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MBF-015 by Medibiofarma for Parkinson’s Disease: Likelihood of Approval

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).

Medibiofarma overview

Medibiofarma is a biotechnology company, develops novel drugs for the treatment of cancer. The company focuses on virtual drug design, medicinal chemistry, in vitro pharmacology, intellectual property. Medibiofarma is headquartered in Noain, Navarra, Spain.

For a complete picture of MBF-015’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 20 February 2024

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GlobalData

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.




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