Enrolling by invitationPhase 2NCT06275620
A Study Comparing Two Doses of AGTC-501 in Male Participants With X-linked Retinitis Pigmentosa Caused by RPGR Mutations (DAWN)
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
- Intervention
- AGTC-501 (high dose and standard corticosteroid regimen)(biological)
- Enrollment
- 24 enrolled
- Eligibility
- 12 years · MALE
- Timeline
- 2023 – 2029
Study locations (7)
- University of Florida, Jacksonville, Florida, United States
- Bascom Palmer Eye Institute, Miami, Florida, United States
- Boston Children's Hospital, Boston, Massachusetts, United States
- Cincinnati Eye Institute, Cincinnati, Ohio, United States
- Cleveland Clinic, Cleveland, Ohio, United States
- 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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