RecruitingNCT06435000

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

Studying Stargardt disease

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Key facts

Sponsor
Splice Bio
Enrollment
75 enrolled
Eligibility
12-65 years · All sexes
Timeline
20242027

Study locations (20)

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT06435000 on ClinicalTrials.gov

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