IMP-17 is under clinical development by Eikon Therapeutics and currently in Phase II for Ovarian Cancer. According to GlobalData, Phase II drugs for Ovarian Cancer have a 26% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how IMP-17’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.

IMP-17 overview

IMP-17 is under development for the treatment of solid tumors, metastatic breast cancer, ovarian cancer, fallopian tube cancer, primary peritoneal cancer and metastatic castrate resistant prostate cancer (mCRPC). It acts by targeting Poly (ADP-Ribose) Polymerase 1. It is administered through oral route.

Eikon Therapeutics overview

Eikon Therapeutics is a clinical-stage biotechnology company that carries out drug discovery and development. The company provides preclinical programs in the fields of oncology, neuroscience and immunology as well as clinic programs designed to improve cancer treatment. Its oncological pipeline products include TLR7/8 – BDB001 and PARP1 selective inhibitors – IMP1734 and IMP17307. The company utilizes technology such as single molecule tracking and super-resolution fluorescence microscopy the interface of biology, engineering and chemistry to discover novel treatments for life-threatening diseases. Eikon Therapeutics is headquartered in Hayward, California, the US.

For a complete picture of IMP-17’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 18 April 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.