OKYO Pharma reports Phase 2a data showing improved quality-of-life scores with 0.05% urcosimod in neuropathic corneal pain patients

Reuters03-18

<a href="https://laohu8.com/S/OKYO">OKYO Pharma</a> reports Phase 2a data showing improved quality-of-life scores with 0.05% urcosimod in neuropathic corneal pain patients

OKYO Pharma reported new findings from an exploratory analysis of patient-reported outcomes in its completed Phase 2a randomized, double-masked, placebo-controlled trial of urcosimod 0.05% for neuropathic corneal pain. The quality-of-life data will be presented in the future at the ARVO 2026 Annual Meeting. In the intent-to-treat population, patients received urcosimod (n=6) or placebo (n=6) for 12 weeks. Reported mean change from baseline included “enjoying life/relationships” of −4.5 with urcosimod versus 0 with placebo on a 0–10 scale. The company also said the Phase 2a results included pain reductions measured by the visual analogue scale and exploratory signals related to corneal nerve structure.

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: 202603180700OMX_____CNEWS_EN_GNW9674336_en) on March 18, 2026, and is solely responsible for the information contained therein.

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