Urcosimod shows promising nerve health improvements in neuropathic corneal pain patients, suggesting potential therapeutic benefits.
Quiver AI Summary
OKYO Pharma Limited announced promising results from its Phase 2 clinical trial of 0.05% urcosimod for treating neuropathic corneal pain, a condition lacking an FDA-approved therapy. Patients receiving urcosimod showed improvements in nerve fiber count and length, indicating potential benefits for corneal nerve health, unlike the placebo group. The study observed median increases in nerve metrics, suggesting urcosimod not only alleviates pain but may also support nerve restoration. These findings bolster the company's belief in targeting the chemerin receptor pathway and lay the groundwork for further research, including a larger upcoming trial planned for early 2026.
Potential Positives
- Patients treated with 0.05% urcosimod showed directionally favorable improvements in nerve fiber count and length, indicating a potential breakthrough in treating neuropathic corneal pain.
- Urcosimod demonstrated a positive impact on corneal nerve health, which may lead to novel therapeutic approaches for a condition with currently no FDA-approved treatments.
- The results reinforce the company’s ongoing belief in the therapeutic potential of targeting the chemerin receptor pathway, bolstering future investigations and development opportunities.
- OKYO plans to initiate a larger multicenter trial for urcosimod in NCP patients, set to start in Q1 2026, indicating continued commitment to bringing the therapy to market.
Potential Negatives
- The press release indicates that the findings, while promising, are based on an exploratory analysis from a small sample size of only 18 patients, which may limit the credibility and generalizability of the results.
- Despite showing favorable trends, the results did not reach statistical significance (p = 0.057), potentially undermining claims of efficacy and the robustness of the therapeutic impact of urcosimod.
- The company operates in a space with no FDA-approved therapies for NCP, which may suggest challenges in regulatory approval and competition in a potentially high-risk market.
FAQ
What is urcosimod and its role in treating neuropathic corneal pain?
Urcosimod is a chemerin peptide agonist being developed to treat neuropathic corneal pain, showing promise in clinical trials for nerve health improvement.
What were the results of the Phase 2 trial for urcosimod?
The Phase 2 trial revealed urcosimod significantly improved nerve fiber count and length compared to the placebo group in patients with neuropathic corneal pain.
How does neuropathic corneal pain (NCP) affect patients?
NCP causes severe pain and sensitivity in the eyes, face, or head, often resulting from corneal nerve damage and inflammation.
Are there any FDA-approved treatments for neuropathic corneal pain currently?
No, there are currently no FDA-approved treatments specifically for neuropathic corneal pain, highlighting the need for new therapeutic options like urcosimod.
When is the next clinical trial for urcosimod planned to start?
A larger multicenter trial of urcosimod for neuropathic corneal pain is planned to begin in Q1 2026, following positive Phase 2 results.
Disclaimer: This is an AI-generated summary of a press release distributed by GlobeNewswire. The model used to summarize this release may make mistakes. See the full release here.
$OKYO Hedge Fund Activity
We have seen 4 institutional investors add shares of $OKYO stock to their portfolio, and 4 decrease their positions in their most recent quarter.
Here are some of the largest recent moves:
- DAUNTLESS INVESTMENT GROUP, LLC removed 313,732 shares (-11.5%) from their portfolio in Q3 2025, for an estimated $627,464
- NORTHERN TRUST CORP added 57,158 shares (+inf%) to their portfolio in Q3 2025, for an estimated $114,316
- RENAISSANCE TECHNOLOGIES LLC added 41,200 shares (+inf%) to their portfolio in Q3 2025, for an estimated $82,400
- FNY INVESTMENT ADVISERS, LLC removed 20,000 shares (-100.0%) from their portfolio in Q2 2025, for an estimated $51,400
- CITADEL ADVISORS LLC added 15,355 shares (+inf%) to their portfolio in Q3 2025, for an estimated $30,710
- OSAIC HOLDINGS, INC. added 152 shares (+inf%) to their portfolio in Q3 2025, for an estimated $304
- UBS GROUP AG removed 115 shares (-100.0%) from their portfolio in Q3 2025, for an estimated $230
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$OKYO Analyst Ratings
Wall Street analysts have issued reports on $OKYO in the last several months. We have seen 1 firms issue buy ratings on the stock, and 0 firms issue sell ratings.
Here are some recent analyst ratings:
- HC Wainwright & Co. issued a "Buy" rating on 09/23/2025
To track analyst ratings and price targets for $OKYO, check out Quiver Quantitative's $OKYO forecast page.
$OKYO Price Targets
Multiple analysts have issued price targets for $OKYO recently. We have seen 2 analysts offer price targets for $OKYO in the last 6 months, with a median target of $6.0.
Here are some recent targets:
- William Woods from B. Riley Securities set a target price of $5.0 on 12/08/2025
- Yi Chen from HC Wainwright & Co. set a target price of $7.0 on 09/23/2025
Full Release
- Patients treated with 0.05% urcosimod demonstrated directionally favorable improvements in nerve fiber count and fiber length, trends not observed in the placebo group
- These findings suggest that urcosimod may have a positive impact on corneal nerve health in patients with neuropathic corneal pain
- Corneal nerve imaging data from the Phase 2 NCP trial were analyzed using in vivo confocal microscopy
LONDON and NEW YORK, Dec. 11, 2025 (GLOBE NEWSWIRE) -- OKYO Pharma Limited (NASDAQ: OKYO ), a clinical-stage biopharmaceutical company developing innovative therapies for the treatment of neuropathic corneal pain, a severe ocular condition without an FDA approved therapy, is pleased to announce new analyses of corneal images from the recently completed placebo-controlled, randomized, double-masked, Phase 2 clinical trial of urcosimod in neuropathic corneal pain (NCP). Patients treated with 0.05% urcosimod demonstrated not only a positive reduction in neuropathic corneal pain, but also favorable changes in corneal nerve structure which were not observed in the placebo group.
Data compiled from nerve growth analyses that were an exploratory endpoint in the recently completed 18-patient trial of urcosimod demonstrated a favorable impact on corneal nerve health. Patients treated with 0.05% urcosimod showed median i ncreases in total nerve fiber count (+2.0 , n/0.16 mm², IQR 0.54 to 3.63 ) and total nerve fiber length ( +2.6 mm/mm² , IQR 1.55 to 5.67; p = 0.057 vs placebo ). In contrast, the placebo group exhibited median decreases in total nerve fiber count ( –1.92, n/0.16 mm², IQR –2.79 to –0.04 ) and total nerve fiber length ( –1.63 mm/mm² , IQR –3.76 to 0.63 ). This exploratory dataset, exhibiting consistent and meaningful directional improvements for 0.05% patients on urcosimod across key anatomical endpoints, highlights urcosimod’s potential to support corneal nerve restoration and reinforces its promise as a first-in-class therapeutic approach for neuropathic corneal pain that warrants further investigations. All values represent median (n = 4).
* IQR = (Inter Quartile Range)
“These early nerve regeneration signals are highly encouraging and biologically meaningful,” said Pedram Hamrah, MD, FARVO, Principal Investigator, and currently Professor of Ophthalmology at University of South Florida. “The fact that we are seeing consistent directional improvements in both nerve fiber count and nerve fiber length, suggests that urcosimod may not only reduce pain but also support the restoration of corneal nerve architecture. This represents an important step toward establishing additional mechanistic insights for urcosimod in NCP.”
“These results provide early evidence that urcosimod may help restore corneal nerve structure in patients suffering from neuropathic corneal pain,” said Raj Patil, PhD, Chief Scientific Officer of OKYO Pharma . “ While exploratory, these findings reinforce our long-standing belief that targeting the chemerin receptor pathway may open a new therapeutic avenue for patients with neuropathic corneal pain. We are encouraged by the biological activity observed and believe they provide an important foundation for the continued development of urcosimod.”
About Neuropathic Corneal Pain (NCP)
NCP
is a condition that causes severe pain and sensitivity of the eyes, face, or head. The exact cause of NCP is unknown but is thought to result from nerve damage to the
cornea
combined with
inflammation
. NCP, which can exhibit as a severe, chronic, debilitating condition in patients suffering from a host of ophthalmic conditions, is presently treated, with limited success by various topical and systemic treatments in an off-label fashion. There is presently no FDA-approved drug to treat NCP.
About Urcosimod (formerly called OK-101)
Urcosimod is a lipid conjugated chemerin peptide agonist of the ChemR23 G-protein coupled receptor which is typically found on immune cells of the eye responsible for the inflammatory response, as well as on neurons and glial cells in the dorsal root ganglion. Urcosimod has been shown to produce anti-inflammatory and pain-reducing activities in a mouse model of dry eye disease and in a corneal neuropathic pain mouse model, respectively. Urcosimod showed clear statistical significance in multiple endpoints in an earlier 240-patient Phase 2, multi-center, double-masked, placebo-controlled trial to treat dry eye disease, and OKYO recently announced positive data on NCP pain reduction in a randomized, placebo-controlled, double-masked Phase 2 trial involving 18 neuropathic corneal pain patients.
About OKYO
OKYO Pharma Limited (NASDAQ: OKYO) is a clinical stage biopharmaceutical company developing innovative therapies for the treatment of neuropathic corneal pain, with ordinary shares listed for trading on the NASDAQ Capital Market. OKYO is focused on the discovery and development of novel molecules to treat neuropathic corneal pain and other ocular diseases. OKYO recently completed a successful phase 2 trial of its flagship drug urcosimod in patients with NCP and is currently planning a second larger, multicenter trial of urcosimod in NCP patients that is planned to start in Q1 2026.
For further information, please visit www.okyopharma.com .
Enquiries:
| OKYO Pharma Limited | Gary S. Jacob, Chief Executive Officer |
+44 (0)20 7495 2379
|
| Business Development & Investor Relations | Paul Spencer |
+44 (0)20 7495 2379
|