Samelisant is under clinical development by Suven Life Sciences and currently in Phase II for Narcolepsy. According to GlobalData, Phase II drugs for Narcolepsy have a 59% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Samelisant’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.
Samelisant overview
Samelisant (SUVNG-3031) is under development for the treatment of narcolepsy with and without cataplexy and cognitive disorders. The drug candidate is administered orally in the form of tablet. The drug candidate acts by targeting histamine 3 (H3) receptor.
It was also under development for cognitive impairment associated with Alzheimer's disease, schizophrenia.
Suven Life Sciences overview
Suven Life Sciences (Suven) is a biopharmaceutical company. It carries out the discovery and development of novel pharmaceutical products. Its pipeline products include masupirdine (SUVN-502), samelisant (SUVN-G3031), usmarapride (SUVN-D4010), ropanicant (SUVN-911), SUVN-I6107, SUVN-M8036 and SUVN-D1044. The company’s product portfolio treats central nervous system (CNS) diseases such as alzheimer’s, dementia, narcolepsy, major depressive disorder (MDD), attention deficient hyperactivity disorder (ADHD), huntington’s disease, parkinson’s, bipolar disorder, and various neuro-psychiatry disorders. Suven also offers drug discovery and development support services (DDDSS) including synthetic and medicinal chemistry, analytical chemistry, in vitro biology, pharmacology, toxicology, bioanalysis, and ncenew chemical entity (NCE) formulations. Suven is headquartered in Hyderabad, Telangana, India.
For a complete picture of Samelisant’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.
