Quoin Pharmaceuticals Announces EMA Orphan Drug Designation for QRX003, Advancing Late-Stage Trials for Netherton Syndrome Treatment

Reuters

2025/05/21

<a href="https://laohu8.com/S/QNRX">Quoin Pharmaceuticals</a> Announces EMA Orphan Drug Designation for QRX003, Advancing Late-Stage Trials for Netherton Syndrome Treatment

Quoin Pharmaceuticals Ltd. has announced that the European Medicines Agency (EMA) has granted Orphan Drug Designation for their lead product, QRX003, for the treatment of Netherton Syndrome. This designation provides Quoin Pharmaceuticals with incentive benefits such as scientific advice on study protocols, fee reductions, and access to EU grants. If approved, QRX003 will receive 10 years of market exclusivity in Europe. QRX003 is currently undergoing multiple late-stage clinical trials as a topical, non-systemic treatment for Netherton Syndrome, a condition for which no approved therapies currently exist.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Quoin Pharmaceuticals Ltd. published the original content used to generate this news brief via EDGAR, the Electronic Data Gathering, Analysis, and Retrieval system operated by the U.S. Securities and Exchange Commission (Ref. ID: 0001104659-25-051324), on May 21, 2025, and is solely responsible for the information contained therein.

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This designation provides Quoin Pharmaceuticals with incentive benefits such as scientific advice on study protocols, fee reductions, and access to EU grants. If approved, QRX003 will receive 10 years of market exclusivity in Europe. QRX003 is currently undergoing multiple late-stage clinical trials as a topical, non-systemic treatment for Netherton Syndrome, a condition for which no approved therapies currently exist.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<em>Disclaimer: <span>This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Quoin Pharmaceuticals Ltd. published the original content used to generate this news brief via EDGAR, the Electronic Data Gathering, Analysis, and Retrieval system operated by the U.S. Securities and Exchange Commission (Ref. ID: 0001104659-25-051324), on May 21, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"BK4139","symbol_name":"生物科技","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250521:nNDL6B9Vc9:1","article_id":"2537382679","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2537382679","pubTimestamp":1747830754,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"Quoin Pharmaceuticals Announces EMA Orphan Drug Designation for QRX003, Advancing Late-Stage Trials for Netherton Syndrome Treatment. 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