APG-157 is under clinical development by Aveta Biomics and currently in Phase II for Gliosarcoma. According to GlobalData, Phase II drugs for Gliosarcoma does not have sufficient historical data to build an indication benchmark PTSR for Phase II. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the APG-157 LoA Report. 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.
APG-157 overview
APG-157 is under development for the treatment of recurrent high-grade glioma squamous cell carcinoma of oral cavity and oropharynx, recurrent glioblastoma multiforme accessible for local and topical administration, anaplastic astrocytoma, anaplastic oligodendroglioma and gliosarcoma. It is also under treatment for head and neck squamous cell cancer (HNSCC) of the oral cavity and/or oropharynx The drug candidates are developed as network modulating drugs. They are administered through oral route and topical route.
Aveta Biomics overview
Aveta Biomics., is a developer of a pain relief medicine that designed to help users recover headaches and body-aches. The company is headquartered in United States.
For a complete picture of APG-157’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.
