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    Home > Medical News > Medical Research Articles > FDA Grants BBT-877 For Orphan Drug For Iapathic Pulmonary Fibrosis

    FDA Grants BBT-877 For Orphan Drug For Iapathic Pulmonary Fibrosis

    • Last Update: 2020-06-10
    • Source: Internet
    • Author: User
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    recently, South Korea's Bridge Bios
    company(http:// announcedthat the u.SFood andDrug(http://Administration (
    FDA(http://) has granted BBT-877 treatment for iacotic pulmonary fibrosis (IPF) orphan drug eligibilityBBT-887
    BBT-887 is a powerful, best-in-class self-secretion motor factor (Autotaxin, ATX) inhibitor, an enzyme that participates in inflammation and fibrosis by generating lipid signaling moleculesEarly compounds of BBT-887 were first discovered by LegoChem Biosciences, a Korean biotech company2017, Bridge Biotherapeutics was granted the exclusive global license to further develop the drugIn August 2018, Bridge Biotherapeutics presented the results of the preclinical study of BBT-877 at the IPF Summit, which raised interest and concern among respiratory experts about the effectiveness and safety of the drug candidateData show that BBT-877 may be the best-in-class compound compared to the compounds currently in the pipeline developed BBT-877 is bridge Biotherapeutics' second molecule to receive FDA approval for clinical studies, and another molecule, BBT-401, is currently in Phase II clinical, the first anti-ubiquinone-connected enzyme Pellino-1 compound to treat ulcerative colitis, and is expected to be the first drug in the selective patient group in February
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