Brexanolone is under clinical development by Seaport Therapeutics and currently in Phase II for Major Depressive Disorder. According to GlobalData, Phase II drugs for Major Depressive Disorder have a 39% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. 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.
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
Brexanolone is under development for the treatment of neurological and neuropsychological conditions, including major depression disorder (MDD) with anxiety, sleep disorders, fragile X tremor-associated syndrome, essential tremor, epileptic disorders, anxiety disorders, postpartum depression, among others. It is administered by oral route. It acts by targeting GABAA receptor. The drug candidate is developed based on Glyph technology. It is a prodrug of allopregnanolone.
Seaport Therapeutics overview
Seaport Therapeutics, a subsidiary of Puretech Health Plc, is a clinical-stage biopharmaceutical company primarily focused on the development of novel neuropsychiatric medicines. The company is headquartered in Boston, Massachusetts, the US.
For a complete picture of Brexanolone’s drug-specific PTSR and LoA scores, buy the report here.
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