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Condition: Inherited Retinal Diseases Caused By Rpe65 Mutations Synced from ClinicalTrials.gov · July 28, 2026

Recruiting studies: Inherited Retinal Diseases Caused By Rpe65 Mutations

Studies currently listed as recruiting on the public registry for this search term. Each page explains the study in plain language, with locations and the study team's contact details. Clinicians: generate a printable list for your patient →

Safety and Efficacy Trial of HG004 for Leber Congenital Amaurosis Related to Rpe65 Gene Mutations (STAR)
Phase 1/Phase 2 · 3 location(s) · HuidaGene Therapeutics Co., Ltd. · NCT05906953
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.