Trial Profile

A Repeat-Dose, Open-Label, Four Arm Safety and Efficacy Study of Two Doses of VP-001 (75ug and 120ug) Administered Intravitreally in Participants with Confirmed PRPF31 Mutation-Associated Retinal Dystrophy and Previously Treated with VP001 in the PLATYPUS Study (Protocol# VP001-101) or WALLABY Study (Protocol #VP001-102) for a Minimum of 8 Weeks

Status: Not yet recruiting

Phase of Trial: Phase I/II

Latest Information Update: 07 Mar 2025

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