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QNCXNasdaq

Quince Therapeutics, Inc.

Biopharma developer (SEC filing verified)·Phase 3·South San Francisco, CA, United States·CEO: Dr. Dirk Thye M.D.
Rare DiseaseNeurology

QNCX evidence brief

What we can confirm

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What it means

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 · QNCX

Quince Therapeutics, Inc. is a biopharmaceutical company focused on developing therapies for rare diseases, currently evaluating strategic alternatives after its lead drug candidate eDSP failed to meet endpoints in a Phase 3 trial.

Key risk: Lead drug failure

4.4/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$34.3M

Cash Runway

18.8 mo

Lead Asset

edsp (Phase 3)

Financial data as of Jun 30, 2026.

Tracking 2 pipeline candidates · 2 clinical trials · 1 catalyst for Quince Therapeutics, Inc..

Similar companies

AI OverviewAI overview is shown in English only.

Quince Therapeutics, Inc. is a biopharmaceutical company focused on developing therapies for rare diseases, currently evaluating strategic alternatives after its lead drug candidate eDSP failed to meet endpoints in a Phase 3 trial.

  • Lead drug candidate eDSP failed to meet primary or secondary endpoints in the Phase 3 NEAT clinical trial for Ataxia-Telangiectasia (A-T) [sec_mda · as of 2026-08-14].
  • Cash and equivalents of $116.0M as of 2026-06-30 [sec].
  • Accumulated deficit of $500.0 million as of June 30, 2026 [sec_mda · as of 2026-08-14].
  • Net income of -$75.5M for the period ending 2026-06-30 [sec].
  • Shareholders' equity of -$35.7M as of 2026-06-30 [sec].

What works

  • Cash position of $116.0M as of 2026-06-30 provides a substantial buffer for evaluating strategic alternatives [sec].
  • The company has a proprietary AIDE technology platform that was previously the focus of its strategic efforts [sec_mda · as of 2025-08-11].

What to weigh

  • Lead drug candidate eDSP failed to meet primary or secondary endpoints in the Phase 3 NEAT trial, and development has been discontinued [sec_mda · as of 2026-08-14].
  • The company has an accumulated deficit of $500.0 million as of June 30, 2026, with no product revenue expected unless marketing approval is obtained [sec_mda · as of 2026-08-14].
  • Shareholders' equity is negative at -$35.7M as of 2026-06-30, indicating a net deficit position [sec].
  • The company has previously disclosed substantial doubt about its ability to continue as a going concern [sec_mda · as of 2025-05-13].

From the filings

Quoted directly from source documents.

  • eDSP failed to meet endpoints in Phase 3 trial

    the primary endpoints of the NEAT trial did not reach statistical significance

    SEC MD&A · August 14, 2026

  • Accumulated deficit as of June 30, 2026

    As of June 30, 2026, we had an accumulated deficit of $500.0 million.

    SEC MD&A · August 14, 2026

Catalyst timeline

  • 2026-12-31 · Phase2_Topline · lam-001 — Phase 2 Readout: lam-001Topline data from the Phase 2 trial of lam-001 will be reported, which may inform the company's future direction.
Risks & what to watch (4)

Key risks

  • Lead drug failureeDSP failed Phase 3 endpoints; development discontinued, leaving no active pipeline candidate [sec_mda · as of 2026-08-14].
  • Going concern uncertainty
  • Negative shareholders' equityShareholders' equity of -$35.7M as of 2026-06-30 indicates liabilities exceed assets [sec].
  • No product revenueNo product revenue expected unless marketing approval is obtained, which is uncertain [sec_mda · as of 2026-08-14].

What to watch

  • Phase 2 topline readout for lam-001 expected on 2026-12-31 [catalyst].
  • Any announcement of strategic alternatives, including potential reverse merger or asset sale [sec_mda · as of 2026-05-11].
  • Cash burn rate and any additional financing activities given the negative equity position [sec].

Sources: SEC filings · SEC MD&A · Generated August 28, 2026 · How we verify sources →

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Evidence & data

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

Cash Runway5.2

18.8 months

Financial Health0.5

OCF -$19M · Net income -$75M

Pipeline Maturity8.5

Lead: Phase 3

Pipeline Breadth4.6

2 candidates

Catalyst Momentum3.0

1 upcoming, next in ~123d

Insider SignalN/A

No insider transactions in the last 180 days

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

2

Total value held

$26K

HolderSharesValue
tudor investment corp et al220,000$22K
gen-wealth partners inc33,018$3K

Short Interest

as of Apr 21, 2026
% of float
27.7%
Days to cover
0.4
Shares short
1,382,655
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 →

QNCX short interest

Governance

Frequently asked questions

What is the AI investment thesis for Quince Therapeutics, Inc.?

Quince Therapeutics, Inc. is a biopharmaceutical company focused on developing therapies for rare diseases, currently evaluating strategic alternatives after its lead drug candidate eDSP failed to meet endpoints in a Phase 3 trial.

What is Quince Therapeutics, Inc.'s lead drug candidate?

Quince Therapeutics, Inc.'s most advanced tracked candidate is edsp (Phase 3) for Duchenne muscular dystrophy (DMD).

What is Quince Therapeutics, Inc.'s next catalyst?

Quince Therapeutics, Inc.'s next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: lam-001" — expected December 31, 2026.

Who is the CEO of Quince Therapeutics, Inc.?

Dr. Dirk Thye M.D. is the chief executive officer of Quince Therapeutics, Inc. (QNCX).

Where is Quince Therapeutics, Inc. headquartered?

Quince Therapeutics, Inc. (QNCX) is headquartered in South San Francisco, 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.