BXU-001 is under clinical development by Baylx and currently in Phase II for Idiopathic Pulmonary Fibrosis. According to GlobalData, Phase II drugs for Idiopathic Pulmonary Fibrosis have a 35% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how BXU-001’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
BXU-001 overview
BXU-001 is under development for the treatment of idiopathic pulmonary fibrosis (IPF), severe COVID-19 pneumonia with mild to moderate acute respiratory distress syndrome and rheumatoid arthritis. The drug candidate consists of allogeneic human umbilical cord tissue-derived mesenchymal stem cell, which is administered through intravenous route. The drug candidate is being developed based on stem cell technology platform.
It was also under development for the treatment of inflammatory bowel disease (IBD) and for multiple sclerosis.
Baylx overview
Baylx is developing stem cell therapeutics for the treatment of rheumatoid arthritis, liver disease and autoimmune diseases. The company is headquartered in Irvine, California, the US.
For a complete picture of BXU-001’s drug-specific PTSR and LoA scores, buy the report here.
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