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BELITE BIO, INC (BLTE)

Belite Bio, Inc. is a clinical-stage biopharmaceutical company focused on the discovery and advancement of novel therapies. The firm's primary therapeutic areas include atrophic age-related macular degeneration and autosomal recessive Stargardt disease. Its flagship drug candidate, LBS-008, is an investigational oral medication administered once daily. Currently undergoing Phase 3 clinical trials, LBS-008 is engineered to modulate vitamin A delivery to the eye, thus preventing the accumulation of detrimental vitamin A metabolites in ocular tissues. Furthermore, Belite Bio is advancing LBS-009, an oral anti-retinol binding protein 4 therapy, through preclinical development. This therapy targets various liver ailments, including non-alcoholic fatty liver disease, nonalcoholic steatohepatitis, and type 2 diabetes. Founded in 2016, Belite Bio, Inc. is headquartered in San Diego, California, and operates as a subsidiary of Lin Bioscience International Ltd.

Sector: Pharmaceutical Preparations

Industry: Biotechnology

Belite Bio, Inc logo

Belite Bio, Inc

NASDAQ:BLTEHealthcare
+2.97%$154.74
AH$154.74+0.00%vs close
Mkt Cap$6.23B
Float22.63M
O/S40.27M
Vol
$ Vol
RVOL
Inst Own23.5%
Earnings
Dilution
Upcoming Catalysts
  • Stargardt Disease Type 1 (STGD1)
    Cash runway at this date: > 5 yr
    Feb 12, 2027in 102 days8-K
Pipeline4 lead-sponsored trials·2 active2 completed(3 more as collaborator)

Trials need funding. See this company's dilution risk and cash position.

Clinical Trials
Sponsor role
Status
Phase
  • Phase 3
    Completed

    Phase 3, Randomized, Placebo-Controlled Study of Tinlarebant to Explore Safety and Efficacy in Adolescent Stargardt Disease

    Tinlarebant, Placebo

    Stargardt Disease 1

    Enrollment
    104
    Start
    Mar 2022
    Primary Completion
    Aug 2025
    Completion
    Sep 2025
    NCT05244304
  • Phase 3
    Active, not recruiting

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

    Tinlarebant, Placebo

    Geographic Atrophy

    Enrollment
    429
    Start
    Jul 2023
    Primary Completion
    Jun 2027est.
    Completion
    Aug 2027est.
    NCT05949593
  • Phase 2/3
    Active, not recruiting

    A Phase 2/3 Study to Evaluate the Efficacy and Safety of Tinlarebant in Subjects With Stargardt Disease

    Tinlarebant, Placebo

    STGD1, Stargardt Disease 1

    Enrollment
    60
    Start
    Jul 2024
    Primary Completion
    Feb 2028est.
    Completion
    Feb 2028est.
    NCT06388083
  • Phase 1
    Completed

    Safety and Tolerability of Escalating Doses of BPN-14967 in Healthy Adults

    BPN-14967, Placebo

    Healthy Volunteers

    Enrollment
    40
    Start
    Jul 2019
    Primary Completion
    Dec 2019
    Completion
    Dec 2019
    NCT04005807