OKYO Pharma to Present Phase 2 Urcosimod Efficacy Data at 2026 ASCRS Annual Meeting

Reuters

01/31

<a href="https://laohu8.com/S/OKYO">OKYO Pharma</a> to Present Phase 2 Urcosimod Efficacy Data at 2026 ASCRS Annual Meeting

OKYO Pharma Ltd. announced that results from its proof-of-concept Phase 2 study of urcosimod (formerly OK-101) for the treatment of neuropathic corneal pain have been accepted for presentation at the 2026 American Society of Cataract and Refractive Surgery (ASCRS) Annual Meeting. The abstract, titled "Evaluation of Urcosimod in Neuropathic Corneal Pain: Efficacy and Safety Results from a Proof-of-Concept Pilot Phase 2 Study," will be presented on April 11, 2026, in Washington, DC. The company also confirmed plans to initiate a 150-patient Phase 2b/3 multiple-dose study of urcosimod in the first half of 2026. Urcosimod has been granted fast track designation by the FDA for the treatment of neuropathic corneal pain.

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. OKYO Pharma Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9646182-en) on January 30, 2026, and is solely responsible for the information contained therein.

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The abstract, titled \"Evaluation of Urcosimod in Neuropathic Corneal Pain: Efficacy and Safety Results from a Proof-of-Concept Pilot Phase 2 Study,\" will be presented on April 11, 2026, in Washington, DC. The company also confirmed plans to initiate a 150-patient Phase 2b/3 multiple-dose study of urcosimod in the first half of 2026. Urcosimod has been granted fast track designation by the FDA for the treatment of neuropathic corneal pain.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<p>\n<i>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. OKYO Pharma Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9646182-en) on January 30, 2026, and is solely responsible for the information contained therein.</span></i>\n</p>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"SG9999014013.SGD","symbol_name":"United Global Durable Equities Fund Dis SGD","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260130:nNDL71tBPc:1","article_id":"2607040604","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2607040604","pubTimestamp":1769790616,"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":"OKYO Pharma Ltd. announced that results from its proof-of-concept Phase 2 study of urcosimod  for the treatment of neuropathic corneal pain have been accepted for presentation at the 2026 American Society of Cataract and Refractive Surgery  Annual Meeting. 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