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tinlarebant

tinlarebant: 3 clinical trials tracked.

tinlarebant evidence translation

What we can confirm

3 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about tinlarebant, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 1 study sponsors
Clinical Trial Registry Records (3)

A Phase 1b Open-label Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety, and Tolerability of Tinlarebant in Japanese Subjects With Stargardt Disease and a Phase 2/3 Randomized, Double-masked, and Placebo-controlled Study to Evaluate the Safety, Tolerability, and Efficacy of Tinlarebant in Subjects With Stargardt Disease

NCT06388083Registry updated 2026-03-12·Phase 2/Phase 3·BLTE
Active, not recruiting

Primary endpoint: To measure the annualized rate of change from baseline lesion size in aggregate area of atrophy

InterventionalRandomizedtriple60 targetStarted 2024-07Completion 2028-0218 sites · Japan, United Kingdom, United StatesBelite Bio, Inc

PHase 3, Multicenter, RandOmized, Double-masked, PlacEbo-CoNtrolled Study of TInlarebant to EXplore Safety and Efficacy in the Treatment of Geographic Atrophy (the PHOENIX Study)

NCT05949593Registry updated 2026-01-07·Phase 3·BLTE
Active, not recruiting

Primary endpoint: To measure the rate of change (growth rate slope) in geographic atrophy (GA) lesion size

InterventionalRandomizeddouble429 targetStarted 2023-07Completion 2027-0849 sites · Australia, China, Czechia, France…Belite Bio, Inc

Phase 3, Multicenter, Randomized, Double-Masked, Placebo-Controlled Study to Evaluate the Safety and Efficacy of Tinlarebant in the Treatment of Stargardt Disease in Adolescent Subjects

NCT05244304Registry updated 2026-07-23·Phase 3·BLTE
Completed

Primary endpoint: To measure change in atrophic lesion size (definitely decreased autofluorescence, DDAF) by fundus autofluorescence (FAF) photography from baseline

InterventionalRandomizeddouble104 enrolledStarted 2022-03Completion 2025-0919 sites · Australia, Belgium, China, France…Belite Bio, Inc