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Clinical Trial Summary

A Phase 1 Open-Label, Multiple Ascending Dose Study to Evaluate the Safety and Tolerability of Intravitreally Administered VP-001 in Participants with Confirmed PRPF31 Mutation-Associated Retinal Dystrophy


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06455826
Study type Interventional
Source PYC Therapeutics
Contact Ora Inc
Phone 5104232680
Email VP001@oraclinical.com
Status Not yet recruiting
Phase Phase 1
Start date June 2024
Completion date November 2025

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