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QNRXNasdaq

Quoin Pharmaceuticals, Ltd.

Biopharma developer (SEC filing verified)·Commercial·Ashburn, VA, United States·CEO: Dr. Michael Myers Ph.D.
OncologyImmunology

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BioSniper AI · QNRX

Quoin Pharmaceuticals, Ltd. is a clinical-stage biopharmaceutical company focused on developing and commercializing treatments for rare and orphan diseases, with its lead candidate QRX003 in late-stage trials for Netherton Syndrome.

Key risk: Cash runway and funding need

5.9/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$12.3M

Cash Runway

10.2 mo

Lead Asset

qrx003 (Phase 2/Phase 3)

Financial data as of Jun 30, 2026.

Tracking 4 pipeline candidates · 4 clinical trials · 3 catalysts for Quoin Pharmaceuticals, Ltd..

Similar companies

AI OverviewAI overview is shown in English only.

Quoin Pharmaceuticals, Ltd. is a clinical-stage biopharmaceutical company focused on developing and commercializing treatments for rare and orphan diseases, with its lead candidate QRX003 in late-stage trials for Netherton Syndrome.

  • Lead product candidate QRX003 is in late-stage clinical testing for Netherton Syndrome (NS), a rare genetic skin disorder with no approved treatments [sec_mda · as of 2026-05-07].
  • Cash and equivalents were $3.8M as of 2026-06-30, with a net loss of -$5.4M for the period [sec].
  • The company has not generated any revenue from product sales and expects to require additional funding to complete development and commercialization [sec_mda · as of 2026-08-14].
  • Quoin has commercial agreements in place for QRX003 in Canada, Australia/New Zealand, Singapore, Israel, Central and Eastern Europe, Turkey, and several Latin American countries [sec_mda · as of 2026-05-07].

What works

  • QRX003 targets Netherton Syndrome, a rare disease with no FDA-approved treatments, potentially addressing a high unmet medical need [sec · filed 2025-11-12].
  • The company has established commercial distribution agreements for QRX003 in multiple territories outside the U.S., Europe, and Japan [sec_mda · as of 2026-05-07].
  • Quoin is advancing QRX003 through late-stage clinical trials with Phase 2 and Phase 3 topline data expected by end of 2026 [catalyst_timeline].

What to weigh

  • The company has no revenue from product sales and has incurred a net loss of -$5.4M as of 2026-06-30, with cash of only $3.8M, indicating a need for near-term funding [sec] [sec_mda · as of 2026-08-14].
  • Quoin will need to obtain further funding through equity offerings, debt, or partnerships, and failure to do so could force delay, reduction, or termination of development programs [sec_mda · as of 2026-08-14].
  • The company's success depends entirely on the clinical and regulatory outcomes of QRX003, with no other late-stage pipeline candidates mentioned.

From the filings

Quoted directly from source documents.

  • QRX003 is in late-stage clinical testing for Netherton Syndrome.

    complete the late-stage clinical testing of QRX003 in NS and, if successful, file for marketing approval in the United States, Europe, Japan and the other territories for which we have commercial agreements in place

    SEC MD&A · May 7, 2026

  • The company has no approved treatments for its target indications.

    clinical indications that have been identified by the Company as targets include Microcystic Lymphatic Malformations and Venous Malformations among others. For each of these initial targets, there are currently no FDA approved treatments or cures.

    SEC filings · November 12, 2025

  • Quoin has not generated revenue and needs additional funding.

    We do not expect to generate revenue from product sales unless and until we successfully complete development and obtain marketing approval for one or more of our product candidates, which we expect will take a number of years and is subject to significant uncertainty.

    SEC MD&A · August 14, 2026

Catalyst timeline

  • 2026-12-31 · Phase2_Topline · qrx003 — Phase 2 Readout: qrx003Topline results from the Phase 2 study of QRX003 in Netherton Syndrome are expected.
  • 2026-12-31 · Phase3_Topline · qrx003 — Phase 3 Topline: A Multicenter, Randomized, Vehicle-Controlled, Double-Blind, Parallel Comparison Study of QRX003 LotTopline results from the vehicle-controlled Phase 3 study of QRX003 are expected.
  • 2027-03-31 · Phase3_Topline · qrx003 — Phase 3 Topline: A Multicenter, Open-label Study of QRX003 Lotion in Participants With Netherton SyndromeTopline results from the open-label Phase 3 study of QRX003 are expected.
Risks & what to watch (4)

Key risks

  • Cash runway and funding needWith $3.8M cash and no revenue, the company must raise additional capital soon to continue operations [sec] [sec_mda · as of 2026-08-14].
  • Single-product pipeline riskQuoin's prospects depend entirely on QRX003; failure in clinical trials or regulatory hurdles would be material [sec_mda · as of 2026-05-07].
  • No approved treatments for targetsWhile no approved treatments exist, this also means no prior regulatory pathway, increasing development risk [sec · filed 2025-11-12].
  • Forward-looking statement uncertaintyThe company's plans are subject to risks and uncertainties that could cause actual results to differ materially [sec_mda · as of 2026-08-14].

What to watch

  • Phase 2 topline data for QRX003 expected by 2026-12-31 [catalyst_timeline].
  • Phase 3 topline data for QRX003 (vehicle-controlled study) expected by 2026-12-31 [catalyst_timeline].
  • Additional Phase 3 topline data for QRX003 (open-label study) expected by 2027-03-31 [catalyst_timeline].
  • Any financing or partnership announcements to extend cash runway beyond $3.8M [sec].

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

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Evidence & data

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

Cash Runway2.8

10.2 months

Financial Health3.9

D/E 2.04

Pipeline Maturity8.5

Lead: Phase 2/Phase 3

Pipeline Breadth7.2

4 candidates

Catalyst Momentum7.0

3 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

14

Total value held

$2.7M

Showing top 10 of 14 institutional holders of Quoin Pharmaceuticals, Ltd.. Open the full 13F history after sign-in.

Short Interest

as of May 22, 2026
% of float
4.8%
Days to cover
2.2
Shares short
85,556
Daily short volume (May 4, 2026)
41.9%

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 →

QNRX short interest

Governance

Frequently asked questions

What is the AI investment thesis for Quoin Pharmaceuticals, Ltd.?

Quoin Pharmaceuticals, Ltd. is a clinical-stage biopharmaceutical company focused on developing and commercializing treatments for rare and orphan diseases, with its lead candidate QRX003 in late-stage trials for Netherton Syndrome.

What is Quoin Pharmaceuticals, Ltd.'s lead drug candidate?

Quoin Pharmaceuticals, Ltd.'s most advanced tracked candidate is qrx003 (Phase 2/Phase 3) for Netherton Syndrome.

What is Quoin Pharmaceuticals, Ltd.'s next catalyst?

Quoin Pharmaceuticals, Ltd.'s next tracked catalyst is a Phase2_Topline event — "Phase 2 Readout: qrx003" — expected December 31, 2026.

Who is the CEO of Quoin Pharmaceuticals, Ltd.?

Dr. Michael Myers Ph.D. is the chief executive officer of Quoin Pharmaceuticals, Ltd. (QNRX).

Where is Quoin Pharmaceuticals, Ltd. headquartered?

Quoin Pharmaceuticals, Ltd. (QNRX) is headquartered in Ashburn, VA, 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.