KB-001 is under clinical development by Keystone Bio and currently in Phase I for Lung Cancer. According to GlobalData, Phase I drugs for Lung Cancer have an 80% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how KB-001’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.

KB-001 overview

KB-001 is under development for the treatment of Alzheimer's disease, nonalcoholic fatty liver disease (NAFLD), non-alcoholic steatohepatitis (NASH), periodontal disease, peri-implantitis, stroke, atherosclerosis, esophageal cancer, non-smokers lung cancer, oral squamous cell cancer, cardiovascular disease, type 2 diabetes, pneumonia. It is administered by oral route.

Keystone Bio overview

Keystone Bio, Inc., is a developer of a suite of antibodies intended to cure Alzheimer’s and Heart Disease. The company is headquartered in United States.

For a complete picture of KB-001’s drug-specific PTSR and LoA scores, buy the report here.

GlobalData

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 its clinical pathway (PTSR), as well as how likely the drug will be approved (LoA). This is based on a proprietary algorithm built from the drugs’ sales forecast, regulatory milestones, cost forecasts, WACC rate and other proprietary data sources found on GlobalData’s Pharmaceutical Intelligence Center.