
Opus Genetics To Present At Upcoming Medical And Industry Conferences In October 2025
“These upcoming presentations highlight the strong momentum across our pipeline, from advancing OPGx-LCA5 for patients living with an LCA5 IRD to sharing pivotal Phase 3 data from LYNX-2 in keratorefractive patients with visual disturbances under mesopic, low-contrast conditions,” said George Magrath, M.D., Chief Executive Officer, Opus Genetics.“We look forward to engaging with the gene therapy, ophthalmology, and investor communities at these key meetings.”
Conference Participation Details:
Cell and Gene Meeting on the Mesa
- Presentation Title: Transformative Gene Therapies for the Treatment of Rare Inherited Retinal Diseases Presentation Content: Three-month pediatric and 18-month adult clinical data from the Phase 1/2 trial of OPGx-LCA5 in patients with Leber congenital amaurosis type 5 (LCA5) Date/Time: Monday, October 6, 2025, 9:15–9:30 am MT Presenter: George Magrath, M.D., Chief Executive Officer, Opus Genetics Location: Arizona Biltmore, Phoenix, AZ
Fierce Biotech Week
- Fireside Chat: Investing with Intention – How Early Vision and Partnership Shaped Opus Genetics Date/Time: Wednesday, October 8, 2025, 12:15–12:45 pm ET Speakers: Ben Yerxa, Ph.D., President, Opus Genetics and Christy Shaffer, Ph.D., General Partner, Hatteras Venture Partners Location: Encore Boston Harbor Hotel, Boston, MA
American Academy of Optometry Annual Meeting 2025
- Poster Presentation: LYNX-2: A Pivotal Phase 3 Trial of Phentolamine Ophthalmic Solution in Post-Keratorefractive Surgery Subjects with Decreased Mesopic Visual Acuity Date: Thursday, October 9, 4:30 PM–6:30 pm ET Presenter: Marc Bloomenstein, O.D. Location: Halls B2/C, Thomas M. Menino Convention & Exhibition Center, Boston, MA
Eyecelerator @ American Academy of Ophthalmology (AAO)
- Presentation Title: Transformative Gene Therapies for the Treatment of Rare Inherited Retinal Diseases Presentation Content: Three-month pediatric and 18-month adult clinical data from the OPGx-LCA5 Phase 1/2 trial Session Date/Time: Thursday, October 16, 2025, 1:15–2:45 pm ET Presenter: Sally Tucker, Ph.D., Senior Vice President of Clinical Development, Opus Genetics Location: Orange County Convention Center, Orlando, FL
About Opus Genetics
Opus Genetics is 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's pipeline features AAV-based gene therapies targeting inherited retinal diseases including Leber congenital amaurosis (LCA), bestrophinopathy, and retinitis pigmentosa. Its lead gene therapy candidates are OPGx-LCA5, which is in an ongoing Phase 1/2 trial for LCA5-related mutations, and OPGx-BEST1, a gene therapy targeting BEST1-related retinal degeneration. Opus Genetics is also advancing Phentolamine Ophthalmic Solution 0.75%, a partnered therapy currently approved in one indication and being studied in two Phase 3 programs for presbyopia and reduced low light vision and nighttime visual disturbances. The Company is based in Research Triangle Park, NC. For more information, please visit .
Contacts
Investors
Jenny Kobin
Remy Bernarda
IR Advisory Solutions
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Media
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KKH Advisors
917-291-5744
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Source: Opus Genetics, Inc.


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