended December 31, 2014 and $3.2 million in the year ended December 31, 2013. As Mr. Gunderson was not one of our directors for the year ended December 31, 2015, he is no longer considered a related party. |
Recently Issued Accounting Pronouncements Not Yet Adopted | Recently Issued Accounting Pronouncements Not Yet Adopted In January 2016, the Financial Accounting Standards Board ("FASB") issued Accounting Standards Update ("ASU") 2016-01, Recognition and Measurement of Financial Assets and Financial Liabilities , which provides guidance for the recognition, measurement, presentation, and disclosure of financial assets and liabilities. This ASU will be effective for us beginning in January 1, 2018. We are evaluating the effects of the adoption of this ASU to our consolidated financial statements. In April 2015, the FASB issued ASU 2015-03, Interest—Imputation of Interest , to simplify the presentation of debt issuance costs. This standard amends existing guidance to require the presentation of debt issuance costs associated with term loans in the balance sheet as a deduction from the carrying amount of the related debt liability instead of a deferred charge. It will be effective for us on January 1, 2016, with early adoption permitted. We plan to adopt ASU 2015-03 on January 1, 2016. Upon adoption of ASU 2015-03, we will apply the guidance retrospectively to all periods presented and classify our debt issuance costs, which are currently included in other assets in the consolidated financial statements, as a deduction to our long-term debt. In May 2014, the FASB issued ASU 2014-09, Revenue from Contracts with Customers ("ASU 2014-09"), which converges the FASB and the International Accounting Standards Board standards on revenue recognition. Areas of revenue recognition that will be affected include, but are not limited to, transfer of control, variable consideration, allocation of transfer pricing, licenses, time value of money, contract costs and disclosures. This guidance is effective for the fiscal years and interim reporting periods beginning after December 15, 2017 (as amended through ASU 2015-14 issued in August 2015), at which time we may adopt the new standard under the full retrospective method or the modified retrospective method. Early adoption is permitted. We are currently evaluating the impact of adopting ASU 2014-09 on our consolidated financial statements and related disclosures. |
Description of Operations and25
Description of Operations and Summary of Significant Accounting Policies (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Description of Operations and Summary of Significant Accounting Policies | |
Schedule of property and equipment useful lives | Leasehold improvements Shorter of remaining lease terms or useful life Equipment, furniture and fixtures 5 - 7 years Software and computer equipment 3 years |
Net Loss per Share (Tables)
Net Loss per Share (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Net Loss per Share | |
Schedule of anti-dilutive securities | The following common equivalent shares were not included in the computation of diluted net loss per share because their effect was anti-dilutive (in thousands): Year Ended December 31, 2015(1) 2014 2013 Outstanding options and awards granted under equity incentive plan and employee stock purchase plan Unvested RSAs Shares issuable upon conversion of convertible subordinated notes Total (1) Includes 4.1 million options, 0.4 million restricted stock units, and 1.0 million unvested RSAs retained by former employees who were transferred to Theravance Biopharma in connection with the Spin-Off during the year ended December 31, 2015. Subsequent to the Spin-Off, stock-based compensation expense associated with the awards held by Theravance Biopharma employees granted prior to the Spin-Off is recognized by Theravance Biopharma. |
Collaborative Arrangements (Tab
Collaborative Arrangements (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Collaborative Arrangements | |
Schedule of net revenue recognized under GSK Agreements | Net revenue recognized under our GSK Agreements was as follows (in thousands): Year Ended December 31, 2015 2014 2013 Royalties from a related party $ $ $ Less: amortization of capitalized fees paid to a related party ) ) ) Royalty revenue LABA collaboration(1) — — Strategic alliance—MABA program Total net revenue from GSK $ $ $ (1) Deferred revenue under this agreement was fully recognized in the year ended December 31, 2013. |
Available-for-Sale Securities28
Available-for-Sale Securities and Fair Value Measurements (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Available-for-Sale Securities and Fair Value Measurements | |
Schedule of available-for-sale securities | The classification of available-for-sale securities in the consolidated balance sheets is as follows (in thousands): December 31, 2015 2014 Cash and cash equivalents $ $ Short-term marketable securities Marketable securities — Total $ $ |
Schedule of amortized cost and estimated fair values for available-for-sale securities | The estimated fair value of available-for-sale securities is based on quoted market prices for these or similar investments that were based on prices obtained from a commercial pricing service. Available-for-sale securities are summarized below (in thousands): December 31, 2015 Amortized Cost Gross Unrealized Gains Gross Unrealized Losses Other Than Temporary Impairment Loss Estimated Fair Value U.S. government agencies $ $ — $ ) $ — $ U.S. corporate notes — ) — U.S. commercial paper — — — Money market funds — — — Total $ $ — $ ) $ — $ December 31, 2014 Amortized Cost Gross Unrealized Gains Gross Unrealized Losses Other Than Temporary Impairment Loss Estimated Fair Value U.S. government securities $ $ $ — $ — $ U.S. government agencies ) — U.S. corporate notes ) — U.S. commercial paper — — — Ordinary shares of Theravance Biopharma — — ) Money market funds — — — Total $ $ $ ) $ ) $ |
Schedule of estimated fair values | Estimated Fair Value Measurements as of December 31, 2015 Using: Quoted Price in Active Markets for Identical Assets Significant Other Observable Inputs Significant Unobservable Inputs Types of Instruments (In thousands) Level 1 Level 2 Level 3 Total Assets U.S. government agencies $ — $ $ — $ Corporate notes — — Commercial paper — — Money market funds — — Total assets measured as of estimated fair value $ $ $ — $ Liabilities Convertible subordinated notes due 2023 $ — $ $ — $ Non-recourse notes due 2029 — — Total fair value of liabilities $ — $ $ — $ Estimated Fair Value Measurements as of December 31, 2014 Using: Quoted Price in Active Markets for Identical Assets Significant Other Observable Inputs Significant Unobservable Inputs Types of Instruments (In thousands) Level 1 Level 2 Level 3 Total Assets U.S. government securities $ $ — $ — $ U.S. government agencies — — Corporate notes — — Commercial paper — — Ordinary shares of Theravance Biopharma — — Money market funds — — Total assets measured as of estimated fair value $ $ $ — $ Liabilities Convertible subordinated notes due 2023 $ — $ $ — $ Non-recourse notes due 2029 — — Total fair value of liabilities $ — $ $ — $ |
Capitalized Fees Paid to a Re29
Capitalized Fees Paid to a Related Party (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Capitalized Fees Paid to a Related Party | |
Schedule of capitalized fees paid to a related party | December 31, 2015 December 31, 2014 (In thousands) Weighted Average Remaining Amortization Period (Years) Gross Carrying Value Accumulated Amortization Net Carrying Value Gross Carrying Value Accumulated Amortization Net Carrying Value Approval and launch related milestone payments under the LABA Collaboration $ $ ) $ $ $ ) $ |
Stock-Based Compensation (Table
Stock-Based Compensation (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Stock-Based Compensation | |
Schedule of stock-based compensation expense included in the consolidated statements of operations | Year Ended December 31, (In thousands) 2015 2014 2013 Research and development $ $ $ General and administrative Stock-based compensation from continuing operations Stock-based compensation from discontinued operations — Total stock-based compensation expense $ $ $ |
Schedule of stock-based compensation expense by award type | Year Ended December 31, (In thousands) 2015 2014 2013 Stock options $ $ $ RSUs RSAs Performance RSUs — Performance RSAs ESPP Total stock-based compensation expense $ $ $ |
Schedule of unrecognized stock-based compensation cost, net of expected forfeitures for awards expected to vest, including performance-contingent RSAs for which the performance milestones were determined to be probable of achievement, and the estimated weighted-average amortization period, using the straight-line attribution method | (In thousands, except amortization period) Unrecognized Compensation Cost Weighted- Average Amortization Period (Years) Stock options $ RSUs RSAs Performance RSAs Total stock-based compensation expense $ |
Summary of equity award activity under the 2012 plan and prior plans | (In thousands) Number of Shares Subject to Outstanding Options Weighted- Average Exercise Price of Outstanding Options Number of Shares Subject to Outstanding RSUs Weighted- Average Fair Value per Share at Grant Number of Shares Outstanding Subject to Vesting or Performance Conditions with Vesting Weighted- Average Fair Value per Share at Grant Balance as of December 31, 2014 Granted — — Exercised ) — — — — Released RSUs/RSAs — — ) ) Forfeited ) ) ) Balance as of December 31, 2015 $ $ $ |
Schedule of weighted-average assumptions used to estimate the fair value of stock options granted and employee stock purchase plan issuances | Year Ended December 31, 2015(1) 2014 2013 Employee stock options Risk-free interest rate — % 1.6% - 2.1% 0.8% - 2.0% Expected term (in years) — 5 - 6 5 - 6 Volatility — % 52% - 60% 58% - 60% Dividend yield — % 3% - 4% — Weighted-average estimated fair value of stock options granted $ — $15.63 $19.96 (1) There were no stock options granted for the year ended December 31, 2015. Year Ended December 31, 2015 2014 2013 Employee stock purchase plan issuances Risk-free interest rate 0.1% - 0.9% 0.1% - 0.5% 0.1% - 0.3% Expected term (in years) 0.5 - 2 0.5 - 2 0.5 - 2 Volatility 44% - 69% 43% - 55% 56% - 61% Dividend yield 0% - 6% 8% — Weighted-average estimated fair value of ESPP shares granted $4.52 $4.49 $16.44 |
Long-Term Debt (Tables)
Long-Term Debt (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Long-Term Debt. | |
Schedule of long-term debt | As of December 31, (In thousands) 2015 2014 Convertible Subordinated Notes due 2023 $ $ Non-Recourse Notes Payable due 2029 Total Long-Term Debt $ $ |
Shareholders' Deficit (Tables)
Shareholders' Deficit (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Shareholders' Deficit | |
Schedule of share repurchase activity and related information on the October 2015 TO | Purchase period end date December 2015 Number of shares purchased and retired (in thousands) 2,576 Average repurchase price per share, including associated fees and expenses $9.56 Share repurchase amount (in millions) $24.6 |
Commitments and Contingencies (
Commitments and Contingencies (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Commitments and Contingencies | |
Schedule of future minimum lease payments under non-cancelable operating lease | Future minimum lease payments under this lease as of December 31, 2015, were as follows: (In thousands) Years Ending December 31: 2016 $ 2017 2018 2019 2020 Thereafter — Total $ |
Income Taxes (Tables)
Income Taxes (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Income Taxes | |
Schedule of significant components of the Company's deferred tax assets | As of December 31, (In thousands) 2015 2014 Deferred tax assets: Net operating loss carryforwards $ $ Deferred revenues Research and development tax credit carryforwards Other Total deferred tax assets Valuation allowance ) ) Net deferred tax assets $ — $ — |
Schedule of the differences between the U.S. federal statutory income tax rate to the Company's effective tax rate | The differences between the U.S. federal statutory income tax rate to our effective tax rate are as follows: Year Ended December 31, 2015 2014 2013 U.S. federal statutory income tax rate % % % Non-deductible executive compensation ) ) ) Stock-based compensation ) ) Federal and state research credits — Effect of Spin-Off Transaction — ) — Other ) ) ) Change in valuation allowance ) ) Effective tax rate )% )% )% |
Reconciliation of gross unrecognized tax benefits | A reconciliation of the beginning and ending balances of the total amounts of unrecognized tax benefits are as follows (in thousands): Unrecognized tax benefits as of December 31, 2012 $ Gross decrease for tax positions for prior years ) Gross increase in tax positions for current year Unrecognized tax benefits as of December 31, 2013 Gross decrease for tax positions for prior years ) Gross increase in tax positions for current year Unrecognized tax benefits as of December 31, 2014 Gross increase in tax positions for current year Unrecognized tax benefits as of December 31, 2015 $ |
Spin-Off of Theravance Biopha35
Spin-Off of Theravance Biopharma, Inc. (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Spin-Off of Theravance Biopharma, Inc. | |
Schedule of net book value of net assets that were contributed in connection with the Spin-Off | (In thousands) June 2, 2014 Cash and cash equivalents $ Marketable investment securities Accounts receivable Reimbursement of certain liabilities Prepaid and other current assets Inventories Fixed assets, net Accrued liabilities ) Deferred revenue ) Other liabilities ) Net book value of assets contributed $ |
Discontinued Operations (Tables
Discontinued Operations (Tables) | 12 Months Ended |
Dec. 31, 2015 | |
Discontinued Operations. | |
Schedule of discontinued operations presented on the condensed consolidated statements of operations | Year Ended December 31, (In thousands) 2015 2014 2013 Net revenues(1) $ — $ $ Income (loss) from discontinued operations(2) — ) ) (1) Net revenues primarily consist of revenue from collaborative arrangements and product sales. Revenue from collaborative arrangements was recognized from our agreement with R-Pharm CJSC, which was transferred to Theravance Biopharma as a part of the Spin-Off. Product sales were generated from sales of VIBATIV in the U.S. through a limited number of distributors, and title and risk of loss transfer upon receipt by these distributors. Healthcare providers ordered VIBATIV through these distributors. Commencing in the first quarter of 2014, revenue on the sale of VIBATIV was recorded on a sell-through basis, once the distributors sold the product to healthcare providers. Product sales were recorded net of estimated government-mandated rebates and chargebacks, distribution fees, estimated product returns and other deductions. (2) Loss from discontinued operations decreased in the year ended December 31, 2014 compared to the year ended December 31, 2013 primarily as there was no impact of discontinued operations after the Spin- Off occurring in June 2014. Included in the loss from discontinued operations for the year ended December 31, 2014 and the year ended December 31, 2013 are external legal and accounting fees in connection with our separation strategy which we started to incur in the year ended December 31, 2013 and the additional stock-based compensation and cash bonus expense recognized due to the achievement of performance conditions under a special long-term retention and incentive equity and cash bonus awarded to certain employees in the year ended December 31, 2011, which we started to incur in the year ended December 31, 2014. |
Description of Operations and37
Description of Operations and Summary of Significant Accounting Policies (Details) $ in Millions | Jun. 02, 2014 | Jun. 01, 2014USD ($) | Dec. 31, 2015 |
Business Separation | |||
Cash, cash equivalents and marketable securities contributed to Theravance Biopharma | $ 393 | ||
Number of ordinary shares of Theravance Biopharma issued for every share of Theravance | 0.286 | ||
GSK | LABA collaboration and Strategic Alliance agreements | |||
Description of Operations and Summary of Significant Accounting Policies | |||
Percentage of economic interest in any future payments made under the agreements | 15.00% |
Description of Operations and38
Description of Operations and Summary of Significant Accounting Policies (Details 2) - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
Description of Operations and Summary of Significant Accounting Policies | |||
Property and equipment, net | $ 221 | $ 324 | |
Depreciation expense | $ 100 | $ 1,100 | $ 2,700 |
Capitalized Fees Paid to a Related Party | |||
Capitalized fees paid to a related party, useful life | 15 years | ||
Equipment, furniture and fixtures | Minimum | |||
Description of Operations and Summary of Significant Accounting Policies | |||
Estimated useful life | 5 years | ||
Equipment, furniture and fixtures | Maximum | |||
Description of Operations and Summary of Significant Accounting Policies | |||
Estimated useful life | 7 years | ||
Software and computer equipment | |||
Description of Operations and Summary of Significant Accounting Policies | |||
Estimated useful life | 3 years | ||
Capitalized software | |||
Description of Operations and Summary of Significant Accounting Policies | |||
Estimated useful life | 3 years |
Description of Operations and39
Description of Operations and Summary of Significant Accounting Policies (Details 3) - USD ($) $ in Millions | 12 Months Ended | |
Dec. 31, 2015 | Apr. 30, 2014 | |
Product Revenues | ||
Revenue from product sales | $ 0 | |
Revenue recognition | ||
Allowance for doubtful accounts | 0 | |
Unrecognized tax benefits would affect our effective income tax rate if recognized | $ 0 | |
9% fixed rate term notes due 2029 | ||
Revenue recognition | ||
Loan amount | $ 450 | |
Interest rate (as a percent) | 9.00% | |
Debt issuance costs | $ 15.3 |
Description of Operations and40
Description of Operations and Summary of Significant Accounting Policies (Details 4) - USD ($) $ in Millions | 12 Months Ended | ||
Dec. 31, 2014 | Dec. 31, 2013 | Dec. 31, 2015 | |
GSK | |||
Related parties | |||
Percentage of common stock owned | 27.90% | ||
Gunderson law firm | |||
Related parties | |||
Fees incurred related to related party | $ 1.3 | $ 3.2 |
Net Loss per Share (Details)
Net Loss per Share (Details) - shares shares in Thousands | 12 Months Ended | ||
Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
Anti-dilutive securities | |||
Anti-dilutive securities (in shares) | 19,838 | 20,340 | 9,239 |
Stock options | Former employees transferred to Theravance Biopharma in connection with Spin Off | |||
Anti-dilutive securities | |||
Anti-dilutive securities (in shares) | 4,100 | ||
RSUs | Former employees transferred to Theravance Biopharma in connection with Spin Off | |||
Anti-dilutive securities | |||
Anti-dilutive securities (in shares) | 400 | ||
RSAs | Former employees transferred to Theravance Biopharma in connection with Spin Off | |||
Anti-dilutive securities | |||
Anti-dilutive securities (in shares) | 1,000 | ||
Equity incentive plans and ESPP | |||
Anti-dilutive securities | |||
Anti-dilutive securities (in shares) | 5,290 | 6,239 | 4,095 |
RSAs | |||
Anti-dilutive securities | |||
Anti-dilutive securities (in shares) | 1,644 | 1,772 | 2,364 |
Convertible subordinated notes | |||
Anti-dilutive securities | |||
Anti-dilutive securities (in shares) | 12,904 | 12,329 | 2,780 |
Collaborative Arrangements (Det
Collaborative Arrangements (Details) $ in Thousands | 1 Months Ended | 3 Months Ended | 12 Months Ended | |||||||||
Oct. 31, 2011item | Dec. 31, 2015USD ($) | Sep. 30, 2015USD ($) | Jun. 30, 2015USD ($) | Mar. 31, 2015USD ($) | Dec. 31, 2014USD ($) | Sep. 30, 2014USD ($) | Jun. 30, 2014USD ($) | Mar. 31, 2014USD ($) | Dec. 31, 2015USD ($)shares | Dec. 31, 2014USD ($)shares | Dec. 31, 2013USD ($)shares | |
Information related to collaborative arrangements | ||||||||||||
Less: amortization of capitalized fees paid to a related party | $ (13,823) | $ (11,066) | $ (743) | |||||||||
Royalty revenue | 53,064 | 7,351 | 1,202 | |||||||||
Revenue from collaborative arrangements | 885 | 1,082 | 3,330 | |||||||||
Total net revenue | $ 22,836 | $ 13,562 | $ 10,655 | $ 6,896 | $ 7,280 | $ 999 | $ 934 | $ (780) | 53,949 | 8,433 | 4,532 | |
Aggregate purchase price of common stock | $ 6,528 | $ 38,095 | $ 126,030 | |||||||||
Common Stock | ||||||||||||
Information related to collaborative arrangements | ||||||||||||
Company's stock purchased by related party (in shares) | shares | 424,000 | 1,665,000 | 3,505,000 | |||||||||
Aggregate purchase price of common stock | $ 4 | $ 17 | $ 35 | |||||||||
GSK | ||||||||||||
Information related to collaborative arrangements | ||||||||||||
Royalties from a related party | 66,887 | 18,417 | 1,945 | |||||||||
Less: amortization of capitalized fees paid to a related party | (13,823) | (11,066) | (743) | |||||||||
Royalty revenue | 53,064 | 7,351 | 1,202 | |||||||||
Total net revenue | $ 53,949 | 8,433 | 4,532 | |||||||||
Contingent payments and royalties receivable (as a percent) | 15.00% | |||||||||||
Reimbursement of certain research and development costs to the entity | $ 0 | 100 | 500 | |||||||||
GSK | Theravance Biopharma | ||||||||||||
Information related to collaborative arrangements | ||||||||||||
Contingent payments and royalties receivable (as a percent) | 85.00% | |||||||||||
GSK | MABA | ||||||||||||
Information related to collaborative arrangements | ||||||||||||
Potential future contingent payments receivable | $ 363,000 | $ 363,000 | ||||||||||
Percentage of milestone payment | 15.00% | |||||||||||
Long-acting beta agonist (LABA) collaboration | GSK | ||||||||||||
Information related to collaborative arrangements | ||||||||||||
Revenue from collaborative arrangements | $ 0 | 0 | 1,815 | |||||||||
Milestone fees paid | 220,000 | |||||||||||
Royalty rate for first level of annual global net sales (as a percent) | 15.00% | |||||||||||
Annual global sales level used to determine royalty rate | $ 3,000,000 | |||||||||||
Royalty rate for sales above first level of annual global net sales (as a percent) | 5.00% | |||||||||||
Long-acting beta agonist (LABA) collaboration | GSK | Minimum | ||||||||||||
Information related to collaborative arrangements | ||||||||||||
Royalty rate for combination products (as a percent) | 6.50% | |||||||||||
Long-acting beta agonist (LABA) collaboration | GSK | Maximum | ||||||||||||
Information related to collaborative arrangements | ||||||||||||
Royalty rate for combination products (as a percent) | 10.00% | |||||||||||
2004 Strategic alliance | GSK | MABA | ||||||||||||
Information related to collaborative arrangements | ||||||||||||
Revenue from collaborative arrangements | $ 885 | $ 1,082 | $ 1,515 | |||||||||
Number of preclinical MABA compounds discovered | item | 6 | |||||||||||
Governance agreement | GSK | Common Stock | ||||||||||||
Information related to collaborative arrangements | ||||||||||||
Company's stock purchased by related party (in shares) | shares | 424,081 | |||||||||||
Aggregate purchase price of common stock | $ 6,500 |
Available-for-Sale Securities43
Available-for-Sale Securities and Fair Value Measurements (Details) - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
Available-for-sale securities | |||
Amortized Cost | $ 176,778 | $ 285,483 | |
Gross Unrealized Gains | 0 | 35 | |
Gross Unrealized Losses | (2) | (122) | |
Other Than Temporary Impairment Loss | 0 | (3,752) | $ 0 |
Estimated Fair Value | $ 176,776 | 281,644 | |
Maturity period for marketable securities | |||
Maximum contractual maturity period | 1 year | ||
Average duration | 1 month | ||
Proceeds from sale of available-for-sale securities | $ 108,077 | 7,211 | $ 22,600 |
Theravance Biopharma | |||
Maturity period for marketable securities | |||
Gain on sales of the securities | 1,200 | ||
Issuer of available-for-securities other than Theravance Biopharma | |||
Maturity period for marketable securities | |||
Proceeds from sale of available-for-sale securities | 100,400 | ||
Cash and cash equivalents | |||
Available-for-sale securities | |||
Estimated Fair Value | 148,673 | 95,090 | |
Short-term investments | |||
Available-for-sale securities | |||
Estimated Fair Value | 28,103 | 143,698 | |
Marketable securities | |||
Available-for-sale securities | |||
Estimated Fair Value | 0 | 42,856 | |
U.S. government securities | |||
Available-for-sale securities | |||
Amortized Cost | 30,019 | ||
Gross Unrealized Gains | 24 | ||
Gross Unrealized Losses | 0 | ||
Other Than Temporary Impairment Loss | 0 | ||
Estimated Fair Value | 30,043 | ||
U.S. government agency securities | |||
Available-for-sale securities | |||
Amortized Cost | 14,406 | 34,756 | |
Gross Unrealized Gains | 0 | 6 | |
Gross Unrealized Losses | (1) | (12) | |
Other Than Temporary Impairment Loss | 0 | 0 | |
Estimated Fair Value | 14,405 | 34,750 | |
Corporate notes | |||
Available-for-sale securities | |||
Amortized Cost | 2,702 | 80,880 | |
Gross Unrealized Gains | 0 | 5 | |
Gross Unrealized Losses | (1) | (110) | |
Other Than Temporary Impairment Loss | 0 | 0 | |
Estimated Fair Value | 2,701 | 80,775 | |
Commercial paper | |||
Available-for-sale securities | |||
Amortized Cost | 10,997 | 34,469 | |
Gross Unrealized Gains | 0 | 0 | |
Gross Unrealized Losses | 0 | 0 | |
Other Than Temporary Impairment Loss | 0 | 0 | |
Estimated Fair Value | 10,997 | 34,469 | |
Equity securities | Theravance Biopharma | |||
Available-for-sale securities | |||
Amortized Cost | 10,269 | ||
Gross Unrealized Gains | 0 | ||
Gross Unrealized Losses | 0 | ||
Other Than Temporary Impairment Loss | (3,752) | ||
Estimated Fair Value | 6,517 | ||
Money market funds | |||
Available-for-sale securities | |||
Amortized Cost | 148,673 | 95,090 | |
Gross Unrealized Gains | 0 | 0 | |
Gross Unrealized Losses | 0 | 0 | |
Other Than Temporary Impairment Loss | 0 | 0 | |
Estimated Fair Value | $ 148,673 | $ 95,090 |
Available-for-Sale Securities44
Available-for-Sale Securities and Fair Value Measurements (Details 2) - USD ($) $ in Thousands | 12 Months Ended | |
Dec. 31, 2014 | Dec. 31, 2015 | |
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | $ 281,644 | $ 176,776 |
U.S. government securities | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 30,043 | |
U.S. government agency securities | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 34,750 | 14,405 |
Corporate notes | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 80,775 | 2,701 |
Commercial paper | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 34,469 | 10,997 |
Equity securities | Theravance Biopharma | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 6,517 | |
Recognized losses | 3,800 | |
Money market funds | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 95,090 | 148,673 |
Recurring basis | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 281,644 | 176,776 |
Recurring basis | U.S. government securities | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 30,043 | |
Recurring basis | U.S. government agency securities | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 34,750 | 14,405 |
Recurring basis | Corporate notes | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 80,775 | 2,701 |
Recurring basis | Commercial paper | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 34,469 | 10,997 |
Recurring basis | Equity securities | Theravance Biopharma | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 6,517 | |
Recurring basis | Money market funds | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 95,090 | 148,673 |
Recurring basis | Quoted Prices in Active Markets for Identical Assets, Level 1 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 131,650 | 148,673 |
Recurring basis | Quoted Prices in Active Markets for Identical Assets, Level 1 | U.S. government securities | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 30,043 | |
Recurring basis | Quoted Prices in Active Markets for Identical Assets, Level 1 | U.S. government agency securities | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | 0 |
Recurring basis | Quoted Prices in Active Markets for Identical Assets, Level 1 | Corporate notes | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | 0 |
Recurring basis | Quoted Prices in Active Markets for Identical Assets, Level 1 | Commercial paper | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | 0 |
Recurring basis | Quoted Prices in Active Markets for Identical Assets, Level 1 | Equity securities | Theravance Biopharma | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 6,517 | |
Recurring basis | Quoted Prices in Active Markets for Identical Assets, Level 1 | Money market funds | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 95,090 | 148,673 |
Recurring basis | Significant Other Observable Inputs, Level 2 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 149,994 | 28,103 |
Recurring basis | Significant Other Observable Inputs, Level 2 | U.S. government securities | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | |
Recurring basis | Significant Other Observable Inputs, Level 2 | U.S. government agency securities | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 34,750 | 14,405 |
Recurring basis | Significant Other Observable Inputs, Level 2 | Corporate notes | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 80,775 | 2,701 |
Recurring basis | Significant Other Observable Inputs, Level 2 | Commercial paper | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 34,469 | 10,997 |
Recurring basis | Significant Other Observable Inputs, Level 2 | Equity securities | Theravance Biopharma | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | |
Recurring basis | Significant Other Observable Inputs, Level 2 | Money market funds | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | 0 |
Recurring basis | Significant Unobservable Inputs, Level 3 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | 0 |
Recurring basis | Significant Unobservable Inputs, Level 3 | U.S. government securities | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | |
Recurring basis | Significant Unobservable Inputs, Level 3 | U.S. government agency securities | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | 0 |
Recurring basis | Significant Unobservable Inputs, Level 3 | Corporate notes | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | 0 |
Recurring basis | Significant Unobservable Inputs, Level 3 | Commercial paper | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | 0 |
Recurring basis | Significant Unobservable Inputs, Level 3 | Equity securities | Theravance Biopharma | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | |
Recurring basis | Significant Unobservable Inputs, Level 3 | Money market funds | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total assets measured at fair value | 0 | 0 |
Nonrecurring basis | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total fair value of liabilities | 653,506 | 660,070 |
Nonrecurring basis | Convertible Subordinated Notes Due 2023 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Convertible subordinated notes due 2023 | 197,095 | 189,100 |
Nonrecurring basis | 9% fixed rate term notes due 2029 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Non-recourse notes due 2029 | 456,411 | 470,970 |
Nonrecurring basis | Quoted Prices in Active Markets for Identical Assets, Level 1 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total fair value of liabilities | 0 | 0 |
Nonrecurring basis | Quoted Prices in Active Markets for Identical Assets, Level 1 | Convertible Subordinated Notes Due 2023 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Convertible subordinated notes due 2023 | 0 | 0 |
Nonrecurring basis | Quoted Prices in Active Markets for Identical Assets, Level 1 | 9% fixed rate term notes due 2029 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Non-recourse notes due 2029 | 0 | 0 |
Nonrecurring basis | Significant Other Observable Inputs, Level 2 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total fair value of liabilities | 653,506 | 660,070 |
Nonrecurring basis | Significant Other Observable Inputs, Level 2 | Convertible Subordinated Notes Due 2023 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Convertible subordinated notes due 2023 | 197,095 | 189,100 |
Nonrecurring basis | Significant Other Observable Inputs, Level 2 | 9% fixed rate term notes due 2029 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Non-recourse notes due 2029 | 456,411 | 470,970 |
Nonrecurring basis | Significant Unobservable Inputs, Level 3 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Total fair value of liabilities | 0 | 0 |
Nonrecurring basis | Significant Unobservable Inputs, Level 3 | Convertible Subordinated Notes Due 2023 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Convertible subordinated notes due 2023 | 0 | 0 |
Nonrecurring basis | Significant Unobservable Inputs, Level 3 | 9% fixed rate term notes due 2029 | ||
Estimated fair values of entity's financial assets and liabilities | ||
Non-recourse notes due 2029 | $ 0 | $ 0 |
Capitalized Fees Paid to a Re45
Capitalized Fees Paid to a Related Party (Details) - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
Capitalized Fees paid to a Related Party | |||
Net Carrying Value | $ 194,368 | $ 208,191 | |
Amortization of capitalized fees paid to a related party | 13,823 | 11,066 | $ 743 |
Estimated amortization expense for the year 2016 | 13,800 | ||
Estimated amortization expense for the year 2017 | 13,800 | ||
Estimated amortization expense for the year 2018 | 13,800 | ||
Estimated amortization expense for the year 2019 | 13,800 | ||
Estimated amortization expense for the year 2020 | 13,800 | ||
Estimated amortization expense thereafter | 125,300 | ||
GSK | |||
Capitalized Fees paid to a Related Party | |||
Amortization of capitalized fees paid to a related party | $ 13,823 | 11,066 | $ 743 |
GSK | LABA Collaboration | |||
Capitalized Fees paid to a Related Party | |||
Weighted Average Remaining Amortization Period | 14 years 1 month 6 days | ||
Gross Carrying Value | $ 220,000 | 220,000 | |
Accumulated Amortization | (25,632) | (11,809) | |
Net Carrying Value | $ 194,368 | $ 208,191 |
Stock-Based Compensation (Detai
Stock-Based Compensation (Details) | Jun. 02, 2014 | May. 31, 2014USD ($) | Jun. 30, 2014USD ($) | Dec. 31, 2015USD ($)installmentitemshares | Dec. 31, 2014USD ($)shares | Dec. 31, 2013USD ($) | Dec. 31, 2011shares |
Stock-based compensation | |||||||
Stock-based compensation expense | $ 6,873,000 | $ 27,390,000 | $ 25,687,000 | ||||
Number of shares of Theravance Biopharma issued for every share of Theravance | 0.286 | ||||||
Performance-contingent | |||||||
Stock-based compensation | |||||||
Outstanding (in shares) | shares | 1,305,000 | 1,772,000 | |||||
Employee Stock Purchase Plan | |||||||
Stock-based compensation | |||||||
Shares remaining available for issuance | shares | 265,711 | ||||||
Purchase price as a percentage of fair market value of stock | 85.00% | ||||||
Consecutive and overlapping offering periods | 24 months | ||||||
Number of offering periods | item | 4 | ||||||
Duration of purchase period | 6 months | ||||||
Maximum contributions as a percentage of employee's eligible compensation | 15.00% | ||||||
Maximum number of shares an employee may purchase during any purchase period | shares | 2,500 | ||||||
Maximum value of shares an employee may purchase | $ 25,000 | ||||||
Stock-based compensation expense | 129,000 | $ 10,000 | 536,000 | ||||
RSAs | |||||||
Stock-based compensation | |||||||
Stock-based compensation expense | 2,850,000 | 7,575,000 | 9,723,000 | ||||
RSAs | Performance-contingent | |||||||
Stock-based compensation | |||||||
Stock-based compensation expense | 613,000 | 10,580,000 | 1,061,000 | ||||
RSUs | |||||||
Stock-based compensation | |||||||
Stock-based compensation expense | $ 2,492,000 | $ 4,564,000 | 10,174,000 | ||||
Outstanding (in shares) | shares | 459,000 | 775,000 | |||||
Additional disclosures | |||||||
Incremental stock-based compensation expense arising out of spin-off | $ 1,200,000 | ||||||
Share based compensation expense included in discontinued operations | $ 900,000 | ||||||
RSUs | Non-employee director | |||||||
Additional disclosures | |||||||
One time grant of shares value | $ 250,000 | ||||||
Pro rata shares grant value | $ 250,000 | ||||||
Number of annual installments | installment | 2 | ||||||
RSUs | Performance-contingent | |||||||
Stock-based compensation | |||||||
Stock-based compensation expense | $ 0 | $ 3,000 | $ 61,000 | ||||
Outstanding (in shares) | shares | 0 | ||||||
2012 Equity Incentive Plan | |||||||
Stock-based compensation | |||||||
Shares remaining available for issuance | shares | 3,466,041 | ||||||
Special Long-Term Retention and Incentive Cash Awards Program | RSAs | Performance-contingent | |||||||
Stock-based compensation | |||||||
Shares of common stock approved and authorized for issuance | shares | 1,290,000 | ||||||
Timeframe for achievement of performance conditions | 6 years | ||||||
Stock-based compensation expense | $ 7,000,000 | ||||||
Outstanding (in shares) | shares | 63,000 |
Stock-Based Compensation (Det47
Stock-Based Compensation (Details 2) - USD ($) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
Stock-based compensation | |||
Stock-based compensation expense | $ 6,873 | $ 27,390 | $ 25,687 |
Total unrecognized compensation cost related to unvested stock-based compensation | 11,258 | ||
Stock options | |||
Stock-based compensation | |||
Stock-based compensation expense | 789 | 4,658 | 4,132 |
Total unrecognized compensation cost related to unvested stock-based compensation | $ 1,531 | ||
Weighted-average remaining service period of recognition of unrecognized compensation cost | 2 years 4 months 24 days | ||
RSUs | |||
Stock-based compensation | |||
Stock-based compensation expense | $ 2,492 | 4,564 | 10,174 |
Total unrecognized compensation cost related to unvested stock-based compensation | $ 1,446 | ||
Weighted-average remaining service period of recognition of unrecognized compensation cost | 1 year 1 month 6 days | ||
RSUs | Performance-contingent | |||
Stock-based compensation | |||
Stock-based compensation expense | $ 0 | 3 | 61 |
RSAs | |||
Stock-based compensation | |||
Stock-based compensation expense | 2,850 | 7,575 | 9,723 |
Total unrecognized compensation cost related to unvested stock-based compensation | $ 8,275 | ||
Weighted-average remaining service period of recognition of unrecognized compensation cost | 3 years 1 month 6 days | ||
RSAs | Performance-contingent | |||
Stock-based compensation | |||
Stock-based compensation expense | $ 613 | 10,580 | 1,061 |
Total unrecognized compensation cost related to unvested stock-based compensation | $ 6 | ||
Weighted-average remaining service period of recognition of unrecognized compensation cost | 2 years 1 month 6 days | ||
Employee Stock Purchase Plan | |||
Stock-based compensation | |||
Stock-based compensation expense | $ 129 | 10 | 536 |
Continuing operations | |||
Stock-based compensation | |||
Stock-based compensation expense | 6,873 | 15,761 | 7,898 |
Discontinued operation | |||
Stock-based compensation | |||
Stock-based compensation expense | 0 | 11,629 | 17,789 |
Research and development | Continuing operations | |||
Stock-based compensation | |||
Stock-based compensation expense | 1,036 | 2,781 | 573 |
General and administrative | Continuing operations | |||
Stock-based compensation | |||
Stock-based compensation expense | $ 5,837 | $ 12,980 | $ 7,325 |
Stock-Based Compensation (Det48
Stock-Based Compensation (Details 3) - USD ($) $ / shares in Units, $ in Millions | 12 Months Ended | ||
Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
Performance-contingent | |||
Number of shares outstanding subject to RSUs and vesting or performance conditions with vesting | |||
Balance at the beginning of the period (in shares) | 1,772,000 | ||
Granted (in shares) | 437,000 | ||
Released RSUs and RSAs (in shares) | (883,000) | ||
Forfeited (in shares) | (21,000) | ||
Balance at the end of the period (in shares) | 1,305,000 | 1,772,000 | |
Weighted-average fair value per share at grant | |||
Balance at the beginning of the period (in dollars per share) | $ 25.78 | ||
Granted (in dollars per share) | 13.76 | ||
Released RSUs and RSAs (in dollars per share) | 25.22 | ||
Forfeited (in dollars per share) | 20.33 | ||
Balance at the end of the period (in dollars per share) | $ 18 | $ 25.78 | |
Stock options | |||
Number of Shares Subject to Outstanding Options | |||
Balance at the beginning of the period (in shares) | 5,422,000 | ||
Exercised (in shares) | (111,000) | ||
Forfeited (in shares) | (1,049,000) | ||
Balance at the end of the period (in shares) | 4,262,000 | 5,422,000 | |
Weighted-average exercise price of outstanding options | |||
Balance at the beginning of the period (in dollars per share) | $ 22.46 | ||
Exercised (in dollars per share) | 13.75 | ||
Forfeited (in dollars per share) | 21.19 | ||
Balance at the end of the period (in dollars per share) | $ 23 | $ 22.46 | |
Additional disclosures | |||
Aggregate intrinsic value of options outstanding | $ 0.1 | ||
Aggregate intrinsic value of options exercisable | 0.1 | ||
Total intrinsic value of options exercised | 0.5 | $ 17.5 | $ 41.4 |
Total estimated fair value of options vested | $ 10 | $ 5.7 | $ 3.7 |
Weighted-average assumptions | |||
Risk-free interest rate, minimum (as a percent) | 1.60% | 0.80% | |
Risk-free interest rate, maximum (as a percent) | 2.10% | 2.00% | |
Volatility, minimum (as a percent) | 52.00% | 58.00% | |
Volatility, maximum (as a percent) | 60.00% | 60.00% | |
Weighted-average estimated fair value of shares granted | $ 15.63 | $ 19.96 | |
Stock options | Minimum | |||
Weighted-average assumptions | |||
Expected life (in years) | 5 years | 5 years | |
Dividend yield (as a percent) | 3.00% | ||
Stock options | Maximum | |||
Weighted-average assumptions | |||
Expected life (in years) | 6 years | 6 years | |
Dividend yield (as a percent) | 4.00% | ||
RSUs | |||
Number of shares outstanding subject to RSUs and vesting or performance conditions with vesting | |||
Balance at the beginning of the period (in shares) | 775,000 | ||
Granted (in shares) | 141,000 | ||
Released RSUs and RSAs (in shares) | (327,000) | ||
Forfeited (in shares) | (130,000) | ||
Balance at the end of the period (in shares) | 459,000 | 775,000 | |
Weighted-average fair value per share at grant | |||
Balance at the beginning of the period (in dollars per share) | $ 18.53 | ||
Granted (in dollars per share) | 15.50 | ||
Released RSUs and RSAs (in dollars per share) | 17.66 | ||
Forfeited (in dollars per share) | 18.07 | ||
Balance at the end of the period (in dollars per share) | $ 18.34 | $ 18.53 | |
RSUs | Performance-contingent | |||
Number of shares outstanding subject to RSUs and vesting or performance conditions with vesting | |||
Balance at the end of the period (in shares) | 0 | ||
Employee Stock Purchase Plan | |||
Weighted-average assumptions | |||
Risk-free interest rate, minimum (as a percent) | 0.10% | 0.10% | 0.10% |
Risk-free interest rate, maximum (as a percent) | 0.90% | 0.50% | 0.30% |
Volatility, minimum (as a percent) | 44.00% | 43.00% | 56.00% |
Volatility, maximum (as a percent) | 69.00% | 55.00% | 61.00% |
Dividend yield (as a percent) | 8.00% | ||
Weighted-average estimated fair value of shares granted | $ 4.52 | $ 4.49 | $ 16.44 |
Employee Stock Purchase Plan | Minimum | |||
Weighted-average assumptions | |||
Expected life (in years) | 6 months | 6 months | 6 months |
Dividend yield (as a percent) | 0.00% | ||
Employee Stock Purchase Plan | Maximum | |||
Weighted-average assumptions | |||
Expected life (in years) | 2 years | 2 years | 2 years |
Dividend yield (as a percent) | 6.00% |
Long-Term Debt (Details)
Long-Term Debt (Details) $ / shares in Units, $ in Thousands | Jul. 15, 2014$ / sharesshares | Jun. 01, 2014$ / shares$ / item | Jan. 31, 2013USD ($)item$ / shares$ / itemshares | Apr. 17, 2017 | Dec. 31, 2015USD ($)$ / shares$ / item | Dec. 31, 2014USD ($)shares | Dec. 31, 2013USD ($)shares | Apr. 17, 2016 | Dec. 31, 2015USD ($)$ / shares$ / item | Apr. 30, 2014USD ($) |
Debt disclosures | ||||||||||
Convertible Subordinated Notes due 2023 | $ 255,109 | $ 255,109 | $ 255,109 | |||||||
Non-Recourse Notes Payable due 2029 | 493,162 | 470,527 | 493,162 | |||||||
Total long term debt | 748,271 | 725,636 | 748,271 | |||||||
Proceeds from issuances of note payable, net of debt issuance costs | 0 | 434,677 | $ 281,622 | |||||||
Interest amount added to principal balance | 22,635 | $ 20,527 | $ 0 | |||||||
Common Stock | ||||||||||
Debt disclosures | ||||||||||
Number of common shares issued upon debt conversion | shares | 1,520,000 | 6,668,000 | ||||||||
Convertible Subordinated Notes Due 2023 | ||||||||||
Debt disclosures | ||||||||||
Convertible Subordinated Notes due 2023 | $ 255,109 | $ 255,109 | $ 255,109 | |||||||
Loan amount | $ 287,500 | |||||||||
Proceeds from issuances of note payable, net of debt issuance costs | $ 281,200 | |||||||||
Interest rate (as a percent) | 2.125% | 2.125% | ||||||||
Conversion rate of shares | 0.0469087 | 0.0359903 | 0.0505818 | |||||||
Conversion price of convertible notes into common stock (in dollars per share) | $ / shares | $ 21.32 | $ 27.79 | $ 19.77 | $ 19.77 | ||||||
Percentage of principal amount at which the entity may be forced to redeem some or all notes as a result of a fundamental change (as defined) | 100.00% | |||||||||
Convertible Subordinated Notes Due 2023 | Common Stock | ||||||||||
Debt disclosures | ||||||||||
Conversion price of convertible notes into common stock (in dollars per share) | $ / shares | $ 21.32 | |||||||||
Number of common shares issued upon debt conversion | shares | 1,519,402 | |||||||||
Number of common stares received | shares | 149,645 | |||||||||
Convertible Subordinated Notes Due 2023 | Privately-negotiated capped call option | ||||||||||
Debt disclosures | ||||||||||
Payments for capped call options | $ 36,800 | |||||||||
Number of derivative instruments purchased | item | 2 | |||||||||
Strike price for the underlying number of shares (in dollars per share) | $ / shares | $ 21.32 | $ 27.79 | $ 19.77 | |||||||
Cap price for the underlying number of shares (in dollars per share) | $ / item | 29.16 | 38 | 27.04 | 27.04 | ||||||
Convertible Subordinated Notes Due 2023 | Stock prices below $27.79 per share | Maximum | ||||||||||
Debt disclosures | ||||||||||
Net shares settlement payable to the entity | shares | 2,779,659 | |||||||||
Convertible Subordinated Notes Due 2023 | Stock prices below $27.79 per share | Minimum | ||||||||||
Debt disclosures | ||||||||||
Net shares settlement payable to the entity | shares | 0 | |||||||||
9% fixed rate term notes due 2029 | ||||||||||
Debt disclosures | ||||||||||
Non-Recourse Notes Payable due 2029 | $ 493,162 | 470,527 | $ 493,162 | |||||||
Loan amount | $ 450,000 | |||||||||
Interest rate (as a percent) | 9.00% | |||||||||
Interest amount added to principal balance | $ 22,700 | $ 20,500 | $ 43,200 | |||||||
Debt issuance costs | $ 15,300 | |||||||||
9% fixed rate term notes due 2029 | GSK | ||||||||||
Debt disclosures | ||||||||||
Percentage of royalties from global net sales to secure debt | 40.00% | |||||||||
9% fixed rate term notes due 2029 | Future | ||||||||||
Debt disclosures | ||||||||||
Debt prepayment premium (as a percent) | 2.50% | 5.00% |
Shareholders' Deficit (Details)
Shareholders' Deficit (Details) - USD ($) $ / shares in Units, $ in Thousands | Oct. 30, 2015 | Jul. 24, 2015 | Apr. 24, 2015 | Feb. 20, 2015 | Oct. 16, 2014 | Jul. 25, 2014 | Dec. 31, 2015 | Nov. 30, 2015 | Dec. 31, 2015 | Sep. 30, 2015 | Jun. 30, 2015 | Mar. 31, 2015 | Dec. 31, 2014 | Sep. 30, 2014 | Jun. 30, 2014 | Mar. 31, 2014 | Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | Oct. 28, 2015 |
Dividends | ||||||||||||||||||||
Cash dividend declared per common share (in dollars per share) | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0 | $ 0 | $ 0.75 | $ 0.50 | $ 0 | ||||
Dividends paid | $ 87,331 | $ 56,988 | $ 0 | |||||||||||||||||
$150 million share repurchase program | ||||||||||||||||||||
Dividends | ||||||||||||||||||||
Amount approved under share repurchase program | $ 150,000 | |||||||||||||||||||
$150 million share repurchase program | Common Stock | ||||||||||||||||||||
Dividends | ||||||||||||||||||||
Number of shares purchased and retired | 100,000 | |||||||||||||||||||
Average repurchase price per share, including associated fees and expenses | $ 9.95 | |||||||||||||||||||
Share repurchase price | $ 1,000 | |||||||||||||||||||
October 2015 TO | ||||||||||||||||||||
Dividends | ||||||||||||||||||||
Amount approved under share repurchase program | $ 75,000 | |||||||||||||||||||
Number of shares purchased and retired | 2,576,000 | |||||||||||||||||||
Average repurchase price per share, including associated fees and expenses | $ 9.56 | |||||||||||||||||||
Share repurchase price | $ 24,600 | |||||||||||||||||||
October 2015 TO | Minimum | ||||||||||||||||||||
Dividends | ||||||||||||||||||||
Price per share under share repurchase program | $ 8.50 | |||||||||||||||||||
October 2015 TO | Maximum | ||||||||||||||||||||
Dividends | ||||||||||||||||||||
Price per share under share repurchase program | $ 9.25 |
Commitments and Contingencies51
Commitments and Contingencies (Details) - Lease payments guarantee $ in Millions | Dec. 31, 2015USD ($) |
Operating Leases | |
Total lease payments | $ 27.6 |
Estimated fair value of the guarantee | $ 1.3 |
Commitments and Contingencies52
Commitments and Contingencies (Details 2) - Theravance Biopharma $ in Thousands | 12 Months Ended | ||
Dec. 31, 2015USD ($)ft² | Dec. 31, 2014USD ($) | Dec. 31, 2013USD ($) | |
Operating Leases | |||
Area of office space in South San Francisco, California (in square feet) | ft² | 4,847 | ||
Operating lease rent expenses | $ 200 | $ 3,000 | $ 6,000 |
Future minimum lease payments | |||
2,016 | 192 | ||
2,017 | 197 | ||
2,018 | 203 | ||
2,019 | 210 | ||
2,020 | 89 | ||
Thereafter | 0 | ||
Total | $ 891 |
Income Taxes (Details)
Income Taxes (Details) $ in Thousands | 12 Months Ended | ||
Dec. 31, 2015USD ($) | Dec. 31, 2014USD ($)item | Dec. 31, 2013USD ($) | |
Income Taxes | |||
Income tax expenses | $ 0 | $ 0 | $ 0 |
Deferred tax assets: | |||
Net operating loss carryforwards | 392,000 | 386,000 | |
Deferred revenues | 1,000 | 2,000 | |
Research and development tax credit carryforwards | 53,000 | 53,000 | |
Other | 17,000 | 18,000 | |
Total deferred tax assets | 463,000 | 459,000 | |
Valuation allowance | (463,000) | (459,000) | |
Net deferred tax assets | 0 | 0 | |
Information related to valuation allowance | |||
Increase (decrease) in valuation allowance | $ 4,700 | (103,800) | $ 70,100 |
Federal net operating losses | 252,700 | ||
Valuation Allowance | 88,600 | ||
Deferred tax assets | $ 9,200 | ||
The differences between the U.S. federal statutory income tax rate to the Company's effective tax rate | |||
U.S. federal statutory income tax rate (as a percent) | 34.00% | 35.00% | 34.00% |
Non-deductible executive compensation (as a percent) | (1.94%) | (0.16%) | (0.07%) |
Stock-based compensation (as a percent) | (0.23%) | (1.11%) | 0.28% |
Federal and state research credits (as a percent) | (0.00%) | 12.66% | 3.63% |
Effect of Spin-Off Transaction (as a percent) | 0.00% | (203.20%) | 0.00% |
Other (as a percent) | (0.56%) | (4.04%) | (2.51%) |
Change in valuation allowance (as a percent) | (31.27%) | 160.85% | (35.33%) |
Effective tax rate (as a percent) | 0.00% | 0.00% | 0.00% |
Gross unrecognized tax benefits | |||
Gross unrecognized tax benefits at the beginning of the period | $ 15,459 | $ 57,420 | $ 52,500 |
Gross decrease for tax positions for prior years | (42,650) | (565) | |
Gross increase in tax positions for current year | 29 | 689 | 5,485 |
Gross unrecognized tax benefits at the end of the period | 15,488 | 15,459 | $ 57,420 |
Accrued interest or penalties due to our net operating losses | 0 | $ 0 | |
Number of ownership changes | item | 2 | ||
Federal | |||
Operating Loss and Tax Credit Carryforward | |||
Net operating loss carryforwards | 1,174,700 | ||
Federal | Research and Development | |||
Operating Loss and Tax Credit Carryforward | |||
Tax credit carryforward amount | 45,200 | ||
State | |||
Operating Loss and Tax Credit Carryforward | |||
Net operating loss carryforwards | 676,500 | ||
State | Research | |||
Operating Loss and Tax Credit Carryforward | |||
Tax credit carryforward amount | $ 32,300 |
Spin-Off of Theravance Biopha54
Spin-Off of Theravance Biopharma, Inc. (Details) $ in Thousands | Jun. 02, 2014USD ($) | Jun. 01, 2014USD ($) |
Spin-Off of Theravance Biopharma, Inc. | ||
Cash, cash equivalents and marketable securities | $ 393,000 | |
Number of shares of Theravance Biopharma issued for every share of Theravance | 0.286 | |
Theravance Biopharma | Discontinued operation | ||
Allocation of net book value of assets transferred pursuant to spin-off | ||
Cash and cash equivalents | $ 277,541 | |
Marketable investment securities | 115,129 | |
Accounts receivable | 125 | |
Reimbursement of certain liabilities | 16,983 | |
Prepaid and other current assets | 3,172 | |
Inventories | 14,328 | |
Fixed assets, net | 9,580 | |
Accrued liabilities | (22,342) | |
Deferred revenue | (6,694) | |
Other liabilities | (4,944) | |
Net book value of assets contributed | $ 402,878 |
Discontinued Operations (Detail
Discontinued Operations (Details) - USD ($) $ in Thousands | 1 Months Ended | 3 Months Ended | 12 Months Ended | |||||
Jun. 30, 2013 | Dec. 31, 2014 | Sep. 30, 2014 | Jun. 30, 2014 | Mar. 31, 2014 | Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 | |
Components of research and drug development operations presented on the condensed consolidated statements of operations | ||||||||
Net revenues | $ 0 | $ 3,129 | $ 226 | |||||
Income (loss) from discontinued operations | $ 0 | $ 0 | $ (43,413) | $ (51,521) | $ 0 | $ (94,934) | $ (140,068) | |
Termination fee received recorded as discontinued operations | $ 10,000 |
Subsequent Events (Details)
Subsequent Events (Details) - Common Stock - Subsequent events $ / shares in Units, $ in Millions | 2 Months Ended |
Feb. 15, 2016USD ($)$ / sharesshares | |
Subsequent Event | |
Number of shares purchased and retired | shares | 1,419,641 |
Average repurchase price (in dollars per share) | $ / shares | $ 9.53 |
Share repurchase price | $ | $ 13.5 |
Supplementary Financial Data (D
Supplementary Financial Data (Details) - USD ($) $ / shares in Units, $ in Thousands | Jul. 24, 2015 | Apr. 24, 2015 | Feb. 20, 2015 | Oct. 16, 2014 | Jul. 25, 2014 | Dec. 31, 2015 | Sep. 30, 2015 | Jun. 30, 2015 | Mar. 31, 2015 | Dec. 31, 2014 | Sep. 30, 2014 | Jun. 30, 2014 | Mar. 31, 2014 | Dec. 31, 2015 | Dec. 31, 2014 | Dec. 31, 2013 |
Supplementary Financial Data | ||||||||||||||||
Net revenue | $ 22,836 | $ 13,562 | $ 10,655 | $ 6,896 | $ 7,280 | $ 999 | $ 934 | $ (780) | $ 53,949 | $ 8,433 | $ 4,532 | |||||
Total operating expenses | (5,543) | (5,128) | (5,547) | (6,151) | (7,150) | (10,541) | (10,728) | (13,943) | (22,369) | (42,362) | (33,327) | |||||
Income (loss) from operations | 17,293 | 8,434 | 5,108 | 745 | 31,580 | (33,929) | (28,795) | |||||||||
Loss from continuing operations | (15,926) | (21,271) | (20,151) | (16,182) | (18,760) | (73,530) | (30,633) | |||||||||
Income (loss) from discontinued operations | 0 | 0 | (43,413) | (51,521) | 0 | (94,934) | (140,068) | |||||||||
Net income (loss) | $ 4,301 | $ (4,584) | $ (7,810) | $ (10,667) | $ (15,926) | $ (21,271) | $ (63,564) | $ (67,703) | $ (18,760) | $ (168,464) | $ (170,701) | |||||
Basic and diluted net loss per common share: | ||||||||||||||||
Continuing operations, net of tax | $ (0.14) | $ (0.19) | $ (0.18) | $ (0.15) | $ (0.16) | $ (0.66) | $ (0.30) | |||||||||
Discontinued operations (in dollars per share) | 0 | 0 | (0.39) | (0.47) | 0 | (0.84) | (1.37) | |||||||||
Basic and diluted net loss per share (in dollars per share) | $ 0.04 | $ (0.04) | $ (0.07) | $ (0.09) | (0.14) | (0.19) | (0.57) | (0.62) | (0.16) | (1.50) | (1.67) | |||||
Cash dividend declared per common share (in dollars per share) | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0.25 | $ 0 | $ 0 | $ 0.75 | $ 0.50 | $ 0 |