OCUP Ocuphire Pharma Inc

Ocuphire Announces Peer-Reviewed Publication in BMC Ophthalmology for Nyxol® and Strategic Partnership with American Society of Ophthalmic Administrators (ASOA)

Ocuphire Announces Peer-Reviewed Publication in BMC Ophthalmology for Nyxol® and Strategic Partnership with American Society of Ophthalmic Administrators (ASOA)

FARMINGTON HILLS, Mich., Nov. 02, 2022 (GLOBE NEWSWIRE) -- Ocuphire Pharma, Inc. (Nasdaq: OCUP), a clinical-stage ophthalmic biopharmaceutical company focused on developing and commercializing therapies for the treatment of refractive and retinal eye disorders, today announced that the positive results in night vision disturbances (NVD) patients from its earlier and first Phase 2 study evaluating the safety and efficacy of phentolamine mesylate eye drops (Nyxol) have been peer-reviewed and published in BMC Ophthalmology.

“High quality clinical data and scientific communications are core strengths at Ocuphire,” said Mina Sooch, Founder and CEO. “The growing body of scientific publications across our front and back of the eye candidates, Nyxol and APX3330, respectively, continues to validate the differentiated MOAs to the medical and scientific community. These Phase 2 data were used to inform the design of the Phase 3 LYNX-1 trial in NVD that met its primary endpoint and key secondary endpoints with statistically significance. We would like to thank Dr. Marguerite McDonald, MD for her early contributions to the development of Nyxol in Night Vision Disturbances (NVD), a challenging condition for tens of millions of patients. There are currently no treatment options for physicians, and Nyxol is the only development stage drug candidate pursuing NVD as an indication for potential regulatory approval."



A manuscript titled “A randomized phase 2 clinical trial of phentolamine mesylate eye drops in patients with severe night vision disturbances,” has been published in for clinical trial and reported Nyxol was well-tolerated and effectively reduced pupil size with improvements in contrast sensitivity and visual acuity.

In addition, Ocuphire is announcing the Strategic Business Partnership with the American Society of Ophthalmic Administrators (ASOA), the largest ophthalmic practice professionals network in eyecare. “Most companies underappreciate the administrative members of the ophthalmic practice and work directly with the physicians,” said Mina Sooch. “In addition to the physicians, we believe the ophthalmic administrators play a key role in engaging with patients and influencing the success of new product adoption. We are pleased to be the first company to join the newly created category for emerging companies.”

About Ocuphire Pharma

Ocuphire is a publicly traded (Nasdaq: OCUP), clinical-stage, ophthalmic biopharmaceutical company focused on developing and commercializing small-molecule therapies for the treatment of refractive and retinal eye disorders. For more information about Ocuphire and its clinical trials, visit

Ocuphire Contacts

Mina Sooch, President & CEO 

Ocuphire Pharma, Inc. 

 

Corey Davis, Ph.D.

LifeSci Advisors

 

Bret Shapiro

Core IR

 



EN
02/11/2022

Underlying

To request access to management, click here to engage with our
partner Phoenix-IR's CorporateAccessNetwork.com

Reports on Ocuphire Pharma Inc

 PRESS RELEASE

Opus Genetics Announces FDA Clearance of IND Application for Gene Ther...

Opus Genetics Announces FDA Clearance of IND Application for Gene Therapy Candidate OPGx-BEST1 – Phase 1/2 trial expected to initiate in 2H 2025 in patients with BEST1 inherited retinal disease RESEARCH TRIANGLE PARK, N.C., Aug. 18, 2025 (GLOBE NEWSWIRE) -- (Nasdaq: IRD), a clinical-stage biopharmaceutical company developing gene therapies for the treatment of inherited retinal diseases (IRDs) and small molecule therapies for other ophthalmic disorders, today announced that the U.S. Food and Drug Administration (FDA) has accepted its Investigational New Drug (IND) application for OPGx-B...

 PRESS RELEASE

Opus Genetics Announces Financial Results for Second Quarter 2025 and ...

Opus Genetics Announces Financial Results for Second Quarter 2025 and Provides Corporate Update - Positive 12-month Phase 1/2 clinical data in adult cohort and early pediatric clinical data support potential for meaningful vision restoration with OPGx-LCA5 -- FDA grants Regenerative Medicine Advanced Therapy (RMAT) designation for OPGx-LCA5 - - Positive topline results reported from VEGA-3 and LYNX-2 Phase 3 trials with Phentolamine Ophthalmic Solution 0.75% - - OPGx-BEST1 on track to enter Phase 1/2 trial in H2 2025 for the treatment of bestrophin-1 related inherited retinal disease - -...

 PRESS RELEASE

Opus Genetics to Participate in the H.C. Wainwright 5th Annual Ophthal...

Opus Genetics to Participate in the H.C. Wainwright 5th Annual Ophthalmology Virtual Conference RESEARCH TRIANGLE PARK, N.C., Aug. 05, 2025 (GLOBE NEWSWIRE) -- . (Nasdaq: IRD), a clinical-stage biopharmaceutical company developing gene therapies for the treatment of inherited retinal diseases (IRDs) and small molecule therapies for other ophthalmic disorders, today announced that George Magrath, M.D., Chief Executive Officer, will participate in a fireside chat during the H.C. Wainwright 5th Annual Ophthalmology Virtual Conference, which will be available on demand on Wednesday, August 13...

 PRESS RELEASE

Opus Genetics and the Global RDH12 Alliance Partner to Advance RDH12 G...

Opus Genetics and the Global RDH12 Alliance Partner to Advance RDH12 Gene Therapy for Inherited Childhood Blindness Collaboration aims to accelerate development of OPGx-RDH12, a gene therapy for RDH12-associated Leber congenital amaurosis (RDH12-LCA) RESEARCH TRIANGLE PARK, N.C., July 23, 2025 (GLOBE NEWSWIRE) --  (Nasdaq: IRD), a clinical-stage biopharmaceutical company developing gene therapies for the treatment of inherited retinal diseases (IRDs) and small molecule therapies for other ophthalmic disorders, today announced a strategic partnership with the Global RDH12 Alliance (the Al...

 PRESS RELEASE

Opus Genetics Announces Inducement Grants Under Nasdaq Listing Rule 56...

Opus Genetics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4) RESEARCH TRIANGLE PARK, N.C., July 03, 2025 (GLOBE NEWSWIRE) -- , Inc. (Nasdaq: IRD), a clinical-stage biopharmaceutical company developing gene therapies for the treatment of inherited retinal diseases (IRDs) and small molecule therapies for other ophthalmic disorders (the “Company”), today announced that, on June 30, 2025, it granted equity awards to two new non-executive employees as a material inducement to employment. The equity awards were granted under the Company’s 2021 Inducement Plan, as amended, and ...

ResearchPool Subscriptions

Get the most out of your insights

Get in touch