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.
Masofaniten overview
Masofaniten (EPI-7386) is under development for the treatment of metastatic castration resistant prostate cancer and AR driven cancers. The drug candidate is administered through oral route. The drug candidate acts by targeting N-Terminus domain (NTD) of the androgen receptor. It was also under development for the treatment of breast cancer.
ESSA Pharma overview
ESSA Pharma is a drug developer that offers oncology therapeutics. The company’s pipeline products include EPI-506 in which it includes the programs 3rd-Generation AR N-terminal domain inhibitor, AR N-terminal domain, tau-1 site inhibitor, AR N-terminal, domain degrader among others. It offers clinical trials. The company has collaboration with the cancer prevention and research institute to advance science for cancer biology developments. It operates in Canada and the US. Essa Pharma is headquartered in Vancouver, British Columbia, Canada.
For a complete picture of Masofaniten’s drug-specific PTSR and LoA scores, buy the report here.
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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.