PART I Innoviva is a diversified holding company with a portfolio of royalties and innovative healthcare assets Item 1. Business Innoviva manages GSK-partnered respiratory royalties and an expanded portfolio of commercial and development-stage healthcare products Overview Innoviva is a diversified holding company with GSK-partnered respiratory royalties and commercial products from recent acquisitions - Innoviva, Inc. is a diversified holding company with a portfolio of royalties and other healthcare assets17 - Key royalty assets include RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA® from a collaboration with GSK17 - Recent acquisitions of Entasis Therapeutics (July 11, 2022) and La Jolla Pharmaceutical (August 22, 2022) expanded the portfolio to include commercial products GIAPREZA® and XERAVA®, and development pipeline assets like SUL-DUR18 Our Strategy Innoviva's strategy maximizes GSK royalty value, optimizes operations, and diversifies through opportunistic healthcare acquisitions - Corporate strategy focuses on increasing stockholder value by maximizing respiratory assets partnered with GSK, optimizing operations, and augmenting capital allocation20 - Diversifying royalty management business through opportunistic acquisitions of promising healthcare companies and assets20 - Recent acquisitions of Entasis and La Jolla created a robust hospital and infectious disease platform20 Our Royalty Product Portfolio Innoviva's royalty portfolio includes GSK-partnered respiratory products RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA®, facing competition - Innoviva's royalty portfolio includes RELVAR®/BREO® ELLIPTA® (FF/VI) and ANORO® ELLIPTA® (UMEC/VI), developed under a LABA Collaboration Agreement with GSK21 GSK Royalty Rates | Product | Royalty Rate (Annual Global Net Sales) | | :------ | :------------------------------------ | | RELVAR®/BREO® ELLIPTA® | 15% on first $3.0 billion, 5% above $3.0 billion | | ANORO® ELLIPTA® | Tiered, ranging from 6.5% to 10% | - The market for these respiratory products is highly competitive, facing numerous approved bronchodilator drugs, combination therapies, and generic versions of established products like Advair® and Symbicort®2325 Our Integrated Hospital / Infectious Disease Business Innoviva's hospital/infectious disease business features commercial products GIAPREZA® and XERAVA®, with regulatory exclusivity - Commercial products include GIAPREZA® (angiotensin II) for septic or other distributive shock and XERAVA® (eravacycline) for complicated intra-abdominal infections (cIAI)1827 - GIAPREZA® was approved based on the ATHOS-3 study, showing a 70% MAP response in treated patients vs. 23% in placebo, with a median time to response of ~5 minutes29333637 - XERAVA® was approved based on IGNITE1 and IGNITE4 studies, demonstrating noninferiority in clinical cure rates for cIAI, including against resistant pathogens434752 - Both GIAPREZA® and XERAVA® are New Chemical Entities (NCEs) and have Qualified Infectious Disease Product (QIDP) designation, granting additional market exclusivity5962124 Our Product Candidates Innoviva's pipeline includes SUL-DUR for carbapenem-resistant infections and zoliflodacin for gonorrhea, both with QIDP designation - SUL-DUR is a novel IV antibiotic for carbapenem-resistant Acinetobacter infections, with positive Phase 3 ATTACK trial data showing 19.0% mortality vs. 32.3% for colistin and significantly lower nephrotoxicity (13.2% vs. 37.6%)6572 - SUL-DUR received FDA Fast Track and QIDP designation in September 2017 and FDA Priority Review for its NDA in November 2022, with a target PDUFA date of May 29, 20237278124 - Zoliflodacin is a potential single oral dose cure for uncomplicated gonorrhea, targeting drug-resistant strains, and is currently in a global Phase 3 registration trial with anticipated enrollment completion in 20238795 - Zoliflodacin has QIDP designation and aims to address the global public health threat of gonorrhea, with 82.4 million cases worldwide in 202090124 Manufacturing Innoviva relies on third-party manufacturers for commercial products and candidates, adhering to cGMPs and regulatory standards - Manufacturing of RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA® is performed by GSK103 - Innoviva relies on third-party manufacturers for GIAPREZA and XERAVA, and for raw materials, drug substance, and finished drug product for preclinical and clinical trials of product candidates104105 - Contract manufacturers must comply with FDA's current Good Manufacturing Practices (cGMPs) and other applicable laws and regulations104 Government Regulation Products are subject to extensive U.S. and international regulations covering development, approval, manufacturing, marketing, and reimbursement - Extensive government regulation in the U.S. and other countries covers all stages of product life, from research and development to marketing and post-approval monitoring106107134 - The U.S. FDA approval process involves preclinical tests, IND submission, three phases of clinical trials (Phase 1, 2, 3), NDA submission, and facility inspections for cGMP compliance110111118121 - Expedited review programs like Fast Track and QIDP (Qualified Infectious Disease Product) designation can accelerate development and review, and provide additional market exclusivity (e.g., XERAVA and SUL-DUR have QIDP)123124128 - Post-approval, products are subject to ongoing review, cGMP compliance, adverse event reporting, and strict regulation of promotional claims, with potential for restrictions or withdrawal if issues arise130131 - Reimbursement by third-party payors (government and commercial) is critical for commercial success, with increasing challenges to prices and cost-effectiveness, especially for hospital-administered drugs140141 - Healthcare laws such as the federal Anti-Kickback Statute, False Claims Act, and HIPAA regulate business activities and marketing practices, with non-compliance leading to significant penalties143144145146147 Intellectual Property Innoviva protects its product candidates and technologies through patents, trademarks, and trade secrets, with patents extending to 2044 - Commercial success depends on obtaining and maintaining proprietary or intellectual property protection for product candidates, core technologies, and know-how159 Intellectual Property Portfolio Summary (as of Feb 15, 2023) | Description | United States (Issued/Pending) | Expiration (US) | Foreign (Issued/Pending) | Expiration (Foreign) | | :---------- | :----------------------------- | :-------------- | :----------------------- | :------------------- | | GIAPREZA | 15 / 10 | 2029 - 2044 | 15 / 25 | 2034 - 2044 | | XERAVA | 4 / 2 | 2029 - 2037 | 17 / 15 | 2029 - 2037 | | Other (Tetracycline) | 5 / 1 | 2030 - 2037 | 32 / 17 | 2033 - 2037 | | Durlobactam | 4 / 2 (incl. PCT) | 2033 - 2043 | 107 / 6 | 2033 - 2043 | | Zoliflodacin| 7 / 0 | 2029 - 2035 | 74 / 2 | 2029 - 2035 | - The company also relies on trademarks, trade secrets, and confidentiality agreements to protect unpatented know-how and maintain its competitive position169 Our Strategic Partnership with Sarissa Capital Innoviva partners with Sarissa Capital for acquisition strategy and invests in ISP Fund LP for healthcare equity securities - Innoviva entered a Strategic Advisory Agreement with Sarissa Capital (a related party) to assist in developing and executing its acquisition strategy170171 - Innoviva Strategic Partners LLC, a wholly-owned subsidiary, became a limited partner in ISP Fund LP, contributing $300.0 million initially and an additional $110.0 million in 2022 for investments in healthcare, pharmaceutical, and biotechnology equity securities172173 Human Capital Innoviva had 101 employees as of December 31, 2022, focusing on recruitment, retention, and DEI through competitive compensation - As of December 31, 2022, Innoviva had 101 full-time employees, none represented by a labor union174 - Key human capital objectives include identifying, recruiting, integrating, retaining, and motivating employees through competitive compensation, benefits, and a focus on Diversity, Equity, and Inclusion (DEI)175176177 Executive Officers (as of Feb 28, 2023) | Name | Age | Positions Held | | :------------ | :-- | :---------------------- | | Pavel Raifeld | 39 | Chief Executive Officer | | Marianne Zhen | 54 | Chief Accounting Officer| - Innoviva is a diversified holding company with a portfolio of royalties and innovative healthcare assets1718400 - The corporate strategy is focused on increasing stockholder value by maximizing respiratory assets, optimizing operations, augmenting capital allocation, and diversifying through opportunistic acquisitions in the healthcare industry20 GSK Royalty Structure | Product | Royalty Rate (Annual Global Net Sales) | | :------ | :------------------------------------ | | RELVAR®/BREO® ELLIPTA® | 15% on first $3.0 billion, 5% above $3.0 billion | | ANORO® ELLIPTA® | Tiered, ranging from 6.5% to 10% | Item 1A. Risk Factors Innoviva faces risks from competition, partner dependence, development uncertainties, acquisitions, debt, and regulatory/economic factors - Significant risks include substantial competition for RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA®, dependence on GSK's commercialization efforts, and potential for reduced royalty revenue due to generic competition or pricing pressures182184188191 - Product development risks involve clinical trial failures, delays in regulatory approval, undesirable side effects, and challenges in achieving market acceptance for new product candidates182230242273 - Operational risks include difficulties integrating acquired businesses (Entasis, La Jolla), reliance on third parties for clinical trials and manufacturing, and the potential for unsuccessful acquisitions or strategic collaborations182251257261291293296 - Financial risks include significant debt obligations ($549.7 million as of Dec 31, 2022), potential limitations on net operating loss carryforwards, and the volatility of the company's stock price182221222209377 - Other risks encompass intellectual property protection challenges, compliance with complex government regulations (including healthcare laws and potential price controls), and adverse impacts from global economic and political conditions182298322335341348355381 Item 1B. Unresolved Staff Comments No unresolved staff comments are reported Item 2. Properties Innoviva maintains headquarters in California and office/lab facilities in Massachusetts, sufficient for current operations - Headquarters: 2,111 sq ft office space in Burlingame, CA, lease expires December 2023384 - Other material property: ~20,000 sq ft office and laboratory facility in Waltham, MA, lease expires December 2025384 - Current facilities are sufficient, and additional space is expected to be available on commercially reasonable terms for expansion384 Item 3. Legal Proceedings Legal proceedings information is incorporated by reference from Note 13, 'Commitments and Contingencies,' in financial statements - Legal proceedings information is incorporated by reference from Note 13, 'Commitments and Contingencies,' in the financial statements385 Item 4. Mine Safety Disclosures This item is not applicable to Innoviva, Inc PART II This section covers market information for common equity, related stockholder matters, and issuer purchases of equity securities Item 5. Market for the Registrant's Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities Innoviva's common stock trades on Nasdaq, with a $100.0 million share repurchase program initiated in October 2022 - Innoviva's common stock trades on Nasdaq under the symbol "INVA" since January 11, 2016 (formerly "THRX")388 - As of February 14, 2023, there were 64 stockholders of record389 Share Repurchases (Q4 2022) | Period | Total Number of Shares Purchased | Average Price Paid per Share | | :------------------------------- | :------------------------------- | :--------------------------- | | December 1, 2022 to Dec 31, 2022 | 647,394 | $13.13 | | Total | 647,394 | $13.13 | - The Board authorized a $100.0 million share repurchase program on October 31, 2022390 - Subsequent to December 31, 2022, and through February 24, 2023, an additional 1,522,947 shares were repurchased for approximately $19.2 million406 Item 6. [Reserved] This item is reserved and contains no information Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations Innoviva's 2022 financial performance reflects strategic acquisitions, divestitures, and operational shifts, impacting net income and cash flows Management Overview Innoviva is a diversified holding company managing royalties and healthcare assets, expanded by recent acquisitions - Innoviva is a diversified holding company with a portfolio of royalties and innovative healthcare assets, including GSK-partnered respiratory products (RELVAR®/BREO® ELLIPTA®, ANORO® ELLIPTA®)399 - Acquisitions of Entasis (July 11, 2022) and La Jolla (August 22, 2022) added commercial products GIAPREZA® and XERAVA®, and a development pipeline (SUL-DUR)400 - The company's structure is tailored to managing respiratory assets, commercializing marketed products, developing product candidates, and optimizing capital allocation401 Financial Highlights Innoviva's 2022 net income decreased to $213.9 million due to investment losses and lower royalties, partially offset by a TRC sale gain Net Income Attributable to Innoviva Stockholders | Year | Net Income (in millions) | | :--- | :----------------------- | | 2022 | $213.9 | | 2021 | $265.9 | - The decrease in net income was mainly driven by a $153.2 million unrealized loss on equity and long-term investments and decreased royalty revenues402 - A gain of $266.7 million was recognized from the sale of TRC, partially offsetting the decreases402 - Cash and cash equivalents totaled $291.0 million as of December 31, 2022402 Corporate Updates Innoviva completed acquisitions of Entasis and La Jolla, divested TRC ownership, and initiated a $100.0 million share repurchase program - Acquired Entasis Therapeutics Holdings Inc. on July 11, 2022, for $42.4 million, adding an infectious disease R&D platform and lead asset SUL-DUR403 - Sold 15% ownership interest in TRC to Royalty Pharma for $282.0 million on July 20, 2022, including a potential $50.0 million sales-based milestone404 - Acquired La Jolla Pharmaceutical Company on August 22, 2022, for $150.5 million, adding commercial products GIAPREZA® and XERAVA®405 - Authorized a new $100.0 million share repurchase program on October 31, 2022406 Clinical Updates SUL-DUR received FDA Priority Review, and zoliflodacin's Phase 3 trial enrollment is on track for 2023 completion - FDA granted Priority Review for SUL-DUR's NDA on November 30, 2022, for carbapenem-resistant Acinetobacter infections, with a target PDUFA date of May 29, 2023409 - Positive safety and efficacy findings from the pivotal Phase 3 ATTACK trial for SUL-DUR were reinforced at the Infectious Disease Society of America annual meeting in October 2022409 - Enrollment in the Phase 3 registrational trial for zoliflodacin (for uncomplicated gonorrhea) is on track, with study completion anticipated in 2023409 Collaborative Arrangements with GSK Innoviva receives tiered royalties from GSK on RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA® sales - LABA Collaboration Agreement with GSK (November 2002) developed once-daily products for COPD and asthma, including RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA®408409 - Innoviva receives tiered royalties from GSK on sales of RELVAR®/BREO® ELLIPTA® (15% on first $3.0 billion, 5% above $3.0 billion) and ANORO® ELLIPTA® (6.5% to 10%)411 - Milestone fees of $220.0 million paid to GSK in 2014 are capitalized and amortized over the products' estimated useful lives410 - Innoviva no longer receives royalties on TRELEGY® ELLIPTA® sales after selling its TRC ownership interest in July 2022411 Strategic Partnership with Sarissa Capital Innoviva partners with Sarissa Capital for acquisition strategy and invests in ISP Fund LP for healthcare equity securities - Strategic Advisory Agreement with Sarissa Capital (a related party) provides strategic services for Innoviva's acquisition strategy, free of charge412 - Innoviva Strategic Partners LLC contributed $300.0 million initially and an additional $110.0 million in March 2022 to ISP Fund LP, managed by Sarissa Capital, for investments in healthcare, pharmaceutical, and biotechnology equity securities413414 - Capital contributions to ISP Fund LP are subject to a 36-month lock-up period from the contribution date413414 Critical Accounting Policies and Estimates Innoviva's financial reporting relies on critical estimates for business combinations, revenue recognition, impairment, and investment valuation - Business combinations use the acquisition method, recording acquired assets and liabilities at fair value, requiring significant estimates for identifiable intangible assets, future revenues, cash flows, and discount rates416417 - Royalty revenue is recognized when earned, net of amortization of capitalized fees, based on partner's net sales reports and estimates for rebates/returns418 - Product sales revenue is recognized when customers obtain control, net of variable consideration (chargebacks, discounts, returns, rebates) estimated using the expected-value method420421 - Capitalized fees are reviewed for impairment by comparing carrying amount to expected undiscounted future cash flows, requiring estimates of useful life and sales projections423 - Equity and long-term investments, particularly Level 3 instruments like InCarda preferred stock/warrants and Gate convertible notes, are measured at fair value using models like Black-Scholes-Merton or Monte Carlo simulation, based on significant unobservable inputs428429 Factors Affecting Comparability Financial comparability is impacted by ASU 2020-06 adoption, Entasis consolidation, TRC sale, and La Jolla acquisition - Comparability of financial results is affected by the adoption of ASU 2020-06 (effective Jan 1, 2022)431 - Consolidation of Entasis (Feb 17, 2022) and purchase of remaining noncontrolling interest (July 11, 2022) impact comparability431 - Sale of 15% ownership interest in TRC (July 20, 2022) and acquisition of La Jolla (August 22, 2022) also affect comparability431 Results of Operations Innoviva's 2022 results show decreased royalty revenue, increased R&D and SG&A expenses, a TRC sale gain, and unrealized investment losses Total Net Royalty Revenue (2022 vs. 2021) | Year | Total Net Royalty Revenue (in thousands) | | :--- | :--------------------------------------- | | 2022 | $311,645 | | 2021 | $391,866 | | Change | $(80,221) | - Decrease in royalty revenue primarily due to the sale of TRC ownership interest and pricing pressures/foreign currency changes on RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA®433 Net Product Sales (2022) | Product | Net Sales (in thousands) | | :-------- | :----------------------- | | GIAPREZA® | $14,200 | | XERAVA® | $5,500 | | Total | $19,700 | Key Expenses (2022 vs. 2021) | Expense Category | 2022 (in thousands) | 2021 (in thousands) | Change ($) (in thousands) | | :------------------------------- | :------------------ | :------------------ | :------------------------ | | Research and development | $41,432 | $576 | $40,856 | | Selling, general and administrative | $63,538 | $16,187 | $47,351 | - Recognized a net gain of $266.7 million from the sale of TRC in July 2022446 - Recorded $152.5 million in unrealized losses on Armata investments in 2022, compared to $78.7 million in unrealized gains in 2021448 Liquidity and Capital Resources Innoviva maintains $291.0 million in cash, with $549.7 million in convertible notes, and sufficient liquidity for near-term needs - Cash and cash equivalents totaled $291.0 million as of December 31, 2022457 - Generated $325.5 million in gross royalty revenues and $19.7 million in net product sales in 2022457 - Total outstanding convertible notes were $549.7 million as of December 31, 2022, with $96.2 million (2023 Notes) fully paid in January 2023458 - Management believes current cash and cash equivalents are sufficient for debt service, operating needs, and share repurchase program for at least the next 12 months461 Cash Flows Summary (2022 vs. 2021) | Cash Flow Activity | 2022 (in thousands) | 2021 (in thousands) | | :--------------------------- | :------------------ | :------------------ | | Operating activities | $201,726 | $363,813 | | Investing activities | $(56,634) | $43,722 | | Financing activities | $(55,568) | $(452,497) | - Net income attributable to Innoviva stockholders decreased to $213.9 million in 2022 from $265.9 million in 2021402 - The decrease in net income was mainly driven by a $153.2 million unrealized loss on equity and long-term investments and decreased royalty revenue, partially offset by a $266.7 million gain from the sale of TRC402 - Innoviva completed the acquisition of Entasis Therapeutics on July 11, 2022, for $42.4 million cash, and La Jolla Pharmaceutical Company on August 22, 2022, for $150.5 million net cash403405 - The company sold its 15% ownership interest in Theravance Respiratory Company, LLC (TRC) to Royalty Pharma for $282.0 million on July 20, 2022, including a potential $50.0 million sales-based milestone404 Key Financial Data (2022 vs. 2021) | Metric | 2022 (in thousands) | 2021 (in thousands) | Change ($) (in thousands) | Change (%) | | :----------------------------------------- | :------------------ | :------------------ | :------------------------ | :--------- | | Total net royalty revenue | $311,645 | $391,866 | $(80,221) | (20)% | | Net product sales | $19,694 | $0 | $19,694 | * | | Research and development expenses | $41,432 | $576 | $40,856 | * | | Selling, general and administrative expenses | $63,538 | $16,187 | $47,351 | 293% | | Net income attributable to Innoviva stockholders | $213,921 | $265,854 | $(51,933) | (20)% | | Cash and cash equivalents (period end) | $291,049 | $201,525 | $89,524 | 44% | Item 7A. Quantitative and Qualitative Disclosures About Market Risk Innoviva faces market risks from investment fair value changes, inflation, and foreign exchange rates, though direct foreign exchange impact is minimal - Debt bears fixed interest rates, so cash flows on debt obligations are not subject to variability from interest rate changes476 - Exposed to changes in the fair value of equity and debt securities investments, which could result in material gains or losses477 - Inflationary factors (e.g., raw material costs, interest rates) could adversely affect operating results, though no material impact has been observed to date478 - Foreign exchange risk is considered insubstantial as most cash, investments, and vendor relationships are U.S. dollar-denominated, despite indirect exposure from international royalty revenue479 Item 8. Financial Statements and Supplementary Data This section presents Innoviva's audited consolidated financial statements, including balance sheets, income statements, and cash flow statements, with notes - Includes Consolidated Balance Sheets as of December 31, 2022 and 2021480 - Includes Consolidated Statements of Income, Comprehensive Income, Stockholders' Equity, and Cash Flows for the three years ended December 31, 2022480 - Contains Notes to Consolidated Financial Statements and Reports of Independent Registered Public Accounting Firms480 Item 9. Changes in and Disagreements with Accountants on Accounting and Financial Disclosure No changes in or disagreements with accountants on accounting and financial disclosure are reported Item 9A. Controls and Procedures Innoviva's disclosure controls and internal control over financial reporting were effective as of December 31, 2022, excluding recent acquisitions - Disclosure controls and procedures were evaluated as effective at reasonable assurance levels as of December 31, 2022805 - Management concluded that internal control over financial reporting was effective as of December 31, 2022, based on the COSO 2013 framework807 - Management's assessment excluded internal controls of recently acquired La Jolla and Entasis, which constituted approximately 33% of total assets and 6% of total revenue808 - Deloitte & Touche LLP, the independent registered public accounting firm, issued an unqualified opinion on the effectiveness of internal control over financial reporting809815 - The company is integrating acquired operations into its internal control environment and implementing necessary changes, including for inventory management, R&D, and product sales811 Item 9B. Other Information No other information is reported under this item Item 9C. Disclosure Regarding Foreign Jurisdictions that Prevent Inspections This item is not applicable to Innoviva, Inc PART III This section incorporates information on directors, executive compensation, security ownership, related transactions, and accountant fees by reference Item 10. Directors, Executive Officers and Corporate Governance Information is incorporated by reference from the 2023 Annual Meeting of Stockholders Proxy Statement - Information is incorporated by reference from the 2023 Annual Meeting of Stockholders Proxy Statement825 Item 11. Executive Compensation Information is incorporated by reference from the 2023 Annual Meeting of Stockholders Proxy Statement - Information is incorporated by reference from the 2023 Annual Meeting of Stockholders Proxy Statement826 Item 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters This section details security ownership and equity compensation plans, including outstanding options and shares available for future issuance Securities Authorized for Issuance under Equity Compensation Plans (as of Dec 31, 2022) | Plan Category | Number of securities to be issued upon exercise of outstanding options and vesting of outstanding restricted stock units and restricted stock awards (a) | Weighted‑average exercise price of outstanding options (b) | Number of securities remaining available for future issuance under equity compensation plans (excluding securities reflected in column (a)) (c) | | :------------------------------------------------ | :------------------------------------------------------------------------------------------------------------------------------------------------ | :--------------------------------------------------------- | :---------------------------------------------------------------------------------------------------------------------------------------------------- | | Equity compensation plans approved by security holders | 1,465,720 | $15.56 | 3,999,265 | - Column (a) includes 947,906 shares from outstanding options and 517,814 shares from outstanding RSUs and RSAs828 - Column (c) includes 160,995 shares of common stock available under the Employee Stock Purchase Plan828 Item 13. Certain Relationships and Related Transactions, and Director Independence Information is incorporated by reference from the 2023 Annual Meeting of Stockholders Proxy Statement - Information is incorporated by reference from the 2023 Annual Meeting of Stockholders Proxy Statement829 Item 14. Principal Accountant Fees and Services Information is incorporated by reference from the 2023 Annual Meeting of Stockholders Proxy Statement - Information is incorporated by reference from the 2023 Annual Meeting of Stockholders Proxy Statement830 PART IV This section lists financial statements, schedules, and exhibits filed as part of the Annual Report on Form 10-K Item 15. Exhibits and Financial Statement Schedules This section details financial statements, schedules, and an index of exhibits required by Regulation S-K for the Annual Report on Form 10-K - Includes Consolidated Balance Sheets, Statements of Income, Comprehensive Income, Stockholders' Equity, and Cash Flows for the periods ended December 31, 2022832 - Contains Notes to Consolidated Financial Statements and Reports of Independent Registered Public Accounting Firms832 - Provides an index of exhibits required by Item 601 of Regulation S-K, including merger agreements, certificates of incorporation, indentures, and various other agreements832836 Item 16. Form 10‑K Summary No Form 10-K Summary is provided
Innoviva(INVA) - 2022 Q4 - Annual Report