Teverelix is under clinical development by Antev and currently in Phase II for Hormone-Sensitive Prostate Cancer. According to GlobalData, Phase II drugs for Hormone-Sensitive Prostate Cancer have a 74% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Teverelix’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.

Teverelix overview

Long acting formulation of Teverelix (B-110) is under development for metastatic prostate cancer, non-metastatic hormone sensitive prostate cancer, acute urinary retention, benign prostatic hyperplasia. Teverelix is a luteinizing hormone-releasing hormone (LHRH) antagonist. It is administered subcutaneously and intramuscularly. The drug candidate is developed based on the microcrystalline suspension technology. It was also under development for uterine fibroids and endometriosis.

For a complete picture of Teverelix’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.