Abiraterone acetate by Tavanta Therapeutics for Hormone-Sensitive Prostate Cancer: Likelihood of Approval

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.

Abiraterone acetate overview

Abiraterone acetate (DRGT-45) is under development for the treatment of metastatic castration-resistant prostate cancer and castrate-sensitive prostate cancer. It is administered through granules for oral suspension. It acts by targeting CYP17. The drug candidate is developed based on Super-API technology.

Tavanta Therapeutics overview

Tavanta Therapeutics is a pharmaceutical company that develops proprietary drugs to treat patients with debilitating or serious diseases with novel small molecules and peptides. The company is headquartered in King of Prussia, Pennsylvania, the US.

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

This content was updated on 1 January 1970

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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.