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Vaxcyte, Inc.

Biopharma developer (SEC filing verified)·Phase 3·San Carlos, CA, United States·CEO: Mr. Grant E. Pickering M.B.A.
OncologyImmunologyInfectious Disease

PCVX evidence brief

What we can confirm

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

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Prepared research question

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BioSniper AI · PCVX

Vaxcyte, Inc. is a clinical-stage biotechnology company developing vaccines to prevent bacterial diseases, with a focus on pneumococcal conjugate vaccines for adults and pediatric populations.

Key risk: No approved products or revenue

6.5/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$8.90B

Cash Runway

18.6 mo

Lead Asset

vax-24 (Phase 2)

Financial data as of Jun 30, 2026.

Tracking 5 pipeline candidates · 7 clinical trials · 3 catalysts for Vaxcyte, Inc..

AI OverviewAI overview is shown in English only.

Vaxcyte, Inc. is a clinical-stage biotechnology company developing vaccines to prevent bacterial diseases, with a focus on pneumococcal conjugate vaccines for adults and pediatric populations.

  • Vaxcyte has incurred net losses each year since inception and expects to continue incurring net losses in the foreseeable future [sec_mda · as of 2025-05-07].
  • As of June 30, 2026, the company reported cash and equivalents of $184.7 million and shareholders' equity of $3,071.3 million [sec].
  • The company is advancing vaccine candidates VAX-31 and VAX-24 through clinical trials, with Phase 3 topline data expected in early 2027 [catalyst].
  • Vaxcyte does not expect to generate revenue from product sales until it obtains regulatory approval for one or more candidates, which is expected to take several years [sec_mda · as of 2026-05-06].
  • The company has raised substantial capital but will need additional funding to complete development, manufacturing, and commercialization of its candidates [sec_mda · as of 2026-02-24].

What works

  • Vaxcyte has a strong cash position with $3.1 billion in shareholders' equity as of June 30, 2026, providing a substantial runway for ongoing operations [sec].
  • The company's lead vaccine candidates, VAX-31 and VAX-24, target large markets in adult and pediatric pneumococcal vaccination, with Phase 3 trials underway [catalyst].
  • Management includes experienced leadership from the pharmaceutical industry, including a former President of Merck Global Vaccines [sec_mda · as of 2026-08-05].

What to weigh

  • Vaxcyte has no approved products or revenue from commercial sales, and it expects to remain pre-revenue for several years [sec_mda · as of 2026-05-06].
  • The company has a history of net losses, with a net loss of $284.3 million for the six months ended June 30, 2026 [sec].
  • Vaxcyte will need to raise substantial additional capital to complete development and commercialization, which may dilute existing shareholders [sec_mda · as of 2026-02-24].
  • The company has discontinued development of certain candidates (VAX-A1, VAX-GI, VAX-PG) due to insufficient efficacy signals, highlighting pipeline risk [sec_mda · as of 2025-08-06].

From the filings

Quoted directly from source documents.

  • Vaxcyte has incurred net losses each year since inception and expects to continue incurring net losses.

    We have incurred net losses in each year since inception and expect to continue to incur net losses in the foreseeable future.

    SEC MD&A · May 7, 2025

  • The company does not expect to generate revenue from product sales until regulatory approval is obtained.

    We do not expect to generate any revenue from commercial product sales unless and until we successfully complete development and obtain regulatory approval for one or more of our vaccine candidates, which we expect will take a number of years.

    SEC MD&A · May 6, 2026

  • Vaxcyte will need to raise substantial additional capital to complete development and commercialization.

    We have raised substantial capital; however, we will need to raise substantial additional capital to complete development, manufacturing and commercialization of our drug candidates.

    SEC MD&A · February 24, 2026

  • The company discontinued development of VAX-PG due to insufficient efficacy signals.

    Additionally, we discontinued further development of VAX-PG. VAX-PG preclinical data demonstrated an acceptable safety profile but not sufficient efficacy signals to warrant further investment.

    SEC MD&A · August 6, 2025

Catalyst timeline

  • 2027-01-01 · Phase 3 Topline for VAX-31/VAX-24 (adult/pediatric)Topline data from a Phase 3 randomized, double-blind, active-controlled study evaluating safety and tolerability of a vaccine candidate.
  • 2027-03-01 · Phase 3 Topline for VAX-31/VAX-24 (pediatric)Topline data from a Phase 3 randomized, double-blind, placebo-controlled study evaluating safety and tolerability of a vaccine candidate.
  • 2027-03-01 · Phase 3 Topline for VAX-31/VAX-24 (adult)Topline data from a Phase 3 randomized, double-blind, active-controlled study evaluating safety and tolerability of a vaccine candidate.
Risks & what to watch (4)

Key risks

  • No approved products or revenueVaxcyte has no commercial products and expects no revenue for several years, relying entirely on funding [sec_mda · as of 2026-05-06].
  • Need for additional capitalThe company will require substantial additional funding to complete development and commercialization, with potential dilution [sec_mda · as of 2026-02-24].
  • Clinical and regulatory uncertaintyPhase 3 trials for VAX-31 and VAX-24 may fail to meet endpoints, delaying or preventing approval [catalyst].
  • Pipeline attritionDiscontinued programs (VAX-A1, VAX-GI, VAX-PG) show risk of candidate failure [sec_mda · as of 2025-08-06].

What to watch

  • Phase 3 topline data for VAX-31 and VAX-24 expected in early 2027 [catalyst].
  • Any updates on regulatory interactions or potential approval timelines for lead candidates [sec_mda · as of 2026-05-06].
  • Future financing events, as the company will need additional capital to fund operations beyond its current cash runway [sec_mda · as of 2026-02-24].
  • Progress in manufacturing scale-up for potential commercial launches [sec_mda · as of 2026-05-06].

Sources: Catalysts · SEC MD&A · Generated August 24, 2026 · How we verify sources →

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Evidence & data

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

Cash Runway5.2

18.6 months

Financial Health9.8

D/E 0.14 · 0% dilution

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth8.5

5 candidates

Catalyst Momentum7.0

3 upcoming, next in ~124d

Insider Signal0.0

0 buys · 41 sells (180d)

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

335

Total value held

$9.82B

HolderSharesValue
janus henderson group plc33,151,750$1.92B
fmr llc16,492,861$958.4M
vanguard capital management llc12,533,402$728.3M
ra capital management, l.p.11,474,599$666.8M
blackrock, inc.10,971,816$637.6M
vanguard portfolio management llc6,279,545$364.9M
wellington management group llp5,614,597$326.3M
state street corp4,440,519$258.0M
deep track capital, lp4,300,000$249.9M
westfield capital management co lp3,646,138$211.9M

Showing top 10 of 335 institutional holders of Vaxcyte, Inc.. Open the full 13F history after sign-in.

Short Interest

as of Apr 30, 2026
% of float
10.0%
Days to cover
10.7
Shares short
14,356,548
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 →

PCVX short interest

Governance

Frequently asked questions

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

Vaxcyte, Inc. is a clinical-stage biotechnology company developing vaccines to prevent bacterial diseases, with a focus on pneumococcal conjugate vaccines for adults and pediatric populations.

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

Vaxcyte, Inc.'s most advanced tracked candidate is vax-24 (Phase 2) for Pneumococcal Vaccines.

What is Vaxcyte, Inc.'s next catalyst?

Vaxcyte, Inc.'s next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: A Phase 3, Randomized, Double-Blind, Active-Controlled Clinical Study to Evaluate the Safety, Tolera" — expected January 1, 2027.

Who is the CEO of Vaxcyte, Inc.?

Mr. Grant E. Pickering M.B.A. is the chief executive officer of Vaxcyte, Inc. (PCVX).

Where is Vaxcyte, Inc. headquartered?

Vaxcyte, Inc. (PCVX) is headquartered in San Carlos, 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.