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Ocuphire Announces Topline Results from ZETA-1 Phase 2 Trial of Oral APX3330 in Diabetic Retinopathy and Plans for End-of-Phase 2 Meeting with FDA

Oral APX3330 Achieved Statistical Significance on a Key Pre-specified Secondary Endpoint of Preventing Clinically Meaningful Progression of Diabetic Retinopathy after 24 Weeks of Treatment Oral... | January 25, 2023
Bret Shapiro Corey Davis Ocuphire Pharma Mina Sooch Peterk Kaiser Early Treatment Diabetic Retinopathy Study Research Group

Nyxol meets endpoint in phase 3 night vision disturbance trial

Nyxol demonstrated positive topline results in subjects with night vision disturbances in the phase 3 LYNX-1 pivotal clinical trial, Ocuphire Pharma announced in a press release.One hundred forty-five subjects who experienced night vision impairment were randomly assigned to receive either Nyxol (0.75% phentolamine ophthalmic solution) or placebo daily for 14 days. The primary endpoint was the
Ocuphire Pharma Mina Sooch
Source: healio.com

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Ocuphire Granted New U.S. Patent for Late-Stage Oral Drug Candidate APX3330 for Use in Diabetics and Announces New Peer-Reviewed APX3330 Publication

Ocuphire Granted New U.S. Patent for Late-Stage Oral Drug Candidate APX3330 for Use in Diabetics and Announces New Peer-Reviewed APX3330 Publication - read this article along with other careers information, tips and advice on BioSpace
United States David Boyer Corey Davis Ocuphire Pharma Mark Kelley Mina Sooch

Ocuphire Announces Positive Topline Results from LYNX-1 Phase 3 Trial Evaluating Nyxol® Eye Drops for Night Vision Disturbances

Ocuphire Announces Positive Topline Results from LYNX-1 Phase 3 Trial Evaluating Nyxol® Eye Drops for Night Vision Disturbances - read this article along with other careers information, tips and advice on BioSpace
Corey Davis Ocuphire Pharma Mina Sooch Ocuphire Pharma Inc Primary Endpoint More Nyxol Subjects Gaining

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