Press Releases June 2, 2026 07:00 AM

Opus Genetics to Host Virtual R&D Science Forum on Tuesday, June 16, 2026 Featuring Multiple Inherited Retinal Disease Experts

Opus Genetics to Host Virtual R&D Science Forum Showcasing Advancements in Gene Therapy for Inherited Retinal Diseases

By Sofia Navarro IRD

Opus Genetics, a clinical-stage biopharmaceutical company focused on gene therapies for inherited retinal diseases, announced a virtual R&D Science Forum on June 16, 2026. The forum will feature expert speakers discussing the company's multi-asset gene therapy pipeline, including upcoming clinical trials targeting RDH12, MERTK, and RHO mutations, recent data presentations, and global market opportunities for IRD treatments.

Opus Genetics to Host Virtual R&D Science Forum on Tuesday, June 16, 2026 Featuring Multiple Inherited Retinal Disease Experts
IRD

Key Points

  • Opus Genetics is advancing multiple gene therapy programs addressing genetic causes of severe inherited retinal diseases, with several candidates entering clinical testing.
  • The virtual forum will feature prominent ophthalmology experts and KOLs discussing the scientific progress and clinical plans.
  • The company aims to address significant unmet medical needs in IRDs, potentially capturing a growing market for gene therapies in ocular disorders.

RESEARCH TRIANGLE PARK, N.C., June 02, 2026 (GLOBE NEWSWIRE) -- Opus Genetics, Inc. (Nasdaq: IRD) (“Opus Genetics” or the “Company”), a clinical-stage biopharmaceutical company developing gene therapies to restore vision and prevent blindness in patients with inherited retinal diseases (IRDs), today announced the guest speakers for its virtual Research & Development (R&D) Science Forum to be held on Tuesday, June 16, 2026, from 10:00 am – 12:00 pm ET.

The R&D Science Forum will feature management and key opinion leaders (KOLs) highlighting Opus Genetics’ multi-asset gene therapy pipeline, which is designed to address the underlying genetic causes of severe IRDs. The Forum will include detailed information on three gene therapy programs entering clinical testing, targeting the RDH12, MERTK, and RHO mutations. In addition, there will be a summary of recently presented data from the ongoing LCA5 and BEST1 clinical programs and an overview of IRD global market opportunities and patient prevalence.

“Our R&D Science Forum brings together leading investigators and scientific experts to highlight the progress we are making within our gene therapy pipeline for inherited retinal diseases,” said George Magrath, M.D., Chief Executive Officer, Opus Genetics. “With significant unmet needs across RDH12, MERTK, RHO, LCA5 and BEST1, we look forward to sharing our preclinical data, our deepening engagement with the clinical community, as well as our strategic development plans as we advance potentially transformative therapies for patients at risk of vision loss.”

Opus Genetics’ R&D Science Forum Guest Speakers:

  • Jean Bennett, MD, PhD
    Emeritus Professor of Ophthalmology, University of Pennsylvania / Scheie Eye Institute
  • Todd Durham, PhD
    Senior Vice President, Clinical & Outcomes Research, Foundation Fighting Blindness
  • Kenneth C. Fan, MD, MBA
    Retina Specialist & Surgeon, Retina Consultants of Texas
  • Bart P. Leroy, MD, PhD
    Professor of Ophthalmology & Head of Department, Ghent University Hospital
  • Robert E. MacLaren, MB ChB, DPhil
    Professor of Ophthalmology, University of Oxford
  • Lejla Vajzovic, MD
    Professor of Ophthalmology, Duke University Eye Center

Webcast Registration:

Registration for the event is available on the Events page of the Opus Genetics website. There will also be an archived replay available following the event.

About Opus Genetics

Opus Genetics is a clinical-stage biopharmaceutical company developing gene therapies to restore vision and prevent blindness in patients with inherited retinal diseases (IRDs). The Company is developing durable, one-time treatments designed to address the underlying genetic causes of severe retinal disorders. The Company’s pipeline includes seven AAV-based programs, led by OPGx-LCA5 for LCA5-related mutations and OPGx-BEST1 for BEST1-related retinal degeneration, with additional candidates targeting RDH12, MERTK, RHO, CNGB1 and NMNAT1. The Company is based in Research Triangle Park, NC. For more information, visit www.opusgtx.com.

Contacts:

Investors
Jenny Kobin
Remy Bernarda
IR Advisory Solutions
[email protected]

Media
Kimberly Ha
KKH Advisors
917-291-5744
[email protected]

Source: Opus Genetics, Inc.


Risks

  • Clinical programs are at early stages and face typical risks of gene therapy trials including safety, efficacy, and regulatory approval.
  • Market adoption and reimbursement uncertainties for novel gene therapies in inherited retinal diseases could impact commercial success.
  • Competition from other companies developing treatments for IRDs may affect Opus Genetics' market positioning and investor sentiment.

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