EC-313 is under clinical development by Evestra and currently in Phase I for Endometriosis. According to GlobalData, Phase I drugs for Endometriosis have a 70% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how EC-313’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. 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.

EC-313 overview

EC-313 is under development for the treatment of breast cancer, heavy menstrual bleeding, fibroids and endometriosis. It is a new molecular entity. It is a selective progesterone receptor modulator (SPRM). The drug candidate acts by targeting progesterone receptor. It is administered through oral and vaginal routes.

Evestra overview

Evestra is a biopharmaceutical research and development company with developing women’s healthcare products. The company can analyze the information and customize the offering to market needs. Evestra is headquartered in Schertz, Texas, the US.

For a complete picture of EC-313’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 10 June 2024

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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.