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YARW

VYNE Therapeutics Inc.

Pharmaceutical preparations·Phase 2·New York, NY, United States·CEO: Ms. Rebecca Velez Frey Pharm.D.
Immunology

YARW evidence brief

What we can confirm

BioSniper Score:
7.3 / 10
Market Cap:
$72.1M
Lead Asset:
repibresib (Phase 2)

What it means

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

What to watch

Market Cap: $72.1M · Lead Asset: repibresib (Phase 2)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · YARW

VYNE Therapeutics Inc. is a clinical-stage biopharmaceutical company focused on developing therapies for chronic inflammatory and immune-mediated conditions, currently undergoing a strategic review and merger with Yarrow Bioscience.

Key risk: Clinical hold on VYN202

7.3/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$72.1M

Cash Runway

—

Lead Asset

repibresib (Phase 2)

Next Catalyst

—

Financial data as of Jun 30, 2026.

Tracking 3 pipeline candidates · 1 clinical trial for VYNE Therapeutics Inc..

AI OverviewAI overview is shown in English only.

VYNE Therapeutics Inc. is a clinical-stage biopharmaceutical company focused on developing therapies for chronic inflammatory and immune-mediated conditions, currently undergoing a strategic review and merger with Yarrow Bioscience.

  • VYNE is developing VYN202, an oral BD2-selective BET inhibitor for immune-mediated diseases, and repibresib gel (VYN201) for vitiligo, which was discontinued after Phase 2b data [sec_mda · as of 2025-11-06].
  • Cash and equivalents were $22.9M as of 2026-06-30, with a net loss of $3.0M for the quarter [sec].
  • In August 2025, the board initiated a strategic review to maximize shareholder value, including pipeline assessment and financing opportunities [sec_mda · as of 2025-11-06].
  • A merger agreement with Yarrow Bioscience was announced in December 2025, aiming to advance Yarrow's lead program YB-101 for Graves' disease and thyroid eye disease [news · published 2025-12-17].
  • VYN202 is under a partial clinical hold for male subjects, with a non-clinical toxicology study in dogs ongoing, expected to complete in the second half of 2026 [sec_mda · as of 2026-05-15].

What works

  • VYN202 is designed for high BD2 selectivity, potentially avoiding hematologic and gastrointestinal side effects of earlier BET inhibitors [sec_mda · as of 2025-11-06].
  • Repibresib gel has composition of matter patent exclusivity into at least 2042 in the U.S. and 2040 in Europe/Japan, providing long-term protection [sec_mda · as of 2025-11-06].
  • The merger with Yarrow Bioscience brings a potentially first-in-class anti-TSHR antibody for Graves' disease and thyroid eye disease, with a planned Phase 1b/2b trial in 2026 [news · published 2025-12-17].

What to weigh

  • Repibresib gel's Phase 2b vitiligo trial was terminated after failing to meet primary endpoints, with only modest efficacy on secondary measures [sec_mda · as of 2025-11-06].
  • VYN202 is under a partial clinical hold for male subjects, requiring a non-clinical toxicology study that may delay development [sec_mda · as of 2026-05-15].
  • The company has a history of net losses and requires significant additional financing to continue operations, with cash runway only into first half of 2027 [news · published 2025-11-06].
  • The strategic review and merger introduce uncertainty about the future direction and potential dilution for existing shareholders [sec_mda · as of 2025-11-06].

From the filings

Quoted directly from source documents.

  • Repibresib gel Phase 2b vitiligo trial was terminated due to lack of efficacy on primary endpoint.

    “Based on these data, we discontinued the ongoing extension phase of the trial and has terminated the trial.”

    SEC MD&A · November 6, 2025

  • VYN202 is under a partial clinical hold for male subjects, requiring a 12-week dog toxicology study.

    “the clinical hold for two doses of VYN202 for female subjects and indicated that sufficient data from a 12-week non-clinical toxicology study of VYN202 in dogs would be required in order to resume studies in male clinical subjects.”

    SEC MD&A · February 27, 2026

  • Merger with Yarrow Bioscience to advance YB-101 for Graves' disease and thyroid eye disease.

    “VYNE Therapeutics and Yarrow Bioscience Announce Merger Agreement”

    News · December 17, 2025

  • Cash runway into first half of 2027.

    “Cash runway into first half of 2027 based on”

    News · November 6, 2025

Risks & what to watch (4)›

Key risks

  • Clinical hold on VYN202 — Partial clinical hold for male subjects requires a non-clinical toxicology study, delaying development [sec_mda · as of 2026-05-15].
  • Repibresib gel failure — Phase 2b vitiligo trial terminated; seeking external partner for further development [sec_mda · as of 2025-11-06].
  • Financing dependency — Requires additional capital to fund operations; cash runway only into first half of 2027 [news · published 2025-11-06].
  • Merger execution risk — Integration with Yarrow Bioscience and advancement of YB-101 may face regulatory and clinical hurdles [news · published 2025-12-17].

What to watch

  • Completion of the non-clinical toxicology study of VYN202 in dogs, expected in the second half of 2026 [sec_mda · as of 2026-05-15].
  • Progress of the merger with Yarrow Bioscience and initiation of the Phase 1b/2b trial for YB-101 in Graves' disease in the first half of 2026 [news · published 2025-12-17].
  • Outcome of the strategic review and any financing or partnering announcements [sec_mda · as of 2025-11-06].
  • Cash runway updates, as current projections extend into first half of 2027 [news · published 2025-11-06].

Sources: News · SEC filings · SEC MD&A · Generated September 24, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 3 of 6 signals · derived from public data

Cash RunwayN/A

Cash runway data unavailable

Financial Health9.9

D/E 0.07 · 0% dilution

Pipeline Maturity6.0

Lead: Phase 2

Pipeline Breadth5.9

3 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Regulatory

Financials

Short Interest

as of Apr 21, 2026
% of float
0.4%
Days to cover
0.6
Shares short
121,535
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 →

YARW short interest

Governance

Frequently asked questions

What is the AI investment thesis for VYNE Therapeutics Inc.?

VYNE Therapeutics Inc. is a clinical-stage biopharmaceutical company focused on developing therapies for chronic inflammatory and immune-mediated conditions, currently undergoing a strategic review and merger with Yarrow Bioscience.

What is VYNE Therapeutics Inc.'s lead drug candidate?

VYNE Therapeutics Inc.'s most advanced tracked candidate is repibresib (Phase 2) for nonsegmental vitiligo (NSV).

Who is the CEO of VYNE Therapeutics Inc.?

Ms. Rebecca Velez Frey Pharm.D. is the chief executive officer of VYNE Therapeutics Inc. (YARW).

Where is VYNE Therapeutics Inc. headquartered?

VYNE Therapeutics Inc. (YARW) is headquartered in New York, NY, United States.

What therapeutic areas does VYNE Therapeutics Inc. focus on?

VYNE Therapeutics Inc. develops therapies across Immunology.

923 companies304,840 SEC filings22,637 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.