K-757 is under clinical development by Kallyope and currently in Phase II for Obesity. According to GlobalData, Phase II drugs for Obesity have a 29% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how K-757’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
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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.
K-757 overview
K-757 is under development for the treatment of metabolic disorders such as obesity (weight loss) in patients with type 2 diabetes. The drug candidate acts by targeting the circuits involved in the gut-brain axis. It is administered through oral route. It is developed based on computational biology through Klarity™ Platform. It acts by targeting GPR40.
Kallyope overview
Kallyope is a biotechnology company that focuses on discovering and developing novel, oral small-molecule therapeutics. Its main activities carry out addressing metabolic, neurological, and gastrointestinal diseases through innovative drug discovery and development. The company’s products include gut-targeted molecules such as K-757 and K-833, that are being evaluated for obesity and type 2 diabetes. Kallyope’s products are designed for patients with significant unmet medical needs in the healthcare industry. The company also offers solutions for diabetes, obesity, inflammatory disease, migraine, and allergies. It markets under Klarity brand. The company operates primarily in the US. Kallyope is headquartered in New York City, New York, the US.
For a complete picture of K-757’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.
