AGX-101 is under clinical development by Angiex and currently in Phase I for Solid Tumor. According to GlobalData, Phase I drugs for Solid Tumor have a 70% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how AGX-101’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.
AGX-101 overview
AGX-101 is under development for the treatment of solid tumors which include triple-negative breast cancer (TNBC) and pancreatic ductal adenocarcinoma (PDAC) . The therapeutic candidate constitutes an antibody drug conjugate which delivers auristatin payload. The drug candidate acts by targeting TM4SF1. It is administered through intravenous route.
Angiex overview
Angiex, a biotechnology company that develop vascular-targeted biotherapeutics. The company is headquartered in United States.
For a complete picture of AGX-101’s drug-specific PTSR and LoA scores, buy the report here.
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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.
