STGD1

1

Review clinical trials related to STGD1. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

An Observational Study in Subjects to Follow the Progression of Stargardt Disease Type 1 (STGD1) Caused by Bi-Allelic Autosomal Recessive Mutations in the ABCA4 Gene

This is an Observational Study to Follow the Progression of Stargardt Disease Type 1 (STGD1) Caused by Bi-Allelic Autosomal Recessive Mutations in the ABCA4 Gene This is a multicenter study which will enroll approximately 75 subjects

Participants needed: 75
Trial details
Age: 12-65Biological sex: AllType: ObservationalSponsor: Splice BioUpdated: Sep 19, 2025Locations: 20
Eligibility criteria

Provide written consent [+9]

Are an immediate family member (e.g., child, sibling) of the Sponsor or study si... [+10]