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OKYO (Nasdaq: OKYO) to present Fast Track NCP therapy data at ARVO 2026

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6-K

Rhea-AI Filing Summary

OKYO Pharma Limited filed a Form 6-K highlighting that its abstract on urcosimod for neuropathic corneal pain (NCP) was accepted for presentation at the ARVO 2026 Annual Meeting in Denver. Chief Scientific Officer Raj Patil, Ph.D., will present first-in-human data showing clinically meaningful pain reduction on the Visual Analogue Scale and improved quality-of-life metrics in NCP patients.

The Phase 2a proof-of-concept trial of urcosimod, a novel non-opioid, preservative-free eye drop with dual pain-relieving and anti-inflammatory activity, also suggested potential restoration of corneal nerve structure. Urcosimod holds FDA Fast Track designation and the first IND clearance specifically for NCP, and OKYO plans to initiate an approximately 150-patient multicenter Phase 2b/3 study in the first half of this year.

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

 

 

FORM 6-K

 

 

 

REPORT OF FOREIGN PRIVATE ISSUER

PURSUANT TO RULE 13a-16 OR 15d-16

UNDER THE SECURITIES EXCHANGE ACT OF 1934

 

February 2026

 

 

 

Commission File Number: 001-41386

 

 

 

OKYO Pharma LTD

(Exact Name of Registrant as Specified in Its Charter)

 

 

 

9th Floor

107 Cheapside

London

EC2V 6DN

(Address of registrant’s principal executive office)

 

 

 

Indicate by check mark whether the registrant files or will file annual reports under cover of Form 20-F or Form 40-F.

 

Form 20-F ☒ Form 40-F ☐

 

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(1): ☐

 

Indicate by check mark if the registrant is submitting the Form 6-K in paper as permitted by Regulation S-T Rule 101(b)(7): ☐

 

 

 

 

 

 

INFORMATION CONTAINED IN THIS REPORT ON FORM 6-K

 

On February 23, 2026, OKYO Pharma LTD (the “Company”) issued this 6K announcing that its abstract has been accepted for presentation at the Association for Research in Vision and Ophthalmology (ARVO) 2026 Annual Meeting, taking place May 3-7, 2026, in Denver, Colorado. Chief Scientific Officer Raj Patil, Ph.D., will share the data in a presentation titled: “First-in-Human Study of Urcosimod to Treat Neuropathic Corneal Pain (NCP) Shows Clinically Meaningful Pain Reduction and Quality-of-Life Improvement in NCP Patients.”

 

The Announcement is furnished herewith as Exhibit 99.1 to this Report on Form 6-K. The information in the attached Exhibits 99.1 is being furnished and shall not be deemed “filed” for the purposes of Section 18 of the Securities Exchange Act of 1934, or otherwise subject to the liabilities of that Section, This report on Form 6-K is hereby incorporated by reference into the Company’s Registration Statement on Form F-3 (Reg. No. 333-293145)

 

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SIGNATURES

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned, thereunto duly authorized.

 

  OKYO Pharma LTD
     
Date: February 23, 2026 By: /s/ Keeren Shah
  Name: Keeren Shah
  Title: Chief Financial Officer

 

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EXHIBIT INDEX

 

Exhibit No.   Description
     
99.1   News Announcement, dated February 23, 2026

 

4

 

Exhibit 99.1

 

 

OKYO Abstract Selected for Presentation at Premier Global Ophthalmology Congress

 

London and New York, NY, February 23, 2026. OKYO Pharma Limited (Nasdaq: OKYO), a clinical-stage biopharmaceutical company developing investigational therapies for the treatment of neuropathic corneal pain (NCP) and for inflammatory eye diseases, today announced that its abstract has been accepted for presentation at the Association for Research in Vision and Ophthalmology (ARVO) 2026 Annual Meeting, taking place May 3-7, 2026, in Denver, Colorado.

 

Chief Scientific Officer Raj Patil, Ph.D., will share the data in a presentation titled: “First-in-Human Study of Urcosimod to Treat Neuropathic Corneal Pain (NCP) Shows Clinically Meaningful Pain Reduction and Quality-of-Life Improvement in NCP Patients.”

 

This presentation highlights positive results from OKYO’s recently completed proof-of-concept Phase 2a clinical trial of urcosimod, a novel, non-opioid, preservative-free eye-drop therapy with dual pain-relieving and anti-inflammatory activity for neuropathic corneal pain (NCP). The first-in-human study in NCP patients demonstrated clinically meaningful reductions in pain—as measured by the Visual Analogue Scale (VAS)—along with improvements in quality-of-life metrics. In addition, urcosimod demonstrated the potential to help restore corneal nerve structure in patients suffering from neuropathic corneal pain.

 

Neuropathic corneal pain is a debilitating chronic ocular condition characterized by severe nerve-related pain without visible surface damage and currently has no FDA-approved treatments. Urcosimod holds FDA Fast Track designation for NCP and is the first candidate to receive IND clearance specifically for this indication. Following encouraging Phase 2a proof-of-concept results, OKYO is advancing urcosimod into a planned larger multicenter Phase 2b/3 trial (approximately 150 patients) to further evaluate its efficacy and safety, with initiation expected in the coming months.

 

“We are honored that our urcosimod data has been selected for presentation at ARVO 2026, one of the world’s leading forums for vision and ophthalmology research,” said Raj Patil, Ph.D., Chief Scientific Officer of OKYO Pharma. “These first-in-human results underscore urcosimod’s potential to address a significant unmet need in NCP by providing meaningful pain relief and enhancing patients’ quality of life. We look forward to sharing these findings with the scientific community and continuing to advance this promising therapy.”

 

The ARVO Annual Meeting attracts thousands of leading researchers, clinicians, and industry professionals focused on advancing eye and vision science.

 

As previously announced, urcosimod was granted the first IND application for the treatment of patients with NCP and was awarded fast track designation by the Food and Drug Administration (FDA). The company expects to initiate a ~150 subject Phase 2b/3 multiple-dose study of urcosimod to treat NCP in the first half of this year.

 

 

 

 

About Neuropathic Corneal Pain (NCP)

 

Neuropathic corneal pain (NCP) is a chronic, often debilitating condition characterized by severe pain and sensitivity of the eyes, and in some cases the face or head. It is thought to result from damage or dysfunction of corneal sensory nerves, often in combination with inflammatory processes, and may occur in patients with a range of underlying ophthalmic conditions. There are currently no FDA-approved therapies specifically for NCP, resulting in patients being treated with limited or no success using various topical and systemic medications in an off-label manner.

 

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 neuropathic corneal pain mouse model, respectively. OKYO recently announced positive data on NCP pain reduction in a randomized, placebo-controlled, double-masked Phase 2a trial involving 18 neuropathic corneal pain subjects. Urcosimod has shown significant pain reduction in an earlier 240 subject Phase 2, multi-center, double-masked, placebo-controlled trial in DED, which supports the development rationale in NCP.

 

About OKYO Pharma

 

OKYO Pharma Limited (Nasdaq: OKYO) is a clinical-stage biopharmaceutical company developing innovative therapies for the treatment of neuropathic corneal pain (NCP) and inflammatory eye diseases, 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 subjects with NCP and plans to initiate a ~150 subject Phase 2b/3 multiple-dose study of urcosimod to treat NCP in the first half of this year.

 

For further information, please visit www.okyopharma.com.

 

Forward-Looking Statements

 

Certain statements made in this announcement are forward-looking statements. These forward-looking statements are not historical facts but rather are based on the Company’s current expectations, estimates, and projections about its industry, its beliefs, and assumptions. Words such as ‘anticipates,’ ‘expects,’ ‘intends,’ ‘plans,’ ‘believes,’ ‘seeks,’ ‘estimates,’ and similar expressions are intended to identify forward-looking statements. These statements are not guarantees of future performance and are subject to known and unknown risks, uncertainties, and other factors, some of which are beyond the Company’s control, are difficult to predict, and could cause actual results to differ materially from those expressed or forecasted in the forward-looking statements. These and additional risks and uncertainties are described more fully in the company’s filings with the SEC, including those factors identified as “Risk Factors” in our most recent Annual Report on Form 20-F, for the fiscal year ended March 31, 2025. The company cautions security holders and prospective security holders not to place undue reliance on these forward-looking statements, which reflect the view of the company only as of the date of this announcement. The forward-looking statements made in this announcement relate only to events as of the date on which the statements are made. The company will not undertake any obligation to release publicly any revisions or updates to these forward-looking statements, except as may be required by law.

 

For further inquiries:

 

OKYO Pharma Ltd

Paul Spencer, Business Development, and Investor Relations

+44 (0) 207 495 2379

Email: info@okyopharma.com

 

 

 

FAQ

What did OKYO (OKYO) disclose in this Form 6-K?

OKYO disclosed that its abstract on urcosimod for neuropathic corneal pain was accepted for presentation at the ARVO 2026 Annual Meeting, featuring first-in-human Phase 2a data showing clinically meaningful pain reduction and improved quality-of-life outcomes in treated patients.

What is urcosimod and what condition is OKYO (OKYO) targeting?

Urcosimod is a novel, non-opioid, preservative-free eye-drop therapy with dual pain-relieving and anti-inflammatory activity. OKYO is developing it to treat neuropathic corneal pain, a debilitating chronic ocular condition with no FDA-approved therapies specifically indicated for this disease.

What were the key Phase 2a results for urcosimod reported by OKYO (OKYO)?

The first-in-human Phase 2a study in neuropathic corneal pain patients showed clinically meaningful reductions in pain on the Visual Analogue Scale and improvements in quality-of-life measures, with additional signals suggesting potential restoration of corneal nerve structure in affected patients.

What are OKYO’s (OKYO) next clinical plans for urcosimod in NCP?

Following encouraging Phase 2a proof-of-concept results, OKYO plans a larger multicenter Phase 2b/3 trial of approximately 150 neuropathic corneal pain patients, a multiple-dose study expected to start in the first half of the year to further evaluate efficacy and safety.

Does urcosimod have any special regulatory designations according to OKYO (OKYO)?

Yes. Urcosimod holds FDA Fast Track designation for neuropathic corneal pain and is described as the first candidate to receive IND clearance specifically for this indication, supporting an expedited development path for this underserved ocular pain condition.

Why is neuropathic corneal pain (NCP) an important focus for OKYO (OKYO)?

Neuropathic corneal pain is a chronic, often debilitating condition with severe nerve-related eye pain and no FDA-approved treatments. Patients are typically treated off-label with limited success, so OKYO views urcosimod as a potential therapy addressing a significant unmet medical need.

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