Skip to main content
QNRX

Quoin Pharmaceuticals, Ltd.

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

QNRX evidence brief

What we can confirm

BioSniper Score:
6.5 / 10
Market Cap:
$13.6M
Lead Asset:
qrx003 (Phase 2/Phase 3)

What it means

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

What to watch

Market Cap: $13.6M · Lead Asset: qrx003 (Phase 2/Phase 3)
BioSniper AIPage evidence connected

Prepared research question

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

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · QNRX

Quoin Pharmaceuticals (QNRX) is a late clinical-stage specialty pharmaceutical company developing QRX003 for Netherton Syndrome and other rare/orphan diseases, with a focus on commercial readiness and global regulatory approvals.

Key risk: Limited cash runway

6.5/10

BioSniper Score

Based on 3 of 6 signals

Limited data coverage

Market Cap

$13.6M

Cash Runway

—

Lead Asset

qrx003 (Phase 2/Phase 3)

Next Catalyst

—

Financial data as of Jun 30, 2026.

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

AI OverviewAI overview is shown in English only.

Quoin Pharmaceuticals (QNRX) is a late clinical-stage specialty pharmaceutical company developing QRX003 for Netherton Syndrome and other rare/orphan diseases, with a focus on commercial readiness and global regulatory approvals.

  • Lead product QRX003 is in pivotal registrational clinical testing for Netherton Syndrome under an open FDA IND, with six U.S. and three UK clinical sites [sec · filed 2026-09-18].
  • Cash and equivalents were $3.8M as of 2026-06-30, with net income of -$5.4M and shareholders' equity of $3.9M [sec].
  • The company secured Orphan Drug Designations for QRX003 in the U.S. and Europe, and Fast Track Designation in the U.S. [news · published 2026-03-26].
  • QRX003 is being tested in eight pediatric NS patients in a Compassionate Use program across Ireland, Austria, the Netherlands, and New Zealand [sec · filed 2026-09-18].
  • Quoin closed a private placement financing of up to $104.5 million to support clinical and commercial activities [news · published 2026-03-26].

What works

  • QRX003 has received Orphan Drug Designations in the U.S. and Europe, and Fast Track Designation in the U.S., which may expedite development and market access [news · published 2026-03-26].
  • The company has established a global commercial infrastructure plan, including sales infrastructure in the U.S., Europe, and Japan, and distribution partners in multiple territories [sec · filed 2026-09-18].
  • Positive long-term efficacy data with no reported safety concerns from ongoing clinical studies support the potential of QRX003 [news · published 2026-03-26].

What to weigh

  • The company reported a net loss of -$5.4M for the period ending 2026-06-30, indicating ongoing operational cash burn [sec].
  • Cash reserves of $3.8M as of 2026-06-30 are relatively limited for a company planning late-stage trials and commercialization [sec].
  • QRX003 is still in clinical testing and has not yet received marketing approval in any territory, creating regulatory and commercial uncertainty [sec · filed 2026-09-18].

From the filings

Quoted directly from source documents.

  • QRX003 is entering pivotal registrational clinical testing for Netherton Syndrome under an open FDA IND.

    “QRX003 is entering pivotal registrational clinical testing under an open IND application with the FDA.”

    SEC filings · September 18, 2026

  • The company closed a private placement financing of up to $104.5 million.

    “Closes Private Placement Financing of Up to $104.5 Million”

    News · March 26, 2026

  • QRX003 is being tested in eight pediatric NS patients in a Compassionate Use program.

    “QRX003 is currently being tested in eight pediatric NS patients in a Compassionate Use program in Ireland, Austria, the Netherlands and New Zealand”

    SEC filings · September 18, 2026

Risks & what to watch (3)›

Key risks

  • Limited cash runway — Cash of $3.8M as of 2026-06-30 may be insufficient to complete late-stage trials and commercialization without additional financing [sec].
  • No approved product yet — QRX003 has not received marketing approval in any jurisdiction, creating regulatory and commercial risk [sec · filed 2026-09-18].
  • Dependence on single lead asset — The company's pipeline is heavily reliant on QRX003, with limited diversification across other programs [sec · filed 2026-09-18].

What to watch

  • Initiation of the first company-sponsored Phase 2/3 study for QRX003 in Peeling Skin Syndrome, expected in 2H 2026 [news · published 2026-08-14].
  • Progress of the pediatric Compassionate Use program for QRX003 in Netherton Syndrome, with additional patients expected [sec · filed 2026-09-18].
  • Regulatory decisions on marketing approval applications for QRX003 in the U.S., Europe, and Japan [sec · filed 2026-09-18].
  • Financial sustainability and potential need for further capital raises given the net loss and cash position [sec].

Sources: News · SEC filings · SEC MD&A · Generated October 10, 2026 · How we verify sources →

Run Quoin Pharmaceuticals, Ltd. through your own thesis

Use the pipeline, catalyst, financial, FDA, and market facts on this page as inputs to a protocol you control.

Your protocol can:

  • Turn available Quoin Pharmaceuticals, Ltd. facts into screen rules or deeper checks
  • Show cited findings, blockers, and unresolved evidence together
  • Save the logic and rerun it as the company evidence changes
Run a thesis on this company — freeRun a thesis on this company

Evidence & data

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

Cash RunwayN/A

Cash runway data unavailable

Financial Health3.9

D/E 2.04

Pipeline Maturity8.5

Lead: Phase 2/Phase 3

Pipeline Breadth7.2

4 candidates

Catalyst MomentumN/A

No upcoming catalysts tracked

Insider SignalN/A

No insider transactions in the last 180 days

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

21

Total value held

$7.8M

Showing top 10 of 21 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 (QNRX) is a late clinical-stage specialty pharmaceutical company developing QRX003 for Netherton Syndrome and other rare/orphan diseases, with a focus on commercial readiness and global regulatory approvals.

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.

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.

What therapeutic areas does Quoin Pharmaceuticals, Ltd. focus on?

Quoin Pharmaceuticals, Ltd. develops therapies across Oncology, Immunology.

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.