UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, DC 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): April 7, 2022
INNOVIVA, INC.
(Exact Name of Registrant as Specified in its Charter)
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Delaware
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000-30319
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94-3265960
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(State or Other Jurisdiction of
Incorporation) |
(Commission File Number)
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(I.R.S. Employer Identification
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1350 Old Bayshore Highway,
Suite 400
Suite 400
Burlingame, California 94010
(650) 238-9600
(Addresses, including zip code, and telephone numbers, including area code, of principal executive offices)
(Former name or former address, if changed since last report)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions (see General Instruction A.2. below):
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Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
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Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
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Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
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Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
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Securities registered pursuant to Section 12(b) of the Act:
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Title of each class
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Trading Symbol(s)
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Name of each exchange on which registered
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Common Stock, par value $0.01 per share
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INVA
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The NASDAQ Global Select Market
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Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933(§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
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. ☐
Item 7.01. Regulation FD Disclosure.
On April 7, 2022, Innoviva, Inc. (the “Company”) made available on its website a revised Company investor presentation. A copy of the presentation is attached hereto as Exhibit 99.1 and is incorporated by reference herein.
The information included in this Current Report on Form 8-K that is furnished pursuant to this Item 7.01, including the information contained in Exhibit 99.1 hereto, shall not be deemed to be “filed” for the purposes of Section 18 of the
Securities Exchange Act of 1934, as amended, or otherwise subject to the liabilities of that section or Sections 11 and 12(a)(2) of the Securities Act of 1933, as amended. In addition, the information included in this Current Report on Form 8-K that
is furnished pursuant to this Item 7.01, including the information contained in Exhibit 99.1 hereto, shall not be incorporated by reference into any filing of the Company, whether made before or after the date hereof, regardless of any general
incorporation language in such filing, unless expressly incorporated by specific reference into such filing
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits
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99.1
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Investor Presentation
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SIGNATURE
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
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INNOVIVA, INC.
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Date: April 7, 2022
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By:
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/s/ Pavel Raifeld
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Pavel Raifeld
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Chief Executive Officer
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CorporatePresentation April 2022
Important information On March 25, 2022, the Company filed a Definitive Proxy Statement on Schedule 14A
and accompanying proxy card with the Securities and Exchange Commission (“SEC”) to be used to in connection with the Company’s 2022 annual meeting of the stockholders.THE COMPANY STRONGLY ADVISE ALL STOCKHOLDERS OF THE COMPANY TO READ THE PROXY
STATEMENT AND OTHER PROXY MATERIALS (IF ANY) AS THEY BECOME AVAILABLE BECAUSE THEY CONTAIN IMPORTANT INFORMATION. SUCH PROXY MATERIALS WILL BE AVAILABLE AT NO CHARGE ON THE SEC’S WEB SITE AT HTTP://WWW.SEC.GOV. IN ADDITION, THE COMPANY WILL
PROVIDE COPIES OF THE PROXY STATEMENT WITHOUT CHARGE UPON REQUEST. 2
Forward-looking statements The information in this presentation 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. Furthermore, if our forward-looking statements prove to be inaccurate, the
inaccuracy may be material. 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 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; our strategies, plans and objectives (related to our growth strategy and corporate development initiatives beyond our existing portfolio); the timing, manner and
amount of capital deployment, including potential capital returns to stockholders; risks related our growth strategy; projections of revenue, expenses and other financial items. 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. Any person reviewing this presentation is advised
to review our “Risk Factors” and other information in our Annual Report on Form 10-K for the year ended December 31, 2021 filed with the Securities and Exchange Commission (“SEC”) on February 28, 2022, (“2021 Form 10-K”), and the information in
the other reports and documents that we file with the SEC from time to time. All information in this presentation should be read in conjunction with the information we have filed with the SEC. All forward-looking statements in this presentation
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. 3
Innoviva overview Company highlights Diversified holding company with a portfolio of royalties and
a growing portfolio of innovative healthcare investments and assetsRoyalty portfolio consists of respiratory products that were jointly developed with, and are licensed to, GSK and collectively make up the majority of GSK’s leading respiratory
franchise (RELVAR®/ BREO® ELLIPTA®, ANORO® ELLIPTA®, TRELEGY® ELLIPTA®)Strategic healthcare investments – investments in areas with high unmet medical need and significant long-term value creation potential, oftentimes with a focus on control
positions 3 Thoughtful, robust approach to capital deployment with long-term horizon 5 Efficient and flexible platform enabling meaningful, sustainable value generation 4 Strong track record of growth and unrelenting value
creation focus 2 Deep and proven healthcare expertise across governance, strategy, R&D, finance, and operations 1 Strongly cashflow-generative, diversified and durable core royalty business 4 Company description
Innoviva combines sustainable royalty cashflows with a long-term capital deployment strategy to drive
innovation and maximize shareholder value Robust, valuable royalty portfolio Thoughtful, accretive capital deployment Long-term shareholder value creation + = Significant royalties from a durable and growing portfolio of blockbuster
respiratory products Strategic healthcare asset acquisitions and capital structure optimization to drive sustainable growth Strong record of growth and capital deployment position the company for continued value creation 5 Over $250M net
income to Innoviva stockholders generated in 2021
Innoviva has a valuable royalty portfolio comprised of robust, durable revenues stemming from widely used
respiratory therapies commercialized by GSK 2021 Global net sales ($B) Key royalty terms 2021 Innoviva royalties1 ($M) Totals 15% on first $3B in annual sales; 5% on sales over $3B 100% economics Tiered 6.5-10.0%100% economics Tiered
6.5-10.0%15% economics1 5-year projected royalties1,2 ($B) ANORO®ELLIPTA® RELVAR®/ BREO®ELLIPTA® TRELEGY®ELLIPTA® 1 – TRELEGY® ELLIPTA® royalties are assigned to Theravance Respiratory Company LLC, a subsidiary of Innoviva, where
Theravance Biopharma holds 85% economic interest; 100% royalty economics shown2 – Projections per analyst consensus on GSK forecast website accessed March 28, 2022; GBP converted to USD using March 28 exchange rate of $1.31; 2022-2026E
royalties shown $3.9B $406M ~$2.4B 6 Royalty portfolio Asthma / COPD COPD Asthma / COPD
Our royalty product portfolio has demonstrated resilience and growth; we remain excited about its
long-term potential while we build out the next generation of high impact products Sizeable and differentiated Resilient anddurable Diversifiedand growing Differentiated respiratory therapies portfolio with over $3B annual salesConsensus
projections imply royalties of $2B+ over the next 5 years1 Robust products have performed well across environments despite competitive pressuresMeaningful longevity afforded by strong IP estate, with the “moat” amplified by manufacturing
complexity Broad portfolio covers all major respiratory drug classes in easy-to-use single daily dose formPortfolio contains products across the life cycle, including relatively mature standard of care therapies (RELVAR®/ BREO® ELLIPTA®,
ANORO® ELLIPTA®) and fast-growing innovative products (TRELEGY® ELLIPTA®)Products approved and launching in multiple geographies and indications, reducing single-market risk 1 – Projections per analyst consensus on GSK forecast website
accessed March 28, 2022; GBP converted to USD using March 28 exchange rate of $1.31; 100% Trelegy royalties included; 2022-2026E 7 Royalty portfolio
Innoviva actively deploys its capital to maximize shareholder value In 2021 we strategically
repurchased GSK’s equity stake for ~$400M and continued to deploy capital into high-potential assets – with ~$480M equity and investments on the balance sheet at year-end Continued active search for strategically attractive opportunities with
external supportLong-term, deliberate approach to direct strategic investments into promising healthcare assets, matching the meaningful duration of our cashflowsConcentrated exposure to fundamentally robust, attractively priced assets with
significant upsidePotential capital return to shareholders as appropriate, especially when strong economic value accretion is coupled with compelling strategic benefitsE.g., GSK’s 32% equity stake repurchase in May 2021 at $12.25 per share for
$392M1 We thoughtfully approach capital deployment with a strong value focus 8 1 – Excludes associated feesNote: $484M equity and long-term investments assets on balance sheet as of Dec 31, 2021. Capital deployment
We approach strategic transactions in a thoughtful and disciplined manner We target fundamentally
attractive, yet often overlooked or contrarian, healthcare areas where our capital and capabilities can make a difference We look for differentiated assets with meaningful value creation potential We structure and negotiate asset acquisitions
on mutually beneficial terms to maximize long-term valueFocus on concentrated, long-term investments, often by purchasing majority or other large stakesOpenness to smaller investments in companies with compelling growth and risk profiles We
proactively manage risks through ongoing asset stewardship and appropriate diversificationOperational and strategic support (across strategy, finance, development, commercial, governance, and other areas) as a key value creation
driver Opportunity identification Strategic investment execution 9 Capital deployment
Strategic investment case study: infectious disease Infectious disease therapeutics have focused
primarily on common bacteria diseases; however, there is a clear need for improved therapeutics for specific bacterial diseases, along with viral and fungal diseasesIdiosyncratic challenges leading to historical underinvestment have resulted in
compelling strategic opportunitiesA player with long-term vision, capital, and expertise can take advantage of market dislocations and facilitate R&D and commercialization of novel, differentiated treatments capable of generating
significant value for patients and health systems – and producing strong returns Infectious disease is a promising area of high unmet medical need with currently scarce capital access Selected Innoviva transactions
(end-2021) Pathogen-specific bacteriophage therapeutics platform for the treatment of drug resistant infections and other usesHighly differentiated novel biologic platform with broad applicability, rooted in a well-known modality and supported
by strong manufacturing capabilitiesBroad development program with lead therapy focused on respiratory Pseudomonas aeruginosa infections in cystic fibrosis patients, an area of high unmet need Novel antibacterial platform validated by lead
asset’s highly differentiated profile in an area of unmet needNovel potential carbapenem-resistant Acinetobacter treatment SUL-DUR has significant commercial promise following favorable efficacy and safety in pivotal trialOngoing Phase 3 trial
for gonorrhea antibiotic“Rational design” platform used to develop earlier stage antibiotics less susceptible to resistance $68M cost basis1 ~60% ownership1 $49M cost basis1 ~60% ownership1 $104M fair value1 $147M fair value1 1 – As of
Dec 31, 2021. On February 1, 2022, Innoviva made an initial non-binding offer to acquire Entasis and made $15M investment on February 18, 2022; on March 15, 2022, Innoviva revised the non-binding Entasis offer. On February 9, 2022, Innoviva
announced $45M investment in Armata, $18.1 million of which closed on February 9, 2022, and the remainder on March 31, 2022 10 Capital deployment
Innoviva is the sole manager of all TRELEGY®ELLIPTA® royalties via TRC, seeking to maximize long-term
equity holder value 11 1 – Projections per analyst consensus on GSK forecast website accessed March 28, 2022; GBP converted to USD using March 28 exchange rate of $1.31; 100% Trelegy royalties included; 2022-2026E An Innoviva subsidiary,
Theravance Respiratory Company LLC (TRC), receives all TRELEGY® ELLIPTA® royalties from GSK$127M in 2021 with approximately $1.1B projected over 5 years based on consensus estimates1Innoviva as Manager of TRC has a broad mandate and
responsibility to maximize the value of TRC both by active management of the TRELEGY® ELLIPTA® royalties and via strategic investmentsUltimately, 15% economics accrue to Innoviva (and 85% to Theravance Biopharma)Theravance Biopharma
unsuccessfully challenged our ability to make investments in arbitrationAdditional active strategic investing anticipated seeking significant value creation with uncertainty removed (due to the successful resolution of the Theravance Biopharma
arbitration) in light of strong current opportunity set, benefiting from our long-term orientation Additional detail in the appendix Capital deployment
Relevant experience Management Team Pavel Raifeld, CFAChief Executive Officer Experienced
finance and life sciences professional; formerly with Sarissa Capital, Credit Suisse, McKinsey and BCG Marianne Zhen, CPAChief Accounting Officer Experienced finance professional with over 20 years in accounting and strategic
operations Board of Directors George Bickerstaff,Chairperson Managing Director at M.M. Dillon & Co.; former CFO of Novartis Pharma AG and IMS Health; director at CareDx Deborah L. Birx, M.D. Physician-scientist and healthcare
leader; former response coordinator of The White House Coronavirus Task Force Mark DiPaolo, Esq. Senior Partner and General Counsel at Sarissa Capital; former senior member Icahn Capital’s investment team Jules Haimovitz Founder,
executive, and director of multiple companies in life sciences and entertainment; former director of Ariad Pharma Odysseas Kostas, M.D. Senior Managing Director at Sarissa Capital; former life sciences analyst at Evercore ISI and
practicing physician Sarah J. Schlesinger, M.D. Professor at Rockefeller University with governance and clinical / medical expertise; former director of The Medicines Company and Ariad Pharma Innoviva’s management and board have
world-class expertise in healthcare and single-minded focus on value creation – brought to bear for the benefit of shareholders Innoviva Team (Icahn Capital) 12 Joined in 2021 World-class expertise Unique and complementary skill
sets Strong value creation focus Proven track record of success Value creation
2021 was a milestone year both in terms of financial performance and strengthening our operating
platform $406M total royalty revenues$364M net cash provided by operating activities$3.24 basic net income per share2$266M net income 13 Value creation Strategically deployed over $450M in 2021Accretively repurchased GSK’s 32% equity
stake for $392M3 (at $12.25 per share)Strategically invested $~65M into innovative healthcare assetsStrengthened Innoviva platformAdded healthcare and infectious disease leader Deborah L. Birx to the BoardIn 20224, continued to strategically
deploy capital and improve capital structureInvested $~70M into healthcare assetsIssued $261M 2.125% convertible notes due 2028, partially using proceeds to retire a portion of 2023 notes 23% CAGR Financial highlights (2021) Business
highlights 1 – Includes 100% TRELEGY® ELLIPTA® royalties2 – $2.87 diluted net income per share; attributable to Innoviva stockholders3 – Excludes associated fees4 – 1Q2022 data shown
Why Innoviva 5 Efficient and flexible platform enabling meaningful, sustainable value
generation 4 Strong track record of growth and unrelenting value creation focus 3 Thoughtful, robust approach to capital deployment with long-term horizon 2 Deep and proven healthcare expertise – across governance, strategy,
R&D, commercial, finance, and operations – brought to bear across everything we do 1 Strongly cashflow-generative, diversified and durable core royalty business 14 Value creation
Appendix 15
RELVAR®/BREO® ELLIPTA® detail: First once-daily inhaled corticosteroid / long-acting beta-agonist for
asthma and chronic obstructive pulmonary disease RELVAR® / BREO®ELLIPTA® Launched in 2013 as first and only once-daily ICS / LABA in the U.S.RELVAR®/ BREO® ELLIPTA® delivers superior, lasting proactive asthma control, with simple once-daily
dosing in an easy-to-use deviceHistorical resilience in a competitive, volatile environment supported by positive demographic trends Net global sales ($B) Implied royalties ($M) (fluticasone furoate 100 mcg and vilanterol 25 mcg inhalation
powder) Indications (US)Long-term, once-daily, maintenance treatment of airflow obstruction and reducing exacerbations in patients with COPDOnce-daily treatment of asthma in patients aged 18 years and older 1 1 – Projections per analyst
consensus on GSK forecast website accessed March 28, 2022; GBP converted to USD using March 28 exchange rate of $1.31 16 100% economics to INVA Royalty portfolio
ANORO® ELLIPTA® detail: Best-in-class long-acting beta-agonist / long-acting muscarinic antagonist for
COPD ANORO®ELLIPTA® (umeclidinium 62.5 mcg and vilanterol 25 mcg inhalation powder) Indications (US)Long-term, once-daily, maintenance treatment of airflow obstruction and reducing exacerbations in patients with COPD Net global sales
($B) Implied royalties ($M) 1 – Projections per analyst consensus on GSK forecast website accessed March 28, 2022; GBP converted to USD using March 28 exchange rate of $1.312 – Superior improvement in lung function has been demonstrated in
clinical trials of ANORO® ELLIPTA® vs. Tiotropium (LAMA) and Spiolto (LAMA/LABA) 17 1 Launched in 2014 as first-in-class LABA / LAMA single inhaler product in the U.S.ANORO® ELLIPTA® delivers superior lung function improvement vs common
initial maintenance therapy options2Class leader in the U.S. due to clear differentiationLong-term prospects supported by positive demographics 100% economics to INVA Royalty portfolio
TRELEGY® ELLIPTA® detail: First 3-in-1 inhaled corticosteroid / long-acting beta-agonist / long-acting
muscarinic antagonist for COPD and asthma TRELEGY®ELLIPTA® Net global sales ($B) Implied royalties ($M) (fluticasone furoate 100 mcg, umeclidinium 62.5 mcg and vilanterol 25 mcg inhalation powder) Indications (US)Long-term, once-daily,
maintenance treatment of patients with COPD, including chronic bronchitis and/or emphysemaOnce-daily treatment of asthma in patients aged 18 years and older 18 1 – Projections per analyst consensus on GSK forecast website accessed March 28,
2022; GBP converted to USD using March 28 exchange rate of $1.312 – FULFIL trial vs. Symbicort (ICS/LABA), IMPACT study vs. ICS/LABA and LAMA/LABA3 – TRELEGY® ELLIPTA® royalties are assigned to Theravance Respiratory Company LLC, a subsidiary
of Innoviva, where Theravance Biopharma holds 85% economic interest; 100% royalty economics shown 1 Launched in 2017 as first-in-class ICS / LABA / LAMA single inhaler product in the U.S.TRELEGY® ELLIPTA® demonstrated superior efficacy in
clinical trials for COPD vs double combination drug classes2Strong growth driven by demographic tailwinds, increasing class adoption, and share increase across geographies 15% economics to INVA3 Royalty portfolio
GSK net global sales1 ($B) Net global sales and royalty revenues have grown over time Innoviva
Royalty Revenue2 ($M) Note: May not sum due to rounding1 – Reflects net sales from RELVAR®/ BREO® ELLIPTA®, ANORO® ELLIPTA®, TRELEGY® ELLIPTA®2 – Excludes the impacts of amortization of capitalized fees and the MABA strategic alliance;
reflects TRELEGY® ELLIPTA® royalties received by TRC at 100%; may not sum due to rounding TRELEGY® ELLIPTA® Royalties @ 15% Economics - - $2mm $6mm $11mm $19mm 19 ’16 – ’21 CAGR: 28% ’16 – ’21 CAGR: 23% Royalty portfolio
Innoviva’s portfolio products are protected by a robust IP estate with meaningful remaining
exclusivity Manufacturing complexity provides further protection Primary US patent ANORO®ELLIPTA® RELVAR®/ BREO®ELLIPTA® TRELEGY®ELLIPTA® Potential expiration Key secondary US patent Potential expiration Vilanterol drug substance1
ELLIPTA device4 Specified LABA/LAMA combination for treatment of COPD and asthma2,3 Process for aggregating particles of umeclidinium and/or vilanterol and/or fluticasone furoate5 Specified LABA/LAMA combination for treatment of COPD and
asthma2,3 1 – US patent 7439393. Original expiration 9/11/2022, granted additional exclusivity to May 2025 through 35 USC §1562 – US patents 9750726 and 110902943 – Umeclidinium (contained in Anoro and Trelegy) is covered by US drug substance
patent 7488827; original expiration 4/27/2025, granted extension to Dec 2027 through 35 USC §156 4 – US patent 87462425 – US patent 9763965 2025 2030 2030 Process for aggregating particles of umeclidinium and/or vilanterol and/or
fluticasone furoate5 2030 2033 2033 The terms of the collaboration agreement with GSK indicate that royalties will be paid until the later of:The expiration of the last patent covering each product in such country 15 years from first
commercial sale of each product in such countryFor each of the portfolio products, the secondary patent expiration date would be the later date for purposes of royaltiesIP protection in international markets is generally longer dated than in
the US 20 Royalty portfolio
Additional TRC information While TRC actively manages its royalty-producing relationship with GSK, under
the LLC Agreement, TRC is permitted to “engage in any lawful business”; additionally, Innoviva was granted broad “decision-making authority as to the LLC”There have been two separate arbitrations brought by Theravance Biopharma against Innoviva
and TRC over the last two years challenging the scope of Innoviva’s authority as Manager of TRC to deploy capital rather than simply distribute royalty incomeThe arbitrator ruled in favor of Innoviva and TRC in both arbitrations. The arbitrator
has confirmed that the LLC Agreement broadly empowers the LLC to engage in any lawful business and that Innoviva has the “discretion” and “freedom” under the LLC Agreement to determine how to use the LLC’s cash, including in investments
unrelated to TRELEGY® ELLIPTA®. The arbitrator did not enjoin TRC from making additional investmentsEach of the arbitrator’s decisions is publicly available Arbitration background Example investments InCarda focuses on cardiovascular
diseases; its lead drug is in late-stage development for large, attractive PAF1 market ImaginAb is a leader in radio-pharmaceutical imaging with a differentiated solution for IO2 patient care and other areas of unmet medical need 21 1 –
Paroxysmal atrial fibrillation2 – Immuno-oncology Gate Neurosciences is developing next-generation therapies for psychiatric and neurological disorders Nanolive is a microscopy company that has developed a method for live cell 3D imaging and
analysis with applications across drug discovery and biotech R&D Capital deployment
Innoviva’s platform optimizes for lean, focused value creation leveraging superior
capabilities Low-cost, efficient operating platform Best-in-class internal capabilities Superior external resources access Our key operations principles are cost discipline, flexibility, and value orientation, while ensuring we are
well-resourced to executeLean expense structure; 2021 G&A expense totaled ~$16MFlexibility and scalability are key Strong revenue conversion to income and cashflows Management team and board members have significant functional and industry
expertise with proven track records in key areas utilized both at Innoviva and our investeesMedicine, science, and R&D; M&A and investments; governance and management; strategy and planning; commercial and operations Deep, multi-year
relationships across healthcare ecosystem enabling differentiated deal flow and talent pool accessExternal advisors, investment community, industry, government, patient groups, and others Innoviva is well positioned for strong
execution 22 Value creation