Valbenazine tosylate is under clinical development by Neurocrine Biosciences and currently in Phase II for Trichotillomania. According to GlobalData, Phase II drugs for Trichotillomania 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 Valbenazine tosylate LoA Report. Buy the report here.
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Valbenazine tosylate overview
Valbenazine tosylate (NBI-98854, Ingrezza, Dysval, Gisbal, Ingrezza Sprinkle) is an anti-dyskinesia agent. It is formulated as hard gelatin capsules for oral route of administration. It is indicated for the treatment of central nervous system disorders including tardive dyskinesia in schizophrenia patients, adjunctive treatment in schizophrenia, for dyskinesia due to cerebral palsy and chorea associated with Huntington's disease. It acts by targeting vesicular monoamine transporter type 2.
Valbenazine tosylate is also under development for the treatment of chorea associated with Huntington's disease, trichotillomania, tardive dyskinesia and tourette syndrome (in adults and pediatrics).
Neurocrine Biosciences overview
Neurocrine Biosciences (Neurocrine) is a biopharmaceutical company that discovers, develops, and markets neurological drugs. The company’s lead product Ingrezza, is a vesicular monoamine transporter 2 (VMAT2) inhibitor to treat adults with tardive dyskinesia and chorea associated with Huntington’s disease. It is developing a pipeline of drug candidates for various indications in neurology, neuroendocrinology, and neuropsychiatry. Neurocrine also conducts clinical trials and studies for diseases such as movement disorders, epilepsy, and congenital adrenal hyperplasia, among others. The company works in collaboration with Mitsubishi Tanabe Pharma and AbbVie for products distribution. Neurocrine is headquartered in San Diego, California, the US.
For a complete picture of Valbenazine tosylate’s drug-specific PTSR and LoA scores, buy the report here.
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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.
