Bezisterim is under clinical development by BioVie and currently in Phase II for Mild Cognitive Impairment. According to GlobalData, Phase II drugs for Mild Cognitive Impairment 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 Bezisterim 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.
Bezisterim overview
BioVie overview
BioVie (BIVI) is a clinical-stage biopharmaceutical company that develops drug therapies for neurodegenerative and liver disease. The company’s pipeline products such as BIV201 (continuous infusion terlipressin), NE3107, and clinical trials for ascites due to advanced liver cirrhosis. BIV201 for hepatorenal syndrome (HRS). It focused on potential future treatment options for patients suffering from ascites and other life-threatening complications of advanced liver cirrhosis caused by hepatitis, NASH, and alcoholism. NE3107 finds application in the treatment of excess cortisol diseases such as Alzheimer’s and Parkinson’s diseases. The company is also focused on the FDA to approve their drug specifically for treating ascites to extend their quality. BioVie is targeting this landmark achievement. BIVI is headquartered in Carson City, Nevada, the US.
For a complete picture of Bezisterim’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.
