PT-217 is under clinical development by Phanes Therapeutics and currently in Phase I for Neuroendocrine Carcinoma. According to GlobalData, Phase I drugs for Neuroendocrine Carcinoma does not have sufficient historical data to build an indication benchmark PTSR for Phase I. GlobalData uses proprietary data and analytics to create drugs-specific PTSR and LoA in the PT-217 LoA Report. 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.

PT-217 overview

PT-217 is under development for the treatment of small-cell lung cancer, large cell neuroendocrine cancer, neuroendocrine prostate cancer and gastroenteropancreatic neuroendocrine tumors (GEP-NET). The drug candidate is a bi-specific monoclonal antibody acts by targeting cells expressing DLL3 and leukocyte surface antigen CD47.

Phanes Therapeutics overview

Phanes Therapeutics is a biotech company focused on discovery and development of therapeutics for metabolic complications and various types of cancer. Our extensive experience and deep scientific know-how strongly position us to discover and advance robust therapeutic molecules. Through scientific innovation, we deliver better treatment options for patients. Our mission is to relentlessly seek scientific and technological solutions to improve the lives of patients globally.

For a complete picture of PT-217’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.