Novel Therapy for
UNMET MEDICAL NEED
Belite Bio™ is a San Diego based clinical stage biopharmaceutical drug development company targeting untreatable eye diseases, such as atrophic age-related macular degeneration (commonly known as dry AMD) and Stargardt disease, and metabolic diseases.
Developed from our RBP4 intellectual property portfolio, our lead candidate, LBS-008, has initiated its phase 3 for Stargardt disease, an inherited juvenile form of macular degeneration, and expects to initiate its phase 3 for dry age-related macular degeneration in 2022. LBS-008 has obtained Orphan Drug Designation in the United States and Europe and has been granted a Rare Pediatric Disease (RPD) designation and Fast Track Designation in the US.
Tinlarebant
LBS-008
Bringing Hope to
INCURABLE BLINDNESS
Dry AMD / Stargardt Disease
PHASE 3
LBS
009
Blocking the Path to
METABOLIC DISEASE
Non-Fatty Liver Disease / Type 2 Diabetes
PRECLINICAL
BRINGING HEALTH INSIGHT
TREAT THE
UNTREATABLE
Our pipeline of novel therapies, which is built on our RBP4 (Retinol Binding Protein 4) IP Portfolio, is focused on meeting the unmet needs of patients suffering from blindness, liver disease and diabetes.
Patient Registry
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Tinlarebant (LBS-008) – Phase 3 trial for Geographic Atrophy (the “Phoenix” trial)
Recruitment Status : Recruiting
Tinlarebant (LBS-008) – Phase 3 trial for Stargardt Disease (the “Dragon” trial)
Recruitment Status : Active: not recruiting
This trial is to assess the efficacy and safety of Tinlarebant in adolescent subjects with childhood-onset Stargardt Disease.
Tinlarebant (LBS-008) – Phase 1b/2 trial for Stargardt Disease
Recruitment Status : Active, not recruiting
This Phase 1b trial is to identify the optimal dose of Tinlarebant in adolescent subjects with childhood-onset Stargardt Disease. The Phase 1b trial is extended to a two year Phase 2 trial in assessing the safety and efficacy of Tinlarebant in adolescent subjects with childhood-onset Stargardt Disease.