Table of Contents

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

WASHINGTON, D.C. 20549

FORM 10-Q

(Mark One)

QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) O

FQUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the quarterly period ended March 31, 20202021

OR

TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934

For the transition period from                    to                   

Commission File Number: 000-30319

INNOVIVA, INC.

(Exact Name of Registrant as Specified in its Charter)

Delaware

94-3265960

(State or Other Jurisdiction of
Incorporation or Organization)

(I.R.S. Employer
Identification No.)

1350 Old Bayshore Highway Suite 400

Burlingame, CA 94010

(Address of Principal Executive Offices)

(650238-9600

(Registrant’s Telephone Number, Including Area Code)

Securities registered pursuant to Section 12(b) of the Act:

Title of each class

    

Trading Symbol(s)

    

Name of each exchange on which registered

Common Stock, par value $0.01 per share

INVA

The NASDAQ Global Select Market

Indicate by check mark whether the registrant: (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90 days.  Yes    No  

Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files).  Yes    No  

Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Act.

Large accelerated filer 

Accelerated filer 

Non-accelerated filer 

Smaller reporting company 

Emerging growth company

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act.  

Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act).  Yes    No  

The number of shares of registrant’s common stock outstanding on April 20, 202019, 2021 was 101,320,233.101,408,012.

Table of Contents

TABLE OF CONTENTS

PART I. FINANCIAL INFORMATION

Item 1. Financial Statements

Consolidated Balance Sheets as of March 31, 20202021 (Unaudited) and December 31, 20192020

3

Unaudited Consolidated Statements of Income for the Three Months Endedended March 31, 20202021 and 20192020

4

Unaudited Consolidated Statements of Comprehensive Income for the Three Months Endedended March 31, 20202021 and 20192020

5

Unaudited Consolidated Statements of Stockholders’ Equity for the Three Months Endedended March 31, 20202021 and 20192020

6

Unaudited Consolidated Statements of Cash Flows for the Three Months Endedended March 31, 20202021 and 20192020

7

Notes to Unaudited Consolidated Financial Statements

8

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations

1519

Item 3. Quantitative and Qualitative Disclosures About Market Risk

2024

Item 4. Controls and Procedures

2025

PART II. OTHER INFORMATION

Item 1. Legal Proceedings

2125

Item 1A. Risk Factors

2126

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds

2226

Item 3. Defaults Upon Senior Securities

2226

Item 4. Mine Safety Disclosure

2226

Item 5. Other Information

2226

Item 6. Exhibits

2227

Signatures

2228

Exhibits

2

Table of Contents

PART I. FINANCIAL INFORMATION

Item 1. Financial Statements

INNOVIVA, INC.

CONSOLIDATED BALANCE SHEETS

(In thousands, except per share data)

    

March 31, 

    

December 31, 

March 31, 

December 31, 

2020

2019

    

2021

    

2020

(unaudited)

*

(unaudited)

*

Assets

Current assets:

Cash and cash equivalents

$

351,981

$

278,096

$

282,890

$

246,487

Short-term marketable securities

 

31,970

 

72,749

Related party receivables from collaborative arrangements

 

82,134

 

79,427

 

88,974

 

93,931

Prepaid expenses and other current assets

 

822

 

962

 

1,069

 

1,640

Total current assets

 

466,907

 

431,234

 

372,933

 

342,058

Property and equipment, net

 

42

 

33

 

24

 

28

Equity investments

46,915

Equity and long-term investments

519,325

438,258

Capitalized fees paid to a related party, net

 

135,620

 

139,076

 

121,797

 

125,253

Deferred tax assets, net

138,239

154,171

74,023

93,759

Other assets

 

288

 

312

 

188

 

214

Total assets

$

788,011

$

724,826

$

1,088,290

$

999,570

Liabilities and Stockholders' Equity

Current liabilities:

Accounts payable

$

122

$

10

$

14

$

66

Accrued personnel-related expenses

 

274

 

647

 

652

 

490

Accrued interest payable

 

1,668

 

4,152

 

1,668

 

4,152

Other accrued liabilities

 

734

 

562

 

1,470

 

1,402

Total current liabilities

 

2,798

 

5,371

 

3,804

 

6,110

Long-term debt, net of discount and issuance costs

 

379,152

 

377,120

 

387,728

 

385,517

Other long-term liabilities

 

192

 

219

77

106

Commitments and contingencies (Note 7)

Commitments and contingencies (Note 8)

Stockholders’ equity:

Preferred stock: $0.01 par value, 230 shares authorized, 0 shares issued and outstanding

 

0

 

0

Common stock: $0.01 par value, 200,000 shares authorized, 101,320 and 101,288 issued and outstanding as of March 31, 2020 and December 31, 2019, respectively

 

1,013

 

1,013

Common stock: $0.01 par value, 200,000 shares authorized, 101,408 and 101,392 issued and outstanding as of March 31, 2021 and December 31, 2020, respectively

 

1,014

 

1,014

Additional paid-in capital

 

1,259,464

 

1,258,859

 

1,261,326

 

1,260,900

Accumulated other comprehensive income

 

33

 

27

Accumulated deficit

 

(880,967)

 

(946,404)

 

(627,879)

 

(722,002)

Total Innoviva stockholders’ equity

379,543

313,495

634,461

539,912

Noncontrolling interest

26,326

28,621

62,220

67,925

Total stockholders’ equity

 

405,869

 

342,116

 

696,681

 

607,837

Total liabilities and stockholders’ equity

$

788,011

$

724,826

$

1,088,290

$

999,570

*Consolidated balance sheet as of December 31, 20192020 has been derived from audited consolidated financial statements.

See accompanying notes to consolidated financial statements.

3

Table of Contents

INNOVIVA, INC.

CONSOLIDATED STATEMENTS OF INCOME

(In thousands, except per share data)

(Unaudited)

Three Months Ended March 31, 

    

2020

    

2019

Royalty revenue from a related party, net of amortization of capitalized fees paid to a related party of $3,456 in the three months ended March 31, 2020 and 2019

$

78,678

$

55,183

Operating expenses:

General and administrative

 

2,563

 

3,015

Total operating expenses

 

2,563

 

3,015

Income from operations

 

76,115

 

52,168

Other income, net

 

68

 

1

Interest income

 

1,302

 

975

Interest expense

 

(4,516)

 

(4,617)

Changes in fair values of equity investments

21,915

Income before income taxes

94,884

48,527

Income tax expense, net

15,932

8,508

Net income

78,952

40,019

Net income attributable to noncontrolling interest

13,515

6,229

Net income attributable to Innoviva stockholders

$

65,437

$

33,790

Basic net income per share attributable to Innoviva stockholders

$

0.65

$

0.33

Diluted net income per share attributable to Innoviva stockholders

$

0.59

$

0.31

Shares used to compute Innoviva basic and diluted net income per share:

Shares used to compute basic net income per share

101,235

101,059

Shares used to compute diluted net income per share

113,509

113,376

Three Months Ended March 31, 

    

2021

    

2020

Royalty revenue from a related party, net of amortization of capitalized fees paid to a related party of $3,456 in three months ended March 31, 2021 and 2020

$

85,518

$

78,678

Operating expenses:

Research and development

 

49

 

0

General and administrative

 

5,986

 

2,563

Total operating expenses

 

6,035

 

2,563

Income from operations

 

79,483

 

76,115

Other income (expense), net

(433)

68

Interest income

 

30

 

1,302

Interest expense

 

(4,694)

 

(4,516)

Changes in fair values of equity and long-term investments, net

55,045

21,915

Income before income taxes

129,431

94,884

Income tax expense, net

19,736

15,932

Net income

109,695

78,952

Net income attributable to noncontrolling interest

15,572

13,515

Net income attributable to Innoviva stockholders

$

94,123

$

65,437

Basic net income per share attributable to Innoviva stockholders

$

0.93

$

0.65

Diluted net income per share attributable to Innoviva stockholders

$

0.84

$

0.59

Shares used to compute Innoviva basic and diluted net income per share:

Shares used to compute basic net income per share

101,365

101,235

Shares used to compute diluted net income per share

113,624

113,509

See accompanying notes to consolidated financial statements.

4

Table of Contents

INNOVIVA, INC.

CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME

(In thousands)

(Unaudited)

Three Months Ended March 31, 

    

2020

    

2019

Three Months Ended March 31, 

    

2021

    

2020

Net income

$

78,952

$

40,019

$

109,695

$

78,952

Unrealized gain on marketable securities, net

 

6

 

13

0

6

Comprehensive income

78,958

40,032

109,695

78,958

Comprehensive income attributable to noncontrolling interest

13,515

6,229

15,572

13,515

Comprehensive income attributable to Innoviva stockholders

$

65,443

$

33,803

$

94,123

$

65,443

See accompanying notes to consolidated financial statements.

5

Table of Contents

INNOVIVA, INC.

CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY

(In thousands)

(Unaudited)

Three months ended March 31, 2020

Accumulated Other

Common Stock

Additional Paid-In

Comprehensive

Accumulated

Noncontrolling

Total Stockholders’

    

Shares

    

Amount

    

Capital

    

Income (Loss)

    

Deficit

    

Interest

    

Equity

Balance as of December 31, 2019

 

101,288

$

1,013

$

1,258,859

$

27

$

(946,404)

$

28,621

$

342,116

Distributions to noncontrolling interest

 

 

 

 

 

 

(15,810)

 

(15,810)

Exercise of stock options, and issuance of common stock units and stock awards, net of repurchase of shares to satisfy tax withholding

 

32

 

 

170

 

 

 

 

170

Stock-based compensation

 

 

 

435

 

 

 

 

435

Net income

 

 

 

 

 

65,437

 

13,515

 

78,952

Other comprehensive income

 

 

 

 

6

 

 

 

6

Balance as of March 31, 2020

 

101,320

$

1,013

$

1,259,464

$

33

$

(880,967)

$

26,326

$

405,869

Three Months ended March 31, 2021

Accumulated

Additional

Other

Total

Common Stock

Paid-In

Comprehensive

Accumulated

Noncontrolling

Stockholders’

    

Shares

    

Amount

    

Capital

    

Income (Loss)

    

Deficit

    

Interest

    

Equity

Balance as of December 31, 2020

 

101,392

$

1,014

$

1,260,900

$

0

$

(722,002)

$

67,925

$

607,837

Distributions to noncontrolling interest

 

0

 

0

 

0

 

0

 

0

 

(21,285)

 

(21,285)

Equity activity of noncontrolling interest from a consolidated variable interest entity

0

0

0

0

0

8

8

Exercise of stock options, and issuance of common stock units and stock awards, net of repurchase of shares to satisfy tax withholding

 

16

 

0

 

(25)

 

0

 

0

 

0

 

(25)

Stock-based compensation

 

0

 

0

 

451

 

0

 

0

 

0

 

451

Net income

 

0

 

0

 

0

 

0

 

94,123

 

15,572

 

109,695

Balance as of March 31, 2021

 

101,408

$

1,014

$

1,261,326

$

0

$

(627,879)

$

62,220

$

696,681

Three months ended March 31, 2019

Accumulated Other

Common Stock

Additional Paid-In

Comprehensive

Accumulated

Noncontrolling

Total Stockholders’

    

Shares

Amount

    

Capital

    

Income (Loss)

    

Deficit

    

Interest

    

Equity

Balance as of December 31, 2018

101,098

$

1,011

$

1,256,267

$

(3)

$

(1,103,692)

$

5,469

$

159,052

Exercise of stock options, and issuance of common stock units and stock awards, net of repurchase of shares to satisfy tax withholding

85

1

253

254

Stock-based compensation

605

605

Net income

33,790

6,229

40,019

Other comprehensive income

13

13

Balance as of March 31, 2019

101,183

$

1,012

$

1,257,125

$

10

$

(1,069,902)

$

11,698

$

199,943

Three Months ended March 31, 2020

Accumulated

Additional

Other

Total

Common Stock

Paid-In

Comprehensive

Accumulated

Noncontrolling

Stockholders’

    

Shares

Amount

    

Capital

    

Income (Loss)

    

Deficit

    

Interest

    

Equity

Balance as of December 31, 2019

101,288

$

1,013

$

1,258,859

$

27

$

(946,404)

$

28,621

$

342,116

Distributions to noncontrolling interest

0

0

0

0

0

(15,810)

(15,810)

Exercise of stock options, and issuance of common stock units and stock awards, net of repurchase of shares to satisfy tax withholding

32

0

170

0

0

0

170

Stock-based compensation

0

0

435

0

0

0

435

Net income

0

0

0

0

65,437

13,515

78,952

Other comprehensive income

0

0

0

6

0

0

6

Balance as of March 31, 2020

101,320

$

1,013

$

1,259,464

$

33

$

(880,967)

$

26,326

$

405,869

See accompanying notes to consolidated financial statements.

6

Table of Contents

INNOVIVA, INC.

CONSOLIDATED STATEMENTS OF CASH FLOWS

(In thousands)

(Unaudited)

Three Months Ended March 31, 

Three Months Ended March 31, 

    

2020

    

2019

    

2021

    

2020

Cash flows from operating activities

Net income

$

78,952

$

40,019

$

109,695

$

78,952

Adjustments to reconcile net income to net cash provided by operating activities:

Deferred income taxes

15,932

8,508

19,736

15,932

Depreciation and amortization

 

3,463

 

3,539

 

3,460

 

3,463

Stock-based compensation

 

435

 

605

 

451

 

435

Amortization of debt discount and issuance costs

2,032

1,889

2,211

2,032

Amortization of discount on short-term investments

(272)

(356)

0

(272)

Amortization of lease guarantee

(81)

(81)

0

(81)

Changes in fair values of equity investments

(21,915)

Changes in fair values of equity and long-term investments, net

(54,673)

(21,915)

Other non-cash items

8

0

Changes in operating assets and liabilities:

Receivables from collaborative arrangements

 

(2,707)

 

24,647

 

4,957

 

(2,707)

Prepaid expenses and other current assets

 

140

 

147

 

571

 

140

Accounts payable

 

112

 

133

 

(52)

 

112

Accrued personnel-related expenses and other accrued liabilities

 

(126)

 

166

 

227

 

(126)

Accrued interest payable

 

(2,484)

 

(2,489)

 

(2,484)

 

(2,484)

Operating lease liability

(72)

Net cash provided by operating activities

 

73,481

 

76,655

 

84,107

73,481

Cash flows from investing activities

Maturities of marketable securities

 

54,000

 

27,875

 

0

 

54,000

Purchases of marketable securities

 

(12,943)

 

(102,042)

 

0

 

(12,943)

Purchases of equity investments

(25,000)

Purchases of equity and long-term investments

 

(26,394)

 

(25,000)

Purchases of property and equipment

(13)

 

0

 

(13)

Net cash provided by (used in) investing activities

16,044

 

(74,167)

 

(26,394)

 

16,044

Cash flows from financing activities

Repurchase of shares to satisfy tax withholding

(55)

(65)

(25)

(55)

Payments of cash dividends to stockholders

(8)

Proceeds from issuances of common stock, net

225

319

0

225

Distributions to noncontrolling interest

(15,810)

(21,285)

(15,810)

Net cash provided by (used in) financing activities

 

(15,640)

 

246

Net cash used in financing activities

 

(21,310)

 

(15,640)

Net increase in cash and cash equivalents

 

73,885

 

2,734

 

36,403

 

73,885

Cash and cash equivalents at beginning of period

 

278,096

 

62,417

 

246,487

 

278,096

Cash and cash equivalents at end of period

$

351,981

$

65,151

$

282,890

$

351,981

Supplemental disclosure of cash flow information

Cash paid for interest

$

4,967

$

5,218

$

4,967

$

4,967

See accompanying notes to consolidated financial statements.

7

Table of Contents

INNOVIVA, INC.

NOTES TO CONSOLIDATED FINANCIAL STATEMENTS

(Unaudited)

1. Description of Operations and Summary of Significant Accounting Policies

Description of Operations

Innoviva Inc. (referred to as "Innoviva", the "Company", or "we" and other similar pronouns) is a company with a portfolio of royalties that includeand other healthcare assets. Our royalty portfolio contains respiratory assets partnered with Glaxo Group Limited (“GSK”), including RELVAR®/BREO® ELLIPTA® (fluticasone furoate/ vilanterol, “FF/VI”), ANORO® ELLIPTA® (umeclidinium bromide/ vilanterol, “UMEC/VI”) and TRELEGY® ELLIPTA® (the combination FF/UMEC/VI). Under the Long-Acting Beta2 Agonist (“LABA”) Collaboration Agreement, Innoviva is entitled to receive 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; and royalties from the sales of ANORO® ELLIPTA®, which tier upward at a range from 6.5% to 10%. Innoviva is also entitled to 15% of royalty payments made by GSK under its agreements originally entered into with us, and since assigned to Theravance Respiratory Company, LLC (“TRC”), including TRELEGY® ELLIPTA® and any other product or combination of products that may be discovered or developed in the future under the LABA Collaboration Agreement and the Strategic Alliance Agreement with GSK (referred to herein as the “GSK Agreements”), which have been assigned to TRC other than RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA®.

Basis of Presentation

The accompanying unaudited consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the United States of America (“US GAAP”) for interim financial information. Accordingly, they do not include all of the information and notes required by US GAAP for complete financial statements. In our opinion, the unaudited consolidated financial statements have been prepared on the same basis as audited consolidated financial statements and include all adjustments, consisting of only normal recurring adjustments, necessary for the fair presentation of our financial position, results of operations, comprehensive income and cash flows. The interim results are not necessarily indicative of the results of operations to be expected for the year ending December 31, 20202021 or any other period.

The accompanying unaudited consolidated financial statements include the accounts of Innoviva, our wholly-owned subsidiaries and certain variable interest entities for which we are the primary beneficiary. All intercompany balances and transactions have been eliminated in consolidation. For consolidated entities where we own or are exposed to less than 100% of the economics, we record net income (loss) attributable to noncontrolling interest in our unaudited consolidated statements of income equal to the percentage of the economic or ownership interest retained in such entities by the respective noncontrolling parties. The accompanying unaudited consolidated financial statements should be read in conjunction with the audited consolidated financial statements and notes thereto included in our Annual Report on Form 10-K for the year ended December 31, 20192020 filed with the Securities and Exchange Commission (“SEC”) on February 19, 25, 2021 (“2020 and as amended on February 21, 2020 (“2019 Form 10-K”).

Variable Interest EntityEntities

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 evaluation, if we determine we are the primary beneficiary of a VIE, we consolidate the entity intoin our financial statements. We consolidate the financial results

8

Table 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. As of March 31, 2020, and December 31, 2019, $16.1 million and $14.4 million, respectively, of the related party receivables from collaborative arrangements were attributable to TRC. The cash balance attributable to TRC as of March 31, 2020 was $15.3 million. The primary source of revenue for TRC is the royalties generated from the net sales of TRELEGYContents® ELLIPTA® by GSK. Total revenue for TRC related to TRELEGY® ELLIPTA® was $16.1 million and $7.3 million for the three months ended March 31, 2020 and 2019, respectively. Total operating expenses were $0.3 million for the three months ended March 31, 2020, compared to minimal amounts for the same period in 2019.

Equity Investments

We invest from time to time in equity securities of private or public companies. If we determine that we have control over these companies under either voting or VIE models, we include them in our consolidated financial statements. If we determine that we do not have control over these companies under either voting or VIE models, we then determine if we have an ability to exercise significant influence via voting interests, board representation or other business relationships.

We may account for the equity investments where we exercise significant influence using either an equity method of accounting or at fair value by electing the fair value option.option under Accounting Standards Codification ("ASC") Topic 825, Financial Instruments. If the fair value option is applied to an investment that would otherwise be accounted for under the equity method, we apply it to all our financial interests in the same entity (equity and debt, including guarantees) that are eligible items. All gains and losses from fair value changes, unrealized and realized, are presented as changes in fair values of equity and long-term investments, net on the consolidated statements of income.

8

Table of Contents

If we conclude that we do not have an ability to exercise significant influence over an investee, we may elect to account for an equity security without a readily determinable fair value using the measurement alternative described in ASC Topic 825. This measurement alternative allows us to measure the equity investment at its cost minus impairment, if any, plus or minus changes resulting from observable price changes in orderly transactions for the identical or a similar investment of the same issuer.

As of March 31, 2020, we accounted for our equity investments in common stock and warrants of Armata Pharmaceuticals, Inc. (NYSE American: ARMP) (“Armata”) at fair value by electing the fair value option and presented the investments as equity investments on the consolidated balance sheets.

Accounting Pronouncement Adopted by the Company

In June 2016,December 2019, the Financial Accounting Standards Board (“FASB”) issued Accounting Standards Update (“ASU”) No. 2016-132019-12, Financial Instruments-Credit Losses: Measurement of Credit Losses on Financial Instruments“Income Taxes (Topic 740): Simplifying the Accounting for Income Taxes”, as clarified in subsequent amendmentswhich is intended to simplify various aspects related to accounting for income taxes by removing certain exceptions to the initial guidance (collectively,general principles in Topic 326). Topic 326 requires measurement and recognition of expected credit losses for financial assets held at the reporting date based on historical experience, current conditions and reasonable and supportable forecast. ASC 326 must be adopted using a modified retrospective approach with a cumulative effect adjustment as of the beginning of the reporting period in which the guidance is adopted. Topic 326740. The pronouncement is effective for fiscal years, and for interim periods within those fiscal years, beginning after December 15, 2019,2020, with early adoption permitted. We adopted Topic 326740 effective January 1, 2020.2021. The adoption did not have a material impact on our consolidated financial statements.

In October 2020, the FASB issued ASU 2020-10, Codification Improvements. This ASU improves the codification by ensuring that all guidance that requires or provides an option for an entity to provide information in the notes to financial statements is codified in the disclosure section of the codification. The ASU also clarifies various topics in the codification so that entities can apply guidance more consistently. The ASU is effective for fiscal years beginning after December 15, 2020. We adopted ASU 2020-10 effective January 1, 2021. The adoption did not have a material impact on our consolidated financial statements.

Recently Issued Accounting Standards or Updates Not Yet Adopted

In August 2020, the FASB issued ASU 2020-06, Debt-Debt with Conversion and Other Options (Subtopic 470-20) and Derivatives and Hedging-Contracts in Entity's Own Equity (Subtopic 815-40): Accounting for Convertible Instruments and Contracts in an Entity's Own Equity, which is intended to simplify the accounting for convertible instruments by removing certain separation models in Subtopic 470-20 for convertible instruments. The ASU is effective for fiscal years beginning after December 15, 2021, and for interim periods within those fiscal years with early adoption permitted. We are currently in the process of evaluating the effects of the provisions of ASU 2020-06 on our consolidated financial statements.

2. Net Income Per Share

Basic net income per share attributable to Innoviva stockholders is computed by dividing net income attributable to Innoviva stockholders by the weighted-average number of shares of common stock outstanding. Diluted net income per share attributable to Innoviva stockholders is computed by dividing net income attributable to Innoviva stockholders by the weighted-average number of shares of common stock and dilutive potential common stock equivalents then outstanding. Dilutive potential common stock equivalents include the assumed exercise, vesting and issuance of employee stock awards using the treasury stock method, as well as common stock issuable upon assumed conversion of our convertible subordinated notes due 2023 (the “2023 Notes”) using the if converted method.

9

Table of Contents

Our convertible senior notes due 2025 (the “2025 Notes”) are convertible, based on the applicable conversion rate, into cash, shares of our common stock or a combination thereof, at our election. Our current intent is to settle the principal amount of the 2025 Notes in cash upon conversion. The impact of the assumed conversion premium to diluted net income per share is computed using the treasury stock method. As the average market price per share of our common stock as reported on The Nasdaq Global Select Market was lower than the initial conversion price of $17.26 per share, there was 0 dilutive effect of the assumed conversion premium for the three months ended March 31, 2021 and 2020, and 2019, respectively.

9

Table of Contents

The following table shows the computation of basic and diluted net income per share for the three months ended March 31, 20202021 and 2019:2020:

Three Months Ended March 31, 

Three Months Ended March 31, 

(In thousands except per share data)

    

2020

    

2019

     

2021

     

2020

Numerator:

Net income attributable to Innoviva stockholders, basic

$

65,437

$

33,790

 

$

94,123

 

$

65,437

Add: interest expense on 2023 Notes

1,180

1,415

 

1,204

 

1,180

Net income attributable to Innoviva stockholders, diluted

$

66,617

$

35,205

 

$

95,327

 

$

66,617

Denominator:

Weighted-average shares used to compute basic net income per share attributable to Innoviva stockholders

 

101,235

 

101,059

 

101,365

 

101,235

Dilutive effect of 2023 Notes

12,189

12,189

 

12,189

 

12,189

Dilutive effect of options and awards granted under equity incentive plan and employee stock purchase plan

85

128

 

70

 

85

Weighted-average shares used to compute diluted net income per share attributable to Innoviva stockholders

 

113,509

 

113,376

 

113,624

 

113,509

Net income per share attributable to Innoviva stockholders

Basic

$

0.65

$

0.33

 

$

0.93

 

$

0.65

Diluted

$

0.59

$

0.31

 

$

0.84

 

$

0.59

Anti-Dilutive Securities

The following common stock equivalents were not included in the computation of diluted net income per share because their effect was anti-dilutive:

Three Months Ended March 31, 

Three Months Ended March 31, 

(In thousands)

    

2020

    

2019

    

2021

    

2020

Outstanding options and awards granted under equity incentive plan and employee stock purchase plan

 

1,094

1,053

$

1,159

 

$

1,094

3. Revenue Recognition and Collaborative Arrangements

Net Revenue from Collaborative Arrangements

Net revenue recognized under our GSK Agreements was as follows:

Three Months Ended March 31, 

Three Months Ended March 31, 

(In thousands)

    

2020

    

2019

    

2021

    

2020

Royalties from a related party - RELVAR/BREO

$

56,149

$

42,740

$

56,390

$

56,149

Royalties from a related party - ANORO

9,850

8,570

 

10,500

 

9,850

Royalties from a related party - TRELEGY

16,135

7,329

22,084

16,135

Total royalties from a related party

82,134

58,639

 

88,974

 

82,134

Less: amortization of capitalized fees paid to a related party

 

(3,456)

 

(3,456)

 

(3,456)

 

(3,456)

Royalty revenue from GSK

$

78,678

$

55,183

$

85,518

$

78,678

10

Table of Contents

4. Consolidated Entities

We consolidate the financial results of TRC and Pulmoquine Therapeutics, Inc. (“Pulmoquine”), which we have determined to be VIEs. As we have the power to direct the economically significant activities of these entities and the obligation to absorb losses of, or the right to receive benefits from them, we are the primary beneficiary of the entities. We also consolidate the financial results of ISP Fund LP (the “Partnership”), our partnership with Sarissa Capital Management LP (“Sarissa Capital”), as we have determined that the Partnership is a VIE and we are its primary beneficiary.

Theravance Respiratory Company, LLC

The primary source of revenue for TRC is the royalties generated from the net sales of TRELEGY® ELLIPTA® by GSK. As of March 31, 2021, TRC held equity investments in InCarda Therapeutics, Inc. (“InCarda”) and ImaginAb, Inc. (“ImaginAb”). Refer to Note 5, “Financial Instruments and Fair Value Measurements,” for more information.

The summarized financial information for TRC is presented as follows:

Balance sheets

    

March 31,

December 31,

(In thousands)

   

2021

2020

Assets

  

Cash and cash equivalents

$

28,444

$

38,081

Receivables from collaborative arrangements

22,084

 

24,946

Prepaid expenses and other current assets

1

 

0

Equity and long-term investments

22,869

 

16,959

Total assets

73,398

 

79,986

Liabilities and LLC Members' Equity

 

  

Current liabilities

640

 

508

LLC members' equity

72,758

 

79,478

Total liabilities and LLC members' equity

$

73,398

$

79,986

Income statements

    

Three Months Ended March 31,

(In thousands)

   

2021

   

2020

Royalty revenue from a related party

$

22,084

$

16,135

Operating expenses

 

3,281

 

271

Income from operations

 

18,803

 

15,864

Other income (expense), net

 

0

 

36

Changes in fair values of equity and long-term investments

 

(483)

 

0

Net income

$

18,320

$

15,900

Pulmoquine Therapeutics, Inc.

In April 2020, we purchased 5,808,550 shares of Series A preferred stock of Pulmoquine for $5.0 million in cash and held a majority voting interest. Pulmoquine is a biotechnology company focused on the research and development of an aerosolized formulation of hydroxychloroquine to treat respiratory infections. As of March 31, 2021, Pulmoquine’s total assets, mainly attributable to cash and cash equivalents, were $3.3 million. Pulmoquine does not currently generate revenue. Total operating expense was de minimis for the three months ended March 31, 2021.

11

Table of Contents

ISP Fund LP

In December 2020, Innoviva Strategic Partners LLC, our wholly owned subsidiary (“Strategic Partners”), contributed $300.0 million to ISP Fund LP (the “Partnership”) for investing in “long” positions in the healthcare, pharmaceutical and biotechnology sectors and became a limited partner. The general partner of the Partnership (“General Partner”) is an affiliate of Sarissa Capital.

As of March 31, 2021, we held 100% of the economic interest of the Partnership. As of March 31, 2021, total assets of the Partnership were $304.7 million, of which all were attributable to equity and long-term investments. During the three months ended March 31, 2021, the Partnership incurred $0.4 million investment-related expenses, net of investment-related income and recorded an unrealized gain of $5.8 million from the changes of fair value as changes in fair values of equity and long-term investments, net on the consolidated statements of income.

5. Financial Instruments and Fair Value Measurements

Equity Investment in Armata

On January 27,During the first quarter of 2020, we entered into a securities purchase agreement to acquireInnoviva acquired 8,710,800 shares of Armata’s common stock and warrants to purchase up to 8,710,800 additional sharesan equal number of its common stockwarrants of Armata Pharmaceuticals, Inc. (“Armata”) for $25.0 million in cash.cash. Armata is a clinical stage biotechnology company focused on precisely targeted bacteriophage therapeutics for antibiotic-resistant infections.

On January 26, 2021, Innoviva Strategic Opportunities LLC (“ISO”), our wholly owned subsidiary, entered into a securities purchase agreement with Armata to acquire 6,153,847 shares of Armata common stock and warrants to purchase 6,153,847 additional shares of Armata common stock for approximately $20.0 million. The investment iswas closed in 2 tranches on January 26, 2021 and March 17, 2021. The investment continues to support Armata’s ongoing advancement of its bacteriophage development programs includingprograms. The additional investment in the expected first quarter of 2021 increased Innoviva and ISO’s combined ownership to 59.6%. Armata entered into a voting agreement with the Company and ISO, pursuant to which the Company and ISO agreed not to vote or take any action by written consent with respect to any common shares held by the Company and ISO that represent, in human studies related to Armata's lead phage candidate, AP-PA02, targeting Pseudomonas aeruginosa, as well as AP-SA02, its phage candidate targeting Staphylococcus Aureus.

The investment was closed in 2 tranches on February 12, 2020 and March 27, 2020. NaNthe aggregate, more than 49.5% of our board members joined Armata’s board. After the second closing, we own approximately 46.7%total number of shares of Armata’s common stock.stock issued and outstanding as of the record date for voting on the matters related to election or removal of Armata’s board members. Currently, 3 of the 8 members of Armata’s board of directors are also members of the board of directors of Innoviva.

The investment in Armata provides Innoviva and ISO the ability to have significant influence, but not control over Armata’s operations. Based on our evaluation, we determined that Armata is a VIE, but Innoviva isand ISO are not the primary beneficiary of the VIE. We electedcontinue to elect the fair value option under Accounting Standards Codification (“ASC”) Topic 825, Financial Instruments, to account for both Armata’s common stock and warrants at fair value.warrants. The fair value of Armata’s common stock is measured based on its closing market price. The warrants purchased in 2020 and 2021 have an exercise price of $2.87 and $3.25 per share, respectively, are exercisable immediately within five years from the issuance date of the warrants and include a cashless exercise option. We use the Black-Scholes-Merton pricing model to estimate the fair value of these warrants with the following input assumptions: Armata’s closing market price on the valuation date, the risk-free interest rate computed based on the U.S. Treasury yield, the remaining contractual term as the expected term, and the expected stock price volatility calculated based on the historical volatility of the common stock of Armata’sArmata and its peer companies.

As of March 31, 2021, the fair values of Armata’s common stock and warrants were estimated at $71.1 million and $54.2 million, respectively. As of December 31, 2020, the fair values of Armata’s common stock and warrants were estimated at $27.0$26.0 million and $19.9$18.0 million, respectively. The total fair value of both financial instruments in the amount of $46.9$125.3 million and $44.0 million was recorded as equity and long-term investments on the consolidated balance sheets.sheets as of March 31, 2021 and December 31, 2020, respectively. The changes in the fair values in the amount of $61.2 million and $21.9 million for the three months ended March 31, 2021 and 2020, respectively, were recorded as changes in fair value of equity and long-term investments, net on the consolidated statements of income.

Equity Investment in Entasis

During the second quarter of 2020, we purchased 14,000,000 shares of common stock as well as warrants to purchase 14,000,000 additional shares of common stock of Entasis Therapeutics, Inc. (“Entasis”) for approximately $35.0 million in cash. Entasis is a clinical-stage biotechnology company focused on the discovery and development of novel antibacterial products.

12

Table of Contents

During the third quarter of 2020, we purchased 4,672,897 shares of Entasis common stock as well as warrants to purchase 4,672,897 additional shares of its common stock for approximately $12.5 million in cash. Innoviva has a right to designate 2 members to Entasis’ board. As of March 31, 2021 and the date hereof, 0 Innoviva designees are serving on Entasis’ six-member board. As of March 31, 2021, we owned approximately 51.0% of Entasis’s common stock.

The investment in Entasis provides Innoviva the ability to have significant influence, but not control over Entasis’ operations. Based on our evaluation, we determined that Entasis is a VIE, but Innoviva is not the primary beneficiary of the VIE. We elected the fair value option to account for both Entasis's common stock and warrants at fair value. The fair value of Entasis's common stock is measured based on its closing market price at each balance sheet date. The warrants have an exercise price of $2.50 per share for those warrants acquired in the second quarter of 2020 and an exercise price of $2.675 per share for the warrants acquired in the third quarter of 2020. The warrants are exercisable immediately within five years from the issuance date of the warrants and include a cashless exercise option. We use the Black-Scholes-Merton pricing model to estimate the fair value of these warrants.

As of March 31, 2021, the fair values of Entasis’s common stock and warrants were estimated at $40.0 million and $26.6 million, respectively. As of December 31, 2020, the fair values of Entasis’s common stock and warrants were estimated at $46.1 million and $31.9 million, respectively. The total fair value of both financial instruments in the amount of $66.6 million and $78.0 million was recorded as equity and long-term investments on the consolidated balance sheets as of March 31, 2021 and December 31, 2020, respectively. We recorded $21.9$11.5 million of unrealized gains andloss from the changes of fair value changes in Armata’s investments as changes in fair values of equity and long-term investments, net on the consolidated statements of income for the three months ended March 31, 2020.2021.

Equity Investment in InCarda

In October, 2020, TRC purchased 20,469,432 shares of Series C preferred stock and warrants to purchase 5,117,358 additional shares of Series C preferred stock of InCarda Therapeutics, Inc. for $15.0 million. $0.8 million was incurred for investment due diligence costs and recorded as part of the equity investment on the consolidated balance sheets. InCarda is a privately held biopharmaceutical company focused on developing inhaled therapies for cardiovascular diseases. As of March 31, 20201 and as of the date hereof, 1 of InCarda’s 8 board members is designated by TRC. As of March 31, 2021, TRC held 13.0% of InCarda‘s outstanding equity.

The investment in InCarda does not provide TRC the ability to control or have significant influence over InCarda's operations. Based on our evaluation, we determined that InCarda is a VIE, but TRC is not the primary beneficiary of the VIE. We account for our investment in the Series C preferred shares in InCarda using the measurement alternative. Under the measurement alternative, the equity investment is initially recorded at its allocated cost, but the carrying value may be adjusted through earnings upon an impairment or when there is an observable price change involving the same or a similar investment with the same issuer. The warrants are recorded at fair value and subject to remeasurement at each balance sheet date. The warrants are exercisable immediately with an exercise price of $0.7328 per share and expire on October 6, 2021, one year from the issuance date. We use the Black-Scholes-Merton pricing model to estimate the fair value of the warrants with the following input assumptions: the exercise price of the warrants, the risk-free interest rate computed based on the U.S. Treasury yield, the remaining contractual term as the expected term, and the expected stock price volatility calculated based on the historical volatility of the common stock of its peer companies.

As of March 31, 2021 and December 31, 2020, the fair value of InCarda’s warrants was estimated at $0.7 million and $1.1 million, respectively, and recorded as equity and long-term investments on the consolidated balance sheets. We recorded $0.5 million unrealized loss from the changes of fair value as changes in fair values of equity and long-term investments, net on the consolidated statements of income for the three months ended March 31, 2021. There was 0 impairment or other change to the value of InCarda’s Series C preferred stock of $15.8 million as of March 31, 2021.

Equity Investment in ImaginAb

On March 18, 2021, TRC entered into a securities purchase agreement with ImaginAb, Inc. to purchase 4,051,724 shares of ImaginAb Series C preferred stock for $4.7 million. On the same day, TRC also entered into a securities purchase agreement with one of ImaginAb’s common stockholders to purchase 4,097,157 shares of ImaginAb common stock for $1.3 million. ImaginAb is a privately held biotechnology company focused on clinically managing cancer and autoimmune diseases via molecular imaging. $0.4 million was incurred for investment due diligence costs and execution and recorded as part of the equity investment on the consolidated balance sheets. As of the date hereof, 1 of ImaginAb’s 7 board members is designated by TRC. As of March 31, 2021, TRC held 13.0% of ImaginAb equity ownership.

13

Table of Contents

The investment in ImaginAb does not provide TRC the ability to control or have significant influence over ImaginAb’s operations. Based on our evaluation, we determined that ImaginAb is a VIE, but TRC is not the primary beneficiary of the VIE. Because ImaginAb’s equity securities are not publicly traded and do not have a readily determinable fair value, we have accounted for our investment in ImaginAb’s Series C preferred stock and common stock using the measurement alternative. Under the measurement alternative, the equity investment is initially recorded at its allocated cost, but the carrying value may be adjusted through earnings upon an impairment or when there is an observable price change involving the same or a similar investment with the same issuer. As of March 31, 2021, $6.4 million was recorded as equity and long-term investments on the consolidated balance sheets.

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:

March 31, 2020

March 31, 2021

    

    

Gross

    

Gross

    

Gross

Gross

Unrealized

Unrealized

Estimated

Unrealized

Unrealized

Estimated

(In thousands)

Amortized Cost

Gains

Losses

Fair Value

    

Amortized Cost

    

Gains

    

Losses

    

Fair Value

U.S. government securities

$

13,958

$

41

$

$

13,999

U.S. commercial paper

 

48,964

 

 

 

48,964

Money market funds

 

285,309

 

 

 

285,309

Money market funds(1)

$

248,932

$

0

$

0

$

248,932

Total

$

348,231

$

41

$

$

348,272

$

248,932

$

0

$

0

$

248,932

(1)Money market funds were included in cash and cash equivalents on the consolidated balance sheets.

December 31, 2019

December 31, 2020

    

    

Gross

    

Gross

    

Gross

Gross

Unrealized

Unrealized

Estimated

Unrealized

Unrealized

Estimated

(In thousands)

Amortized Cost

Gains

Losses

Fair Value

    

Amortized Cost

    

Gains

    

Losses

    

Fair Value

U.S. government securities

$

53,799

$

35

$

$

53,834

U.S. commercial paper

 

18,915

 

 

 

18,915

Money market funds

 

233,992

 

 

 

233,992

Money market funds (1)

$

204,808

$

0

$

0

$

204,808

Total

$

306,706

$

35

$

$

306,741

$

204,808

$

0

$

0

$

204,808

(1)Money market funds were included in cash and cash equivalents on the consolidated balance sheets.

As of March 31, 2020, 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.

There was 0no credit loss of these securitiesto the money market funds as of March 31, 2020.2021.

1114

Table of Contents

Fair Value Measurements

Our available-for-sale securities and equity investments are measured at fair value on a recurring basis and our debt is carried at amortized cost basis. The estimated fair values were as follows:

Estimated Fair Value Measurements as of March 31, 2020 Using:

Estimated Fair Value Measurements as of March 31, 2021 Using:

Quoted Price in

Quoted Price

Significant

Active Markets

Significant Other

Significant

in Active 

Other

Significant

for Identical

Observable

Unobservable

Markets for 

Observable

Unobservable

Types of Instruments

Assets

Inputs

Inputs

Identical Assets

Inputs

Inputs

(In thousands)

    

Level 1

    

Level 2

    

Level 3

    

Total

    

Level 1

    

Level 2

    

Level 3

    

Total

Assets

U.S. government securities

$

$

13,999

$

$

13,999

U.S. commercial paper

 

 

48,964

 

 

48,964

Money market funds

 

285,309

 

 

 

285,309

$

248,932

$

0

$

0

$

248,932

Investments held by ISP Fund LP (1)

304,696

0

0

304,696

Equity investment - Armata Common Stock

27,003

27,003

71,053

0

0

71,053

Equity investment - Armata Warrants

19,912

19,912

0

54,166

0

54,166

Equity investment - Entasis Common Stock

39,960

0

0

39,960

Equity investment - Entasis Warrants

0

26,580

0

26,580

Equity investment - InCarda Warrants

0

0

664

664

Total assets measured at estimated fair value

$

312,312

$

82,875

$

$

395,187

$

664,641

$

80,746

$

664

$

746,051

Debt

2023 Notes

$

$

216,886

$

$

216,886

$

0

$

242,336

$

0

$

242,336

2025 Notes

 

 

191,538

 

 

191,538

0

203,513

0

203,513

Total fair value of debt

$

$

408,424

$

$

408,424

$

0

$

445,849

$

0

$

445,849

(1)The investments, which consisted of equity investments of $130.5 million and money market funds of $174.2 million, held by ISP Fund LP were subject to a 36-month lock-up period from our initial contribution date, December 11, 2020.

Estimated Fair Value Measurements as of December 31, 2019 Using:

Estimated Fair Value Measurements as of December 31, 2020 Using:

Quoted Price in

Quoted Price

Significant

Active Markets

Significant Other

Significant

in Active 

Other

Significant

for Identical

Observable

Unobservable

Markets for 

Observable

Unobservable

Types of Instruments

Assets

Inputs

Inputs

Identical Assets

Inputs

Inputs

(In thousands)

    

Level 1

    

Level 2

    

Level 3

    

Total

    

Level 1

    

Level 2

    

Level 3

    

Total

Assets

U.S. government securities

$

$

53,834

$

$

53,834

U.S. commercial paper

 

 

18,915

 

 

18,915

Money market funds

 

233,992

 

 

 

233,992

$

204,808

$

0

$

0

$

204,808

Investments held by ISP Fund LP (1)

299,288

0

0

299,288

Equity investment - Armata Common Stock

25,958

 

0

 

0

 

25,958

Equity investment - Armata Warrants

0

 

18,049

 

0

 

18,049

Equity investment - Entasis Common Stock

46,122

 

0

 

0

 

46,122

Equity investment - Entasis Warrants

0

 

31,882

 

0

 

31,882

Equity investment - InCarda Warrants

0

0

1,147

1,147

Total assets measured at estimated fair value

$

233,992

$

72,749

$

$

306,741

$

576,176

$

49,931

$

1,147

$

627,254

Debt

2023 Notes

$

$

243,394

$

$

243,394

$

0

$

239,779

$

0

$

239,779

2025 Notes

208,976

208,976

0

206,135

0

206,135

Total fair value of debt

$

$

452,370

$

$

452,370

$

0

$

445,914

$

$

445,914

(1)The investments, which consisted of equity investments of $14.5 million and money market funds of $284.8 million, held by ISP Fund LP were subject to a 36-month lock-up period from our initial contribution date, December 11, 2020.

The fair valuevalues of our marketable securitiesequity investments in Armata and Entasis's common stock and those investments held by ISP Fund LP are based on the quoted prices in active markets and are classified as Level 1 financial instruments. The fair values of the warrants of Armata and Entasis classified within Level 2 isare 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.

15

Table of Contents

The fair value of our equity investment in Armata’s commons stock is based on Armata’s closing market price per share at the reporting date and is a Level 1 financial instrument. The fair value of our equity investment in Armata’sInCarda’s warrants is classified withinas Level 23 financial instruments as InCarda’s securities are not publicly traded and the assumptions used in the valuation model are based on thesignificant unobservable and observable inputs that include Armata’s closing market price, its comparable companies’ market data and U.S. Treasury yield.including those of publicly traded peer companies.

The fair valuevalues of our 2023 Notes and of our 2025 Notes isare based on recent trading prices of the respective instruments.

5. Stock-Based Compensation

Stock-based compensation expense is included in the consolidated statements of income as follows:

Three Months Ended March 31, 

(In thousands)

    

2020

    

2019

General and administrative

$

435

$

605

12

Table of Contents

6. Stock-Based Compensation

Stock- Based Compensation Expense

Stock-based compensation expense was included in the consolidated statements of income as follows:

Three Months Ended March 31, 

(In thousands)

    

2021

    

2020

General and administrative

$

451

$

435

Valuation Assumptions

Black-Scholes-Merton assumptions used in calculating the estimated value of our stock options on the date of grant were as follows:

Three Months Ended 

 

    

March 31, 2021

 

Risk-free interest rate

 

1.1

%

Expected term (in years)

 

6.11

Volatility

 

45.6

%

Dividend yield

 

0.0

%

Weighted-average estimated fair value of stock options granted

$

5.42

There were 0 grants of stock options during the three months ended March 31, 2020.

6.7. Debt

Our debt consists of:

March 31, 

December 31, 

March 31, 

December 31, 

(In thousands)

    

2020

    

2019

    

2021

    

2020

2023 Notes

 

$

240,984

 

$

240,984

$

240,984

$

240,984

2025 Notes

192,500

192,500

192,500

192,500

Total debt

433,484

433,484

433,484

433,484

Unamortized debt discount and issuance costs

(54,332)

(56,364)

(45,756)

(47,967)

Net long-term debt

 

$

379,152

 

$

377,120

$

387,728

$

385,517

Convertible Senior Notes Due 2025

In accordance with accounting guidance for debt with conversion and other options, we separately account for the liability and equity components of the 2025 Notes by allocating the proceeds between the liability component and the embedded conversion option (“equity component”) due to our ability to settle the conversion obligation of the 2025 Notes in cash, common stock or a combination of cash and common stock, at our option. The carrying amount of the liability component was calculated by measuring the fair value of a similar liability that does not have an associated convertible feature using the income approach. The allocation was performed in a manner that reflected our non-convertible debt borrowing rate for similar debt. The equity component of the 2025 Notes was recognized as a debt discount and represents the difference between the proceeds from the issuance of the 2025 Notes and the fair value of the liability of the 2025 Notes on the date of issuance. The excess of the principal amount of the liability component over its carrying amount (“debt discount”) is amortized to interest expense using the effective interest method over the term of the 2025 Notes. The equity component is not remeasured as long as it continues to meet the conditions for equity classification.

16

Table of Contents

Our outstanding 2025 Notes balances consisted of the following:

March 31, 

December 31, 

March 31, 

December 31, 

(In thousands)

    

2020

    

2019

    

2021

    

2020

Liability component

 

 

 

  

Principal

$

192,500

$

192,500

$

192,500

$

192,500

Debt discount and issuance costs, net

 

(52,703)

 

(54,597)

 

(44,697)

 

(46,766)

Net carrying amount

 

$

139,797

 

$

137,903

$

147,803

$

145,734

Equity component, net

$

65,361

$

65,361

$

65,361

$

65,361

The following table sets forth total interest expense recognized related to the 2025 Notes for the three months ended March 31, 20202021 and 2019:2020:

Three Months Ended March 31, 

Three Months Ended March 31, 

(In thousands)

    

2020

2019

    

2021

    

2020

Contractual interest expense

$

1,203

$

1,203

$

1,203

$

1,203

Amortization of debt issuance costs

145

133

 

159

 

145

Amortization of debt discount

 

1,749

1,601

 

1,911

 

1,749

Total interest and amortization expense

 

$

3,097

$

2,937

$

3,273

$

3,097

13

Table of Contents

Debt Maturities

The aggregate scheduled maturities of our long-term debt as of March 31, 2020, are2021 were as follows:

(In thousands)

    

 

    

Years ending December 31:

 

2020 to 2022

$

2021 to 2022

$

0

2023

240,984

 

240,984

2024

 

0

Thereafter

192,500

2025

192,500

Total

 

$

433,484

$

433,484

7.8. Commitments and Contingencies

Operating Lease

Future minimum operating lease payments on our corporate headquarters as of March 31, 2020 are2021 were as follows:

(In thousands)

    

Years ending December 31:

Remainder of 2020

$

90

2021

 

123

2022

 

109

Thereafter

 

Total

$

322

(In thousands)

    

Years ending December 31:

Remainder of 2021

$

92

2022

109

2023

0

Thereafter

0

Total

$

201

LegalProceedings

From time to time, the Company is involved in legal proceedings in the ordinary course of its business. Currently, we believe that no litigation or arbitration, either individually or in the aggregate, to which we are presently a party is likely to have a material adverse effect on our operating results or financial position.

17

Table of Contents

8.9. Income Taxes

Provisional income tax expense for the three months ended March 31, 2021 and 2020 and 2019 was $15.9$19.7 million and $8.5$15.9 million, respectively. The Company’s effective income tax rate for the three months ended March 31, 20202021 was 16.8%15.2%, compared to 17.5%16.8% for the same period in 2019.2020. The difference betweenincome tax expense for the Company’sthree months ended March 31, 2021 and 2020 was determined based upon estimates of the Company's effective income tax rates in various jurisdictions. Our effective income tax rate andfor the three months ended March 31, 2021 was lower than the U.S. federal statutory income tax rate of 21% is21% due primarily attributable to state income tax, non-deductible expenses and noncontrolling interest.

9. Subsequent Events

On April 12, 2020, Innoviva and Entasis Therapeutics Holdings Inc. (“Entasis”), a clinical-stage biotechnology company focused on the discovery and development of novel antibacterial products, entered into a securities purchase agreement pursuant to which Innoviva will purchase up to approximately $35.0 million in Entasis common stock and warrants upon satisfaction of certain closing conditions. This transaction is expected to occur in 2 tranches during the second quarter of 2020. Innoviva will be entitled to appoint 2 directors to serve on Entasis's Board of Directors for so long as Innoviva and its affiliates hold at least 15% of the outstanding shares of Entasis’ common stock on a fully-diluted basis, or 1 director for so long as Innoviva and its affiliates hold at least 8% of the outstanding shares of Entasis’ common stock on a fully-diluted basis.

1418

Table of Contents

Item 2. Management’s Discussion and Analysis of Financial Condition and Results of Operations

Forward-Looking Statements

The information in this Quarterly Report on Form 10-Q contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended (“Securities Act”), and Section 21E of the Securities Exchange Act of 1934, as amended. Such forward-looking statements involve substantial risks, uncertainties, and assumptions. All statements contained herein that are not of historical fact, including, without limitation, statements regarding our strategy, future operations, future financial position, future revenue, projected costs, prospects, plans, intentions, expectations, goals and objectives, may be forward-looking statements. The words “anticipates,” “believes,” “could,” “designed,” “estimates,” “expects,” “goal,” “intends,” “may,” “objective,” “plans,” “projects,” “pursue,” “will,” “would” and similar expressions (including the negatives thereof) are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. We may not actually achieve the plans, intentions, expectations or objectives disclosed in our forward-looking statements and the assumptions underlying our forward-looking statements may prove incorrect. Therefore, you should not place undue reliance on our forward-looking statements. Actual results or events could differ materially from the plans, intentions, expectations and objectives disclosed in the forward-looking statements that we make. All written and verbal forward-looking statements attributable to us or any person acting on our behalf are expressly qualified in their entirety by the cautionary statements contained or referred to in this section. Important factors that we believe could cause actual results or events to differ materially from our forward-looking statements include, but are not limited to, risks related to: lower than expected future royalty revenue from respiratory products partnered with GSK; the commercialization of RELVAR®/BREO® ELLIPTA®, ANORO® ELLIPTA® and TRELEGY® ELLIPTA® in the jurisdictions in which these products have been approved; substantial competition from products discovered, developed, launched and commercialized both by GSK and by other pharmaceutical companies; the strategies, plans and objectives of the Company (including(related to the Company’s growth strategy and corporate development initiatives beyond the Company’s existing respiratory portfolio); the timing, manner and amount of capital deployment, including potential capital returns to stockholders; risks related to the status and timing of clinical studies, data analysis and communication of results; the potential benefits and mechanisms of action of product candidates; expectations for product candidates through development and commercialization; the timing of regulatory approval of product candidates;Company’s growth strategy; projections of revenue, expenses and other financial items; the impact of the COVID-19 pandemic;items and risks discussed in “Risk Factors” in Item 1A of Part I of our Annual Report on Form 10-K for the year ended December 31, 20192020 filed with the Securities and Exchange Commission (“SEC”) on February 19, 25, 2021, (“2020 (“2019 Form 10-K”) and Item 1A of Part II of our Quarterly Reports on Form 10-Q and below in “Management’s Discussion and Analysis of Financial Condition and Results of Operations” in this Item 2 of Part I. All forward-looking statements in this Quarterly Report on Form 10-Q are based on current expectations as of the date hereof and we do not assume any obligation to update any forward-looking statements on account of new information, future events or otherwise, except as required by law.

We encourage you to read our consolidated financial statements contained in this Quarterly Report on Form 10-Q. We also encourage you to read Item 1A of Part I of our 20192020 Form 10-K and Item 1A of Part II of our Quarterly Reports on Form 10-Q entitled “Risk Factors,” which contain a more complete discussion of the risks and uncertainties associated with our business. In addition to the risks described above and in Item 1A of Part I of our 20192020 Form 10-K and Item 1A of Part II of this report, other unknown or unpredictable factors also could affect our results. Therefore, the information in this report should be read together with other reports and documents that we file with the SEC from time to time, including on Form 10-K, Form 10-Q and Form 8-K, which may supplement, modify, supersede or update those risk factors. As a result of these factors, we cannot assure you that the forward-looking statements in this report will prove to be accurate. Furthermore, if our forward-looking statements prove to be inaccurate, the inaccuracy may be material. In light of the significant uncertainties in these forward-looking statements, you should not regard these statements as a representation or warranty by us or any other person that we will achieve our objectives and plans in any specified time frame, or at all.

1519

Table of Contents

OVERVIEW

Executive Summary

Innoviva, Inc. (“Innoviva”, the “Company”, the “Registrant” or “we” and other similar pronouns) is a company with a portfolio of royalties that includeand other healthcare assets. Our royalty portfolio contains respiratory assets partnered with Glaxo Group Limited (“GSK”), including RELVAR®/BREO® ELLIPTA® (fluticasone furoate/ vilanterol, “FF/VI”), ANORO® ELLIPTA® (umeclidinium bromide/ vilanterol, “UMEC/VI”) and TRELEGY® ELLIPTA® (the combination FF/UMEC/VI). Under the Long-Acting Beta2 Agonist (“LABA”) Collaboration Agreement, Innoviva is entitled to receive 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; and royalties from the sales of ANORO® ELLIPTA®, which tier upward at a range from 6.5% to 10%. Innoviva is also entitled to 15% of royalty payments made by GSK under its agreements originally entered into with us, and since assigned to Theravance Respiratory Company, LLC (“TRC”), including TRELEGY® ELLIPTA® and any other product or combination of products that may be discovered or developed in the future under the LABA Collaboration Agreement and the Strategic Alliance Agreement with GSK (referred to herein as the “GSK Agreements”), which have been assigned to TRC other than RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA®.

Our company structure and organization are tailored to our focused activities of managing our respiratory assets partnered with GSK, the commercialoptimizing our operations and developmental obligations associated with the GSK Agreements, intellectual property, licensing operations, business development activities and providing for certain essential reporting and management functions of a public company. As of March 31, 2020, we had five employees.augmenting capital allocation. Our revenues consist of royalties and potential milestone payments, if any, from our respiratory partnership agreements with GSK.

Recent Highlights

GSK Net Sales:
oFirst quarter 20202021 net sales of RELVAR®/BREO® ELLIPTA® by GSK were $374.3$375.9 million, up 31%slightly from $284.9$374.3 million in the firstsame quarter of 2019,2020, with $147.5$154.6 million in net sales from the U.S. market and $226.8$221.3 million from non-U.S. markets.
oFirst quarter 20202021 net sales of ANORO® ELLIPTA® by GSK were $151.6$161.5 million, up 15%7% from $131.8$151.6 million in the firstsame quarter of 2019,2020, with $81.8$88.4 million net sales from the U.S. market and $69.8$73.1 million from non-U.S. markets.
oFirst quarter 20202021 net sales of TRELEGY® ELLIPTA® by GSK were $248.2$339.8 million, up significantly37% from $112.7$248.2 million in the firstsame quarter of 2019,2020, with $172.4$237.5 million in net sales from the U.S. market and $75.8$102.3 million in net sales from non-U.S. markets.
Capital Allocation:
oOn April 12, 2020, Innoviva, Inc. entered into a securities purchase agreement with Entasis Therapeutics, Inc. (NASDAQ: ETTX), pursuant to which it will purchase, upon satisfaction of certain closing conditions, approximately $35.0 million of Entasis common stock and warrant securities.
oDuring the first quarter of 2020,2021, the Company’s wholly owned subsidiary, Innoviva Strategic Opportunities LLC, invested $25.0$20.0 million in 8,710,800to acquire 6.2 million shares of Armata's common stock and warrants to purchase up to 8,710,800an additional 6.2 million shares of the common stock at $3.25 per share. With this additional investment, Innoviva collectively owned approximately 59.6% of Armata Pharmaceutical Inc.Armata's common stock as of March 31, 2021.
New Director:
oOn March 9, 2021, the Company appointed Deborah L. Birx, M.D., to its Board of Directors, where she serves as an independent director. Dr. Birx is a world renowned medical expert and leader who most recently served as the response coordinator of the White House Coronavirus Task Force. Dr. Birx’s career highlights also include having served as Ambassador-at-Large, when she assumed the role of the Coordinator of the United States Government Activities to Combat HIV/AIDS and U.S. Special Representative for Global Health Diplomacy. Dr. Birx also served as the U.S. Global AIDS Coordinator where she oversaw the President’s Emergency Plan for AIDS Relief (PEPFAR) at the Centers for Disease Control and Prevention and as the Director of the U.S. Military HIV Research Program (USMHRP) at the Walter Reed Army Institute of Research.

1620

Table of Contents

Collaborative Arrangements with GSK

LABA Collaboration

In November 2002, we entered into ourthe LABA Collaboration Agreementcollaboration with GSK to develop and commercialize once-daily LABA products for the treatment of chronic obstructive pulmonary diseasedisorder (“COPD”) and asthma. Theasthma (the “LABA Collaboration Agreement”). For the treatment of COPD, the collaboration has developed three combination products: (1) RELVAR®/BREO® ELLIPTA® (FF/VI) (BREO® ELLIPTA® is the proprietary name in the U.S. and Canada and RELVAR® ELLIPTA® is the proprietary name outside the U.S. and Canada), a once-daily combination medicine consisting of a LABA, vilanterol (VI), and an inhaled corticosteroid (ICS), fluticasone furoate (FF), (2) ANORO® ELLIPTA® (UMEC/VI), a once-daily medicine combining a long-acting muscarinic antagonist (“LAMA”), umeclidinium bromide (UMEC), with a LABA, VI and (3) TRELEGY® ELLIPTA®, fluticasone furoate/umeclidinium/vilanterol (FF/UMEC/VI), a once-daily combination medicine consisting of an ICS, LAMA and LABA.

RELVAR®/BREO® ELLIPTA® (“FF/VI”) (BREO® ELLIPTA® is the proprietary name in the U.S. and Canada and RELVAR® ELLIPTA® is the proprietary name outside the U.S. and Canada), a once-daily combination medicine consisting of a LABA, vilanterol (VI), and an inhaled corticosteroid (“ICS”), fluticasone furoate (“FF”),
ANORO® ELLIPTA® (“UMEC/VI”), a once-daily medicine combining a long-acting muscarinic antagonist (“LAMA”), umeclidinium bromide (“UMEC”), with a LABA, vilanterol (VI), and
TRELEGY® ELLIPTA® (the combination FF/UMEC/VI), a once-daily combination medicine consisting of an ICS, LAMA and LABA.

As a result of the launch and approval of RELVAR®/BREO® ELLIPTA® and ANORO® ELLIPTA® in the U.S., Japan and Europe, in accordance with the LABA Collaboration Agreement, we paid milestone fees to GSK totaling $220.0 million during the year ended December 31, 2014. 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 products.

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 Bifunctional Muscarinic Antagonist-Beta2 Agonist ("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 was funded in full by GSK. GSK is in the process of determining the next steps for the program. For a detailed discussion of our alliance with GSK, see Management’s Discussion and Analysis of Financial Condition and Results of Operations contained in Part II, Item 7 of our 2019 Form 10-K.

Critical Accounting Policies and Estimates

Our management’s discussion and analysis of our financial condition and results of operations is based on our financial statements, which have been prepared in accordance with accounting principles generally accepted in the United States of America (“US GAAP”). The preparation of these financial statements requires us to make estimates and assumptions that affect the reported amounts of assets and liabilities and the disclosure of contingent assets and liabilities as of the date of the financial statements, as well as the reported revenue generated and expenses incurred during the reporting periods. Our estimates are based on our historical experience and on various other factors that we believe are reasonable under the circumstances, the results of which form the basis for making judgments about the carrying value of assets and liabilities that are not readily apparent from other sources. Actual results may differ from these estimates under different assumptions or conditions.

As part of our capital allocation strategies, we invest from time to time in equity securities of private or public companies. We also enter into strategic partnerships in order to accelerate the execution of our strategy and enhance returns on our capital. If we determine that we have control over these companies or partnerships, we consolidate the financial statements of these companies or partnerships. If we determine that we do not have control over these companies or partnerships under either voting or variable interest entity (“VIE”)VIE models, we then determine if we have an ability to exercise significant influence via voting interests, board representation or other business relationships.

We may account for the equity investments where we exercise significant influence using either an equity method of accounting or at fair value by electing the fair value option.option under Accounting Standards Codification ("ASC") Topic 825, Financial Instruments. If the fair value option is applied to an investment that would otherwise be accounted for under the equity method, we apply it to all our financial interests in the same entity (equity and debt, including guarantees) that are eligible items. All gains and losses from fair value changes, unrealized and realized, are presented as changes in fair values of equity and long-term investments, net on the consolidated statements of income.

If we conclude that we do not have an ability to exercise significant influence over an investee, we may elect to account for an equity security without a readily determinable fair value using the measurement alternative as prescribed by ASC Topic 825. This measurement alternative allows us to measure the equity investment at its cost minus impairment, if any, plus or minus changes resulting from observable price changes in orderly transactions for the identical or a similar investment of the same issuer.

There were no other significant changes to our critical accounting policies and estimates. Management’s Discussion and Analysis of Financial Condition and Results of Operations contained in Part II, Item 7 of our Annual Report on Form 10-K for the year ended December 31, 20192020 filed with the SEC on February 19, 202025, 2021 provides a more complete discussion of our critical accounting policies and estimates.

1721

Table of Contents

Results of Operations

Net Revenue

Total net revenue, as compared to the prior year period, was as follows:

Three Months Ended March 31, 

Change

 

Three Months Ended March 31, 

Change

 

(In thousands)

    

2020

    

2019

    

$

    

%

 

    

2021

    

2020

    

$

    

%

 

Royalties from a related party - RELVAR/BREO

$

56,149

$

42,740

$

13,409

31

%

$

56,390

$

56,149

$

241

0

%

Royalties from a related party - ANORO

 

9,850

 

8,570

 

1,280

15

%

 

10,500

 

9,850

 

650

7

%

Royalties from a related party - TRELEGY

 

16,135

 

7,329

 

8,806

120

%

 

22,084

 

16,135

 

5,949

37

%

Total royalties from a related party

 

82,134

 

58,639

 

23,495

40

%

 

88,974

 

82,134

 

6,840

8

%

Less: amortization of capitalized fees paid to a related party

 

(3,456)

 

(3,456)

 

 

(3,456)

 

(3,456)

 

0

%

Royalty revenue from GSK

$

78,678

$

55,183

$

23,495

43

%

$

85,518

$

78,678

$

6,840

9

%

Total net revenue increased to $78.7$85.5 million for the three months ended March 31, 2020,2021, compared to $55.2$78.7 million for the same period a year ago primarily due to favorable adjustments and the growth in prescriptions for our royalty productsrespiratory products.

Research & Development

Research and a one-time favorable rebate adjustmentdevelopment (“R&D”) expenses attributable to Pulmoquine’s product development efforts were de minimis for sales of RELVAR®/BREO® ELLIPTA® in the U.S.three months ended March 31, 2021. We did not incur any R&D expenses during the three months ended March 31, 2020.

General & Administrative

General and administrative expenses, as compared to the prior year period, were as follows:

Three Months Ended March 31, 

Change

 

Three Months Ended March 31, 

Change

(In thousands)

    

2020

    

2019

    

$

    

%

 

    

2021

    

2020

    

$

    

%

General and administrative expenses

$

2,563

$

3,015

$

(452)

(15)

%

General and administrative

$

5,986

$

2,563

$

3,423

*

*Not Meaningful

General and administrative expenses for the three months ended March 31, 2020 decreased2021 increased compared to the same period in 2019, attributable2020 mainly due to overall lower operating$3.1 million legal and related expenses incurred.incurred for the arbitration initiated by Theravance Biopharma against the Company and TRC. These arbitration related legal fees were recognized in TRC’s statement of income.

Other Income, net and Interest Income

Other income, net and interest income, as compared to the prior year period, were as follows:

Three Months Ended March 31, 

Change

Three Months Ended March 31, 

Change

(In thousands)

    

2020

    

2019

    

$

    

%

    

2021

    

2020

    

$

    

%

Other income, net

$

68

$

1

$

67

*

Other income (expense), net

$

(433)

$

68

$

(501)

*

Interest income

 

1,302

 

975

327

34%

$

30

$

1,302

$

(1,272)

(98)

%

*Not Meaningful

Interest income increaseddecreased for the three months ended March 31, 2020, as2021 compared to the same period a year ago primarily due to higher cash and investment balances.lower interest rates impacted by the COVID-19 pandemic.

22

Table of Contents

Interest Expense

Interest expense, as compared to the prior year period, was as follows:

Three Months Ended March 31, 

Change

 

Three Months Ended March 31, 

Change

 

(In thousands)

    

2020

    

2019

    

$

    

%

 

    

2021

    

2020

    

$

    

%

 

Interest expense

$

4,516

$

4,617

$

(101)

(2)

%

$

4,694

$

4,516

$

(178)

4

%

Interest expense decreased slightlyincludes the amortization of debt discount and issuance costs for the three months ended March 31, 2020, compared to the same period a year ago primarilyour convertible notes. The increase in interest expense was mainly due to the lower average outstandingmore debt balance.discount and issuance costs being recognized through amortization.

18

Table of Contents

Changes in Fair Values of Equity and Long-Term Investments

DuringChanges in fair values of equity and long-term investments, as compared to the prior year period, were as follows:

Three Months Ended March 31,

Change

(In thousands)

    

2021

    

2020

    

$

    

%

Changes in fair values of equity and long-term investments

$

55,045

$

21,915

$

33,130

*

*Not Meaningful

The changes in fair values of $55.0 million for the quarter ended March 31, 2021 reflect the net unrealized gain in the stock and warrants of our investments in Armata, Entasis, and InCarda, and those equity investments managed by ISP Fund LP. The changes in fair value of $21.9 million for the quarter ended March 31, 2020 Innoviva invested $25.0 millionreflect the net changes in 8,710,800 shares of Armata’s common stock and warrants to purchase up to an additional 8,710,800 shares of the common stock at $2.87 per share. As a result of thisour initial investment Innoviva owns approximately 46.7% of Armata’s common stock as of March 31, 2020. The total fair value of the common stock and warrants was estimated at $46.9 million. During the quarter ended March 31, 2020, $21.9 million was recognized as unrealized gains and fair value changes and is presented in changes in fair values of equity investments on the consolidated statements of income.Armata.

Provision for Income Taxes

The provisional income tax expense for the three months ended March 31, 20202021 was $15.9$19.7 million with an effective income tax rate of 16.8%15.2%, compared to $8.5$15.9 million with an effective interest rate of 17.5%16.8% in the same period a year ago.

Net Income Attributable to Noncontrolling Interest

Net income attributable to noncontrolling interest, as compared to the prior period, was as follows:

Three Months Ended March 31, 

Change

Three Months Ended March 31, 

Change

(In thousands)

    

2020

    

2019

    

$

    

%

    

    

2021

    

2020

    

$

    

%

    

Net income attributable to noncontrolling interest

$

13,515

$

6,229

$

7,286

117

%

$

15,572

$

13,515

$

2,057

15

%

This represents the 85% share of net income in Theravance Respiratory Company, LLC for Theravance Biopharma for the three months ended March 31, 20202021 and 2019.2020. The increase was primarily due to the increase in the growth in prescriptions and market share for TRELEGY® ELLIPTA®.

Liquidity and Capital Resources

Liquidity

Since our inception, we have financed our operations primarily through private placements and public offerings of equity and debt securities and payments received under collaborative arrangements. For the three months ended March 31, 2020,2021, we generated gross royalty revenues from GSK of $82.1$89.0 million. Net cash and cash equivalents, short term investments and marketable securities totaled $384.0$282.9 million, and royalties receivablereceivables from GSK totaled $82.1$89.0 million as of March 31, 2020.2021.

23

Table of Contents

Adequacy of Cash Resources to Meet Future Needs

We believe that cash from projected future royalty revenues and our cash, cash equivalents and marketable securities will be sufficient to meet our anticipated debt service and operating needs for at least the next 12 months based upon current operating plans and financial forecasts. If our current operating plans and financial forecasts change, we may require additional funding sooner in the form of public or private equity offerings or debt financings. Furthermore, if in our view favorable financing opportunities arise, we may seek additional funding at any time. However, future financing may not be available in amounts or on terms acceptable to us, if at all. This could leave us without adequate financial resources to fund our operations as currently planned. In addition, from time to time we may restructure or reduce our debt, including through tender offers, redemptions, amendments, repurchases or otherwise, all allowable with the terms of our debt agreements.

Cash Flows

Cash flows, as compared to the prior year period, were as follows:

Three Months Ended March 31, 

    

Three Months Ended March 31, 

    

(In thousands)

    

2020

    

2019

    

Change

    

2021

    

2020

    

Change

Net cash provided by operating activities

$

73,481

$

76,655

$

(3,174)

$

84,107

$

73,481

$

10,626

Net cash provided by (used in) investing activities

 

16,044

 

(74,167)

 

90,211

 

(26,394)

 

16,044

 

(42,438)

Net cash provided by (used in) financing activities

 

(15,640)

 

246

 

(15,886)

Net cash used in financing activities

 

(21,310)

 

(15,640)

 

(5,670)

19

Table of Contents

Cash Flows from Operating Activities

Net cash provided by operating activities for the three months ended March 31, 2021 was $84.1 million, consisting primarily of our net income of $109.7 million, adjusted for net non-cash items such as $19.7 million of deferred income taxes and $3.5 million of depreciation and amortization, partially offset by $54.7 million increase in the fair values of our equity investments, an increase in receivables from collaborative arrangements of $5.0 million and a reduction in accrued interest payable of $2.5 million.

Net cash provided by operating activities for the three months ended March 31, 2020 was $73.5 million, consisting primarily of our net income of $79.0 million, adjusted for net non-cash items of $0.4 million, an increase in receivables from collaborative arrangements of $2.7 million and a reduction in accrued interest payable of $2.5 million.

Cash Flows from Investing Activities

Net cash provided by operatingused in investing activities for the three months ended March 31, 20192021 of $26.4 million was $76.7 million, consisting primarily ofdue to our net income of $40.0 million, adjusted for non-cash items such as $8.5 million of deferred income taxes, $3.5 million of depreciationinvestments in Armata and amortization and $1.9 million amortization of debt discount and issuance costs, as well as decrease in receivables from collaborative arrangements of $24.6 million, partially offset by a reduction in accrued interest payable of $2.5 million.

Cash Flows from Investing ActivitiesImaginAb.

Net cash provided by investing activities for the three months ended March 31, 2020 of $16.0 million was primarily due to $54.0 million received from maturities of marketable securities, partially offset by $12.9 million in purchases of marketable securities and $25.0 million for our investments in Armata.

Cash Flows from Financing Activities

Net cash used in investingfinancing activities for the three months ended March 31, 20192021 of $74.2$21.3 million was primarily due to $102.0 million in purchases of marketable securities, partially offset by $27.9 million proceeds received from maturities of marketable securities.

Cash Flows from Financing Activitiesdistributions to noncontrolling interest.

Net cash used in financing activities for the three months ended March 31, 2020 of $15.6 million was primarily due to $15.8 million distributions to noncontrolling interest.

Net cash provided by financing activities for the three months ended March 31, 2019 of $0.2 million was primarily due to $0.3 million net proceeds from issuance of common stock.

Off-Balance Sheet Arrangements

In June 2014, our facility leases in South San Francisco, California were assigned to Theravance Biopharma, Inc. (“Theravance Biopharma”) in connection with the spin-off of Theravance Biopharma. However, if Theravance Biopharma were to default on its lease obligations, we would be held liable by the landlord and thus, 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 March 31, 2020, the total remaining lease payments for the duration of the lease, which runs through May 2020, were $1.1 million. The carrying value of this lease guarantee was immaterial as of March 31, 2020.

Item 3. Quantitative and Qualitative Disclosure about Market Risk

There have been no significant changes in our market risk or how our market risk is managed compared to those disclosed in our Annual Report on Form 10-K for the year ended December 31, 2019.2020.

24

Table of Contents

Item 4. Controls and Procedures

Evaluation of Disclosure Controls and Procedures.

We conducted an evaluation as of March 31, 2020,2021, under the supervision and with the participation of our management, of the effectiveness of the design and operation of our disclosure controls and procedures, which are defined under SEC rules as controls and other procedures of a company that are designed to ensure that information required to be disclosed by a company in the reports that it files under the Securities Exchange Act of 1934 (“Exchange Act”) is recorded, processed, summarized and reported within required time periods. Based upon that evaluation, our Interim PrincipalChief Executive Officer and Chief Accounting Officer, concluded that, as of such date, our disclosure controls and procedures were effective at the reasonable assurance levels.

20

Table of Contents

Limitations on the Effectiveness of Controls

Our management does not expect that our disclosure controls and procedures or our internal control over financial reporting will prevent all errors and all frauds. A control system, no matter how well conceived and operated, can provide only reasonable, not absolute, assurance that the objectives of the control system are met. Further, the design of a control system must reflect the fact that there are resource constraints, and the benefit of controls must be considered relative to their costs. Because of the inherent limitations in all control systems, no evaluation of controls can provide absolute assurance that all control issues and instances of fraud, if any, within Innoviva have been detected. Also, projections of any evaluation of effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.

Changes in Internal Control over Financial Reporting

There werehave been no material changes in our internal control over financial reporting (as defined in Rule 13a-15(f) of the Exchange Act) that occurred during the quarter ended March 31, 20202021 that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.

PART II. OTHER INFORMATION

Item 1. LegalProceedings

In May 2019, Theravance Biopharma, whowhich is the owner of 85% of the economic interests in TRC, initiated arbitration against the Company and TRC, relating to a dispute as to the determination by Innoviva (as manager of TRC) to cause TRC to explore potential reinvestment opportunities for the royalty proceeds received by GSK into initiatives that Innoviva believes will increase the value of TRC and TRELEGY® ELLIPTA®. Theravance Biopharma alleged that, in causing TRC to not distribute substantially all royalty proceeds received from GSK, Innoviva breached the limited liability company operating agreement governing TRC (the “Operating Agreement”), as well as the fiduciary duties applicable to Innoviva as manager of TRC. The hearing in respect of the arbitration was conducted from July 23, 2019 through July 25, 2019. Post-arbitration oral argument was heard on August 14, 2019. On September 26, 2019, the arbitrator issued a final decision. The arbitrator ruled that Innoviva did not breach the Operating Agreement or its fiduciary duties by withholding royalties or pursuing reinvestment opportunities. Accordingly, the Company is permitted to continue to pursue development and commercialization initiatives. The arbitrator did conclude that Innoviva breached a provision of the Operating Agreement requiring Innoviva to deliver quarterly financial plans to Theravance Biopharma. However, the arbitrator concluded that this technical breach did not cause any damages to Theravance Biopharma and the arbitrator awarded limited injunctive relief to expand and clarify the disclosure obligations under the Operating Agreement related to the delivery of financial plans and the pursuit of investment opportunities.opportunities (if those opportunities related to TRELEGY® ELLIPTA®). Finally, the arbitrator ruled that the Company is entitled to indemnification from TRC for 95% of its fees and expenses incurred in connection with the arbitration.

On September 30, 2019, the Company and TRC filed a Verified Complaint in the Court of Chancery of the State of Delaware (“Court of Chancery”) to confirm the arbitration award. That matterThe award was confirmed by the Court of Chancery on May 4, 2020.

25

Table of Contents

On July 16, 2020, Innoviva and TRC initiated a lawsuit in the Court of Chancery against Theravance Biopharma, seeking a permanent injunction preventing Theravance Biopharma from interfering with Innoviva's ability to cause TRC to reserve cash to pursue non-Trelegy related investments opportunities and a declaration that the arbitration award conclusively established that Innoviva, as manager of TRC, has such authority. The Court of Chancery directed the parties to obtain the arbitrator's opinion as to whether the arbitration award addressed non-Trelegy related investment opportunities. On July 31, 2020, the arbitrator, while reiterating that Innoviva has broad authority as manager of TRC, found that this award did not specifically address this situation. Accordingly, on August 5, 2020, the parties stipulated to the dismissal of the Court of Chancery action.

On October 6, 2020, Theravance Biopharma initiated a new arbitration against the Company and TRC, challenging Innoviva’s authority as manager of TRC to cause TRC to pursue non-Trelegy related investment opportunities and again alleging that Innoviva is still pending.required to cause TRC to distribute substantially all royalty proceeds from GSK. The hearing in respect of the arbitration was conducted from February 16, 2021 through February 19, 2021. Post-arbitration oral argument was heard on March 8, 2021. On March 30, 2021, the arbitrator issued a final decision. The arbitrator ruled that Innoviva did not breach the Operating Agreement or its fiduciary duties by withholding royalties to pursue non-Trelegy-related investment opportunities. Additionally, the arbitrator ruled that the Company is entitled to indemnification from TRC for 100% of its fees and expenses reasonably incurred in connection with the arbitration.

On April 15, 2021, the Company filed a Verified Complaint in the Court of Chancery to confirm the arbitration award. Theravance Biopharma must respond to the Verified Complaint by May 19, 2021.

Item 1A. Risk Factors

Our business is subject to a number of risks, including those identified in Item 1A of Part I of our 20192020 Form 10-K. Except as set forth under “Item 1. Legal Proceedings” above and as discussed below, thereThere have been no other material changes to the risk factors described in our 20192020 Form 10-K which is incorporated by reference herein..

The widespread outbreak of an illness or any other communicable disease, or any other public health crisis, could adversely affect our business, results of operations and financial condition.

We could be negatively affected by the widespread outbreak of an illness or any other communicable disease, or any other public health crisis that results in economic and trade disruptions, including the disruption of global supply chains. In December 2019, an outbreak of COVID-19 began in Wuhan, Hubei Province, China. In March 2020, the World Health Organization declared COVID-19 a pandemic. The COVID-19 pandemic has negatively impacted the global economy, disrupted global supply chains, and created significant volatility and disruption of financial markets. At this time, based on the information available to us, we cannot yet predict the extent of the impact of the COVID-19 pandemic on our royalty revenues derived from GSK upon which we significantly rely; however, it is possible that an extended period of global supply chain and economic disruption could materially affect such revenues and therefore our results of operations and financial condition.

21

Table of Contents

Item 2. Unregistered Sales of Equity Securities and Use of Proceeds

None.

Item 3: Defaults Upon Senior Securities

None.

Item 4: Mine Safety Disclosures

None.

Item 5: Other Information

None.

26

Table of Contents

Item 6. Exhibits

(a)Index to Exhibits

Exhibit
Number

    

Description

    

Form

    

Exhibit

    

Incorporated
by Reference
Filing
Date/Period
End Date

10.1

Indemnification Agreement, dated as of March 9, 2021, by and between Innoviva, Inc. and Deborah L. Birx, M.D.

31.1

Certification of Principal Executive Officer pursuant to Rules 13a-14 pursuant to the Securities Exchange Act of 1934

31.2

Certification of Principal Financial Officer pursuant to Rules 13a-14 pursuant to the Securities Exchange Act of 1934

32

Certifications Pursuant to 18 U.S.C. Section 1350

101

Interactive Data File (Quarterly Report on Form 10-Q, for the quarterly period ended March 31, 2020)2021) formatted in iXBRL (Inline eXtensible Business Reporting Language).

104

Cover Page Interactive Data File (embedded within the Inline XBRL document and included in Exhibit 101).

27

Table of Contents

SIGNATURES

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned thereunto duly authorized.

Innoviva, Inc.

Date: April 29, 202028, 2021

/s/ Geoffrey HulmePavel Raifeld

Geoffrey HulmePavel Raifeld

Interim PrincipalChief Executive Officer

(Principal Executive Officer)

Date: April 29, 202028, 2021

/s/ Marianne Zhen

Marianne Zhen

Chief Accounting Officer

(Principal Financial Officer)

2228