Recent 8-K filings for QNRX
Highest-materiality recent filing
Quoin reports positive QRX003 interim data, raises up to $50M in private placement
- Private placement up to $50M: $30.8M upfront at $4.88/ADS+warrant, 6,305,300 ADSs and warrants for 3,152,650 ADSs.
- Net proceeds ~$29M at Aug 31 close; funds into 2H 2029; proceeds for QRX003 development and general corporate.
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Quoin publishes peer-reviewed QRX003 paper; pediatric Netherton case clear at 21 months
Peer-reviewed paper in Dermatology and Therapy, published online Oct 13, 2026, introduces QRX003 and reports Prof. Alan Irvine's pediatric compassionate-use case.
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Quoin's QRX003 wins EMA Orphan Drug Designation for Peeling Skin Syndrome
EMA granted Orphan Drug Designation to lead candidate QRX003 for Peeling Skin Syndrome on Oct 14, 2026, giving 10 years of EU market exclusivity if approved.
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FDA grants Fast Track to Quoin's QRX003 for Peeling Skin Syndrome
FDA granted Fast Track Designation to QRX003 for Peeling Skin Syndrome (PSS) on Sept 22, 2026.
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FDA grants Rare Pediatric Disease Designation for QRX003 in Peeling Skin Syndrome
Second RPD designation for QRX003; first was for Netherton Syndrome.
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Quoin reports positive QRX003 interim data, raises up to $50M in private placement
Private placement up to $50M: $30.8M upfront at $4.88/ADS+warrant, 6,305,300 ADSs and warrants for 3,152,650 ADSs.
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Quoin shareholders approve NED compensation increase to $250k base retainer
Annual base retainer for non-employee directors increased to up to $250,000, set annually by Compensation Committee.
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Quoin Q2 net loss $5.4M; FDA clears first-ever IND for Peeling Skin Syndrome
Q2 2026 net loss $5.4M vs $3.7M in Q2 2025; six-month loss $10.4M vs $7.5M.
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Quoin Pharma gets FDA conditional approval of brand name QYLEKI for Netherton Syndrome candidate
FDA conditionally approved QYLEKI as proposed brand name for QRX003, an investigational treatment for Netherton Syndrome.
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Quoin Pharma gets Japan MHLW Orphan Drug Designation for QRX003 in Netherton Syndrome
Japan MHLW granted Orphan Drug Designation to QRX003 lotion (4%) for Netherton Syndrome, a rare genetic skin disorder with no approved treatments.
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Quoin Q1 net loss $5M; FDA says single Phase 3 may suffice for QRX003
Net loss $5.0M in Q1 2026 vs $3.8M in Q1 2025; cash $14M expected to fund operations into 2027.
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Quoin raises up to $104.5M, advances QRX003 regulatory path, reports 2025 net loss $15.8M
Closed private placement for up to $104.5M ($16.5M at closing, $88M warrant potential).
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FDA grants Fast Track Designation to Quoin's QRX003 for Netherton Syndrome
Fast Track Designation granted to QRX003 lotion (4%) for Netherton Syndrome, a rare genetic skin disorder with no approved treatments.
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Filed application with Saudi FDA for Breakthrough Medicine Designation for QRX003 for Netherton Syndrome.
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Quoin Pharmaceuticals approves stock option award agreement forms under 2025 Equity Plan
Compensation Committee approved forms of Incentive and Non-Qualified Stock Option Award Agreements on Nov 14, 2025.
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Quoin achieves 4% and 5% rapamycin loadings in topical and patch; clinical testing planned H1 2026
Rapamycin loading 4% w/w in proprietary topical formulation; 5% w/w in dermal patch system.
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Quoin Pharma reports Q3 net loss of $3.9M, raises up to $105.3M in private placement
Net loss of $3.9M for Q3 2025 ($11.5M YTD) vs $2.3M and $6.7M in prior-year periods; R&D spend increased to $2.3M for Q3.
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Quoin Pharmaceuticals receives FDA Orphan Drug Designation for QRX003 in Netherton Syndrome
FDA grants Orphan Drug Designation to QRX003 for Netherton Syndrome; 7-year US exclusivity if approved.
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Quoin raises $16.6M upfront in PIPE; up to $104.6M total with milestone warrants
Upfront gross proceeds of $16.6M ($15M net) from private placement; proceeds for QRX003 development and general corporate.
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Quoin finalizes CFO exit: $433K lieu of notice, $108K bonus, extended options
Separation agreement signed August 21; effective August 15, 2025.
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Quoin shareholders approve increase in shares from 100M to 5B; Sally Lawlor named new CFO
Shareholders approved amendment to increase authorized ordinary shares from 100,000,000 to 5,000,000,000 (50x).
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Quoin Pharma Q2 net loss $3.7M; QRX003 advances with FDA/EMA designations
Net loss Q2 2025 $3.7M vs $2.0M YoY; cash $7.8M supports operations into Q1 2026.
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CFO Gordon Dunn to depart Quoin Pharmaceuticals; will continue until successor named
Mutual separation agreed on July 3, 2025; CFO Gordon Dunn to leave later this year.
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Quoin Pharma receives FDA Rare Pediatric Disease Designation for QRX003 in Netherton Syndrome
FDA granted Rare Pediatric Disease Designation (RPDD) on June 24, 2025 for QRX003.
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Quoin Pharmaceuticals sets 2025 AGM for August 21; shareholder proposal deadline June 30
2025 Annual General Meeting scheduled for August 21, 2025.
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Quoin Pharma awards CEO $331k and COO $265k in 2024 cash bonuses
Compensation Committee approved 2024 annual cash bonus of $331,238 for CEO Dr. Michael Myers.
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Quoin Pharma gets FDA clearance to start second pivotal Netherton Syndrome study for QRX003
FDA cleared Study CL-QRX003-002, testing whole-body QRX003 (~80% BSA) with off-label systemic therapy in ~12-15 subjects.
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Quoin Pharma gets EMA Orphan Drug Designation for QRX003 for Netherton Syndrome
EMA grants Orphan Drug Designation for QRX003, a topical treatment for Netherton Syndrome, a rare disease with no approved therapies.
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Quoin Pharma Q1 net loss $3.8M; positive QRX003 data and patent expansion
Cash of $11.6M at March 31, 2025; expected to fund operations into Q1 2026.
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Quoin Pharma regains Nasdaq minimum bid price compliance; delisting risk removed
Received Nasdaq Compliance Notice on April 29, 2025 confirming minimum bid price compliance.
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Quoin Pharma announces 1-for-20 reverse ADS split to regain Nasdaq compliance
ADS ratio changed from 1:1 to 1:20 (one ADS now represents 20 ordinary shares) effective April 8, 2025.
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Quoin Pharma approves 1-for-35 reverse ADS split effective April 9 to meet Nasdaq bid price rule
ADS ratio changes from 1 ADS = 1 ordinary share to 1 ADS = 35 ordinary shares, effective April 9, 2025.
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After 6 weeks of daily whole-body QRX003, the pediatric Netherton patient's skin is almost completely healed.
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Quoin Pharmaceuticals replaces auditor Marcum LLP with CBIZ CPAs after attest business acquisition
Marcum LLP resigned as auditor on March 18, 2025; CBIZ CPAs P.C. engaged effective immediately for FY 2025.
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Quoin reports FY2024 net loss $9.0M; cash $14.1M; positive QRX003 whole-body data in Netherton
Cash of $14.1M at Dec 31, 2024 expected to fund operations into Q2 2026.
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IGA score improved from 7 to 1-2 (0-10 scale) after two weeks of whole-body QRX003 treatment.
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Quoin launches Netherton NOW campaign for rare disease awareness
Campaign 'NETHERTON NOW' launched Feb 4, 2025 to raise awareness for Netherton Syndrome.
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Quoin reports reversal of QRX003 benefits 4 weeks post-discontinuation in Netherton syndrome study
M-IASI score returned from 3 (12 weeks) to 18 at 4 weeks post-discontinuation, equaling baseline of 18.
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IGA score improved from 'severe' at baseline to 'mild' after six weeks of twice-daily QRX003 dosing.
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M-IASI score improved from 18 to 3; WINRS from 7 to 2; IGA from Moderate to Almost Clear after 12 weeks.
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Quoin Pharmaceuticals prices $6.8M public offering of ADSs and warrants
Gross proceeds ~$6.8M from offering of 15,111,110 ADSs (or pre-funded warrants) and Series F/G warrants at $0.45 per unit.
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Quoin Pharma gets FDA clearance for whole-body QRX003 study in Netherton Syndrome
FDA clearance for new Netherton Syndrome study of QRX003 applied to >80% BSA twice daily for 12 weeks in up to 8 patients.
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Quoin shareholders approve charter amendments and executive compensation; board grants options
Shareholders approved amendments to Articles reducing quorum to 33 1/3% (25% for foreign private issuers) and aligning special meeting provisions.
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Quoin Q3 net loss $2.3M; initiates Peeling Skin Syndrome study; management buys shares
Net loss of $2.3M for Q3 2024 vs $1.9M in Q3 2023; nine-month net loss $6.7M vs $6.6M.
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Quoin Pharma gets Nasdaq bid-price extension to April 28, 2025
Nasdaq granted additional 180-day grace period until April 28, 2025 to regain $1.00 minimum bid price compliance.
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Quoin Pharma sets 2024 AGM for Dec 5; shareholder proposals due Oct 10
Annual meeting scheduled for December 5, 2024, more than 30 days after last year's anniversary.
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Quoin posts Q2 net loss of $2.0M; cash $12.6M; expands Netherton trials internationally
Cash, cash equivalents and marketable securities of $12.6M as of June 30, 2024; expected to fund operations into late 2025.
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Quoin Pharma receives Nasdaq notice for non-compliance with $1.00 minimum bid price
Received Nasdaq notice on April 29, 2024 for failing to maintain minimum bid price of $1.00 per ADS for 31 consecutive business days through April 26, 2024.
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Quoin shareholders approve issuance of shares to Alumni Capital LP
Special meeting on April 5, 2024 approved Alumni Issuance Proposal.
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Quoin Pharma reports Q4/FY2023 net loss $8.7M; cash runway to H2 2025; positive QRX003 data
Net loss Q4 2023 $2.0M (flat YoY); FY2023 $8.7M vs $9.4M in 2022.
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Raised $6.5M gross from public offering of ADSs, pre-funded and Series D/E warrants at $1.60 combined per unit.
Materiality & sentiment trend
Max materiality 0.90 · Median 0.60 · Most common event other_material