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Clinical Trial Summary

The primary objective of this trial is to assesses the efficacy of tinlarebant in slowing the rate of growth of atrophic lesion(s) in adolescent subjects with STGD1


Clinical Trial Description

Approximately 90 subjects will be enrolled in this study. Subjects will be assigned to study drug (tinlarebant 5 mg/placebo) with treatment period of upto 24 months with 28 days of follow-up. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05244304
Study type Interventional
Source Belite Bio, Inc
Contact
Status Active, not recruiting
Phase Phase 3
Start date March 28, 2022
Completion date October 2025

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