RecruitingPhase 2NCT07174726
A Phase 2 Open-label Study to Evaluate the Safety of Laruparetigene Zovaparvovec Administered Bilaterally in Male Participants With X-Linked Retinitis Pigmentosa
Studying Retinitis pigmentosa
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Beacon Therapeutics
- Principal Investigator
- None None
- Intervention
- Adeno-associated virus vector expressing a human RPGR gene(biological)
- Enrollment
- 10 enrolled
- Eligibility
- 12-50 years · MALE
- Timeline
- 2025 – 2030
Study locations (6)
- University of Florida Jacksonville Ophthalmology, Jacksonville, Florida, United States
- Bascom Palmer Eye Institute, Miami, Florida, United States
- Duke Eye Center, Durham, North Carolina, United States
- Cincinnati Eye Institute, Cincinnati, Ohio, United States
- OHSU Casey Eye Institute, Portland, Oregon, United States
- Retina Foundation of the Southwest, Dallas, Texas, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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