Quoin Pharmaceuticals
QNRXNASDAQUSD
- Source valuation snapshot. Not a live recalculation.
- Latest filed annual earnings; price snapshot date unavailable. Not forward P/E.
- Diluted earnings per share from the latest filed annual.
- $3.81 Prior regular-session close from the quote source.
- $3.73–$3.81 Regular-session low and high so far today.
- 4.3K Regular-session shares traded · Nov 11, 4:00 PM ET.
- Not yet confirmed The company has not confirmed its next report date. Reported quarters are available in the chart’s Earnings view.
- $3.25–$23.50 52-week trading low and high returned by the quote source.
Understand the Business
Why the Stock Moved
Period-matched expectations history is not yet available. Current metrics are not a substitute for a historical explanation.
The core investment thesis
Own QNRX if Quoin is a pre-commercial, late-stage rare-disease drug developer whose equity value depends less on current financial performance than on whether clinical/regulatory milestones arrive before financing dilution overwhelms shareholders.
QNRX price history
Loading recent earnings…
Investment thesis
What must happen next
QNRX’s value creation depends on rare/orphan disease programs converting high unmet medical need into an approvable regulatory package, not on broad-market sales infrastructure.HoldingMateriality: High
The company describes itself as a late-stage clinical specialty pharmaceutical company. If this holds, a small company can create large option value from one successful asset; if it breaks, the unmet-need narrative never becomes an economic asset.
Watch: FDA or another lead regulator indicates the pivotal endpoints or evidence package are not acceptable for approval.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
The company describes itself as a late-stage clinical specialty pharmaceutical company.
Open source ↗The pipeline can only reach value-inflecting data if QNRX can keep funding development before cash runs out; access to capital is therefore a core operating dependency.WeakeningMateriality: High
Cash and cash equivalents were $3.8 million at FY2025 year-end. If funding remains available, shareholders retain exposure to clinical upside; if funding closes or becomes punitive, even promising science may not accrue to current owners.
Watch: Equity markets become unavailable to QNRX or require deeply discounted issuance with heavy warrant coverage.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
Cash and cash equivalents were $3.8 million at FY2025 year-end.
Open source ↗With only a very small employee base, QNRX’s execution edge must come from managing outsourced clinical, regulatory, and manufacturing partners rather than from internal scale.HoldingMateriality: Medium
The profile reports 10 employees as of 2026-03-26. If outsourced execution works, fixed costs can stay relatively lean through development; if partners fail, delays and rework consume scarce cash before value-inflecting events arrive.
Watch: A CRO misses enrollment targets or produces data-quality issues that delay a pivotal study.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
The profile reports 10 employees as of 2026-03-26.
Open source ↗Per-share upside requires management to fund trials and commercialization without transferring most of the economics to new investors, lenders, warrant holders, or partners.HoldingMateriality: Medium
Stockholders’ equity increased from $5.7 million at FY2023 year-end to $9.2 million at FY2024 year-end and $13.1 million at FY2025 year-end. The company can make clinical progress while existing holders still lose if the financing structure captures too much of the eventual value.
Watch: A deeply discounted equity or warrant-heavy financing materially shifts upside away from existing shareholders.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
Stockholders’ equity increased from $5.7 million at FY2023 year-end to $9.2 million at FY2024 year-end and $13.1 million at FY2025.
Open source ↗Rare-disease demand remains unproven economically until QNRX secures an approval, launch, or monetizing partnership that converts medical need into customer or partner revenue.HoldingMateriality: Medium
GAAP annual revenue was $0 in FY2019. Until that conversion happens, valuation rests on milestones and probability, not on observable customer adoption or recurring cash generation.
Watch: A product approval enables initial commercial orders in the target rare/orphan disease market.
Supporting sources
Source notes are factual paraphrases; read the original disclosures below.
GAAP annual revenue was $0 in FY2019.
Open source ↗
Full investment case & evidence
Loading the original research archive…
Original research
QNRX’s value creation depends on rare/orphan disease programs converting high unmet medical need into an approvable regulatory package, not on broad-market sales infrastructure. If this holds, a small company can create large option value from one successful asset; if it breaks, the unmet-need narrative never becomes an economic asset.
The pipeline can only reach value-inflecting data if QNRX can keep funding development before cash runs out; access to capital is therefore a core operating dependency. If funding remains available, shareholders retain exposure to clinical upside; if funding closes or becomes punitive, even promising science may not accrue to current owners.
With only a very small employee base, QNRX’s execution edge must come from managing outsourced clinical, regulatory, and manufacturing partners rather than from internal scale. If outsourced execution works, fixed costs can stay relatively lean through development; if partners fail, delays and rework consume scarce cash before value-inflecting events arrive.
Per-share upside requires management to fund trials and commercialization without transferring most of the economics to new investors, lenders, warrant holders, or partners. The company can make clinical progress while existing holders still lose if the financing structure captures too much of the eventual value.
Rare-disease demand remains unproven economically until QNRX secures an approval, launch, or monetizing partnership that converts medical need into customer or partner revenue. Until that conversion happens, valuation rests on milestones and probability, not on observable customer adoption or recurring cash generation.
All standing thesis claims
Original report summary
Quoin is a pre-commercial, late-stage rare-disease drug developer whose equity value depends less on current financial performance than on whether clinical/regulatory milestones arrive before financing dilution overwhelms shareholders.
Bull case and bear case
Bull case and bear case for Quoin Pharmaceuticals
Where the evidence on Quoin Pharmaceuticals disagrees: Mixed on the latest evidence (Nov 12, 2026). Of its 5 thesis points, 4 holding and 1 weakening.
Bull case: what the evidence supports
QNRX’s value creation depends on rare/orphan disease programs converting high unmet medical need into an approvable regulatory package, not on broad-market sales infrastructure.
With only a very small employee base, QNRX’s execution edge must come from managing outsourced clinical, regulatory, and manufacturing partners rather than from internal scale.
Per-share upside requires management to fund trials and commercialization without transferring most of the economics to new investors, lenders, warrant holders, or partners.
Rare-disease demand remains unproven economically until QNRX secures an approval, launch, or monetizing partnership that converts medical need into customer or partner revenue.
Bear case: what the evidence questions
The pipeline can only reach value-inflecting data if QNRX can keep funding development before cash runs out; access to capital is therefore a core operating dependency.
Thesis-Break Engine
Thesis-break watch · Quoin Pharmaceuticals
Loading the break-condition record for Quoin Pharmaceuticals.
MARKET + FINANCIAL SNAPSHOT
The numbers behind the thesis
What Changed
- MixedReported results of operations (earnings release).
Quoin Pharmaceuticals filed an SEC 8-K on 2026-11-06: Reported results of operations (earnings release). It is a dated development that tests the current thesis.
- MixedEntered a material definitive agreement.
Quoin Pharmaceuticals filed an SEC 8-K on 2026-11-04: Entered a material definitive agreement. It is a dated development that tests the current thesis.
- MixedRegulation FD disclosure.
Quoin Pharmaceuticals filed an SEC 8-K on 2026-10-20: Regulation FD disclosure. It is a dated development that tests the current thesis.
Risks / falsifiers
What could break the thesis
- FDA or another lead regulator indicates the pivotal endpoints or evidence package are not acceptable for approval.
- Equity markets become unavailable to QNRX or require deeply discounted issuance with heavy warrant coverage.
- A CRO misses enrollment targets or produces data-quality issues that delay a pivotal study.
- A deeply discounted equity or warrant-heavy financing materially shifts upside away from existing shareholders.
- A product approval enables initial commercial orders in the target rare/orphan disease market.
QNRX news
Loading headlines…
Financial statements
QNRX income statement
Annual filed results · USD · Oldest to newest. Margins are calculated from the reported figures.
