SEONGNAM, South Korea, Dec. 16, 2018 /PRNewswire/ -- Bridge Biotherapeutics Inc., a clinical stage biotech company headquartered
Bridge Biotherapeutics now plans to initiate a Phase I study of BBT-877 in the U.S. in January 2019 to assess the safety, tolerability, pharmacokinetics and pharmacodynamics of the drug candidate in healthy volunteers. The planned study will be performed in two phases, a Single Ascending Dose (SAD) phase with 5 cohorts and a Multi Ascending Dose (MAD) phase with 3 cohorts. The estimated primary completion date is currently expected in late 2019.
"We are proud of the IND clearance for BBT-877, which has shown a strong potential to be developed as the best-in-class Autotaxin inhibitor for IPF treatment," and "Our team will continue to focus on developing a breakthrough drug to address huge unmet medical needs in IPF," stated Dr. Gwang-hee Lee, the Head of Translational Research at Bridge Biotherapeutics.
BBT-877 has been originally discovered by LegoChem Biosciences, a publicly traded Korean biotech, and was licensed to Bridge Biotherapeutics in 2017 for the worldwide exclusive right for further development. In August 2018, Bridge Biotherapeutics presented the results of the preclinical study on BBT-877 at the IPF Summit, attracting pulmonologists' interest on the efficacy and safety of the drug candidate. The data has demonstrated the best-in-class opportunity in comparison to a current development pipeline compound.
BBT-877 is the second molecule from Bridge Biotherapeutics with the US FDA clearances of IND for proceeding clinical studies. The company is also developing BBT-401, the first anti-Pellino-1 compound for the ulcerative colitis and aims to initiate the Phase II study in the U.S. within this year.
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1. Bridge Biotherapeutics, Inc.Bridge Biotherapeutics is a virtually-operated, venture-backed clinical stage biotech engaged in the development of novel therapeutics in the therapeutic areas of high unmet needs such as ulcerative colitis, fibrotic diseases and cancers. Following its first compound BBT-401, BBT-877, a potent and selective Autotaxin (ENPP) inhibitor is being developed potentially for the treatment of various fibrotic diseases such as idiopathic pulmonary fibrosis (IPF) and non-alcoholic steatohepatitis (NASH). Bridge Biotherapeutics is a JLABS tenant company at JLABS@TMC, Houston, TX.
2. AutotaxinAutotaxin (ATX) is a protein of approximately 900 amino acids discovered in the early 1990s, and an enzyme important for generating the lipid signaling molecule, lysophosphatidic acid (LPA). Autotaxin has lysophospholipase D activity that converts lysophosphatidylcholine (LPC) into LPA. LPA, the bioactive lipid catalyzed by Autotaxin, engages in signaling via LPA receptors and the LPA signaling results in cell proliferation, migration, secretion of cytokine and chemokine and reduction of cell apoptosis. Pathologically, Autotaxin has been found to be engaged in inflammation and fibrosis and it emerges as one of attractive drug targets.
3. Idiopathic Pulmonary Fibrosis (IPF)Idiopathic Pulmonary Fibrosis (IPF) is a progressive, irreversible and fatal lung disease. A number of investigational drugs are being developed while only two therapeutics, pirfenidone, and nintedanib, were approved by the U.S. FDA.
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SOURCE Bridge Biotherapeutics, Inc.
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