OKYO Pharma Receives FDA Approval of IND for OK-101 in Neuropathic Corneal Pain
09 Febbraio 2024 - 1:00PM
OKYO Pharma Limited (NASDAQ: OKYO), a clinical-stage
biopharmaceutical company developing innovative ocular therapies
for the treatment of inflammatory dry eye disease (DED), a
multi-billion-dollar market, and for neuropathic corneal pain
(NCP), an ocular condition associated with pain but without an FDA
approved therapy, announced today that the U.S. Food and Drug
Administration (FDA) has cleared OK-101 as its first
Investigational New Drug (IND) application for the treatment of
NCP.
Notably, the initial IND submission to FDA proposed an
open-label design for the clinical trial. Based on positive
feedback from FDA, the Phase 2 study is now designed as a
double-masked, randomized, 12-week placebo-controlled trial
comparing OK-101 to placebo in NCP patients. A total of 54 patients
are planned for the study, with NCP disease confirmed via confocal
microscopy. The primary endpoint will be measured utilizing VAS
pain relief scores. These protocol changes will enable a
statistically valid demonstration of a true drug effect of OK-101
on NCP symptoms. OKYO Pharma is scheduling this trial to begin in
Q2 2024.
The OK-101 trial, designed as a single-center trial, will be led
by Pedram Hamrah, MD, of Tufts Medical Center, as Principal
Investigator. Dr. Hamrah is Professor and Vice Chair of Research
and Academic Programs, Co-Director of the Cornea Service and
Director of the Center for Translational Ocular Immunology at Tufts
Medical Center. An ophthalmologist and a clinician-scientist, Dr.
Hamrah is a leading expert in NCP and co-inventor on the OK-101
patent. He is also a member of OKYO’s Scientific Advisory
Board.
“I am very pleased that we have gained FDA IND clearance for the
first drug to be tested for NCP, a debilitating disease,” said Dr.
Hamrah. “Receiving the IND clearance in an important and novel
indication was not a trivial hurdle to overcome. Now that the path
has been opened for drugs to be tested in NCP, I am looking forward
to working with the OKYO team to launch this important trial.”
“We are pleased to gain IND clearance for OK-101 to treat NCP as
a second important disease target for the Company,” said Dr. Gary
S. Jacob, CEO of OKYO. “OK-101 recently demonstrated favorable
tolerability in a Phase 2 trial of dry eye patients along with
statistically significant improvements in dry eye symptoms such as
stinging/burning and blurred vision, which are also hallmarks of
NCP. OK-101 was also shown in a cutting-edge mouse model of NCP to
significantly reduce ocular neuropathic pain. We are looking
forward to advancing OK-101 to potentially treat NCP, a chronically
painful ocular disease with no FDA-approved therapy and a major
unmet medical need for patients suffering from this condition.”
About NCPNeuropathic corneal pain (NCP) is
a condition that causes pain and sensitivity of the eyes, face, or
head. The exact cause of NCP is unknown but thought to result from
nerve damage to the cornea combined
with inflammation. NCP, which can exhibit as a severe,
chronic, or debilitating condition in patients suffering from a
host of ophthalmic conditions, is presently treated by various
topical and systemic treatments in an off-label fashion. There are
no approved commercial treatments currently available for this
condition.
About OK-101OK-101 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. OK-101 was developed using a
membrane-anchored-peptide technology to produce a novel long-acting
drug candidate for treating dry eye disease. OK-101 has been shown
to produce anti-inflammatory and pain-reducing activities in mouse
models of dry eye disease and corneal neuropathic pain (NCP),
respectively, and is designed to combat washout through the
inclusion of the lipid anchor built into the drug molecule to
enhance the residence time of OK-101 within the ocular environment.
OK-101 recently showed clear statistical significance in multiple
endpoints in a recently completed Phase 2, multi-center,
double-blind, placebo-controlled trial of OK-101 to treat DED.
About OKYOOKYO Pharma Limited (NASDAQ: OKYO) is
a clinical stage biopharmaceutical company developing innovative
therapies for the treatment of DED and NCP, with ordinary shares
listed for trading on the NASDAQ Capital Market. OKYO is focused on
the discovery and development of novel molecules to treat
inflammatory DED and ocular pain. In addition to the recently
completed Phase 2 DED trial, OKYO also has plans underway for the
opening of a Phase 2 trial for OK-101 to treat NCP in patients with
this debilitating condition. For further information, please
visit www.okyopharma.com.
Forward-Looking StatementsCertain statements
made in this announcement are forward-looking statements, including
with respect to the anticipated timing of completion of enrolment
of the Company’s Phase 2 trial of topical ocular OK-101 to treat
DED and the release of top-line data therefrom. 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. 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 to reflect
events, circumstances, or unanticipated events occurring after the
date of this announcement except as required by law or by any
appropriate regulatory authority.
Enquiries:
OKYO Pharma
Limited |
Gary S. Jacob, Chief Executive
Officer |
917-497-7560 |
Business Development
& Investor Relations |
Paul Spencer |
+44 (0)20 7495 2379 |
Grafico Azioni OKYO Pharma (NASDAQ:OKYO)
Storico
Da Ott 2024 a Nov 2024
Grafico Azioni OKYO Pharma (NASDAQ:OKYO)
Storico
Da Nov 2023 a Nov 2024