BHV-7000 is under clinical development by Biohaven and currently in Phase III for Bipolar I Disorder. According to GlobalData, Phase III drugs for Bipolar I Disorder have an 80% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how BHV-7000’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.
BHV-7000 overview
BHV-7000 is under development for the treatment of neonatal encephalopathy (KCNQ2-EE), neuropathic pain, partial seizures (Adult focal epilepsy/refractory focal onset epilepsy), generalized seizures with generalized tonic-clonic seizures and mood disorders such as major depressive disorder, bipolar disorder. The drug candidates acts by targeting potassium channels Kv7.2/7.3 and are developed based on ion channel discovery platform.
It was also under development for tinnitus.
Biohaven overview
Biohaven formerly Biohaven Research, is biopharmaceutical company discovering, developing, and commercializing novel therapies for the treatment of neurological and neuropsychiatric diseases. Biohaven is headquartered in Tortola, British Virgin Islands.
For a complete picture of BHV-7000’s drug-specific PTSR and LoA scores, buy the report here.
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