Brexanolone is under clinical development by NeuTherapeutics and currently in Phase I for Parkinson’s Disease. According to GlobalData, Phase I drugs for Parkinson’s Disease have a 72% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how Brexanolone’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.
Brexanolone overview
Allopregnanolone (brexanolone) is under development for the treatment of Alzheimer's disease and Parkinson's disease. It is administered through intravenous and intranasal routes. It acts by targeting gamma-aminobutyric acid type A receptor subunit (GABA(A) receptor).
NeuTherapeutics overview
NeuTherapeutics a company which bridge discovery to cure through the development of regenerative treatments for neurodegenerative diseases and precision therapies that preserve women’s brain health. NeuTherapeutics is headquartered in the US.
For a complete picture of Brexanolone’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.
