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VIR

Vir Biotechnology, Inc.

Biological products·Phase 3·San Francisco, CA, United States·CEO: Dr. Marianne De Backer M.B.A., M.Sc., Ph.D.
OncologyNeurologyInfectious DiseaseGastroenterology

VIR evidence brief

What we can confirm

BioSniper Score:
7.7 / 10
Market Cap:
$1.83B
Lead Asset:
elebsiran (Phase 3)

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Market Cap: $1.83B · Lead Asset: elebsiran (Phase 3)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · VIR

Vir Biotechnology, Inc. (VIR) is a publicly traded biopharmaceutical company developing therapies for infectious diseases (hepatitis B and delta, HIV) and oncology (prostate cancer, HER2-expressing cancers, solid tumors), with its lead hepatitis delta program in Phase 3 and multiple oncology candidates in Phase 1/2.

Key risk: Early-stage oncology pipeline

7.7/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$1.83B

Cash Runway

—

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 6 pipeline candidates · 14 clinical trials for Vir Biotechnology, Inc..

AI OverviewAI overview is shown in English only.

Vir Biotechnology, Inc. (VIR) is a publicly traded biopharmaceutical company developing therapies for infectious diseases (hepatitis B and delta, HIV) and oncology (prostate cancer, HER2-expressing cancers, solid tumors), with its lead hepatitis delta program in Phase 3 and multiple oncology candidates in Phase 1/2.

  • Cash & equivalents of $278.7M as of 2026-06-30 [sec].
  • Total revenue of $238.9M and net income of $80.1M as of 2026-06-30 [sec].
  • Lead hepatitis delta combination (tobevibart + elebsiran) in Phase 3 with Breakthrough Therapy and Fast Track designations [pipeline].
  • Oncology pipeline includes VIR-5500 (Phase 1, PSMA-targeting T-cell engager for mCRPC), VIR-5818 (Phase 2, HER2-targeted T-cell engager), and VIR-5525 (Phase 1, EGFR-targeted T-cell engager) [pipeline].
  • Partnerships with Sanofi (oncology and infectious disease rights) and Norgine (Europe/Australia/New Zealand rights for tobevibart) [pipeline].

What works

  • Strong cash position of $278.7M as of 2026-06-30 provides runway into 2028 [sec][news].
  • Lead hepatitis delta program has regulatory momentum with Breakthrough Therapy and Fast Track status [pipeline].
  • Multiple near-term catalysts in 2026 across hepatitis and oncology programs [news].

What to weigh

  • Oncology candidates are early-stage (Phase 1/2) and face crowded competitive landscapes (e.g., VIR-5500 has 48 competitors, VIR-5525 has 163) [pipeline].
  • HIV program is preclinical and has no disclosed clinical timeline [pipeline].
  • Revenue of $238.9M as of 2026-06-30 is modest relative to shareholders' equity of $982.5M, suggesting limited product revenue [sec].

From the filings

Quoted directly from source documents.

  • Cash runway into 2028

    “Vir Biotechnology has a cash runway into 2028”

    News · May 16, 2026

  • Partnership with Sanofi for oncology and infectious disease rights

    “Partner: Sanofi Collaboration Terms: In-licensed worldwide rights in oncology and infectious diseases.”

    Pipeline

Risks & what to watch (3)›

Key risks

  • Early-stage oncology pipeline — All oncology candidates are Phase 1/2; VIR-5500 faces 48 competitors, VIR-5525 faces 163 [pipeline].
  • Preclinical HIV program — HIV bnAb program is preclinical with no disclosed clinical timeline [pipeline].
  • Modest product revenue — Revenue of $238.9M as of 2026-06-30 is low relative to equity of $982.5M [sec].

What to watch

  • Phase 2 SOLSTICE data for tobevibart + elebsiran in chronic hepatitis delta at upcoming EASL meeting [news·2026-05-18].
  • VIR-5500 Phase 1 expansion cohort data and ASCO GU update in 2026 [news·2026-02-05].
  • VIR-5818 Phase 2 update expected H2 2026 [news·2026-02-05].
  • ECLIPSE 1 hepatitis delta readout in Q4 2026 [news·2026-02-05].

Sources: Catalysts · News · Pipeline · Generated October 3, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 4 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.6

D/E 0.24 · 1% dilution

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth9.8

6 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal2.9

0 buys · 3 sells (180d)

Pipeline

Regulatory

Financials

Short Interest

as of May 22, 2026
% of float
9.7%
Days to cover
9.0
Shares short
16,117,209
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 →

VIR short interest

Governance

Frequently asked questions

What is the AI investment thesis for Vir Biotechnology, Inc.?

Vir Biotechnology, Inc. (VIR) is a publicly traded biopharmaceutical company developing therapies for infectious diseases (hepatitis B and delta, HIV) and oncology (prostate cancer, HER2-expressing cancers, solid tumors), with its lead hepatitis delta program in Phase 3 and multiple oncology candidates in Phase 1/2.

What is Vir Biotechnology, Inc.'s lead drug candidate?

Vir Biotechnology, Inc.'s most advanced tracked candidate is elebsiran (Phase 3) for Viral Hepatitis.

Who is the CEO of Vir Biotechnology, Inc.?

Dr. Marianne De Backer M.B.A., M.Sc., Ph.D. is the chief executive officer of Vir Biotechnology, Inc. (VIR).

Where is Vir Biotechnology, Inc. headquartered?

Vir Biotechnology, Inc. (VIR) is headquartered in San Francisco, CA, United States.

What therapeutic areas does Vir Biotechnology, Inc. focus on?

Vir Biotechnology, Inc. develops therapies across Oncology, Neurology, Infectious Disease, Gastroenterology.

923 companies304,846 SEC filings22,720 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.