KP-201 is under clinical development by Korea Pharma and currently in Phase I for Reflux Esophagitis (Gastroesophageal Reflux Disease). According to GlobalData, Phase I drugs for Reflux Esophagitis (Gastroesophageal Reflux Disease) have a 78% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how KP-201’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.

KP-201 overview

KP-201 is under development for the treatment of gastric ulcers, duodenal ulcers and ulcerative gastroesophageal reflux disease, Alzheimer's disease. It is administered by oral route.

Korea Pharma overview

Korea Pharma manufactures and sells drugs, it develops and sells dementia drugs, inflammatory diseases prescription drugs, gastrointestinal diseases drugs, and other products. Korea Pharma is headquartered in Seoul, South Korea.

For a complete picture of KP-201’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.