RecruitingPHASE1, PHASE2NCT06852963
A Repeat-Dose, Open-Label, Two Arm Safety and Efficacy Study of Two Doses of VP-001 Administered Intravitreally in Participants With Confirmed PRPF31 Mutation-Associated Retinal Dystrophy, Including Participants Previously Treated With VP001
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
- PYC Therapeutics
- Intervention
- VP-001(drug)
- Enrollment
- 16 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2025 – 2028
Study locations (6)
- University of Florida College of Medicine, Jacksonville, Florida, United States
- Bascom Palmer Eye Institute - University of Miami, Miami, Florida, United States
- Kellogg Eye Center - University of Michigan, Ann Arbor, Michigan, United States
- Casey Eye Institute - OHSU, Portland, Oregon, United States
- Retina Foundation of the Southwest, Dallas, Texas, United States
- Baylor College of Medicine, Houston, 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 NCT06852963 on ClinicalTrials.govOther trials for OBSOLETE: Inherited retinal disorder
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