YENEO-001 is under clinical development by NantBioScience and currently in Phase I for Non-Small Cell Lung Cancer. According to GlobalData, Phase I drugs for Non-Small Cell Lung Cancer have an 80% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how YENEO-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.
YENEO-001 overview
YENEO-001 is under development for the treatment of solid tumor including colorectal cancer, head and neck cancer squamous cell carcinoma, non-small cell lung cancer, hormone receptor positive, HER2-positive or negative and triple-negative breast cancer, pancreatic cancer, liver cancer and melanoma. The drug candidate is a yeast-based personalized cancer vaccine formulated as a suspension and administered through parenteral route.
For a complete picture of YENEO-001’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.
