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Quoin Pharmaceuticals Ltd.Bullish
Quoin Pharmaceuticals announced the publication of a peer-reviewed manuscript in 'Dermatology and Therapy' detailing a pediatric compassionate-use case for its Netherton Syndrome treatment, QRX003. The patient achieved clear skin and complete itch relief over 21 months of treatment, while the company expects to complete recruitment for its ongoing Phase 2/3 study by the end of 2026 and report topline data in Q2 2027.…more
Quoin Pharmaceuticals Ltd.
Quoin Pharmaceuticals announced that its lead product candidate, QRX003, has been granted Orphan Drug Designation by the European Medicines Agency (EMA) for the treatment of Peeling Skin Syndrome. This designation provides the company with benefits including scientific advice, fee reductions, and 10 years of market exclusivity in Europe upon marketing authorization. The company remains on track to initiate its first formal clinical trial for this indication before the end of the year.…more
Quoin Pharmaceuticals Ltd.
This is a SCHEDULE 13G/A filing by Ikarian Capital, LLC regarding its beneficial ownership in Quoin Pharmaceuticals Ltd. The reporting entity has submitted an update to the SEC concerning its existing equity position.…more
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Quoin Pharmaceuticals Publishes Peer-Reviewed Case Report on QRX003 for Netherton Syndrome…more
Quoin Pharmaceuticals announced the publication of a peer-reviewed case report demonstrating the efficacy of QRX003 in treating Netherton Syndrome. The company expects to report topline data from its ongoing Phase 2/3 study in the second quarter of 2027.…more
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Quoin Pharmaceuticals' lead candidate QRX003 has been granted Orphan Drug Designation by the EMA for treating Peeling Skin Syndrome. This milestone provides the company with 10 years of market exclusivity in Europe and various regulatory incentives.…more
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Quoin Pharmaceuticals announced that a peer-reviewed paper on its investigational Netherton Syndrome treatment, QRX003, has been accepted for publication. While the company reports positive clinical progress, the drug remains in late-stage clinical trials pending final regulatory approval.…more
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