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)
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 |
EXHIBIT
INDEX
| Exhibit
No. |
|
Description |
| |
|
|
| 99.1 |
|
News Announcement, dated February 23, 2026 |
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