Monlunabant is under clinical development by Inversago Pharma and currently in Phase II for Hypertriglyceridemia. According to GlobalData, Phase II drugs for Hypertriglyceridemia have a 52% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Monlunabant’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.
Monlunabant overview
Monlunabant is under development for the treatment of type I diabetes, asthma, pre-diabetes/impaired glucose tolerance, abdominal obesity, hypertriglyceridemia, diabetic nephropathy, type 2 diabetes, metabolic dysfunction-associated steatohepatitis (non-alcohol related steatohepatitis or MASH or NASH), obesity and metabolic syndrome. The drug candidates are administered through oral route in the form of a tablet. They act by targeting cannabinoid receptor 1 (CB1R).
Inversago Pharma overview
Inversago Pharma is a preclinical-stage biotech company. The company develops peripherally-restricted cannabinoid receptor 1, a G protein-coupled cannabinoid receptor that is encoded by the CNR1 gene for the treatment of Prader-Willi Syndrome, Type-1 Diabetes, obesity and other metabolic disorders such as non-alcoholic steatohepatitis.
For a complete picture of Monlunabant’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.
