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Clinical Trial Summary

This Phase 3, multicenter, double-masked, parallel-group, placebo-controlled, randomized, fixed-dose clinical study is designed to evaluate the efficacy and safety of tinlarebant (LBS-008) in subjects diagnosed with GA.


Clinical Trial Description

Subjects will be randomized in a 2:1 ratio to receive either tinlarebant or placebo. The study treatment will be administered orally once daily from baseline (Day 1) through the final day of Month 24. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05949593
Study type Interventional
Source Belite Bio, Inc
Contact Belitebio Clinical Operations
Phone +886 972 080 097
Email clinicaltrial@belitebio.com
Status Recruiting
Phase Phase 3
Start date July 27, 2023
Completion date November 30, 2027

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