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Opus Genetics

NASDAQ: IRD $4.83 USDMicro-cap (~$5.73/share, Sep 2026) MCAP

Opus Genetics (NASDAQ: IRD), formerly Ocuphire Pharma and renamed in November 2020, is a Durham, North Carolina-based clinical-stage biopharmaceutical company (founded 2018) developing gene therapies to restore vision and prevent blindness in patients with inherited retinal diseases (IRDs) and other ophthalmic disorders. Lead clinical programs are OPGx-LCA5, an AAV gene therapy in Phase 1/2 for LCA5-associated retinal degeneration, and OPGx-BEST1, in a Phase 1/2 trial (BIRD-1) for BEST1-associated retinal disease — which reported positive low-dose Cohort 1 data in September 2026 and advanced to a higher-dose Cohort 2. Preclinical IRD programs include OPGx-RHO (autosomal dominant retinitis pigmentosa), OPGx-RDH12, OPGx-MERTK, OPGx-NMNAT1 and OPGx-CNGB1. The company also develops phentolamine ophthalmic solution for presbyopia and dim-light vision disturbances and APX3330, a small-molecule Ref-1 inhibitor for diabetic retinopathy. In August 2026 Opus Genetics reported a successful FDA Type C meeting on OPGx-BEST1 that aligned on pivotal-trial endpoints and a development path with potential Phase 3 dosing in 2027.

Company Info

Sector:Gene Therapy — Inherited Retinal Disease
Headquarters:Durham, North Carolina, United States
Founded:2018
Website:opusgtx.com/

Upcoming Milestones & Key Dates

2026-Q4
Clinical

OPGx-BEST1 higher-dose Cohort 2 dosing expected to complete

2027-Q2
Clinical

OPGx-BEST1 Cohort 2 topline three-month data expected

2027
Regulatory

Potential Phase 3 dosing for OPGx-BEST1 (FDA Type C path)

Clinical Development Pipeline

OPGx-BEST1

Target: BEST1 gene augmentation (AAV, subretinal)
BEST1-associated retinal disease (incl. BVMD)
Preclinical
Phase 1
Phase 2
Phase 3
Approved

OPGx-LCA5

Target: LCA5 gene augmentation (AAV)
LCA5-associated inherited retinal degeneration
Preclinical
Phase 1
Phase 2
Phase 3
Approved

APX3330

Target: Ref-1 (APE1/Ref-1) small-molecule inhibitor
Diabetic retinopathy
Preclinical
Phase 1
Phase 2
Phase 3
Approved

Phentolamine ophthalmic solution

Target: Alpha-adrenergic receptor antagonist
Presbyopia, reversal of mydriasis, dim-light vision
Preclinical
Phase 1
Phase 2
Phase 3
Approved

Recent News

No recent news updates available for this company.

Leadership Team

George Magrath

Chief Executive Officer and Director

Benjamin R. Yerxa

President and Director

Ashwath Jayagopal

Chief Scientific and Development Officer

Joseph K. Schachle

Chief Operating Officer

Robert E. Gagnon

Chief Financial Officer

Careers & Job Openings

No active job listings. Check back later.