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VIRNasdaq

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 Disease

VIR evidence brief

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Prepared research question

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BioSniper AI · VIR

Vir Biotechnology is a clinical-stage biopharmaceutical company focused on developing transformative therapies for infectious diseases and oncology, with a pipeline including chronic hepatitis delta and other viral programs.

Key risk: No approved products

7.4/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$1.83B

Cash Runway

Financial data as of Jun 30, 2026.

Tracking 5 pipeline candidates · 13 clinical trials · 3 catalysts for Vir Biotechnology, Inc..

AI OverviewAI overview is shown in English only.

Vir Biotechnology is a clinical-stage biopharmaceutical company focused on developing transformative therapies for infectious diseases and oncology, with a pipeline including chronic hepatitis delta and other viral programs.

  • Cash & equivalents of $287.6M as of 2026-06-30 [sec].
  • Total revenue of $238.9M and net income of $80.1M for the period ended 2026-06-30 [sec].
  • Shareholders' equity of $947.5M as of 2026-06-30 [sec].
  • Accumulated deficit of $1.2 billion as of 2026-02-23 [sec_mda].
  • Received $315.0M from Astellas in 2024, including a $240.0M upfront payment [sec_mda · as of 2026-08-05].

What works

  • Strong cash position of $287.6M as of 2026-06-30 provides runway for at least 12 months [sec].
  • Recent net income of $80.1M for the period ended 2026-06-30 indicates improved financial performance [sec].
  • Strategic collaboration with Sanofi and Astellas provides non-dilutive capital and development support [sec_mda · as of 2026-08-05].
  • Industry-leading management team with experience in immunology, infectious diseases, and oncology [sec_mda · as of 2025-02-27].

What to weigh

  • Accumulated deficit of $1.2 billion as of 2026-02-23 reflects historical losses [sec_mda].
  • No approved products generating revenue; company expects to incur net losses for the foreseeable future [sec_mda · as of 2026-05-07].
  • Clinical development costs and milestone payments are uncertain and may require additional capital [sec_mda · as of 2026-08-05].
  • FDA revoked EUA for sotrovimab in December 2024, eliminating a prior revenue source [sec_mda · as of 2025-11-05].

From the filings

Quoted directly from source documents.

  • Accumulated deficit of $1.2 billion as of 2026-02-23

    deficit of $1.2 billion

    SEC MD&A · February 23, 2026

  • Received $315.0M from Astellas in 2024

    we received $315.0 million from Astellas, including a $240.0 million upfront payment

    SEC MD&A · August 5, 2026

Catalyst timeline

  • 2026-12-31 · Phase2_Topline · vir-5818Phase 2 readout for vir-5818 will provide efficacy and safety data.
  • 2031-05-01 · Phase3_Topline — Phase 3 Topline: A Phase 3 Randomized, Open-Label Study to Evaluate the Efficacy and Safety of Tobevibart + ElebsiranPhase 3 topline results for tobevibart + elebsiran will inform regulatory potential.
  • 2031-07-01 · Phase3_Topline — Phase 3 Topline: A Phase 3 Randomized, Open-Label Study to Evaluate the Efficacy and Safety of Tobevibart+Elebsiran CAdditional Phase 3 topline data for tobevibart + elebsiran C will be reported.
Risks & what to watch (4)

Key risks

  • No approved productsCompany does not expect significant revenue from product sales until regulatory approvals, if ever [sec_mda · as of 2026-05-07].
  • Clinical development uncertaintyCosts and timelines for clinical programs are unpredictable; may need additional capital [sec_mda · as of 2026-08-05].
  • Historical accumulated deficitAccumulated deficit of $1.2 billion as of 2026-02-23 indicates long-term unprofitability [sec_mda].
  • Dependence on collaborationsSuccess depends on collaborators' ability to develop licensed product candidates [sec_mda · as of 2026-08-05].

What to watch

  • Phase 2 topline data for vir-5818 expected by 2026-12-31 [catalyst].
  • Phase 3 topline data for tobevibart + elebsiran expected by 2031-05-01 [catalyst].
  • Additional Phase 3 topline data for tobevibart + elebsiran C expected by 2031-07-01 [catalyst].
  • Cash runway updates and potential need for additional financing [sec_mda · as of 2026-05-07].

Sources: SEC filings · SEC MD&A · Generated August 29, 2026 · How we verify sources →

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Evidence & data

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

Cash Runway10.0

Profitable (positive operating cash flow)

Financial Health9.6

D/E 0.24 · 1% dilution

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth8.5

5 candidates

Catalyst Momentum7.0

3 upcoming, next in ~123d

Insider Signal0.8

0 buys · 6 sells (180d)

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

254

Total value held

$1.23B

HolderSharesValue
blackrock, inc.17,998,329$161.3M
arch venture management, llc12,916,663$115.7M
sb investment advisers (uk) ltd10,948,093$98.1M
vanguard capital management llc10,764,206$96.4M
vanguard portfolio management llc9,215,577$82.6M
state street corp7,141,094$64.0M
goldman sachs group inc3,250,227$29.1M
morgan stanley2,854,205$25.6M
adar1 capital management, llc2,744,714$24.6M
geode capital management, llc2,657,843$23.8M

Showing top 10 of 254 institutional holders of Vir Biotechnology, Inc.. Open the full 13F history after sign-in.

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 is a clinical-stage biopharmaceutical company focused on developing transformative therapies for infectious diseases and oncology, with a pipeline including chronic hepatitis delta and other viral programs.

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

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

What is Vir Biotechnology, Inc.'s next catalyst?

Vir Biotechnology, Inc.'s next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: vir-5818" — expected December 31, 2026.

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.

925 companies232,681 SEC filings21,417 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.