Inherited Retinal Diseases Caused by RPE65 Mutations (DBCOND0161859)
Identifiers
- Synonyms
- Inherited Retinal Disease caused by RPE65 Mutation
Associated Data
- Indicated Drugs and Targets
- Not Available
- Clinical Trials
Identifier Title Drug(s) Purpose Phase Status NCT05906953 Safety and Efficacy Trial of HG004 for Leber Congenital Amaurosis Related to Rpe65 Gene Mutations (STAR) treatment 1 / 2 recruiting