Condition: Geographic Atrophy · Stargardt Disease · RPE-mediated Maculopathy · Sponsor: Cellio Therapeutics Inc
This is a first-in-human Phase 1 study evaluating the safety and tolerability of C.001 in patients with retinal diseases involving degeneration of the retinal pigment epithelium. Participants will receive a single administration of C.001 delivered by subretinal injection. The study will evaluate three dose levels in a sequential manner. The primary objective is to assess the safety of C.001 over a 3-month period following administration. Participants will be followed for up to 12 months to further evaluate safety and explore changes in visual function and retinal structure.
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| Clinical Trial Site 1 | Beverly Hills, California, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07594236