drugset / Trial / NCT05949593

Phase 3, Randomized, Placebo-Controlled Study of Tinlarebant to Explore Safety and Efficacy in Geographic Atrophy

NCT05949593 ↗

Phase 3 Active not recruiting 429 enrolled Belite Bio, Inc
RandomizedParallel-groupDouble-blindTreatment

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.

Timeline

Start
2023-07-27
Primary completion
2027-06-30
Completion
2027-08-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Tinlarebant Small molecule 5 mg Oral