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INVANasdaq

Innoviva, Inc.

Biopharma developer (SEC filing verified)·Commercial·Burlingame, CA, United States·CEO: Mr. Pavel Raifeld C.F.A.
Infectious DiseaseMetabolicGastroenterology

INVA evidence brief

What we can confirm

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What it means

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What to watch

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BioSniper AIPage evidence connected

Prepared research question

What matters most for INVA—catalysts, financial risk and supporting evidence?

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BioSniper AI · INVA

Innoviva, Inc. (INVA) is a diversified biopharmaceutical company with a wholly owned critical care and infectious disease platform, royalty interests in respiratory products partnered with GSK, and strategic equity investments in healthcare companies.

Key risk: Royalty revenue dependence

8.5/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$1.51B

Cash Runway

Lead Asset

XACDURO (Approved)

Financial data as of Jun 30, 2026.

Tracking 1 pipeline candidate · 4 clinical trials · 5 catalysts for Innoviva, Inc..

AI OverviewAI overview is shown in English only.

Innoviva, Inc. (INVA) is a diversified biopharmaceutical company with a wholly owned critical care and infectious disease platform, royalty interests in respiratory products partnered with GSK, and strategic equity investments in healthcare companies.

  • Wholly owned critical care and infectious disease platform anchored by four commercial products: GIAPREZA, XACDURO, XERAVA, and ZEVTERA, plus an FDA-approved product expected to launch in H2 2026 [sec_mda · as of 2026-08-05].
  • Royalty revenue from respiratory products partnered with GSK, including ANORO ELLIPTA, with tiered royalties ranging from 6.5% to 10% [sec_mda · as of 2026-08-05].
  • Cash and equivalents of $570.4M as of 2026-06-30 [sec].
  • Total revenue of $119.6M as of 2026-06-30 [sec].
  • Significant equity stake in Armata Pharmaceuticals, a leader in bacteriophage development for infectious diseases [sec_mda · as of 2026-02-25].

What works

  • Diversified revenue streams from both royalty-based respiratory assets and wholly owned commercial infectious disease products reduce dependence on a single source [sec_mda · as of 2026-08-05].
  • Strong cash position of $570.4M as of 2026-06-30 provides financial flexibility for operations and strategic investments [sec].
  • Late-stage pipeline includes zoliflodacin, a potential first-in-class single oral dose treatment for uncomplicated gonorrhea, with NDA submission planned [sec_mda · as of 2025-02-26].
  • Equity stake in Armata Pharmaceuticals offers exposure to innovative bacteriophage therapies with potential across serious infectious diseases [sec_mda · as of 2026-02-25].

What to weigh

  • Royalty revenue from GSK-partnered respiratory products is subject to commercial performance and market risks, including lower-than-expected sales [sec_mda · as of 2026-08-05].
  • Commercialization of multiple products (GIAPREZA, XACDURO, XERAVA, ZEVTERA, NUZOLVENCE) depends on successful market adoption and regulatory approvals in various jurisdictions [sec_mda · as of 2026-08-05].
  • Significant equity investments, such as in Armata, expose the company to market volatility and valuation fluctuations, as seen in fair value changes [sec_mda · as of 2025-11-05].
  • Patent expirations for key products (ANORO ELLIPTA in 2030, ZEVTERA in 2034, NUZOLVENCE in 2035) could erode future revenue exclusivity [catalyst].

From the filings

Quoted directly from source documents.

  • Wholly owned critical care and infectious disease platform with four commercial products and an FDA-approved product expected in H2 2026.

    Our wholly owned, critical care and infectious disease operating platform with a hospital focus, is anchored by a portfolio of four commercial and marketed products, as well as an FDA-approved product which is expected to be available to patients in the second half of 2026

    SEC MD&A · August 5, 2026

  • Royalties from ANORO ELLIPTA tier upward from 6.5% to 10%.

    royalties from the sales of ANORO ® ELLIPTA ® , which tier upward at a range from 6.5% to 10%

    SEC MD&A · August 5, 2026

  • Significant equity stake in Armata Pharmaceuticals.

    a significant stake in Armata Pharmaceuticals, Inc. ("Armata"), a leader in development of bacteriophages with potential use across a range of infectious and other serious diseases

    SEC MD&A · February 25, 2026

  • Zoliflodacin is an investigational first-in-class single oral dose antibiotic for uncomplicated gonorrhea.

    Zoliflodacin: an investigational, first-in-class, single oral dose, spiropyrimidinetrione antibiotic for the treatment of uncomplicated gonorrhea in adults and pediatric patients 12 years and older

    SEC MD&A · November 5, 2025

Catalyst timeline

  • 2030-11-29 · Patent_Expiry · ANORO ELLIPTAPatent/exclusivity expiry for ANORO ELLIPTA, a key respiratory product partnered with GSK, could affect future royalty revenue.
  • 2034-04-03 · Patent_Expiry · ZEVTERAPatent/exclusivity expiry for ZEVTERA, a wholly owned antibiotic, may impact market exclusivity.
  • 2035-12-12 · Patent_Expiry · NUZOLVENCEPatent/exclusivity expiry for NUZOLVENCE, a wholly owned product, could reduce competitive barriers.
  • 2037-01-06 · Patent_Expiry · GIAPREZAPatent/exclusivity expiry for GIAPREZA, a critical care product, may affect revenue stream.
  • 2037-10-19 · Patent_Expiry · XERAVAPatent/exclusivity expiry for XERAVA, an infectious disease product, could open market to generics.
Risks & what to watch (4)

Key risks

  • Royalty revenue dependenceLower-than-expected future royalty revenue from respiratory products partnered with GSK could impact financial performance [sec_mda · as of 2026-08-05].
  • Commercialization risksCommercial success of GIAPREZA, XACDURO, XERAVA, ZEVTERA, and NUZOLVENCE depends on market adoption and regulatory approvals [sec_mda · as of 2026-08-05].
  • Equity investment volatilityFair value of equity investments, including Armata, is subject to market fluctuations, as seen in prior periods [sec_mda · as of 2025-11-05].
  • Patent expirationsPatent expirations for ANORO ELLIPTA (2030), ZEVTERA (2034), and others may reduce exclusivity and revenue [catalyst].

What to watch

  • FDA approval and launch of zoliflodacin for uncomplicated gonorrhea, with NDA submission planned [sec_mda · as of 2025-02-26].
  • Commercial performance of GIAPREZA, XACDURO, XERAVA, ZEVTERA, and NUZOLVENCE in approved markets [sec_mda · as of 2026-08-05].
  • Royalty revenue trends from GSK-partnered respiratory products, including ANORO ELLIPTA [sec_mda · as of 2026-08-05].
  • Valuation changes in equity investments, particularly Armata Pharmaceuticals [sec_mda · as of 2025-11-05].

Sources: Catalysts · SEC MD&A · Generated August 23, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway10.0

Profitable (positive operating cash flow)

Financial Health9.4

D/E 0.38 · 0% dilution

Pipeline Maturity10.0

Lead: Approved

Pipeline Breadth3.3

1 candidate

Catalyst Momentum10.0

5 upcoming, next in ~1552d

Insider SignalN/A

No insider transactions in the last 180 days

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

284

Total value held

$1.80B

Showing top 10 of 284 institutional holders of Innoviva, Inc.. Open the full 13F history after sign-in.

Short Interest

as of May 21, 2026
% of float
11.5%
Days to cover
9.7
Shares short
6,282,273
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

INVA short interest

Governance

Frequently asked questions

What is the AI investment thesis for Innoviva, Inc.?

Innoviva, Inc. (INVA) is a diversified biopharmaceutical company with a wholly owned critical care and infectious disease platform, royalty interests in respiratory products partnered with GSK, and strategic equity investments in healthcare companies.

What is Innoviva, Inc.'s lead drug candidate?

Innoviva, Inc.'s most advanced tracked candidate is XACDURO (Approved) for hospital-acquired and ventilator-associated bacterial pneumonia caused by Acinetobacter.

What is Innoviva, Inc.'s next catalyst?

Innoviva, Inc.'s next tracked catalyst is a Patent_Expiry event — "Patent/Exclusivity Expiry: ANORO ELLIPTA" — expected November 29, 2030.

Who is the CEO of Innoviva, Inc.?

Mr. Pavel Raifeld C.F.A. is the chief executive officer of Innoviva, Inc. (INVA).

Where is Innoviva, Inc. headquartered?

Innoviva, Inc. (INVA) is headquartered in Burlingame, CA, United States.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.