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CRVS

Corvus Pharmaceuticals, Inc.

Pharmaceutical preparations·Commercial·South San Francisco, CA, United States·CEO: Dr. Richard A. Miller M.D.
OncologyImmunologyInfectious DiseaseMetabolicDermatology

CRVS evidence brief

What we can confirm

BioSniper Score:
8.8 / 10
Market Cap:
$1.12B
Lead Asset:
ciforadenant (Phase 2)

What it means

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

What to watch

Market Cap: $1.12B · Lead Asset: ciforadenant (Phase 2)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · CRVS

Corvus Pharmaceuticals is a clinical-stage biotech developing its oral ITK inhibitor soquelitinib across oncology and immune indications, with a Phase 3 PTCL trial and a Phase 1 atopic dermatitis trial ongoing.

Key risk: Single-asset dependency

8.8/10

BioSniper Score

Based on 4 of 6 signals

Market Cap

$1.12B

Cash Runway

—

Lead Asset

ciforadenant (Phase 2)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 4 pipeline candidates · 5 clinical trials for Corvus Pharmaceuticals, Inc..

AI OverviewAI overview is shown in English only.

Corvus Pharmaceuticals is a clinical-stage biotech developing its oral ITK inhibitor soquelitinib across oncology and immune indications, with a Phase 3 PTCL trial and a Phase 1 atopic dermatitis trial ongoing.

  • Cash & equivalents of $18.9M as of 2026-06-30 [sec].
  • Net loss of $18.0M for the six months ended 2026-06-30 [sec].
  • Shareholders' equity of $225.3M as of 2026-06-30 [sec].
  • Lead asset soquelitinib is being tested in five different diseases, including a Phase 3 registrational trial in PTCL and a Phase 1 trial in atopic dermatitis [sec_mda · as of 2026-03-12].
  • Cash runway expected to support operations into Q2 2028 [news · published 2026-08-10].

What works

  • Soquelitinib is being studied across multiple indications (PTCL, atopic dermatitis, asthma, etc.), which diversifies pipeline risk [news · published 2026-08-17].
  • The company has a Phase 3 registrational trial underway for soquelitinib in PTCL, a potential path to approval [sec_mda · as of 2026-03-12].
  • Cash runway extends into Q2 2028, providing a multi-year operational buffer [news · published 2026-08-10].

What to weigh

  • The company reported a net loss of $18.0M for the first half of 2026, with a Q1 2026 net loss of $13.69M [sec] [news · published 2026-05-10].
  • Corvus is a single-asset biotech heavily reliant on soquelitinib, creating concentration risk [news · published 2026-08-17].
  • A $46.16M shelf registration filed in May 2026 could lead to shareholder dilution [news · published 2026-05-10].

From the filings

Quoted directly from source documents.

  • Soquelitinib Phase 3 registrational trial in PTCL

    “enrollment and completion of our ongoing Phase 3 registrational clinical trial for soquelitinib in PTCL”

    SEC MD&A · March 12, 2026

Catalyst timeline

  • 2024-04-16 · Phase 1 atopic dermatitis trial start — A Phase 1, randomized, blinded, placebo-controlled dose escalation/expansion study of soquelitinib in moderate-to-severe atopic dermatitis.
  • 2024-10-02 · Phase 3 PTCL trial start — A Phase 3, randomized, open-label study of soquelitinib versus physician's choice in relapsed/refractory PTCL.
  • 2026-02-01 · Phase 2 start (indication not fully specified in chunk) — A Phase 2 multicenter, randomized, double-blind, placebo-controlled study initiated.
Risks & what to watch (3)›

Key risks

  • Single-asset dependency — Corvus is heavily reliant on soquelitinib; failure in one indication could severely impact the company. [news · published 2026-08-17]
  • Net losses and cash burn — Net loss of $18.0M in H1 2026; Q1 2026 net loss of $13.69M. [sec] [news · published 2026-05-10]
  • Potential dilution from shelf offering — A $46.16M shelf registration for ~2.99M shares was filed in May 2026. [news · published 2026-05-10]

What to watch

  • Interim futility analysis for soquelitinib in PTCL expected in Q1 2027 [news · published 2026-08-10].
  • Advancement of soquelitinib in atopic dermatitis, with Phase 1 completion planned [sec_mda · as of 2026-03-12].
  • Cash runway into Q2 2028 and any changes in operating expenses [news · published 2026-08-10].

Sources: Catalysts · News · SEC MD&A · Generated October 13, 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 Health9.9

D/E 0.06 · 0% dilution

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth7.2

4 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider Signal9.5

3 buys · 0 sells (180d)

Pipeline

Regulatory

Financials

Short Interest

as of May 20, 2026
% of float
24.9%
Days to cover
14.9
Shares short
18,385,941
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 →

CRVS short interest

Governance

Frequently asked questions

What is the AI investment thesis for Corvus Pharmaceuticals, Inc.?

Corvus Pharmaceuticals is a clinical-stage biotech developing its oral ITK inhibitor soquelitinib across oncology and immune indications, with a Phase 3 PTCL trial and a Phase 1 atopic dermatitis trial ongoing.

What is Corvus Pharmaceuticals, Inc.'s lead drug candidate?

Corvus Pharmaceuticals, Inc.'s most advanced tracked candidate is ciforadenant (Phase 2) for metastatic RCC.

Who is the CEO of Corvus Pharmaceuticals, Inc.?

Dr. Richard A. Miller M.D. is the chief executive officer of Corvus Pharmaceuticals, Inc. (CRVS).

Where is Corvus Pharmaceuticals, Inc. headquartered?

Corvus Pharmaceuticals, Inc. (CRVS) is headquartered in South San Francisco, CA, United States.

What therapeutic areas does Corvus Pharmaceuticals, Inc. focus on?

Corvus Pharmaceuticals, Inc. develops therapies across Oncology, Immunology, Infectious Disease, Metabolic, Dermatology.

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.