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Articles published by OKYO Pharma LTD

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OKYO Pharma Announces Positive Data in Long-Term Stability of Urcosimod
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Files for Fast Track Designation with FDA for Urcosimod to Treat Neuropathic Corneal Pain
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces OK-101 Officially Assigned USAN : Urcosimod
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Chairman and CEO Acquire Shares
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma to Complete Enrollment of Neuropathic Corneal Pain Trial by End of Second Quarter
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Receives $1.4 Million in Non-Dilutive Funding
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma to Participate at the 4th Annual BTIG Ophthalmology Conference
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma to Present at International Tear Film and Ocular Surface Society Conference
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces First Patient Dosed in the First Clinical Trial to Treat Neuropathic Corneal Pain
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Start of Phase 2 Clinical Trial to Treat Patients with Neuropathic Corneal Pain
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Chairman Acquires Shares
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Chairman Acquires Shares
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Granted U.S. Patent Covering OK-101’s Potential for Treating Symptoms of Dry Eye Disease
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma CEO Interview to Air on Bloomberg TV
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Chairman Acquires Shares
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Chairman Acquires Shares
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Participates in H.C. Wainwright 4th Annual Ophthalmology Virtual Conference
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Granted European Patent Covering OK-101 Chemerin Analogs and Their Method of Use
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma to Initiate Neuropathic Corneal Pain Trial for OK-101
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Promising Categorical Data from OK-101 Phase 2 Trial in Dry Eye Disease
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Participation in May 2024 Investor Conferences
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Upcoming Presentation of OK-101 Phase 2 Data for Dry Eye Disease at the Dry Horizons Symposium, a Partner Meeting of the Association for Research in Vision and Ophthalmology (ARVO)
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma to Reschedule Key Opinion Leader Event in Dry Eye Disease to May 2024
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Upcoming Presentation of OK-101 Phase 2 Data for Dry Eye Disease at Eyecelerator 2024, a Partner Meeting of the American Society for Cataract and Refractive Surgery
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces OK-101 Successfully Achieved Statistical Significance for Multiple Signs and Symptoms of Dry Eye Disease including Ocular Pain Relief in its First-in-Human Phase 2 Trial of OK-101
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma to Host Key Opinion Leader Event to Discuss New and Comprehensive Data from Phase 2 Dry Eye Disease Trial
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma to Release New and Comprehensive Data from Phase 2 Dry Eye Disease Trial and Host Key Opinion Leader Event
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Receives FDA Approval of IND for OK-101 in Neuropathic Corneal Pain
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces Distinguished Ophthalmologists with Expertise in the Medical and Surgical Treatment of Ocular Surface Diseases Join its Scientific Advisory Board
From OKYO Pharma LTD
Via GlobeNewswire
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OKYO Pharma Announces OK-101 Successfully Achieved Statistical Significance for Both Sign and Symptom Endpoints in its First-in-Human Phase 2 Trial of OK-101 in Patients with Dry Eye Disease
From OKYO Pharma LTD
Via GlobeNewswire
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