Active, not recruitingPHASE1, PHASE2NCT05203939
Study to Assess the Safety and Efficacy of OCU400 for Retinitis Pigmentosa and Leber Congenital Amaurosis
Studying OBSOLETE: Inherited retinal disorder
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
- Ocugen
- Principal Investigator
- Huma Qamar, MD, MPH, CMIOcugen
- Intervention
- OCU400 Low Dose(drug)
- Enrollment
- 22 enrolled
- Eligibility
- 6 years · All sexes
- Timeline
- 2022 – 2027
Study locations (7)
- Associated Retina Consultants, Phoenix, Arizona, United States
- Ocugen Site 5 - University of California, San Diego (UCSD) - Shiley Eye Institute, La Jolla, California, United States
- Ocugen Site 3 - Bascom Palmer Eye Institute, Miami, Florida, United States
- Ocugen Site 6 - Emory University, Atlanta, Georgia, United States
- Ocugen Site 2 - Casey Eye Institute - OHSU, Portland, Oregon, United States
- Ocugen Site 8 - Mid Atlantic Retina - Wills Eye Hospital, Philadelphia, Pennsylvania, United States
- Ocugen Site 1 - 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.
Open NCT05203939 on ClinicalTrials.govOther trials for OBSOLETE: Inherited retinal disorder
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