MBX-1416 is under clinical development by MBX Biosciences Inc and currently in Phase I for Hypoglycemia. According to GlobalData, Phase I drugs for Hypoglycemia have a 65% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how MBX-1416’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
MBX-1416 overview
MBX-1416 is under development for the treatment of post-bariatric hypoglycemia (PBH). The drug candidate is a precision endocrine peptide (PEP). It acts by targeting glucagon-like peptide 1 (GLP-1). It is being developed based on PEP platform. It is administered through subcutaneous route.
MBX Biosciences Inc overview
MBX Biosciences Inc., is a biopharmaceutical company that develops therapies to treat rare endocrine diseases. The company is headquartered in United States.
For a complete picture of MBX-1416’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
