MBF-015 is under clinical development by Medibiofarma and currently in Phase II for Huntington Disease. According to GlobalData, Phase II drugs for Huntington Disease does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the MBF-015 LoA Report. 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.
MBF-015 overview
MBF-015 is under development for the treatment of synaptopathies (huntington disease, alzheimer's disease and parkinson's disease) . It acts by targeting histone deacetylase 1/2 (HDAC 1/2). It ia administered through oral route.
Medibiofarma overview
Medibiofarma is a biotechnology company that develops novel drugs for the treatment of cancer. It focuses on virtual drug design, medicinal chemistry, in vitro pharmacology, and intellectual property. The company is headquartered in Noain, Navarra, Spain.
For a complete picture of MBF-015’s drug-specific PTSR and LoA scores, buy the report here.
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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.
