pre-IPO PHARMA

COMPANY OVERVIEW

Biosight is a private Phase 2 clinical stage biotech company developing innovative therapeutics for hematological malignancies and disorders. Biosight’s lead product, aspacytarabine (BST-236), is an innovative proprietary anti-metabolite which addresses unmet medical needs by enabling high-dose chemotherapy with reduced systemic toxicity. Aspacytarabine is currently being investigated as a single agent in a Phase 2b for first-line treatment of acute myeloid leukemia (AML), following completion of a Phase 1/2a study which demonstrated tolerability with promising efficacy in the challenging population of AML patients unfit for standard of care chemotherapy. Additional Phase 2 studies to be initiated 2021 include a study in relapsed/refractory AML and myelodysplastic syndrome (MDS) under a collaboration agreement recently signed with the European cooperative group, GFM.


LOCATION

  • Lod, None, Israel

  • THERAPEUTIC AREAS


    WEBSITE

    https://www.biosight-pharma.com/


    CAREER WEBSITE

    None


    SOCIAL MEDIA


    INVESTORS


    PRESS RELEASES


    Nov 22, 2022

    Biosight Launches a Phase 1/2 Clinical Trial of Aspacytarabine in Combination with Venetoclax for First-Line AML Induction Therapy, Followed by Aspacytarabine Consolidation


    Aug 1, 2022

    Biosight Granted Orphan Drug Designation from the FDA for Aspacytarabine for the Treatment of Myelodysplastic Syndromes


    Nov 22, 2021

    Nasdaq Grants Advaxis, Inc. an Extension to December 20, 2021, to Complete Merger Transaction with Biosight, Ltd. and Satisfy Initial Listing Requirements


    Nov 18, 2021

    Leading Independent Proxy Advisory Firm Glass Lewis Joins ISS in Recommending Advaxis Stockholders Vote “FOR” Proposed Merger with Biosight


    Nov 12, 2021

    Biosight Announces Initiation of Phase 2 Clinical Trial of Aspacytarabine for MDS and AML


    For More Press Releases


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