DPXE-7 is under clinical development by BioVaxys Technology and currently in Phase II for Cervical Cancer. According to GlobalData, Phase II drugs for Cervical Cancer have a 35% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how DPXE-7’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.
DPXE-7 overview
DPXE-7 is under development for the treatment of HPV associated cervical, oropharyngeal, anal, and head and neck cancers. The drug candidate is formulated as a powder to be reconstituted as oil-based formulation and administered through parenteral route. It is developed based on Depovax technology platform. It acts by targeting human papillomavirus protein E7.
BioVaxys Technology overview
BioVaxys Technology is a biotechnology company that develops immunotherapeutic vaccines to treat various solid tumor types. The company is headquartered in Canada.
For a complete picture of DPXE-7’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.
