Active, not recruitingPHASE1, PHASE2NCT04123626
A Study to Evaluate the Safety and Tolerability of QR-1123 in Subjects With Autosomal Dominant Retinitis Pigmentosa Due to the P23H Mutation in the RHO Gene
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
- ProQR Therapeutics
- Principal Investigator
- ProQR Medical MonitorProQR Therapeutics
- Intervention
- QR-1123(drug)
- Enrollment
- 11 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2019 – 2022
Study locations (5)
- Sue Anschutz-Rogers Eye Center, University of Colorado - Dept. of Ophthalmology, Aurora, Colorado, United States
- VitreoRetinal Associates, Gainesville, Florida, United States
- Shriners UK Ophthalmology - University of Kentucky, Lexington, Kentucky, United States
- Casey Eye Institute, OHSU, 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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