AG-01 is under clinical development by A&G Pharmaceutical and currently in Phase I for Triple-Negative Breast Cancer (TNBC). According to GlobalData, Phase I drugs for Triple-Negative Breast Cancer (TNBC) have an 83% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how AG-01’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.

AG-01 overview

AG-01 is under development for the treatment of triple negative breast cancer, mesothelioma and non-small cell lung cancer. It is administered through parenteral route.

A&G Pharmaceutical overview

A&G Pharmaceutical operates as a medical device company that discovers and develops theranostics products. It offers personalized medicines for cancer, integrated Rx-Dx products, biomarkers, GP88-based breast cancer diagnostic testing kits, GP88 diagnostic kits, and anti-GP88 monoclonal antibody therapeutic products. It also provides breast cancer treatments, progranulin, molecular diagnostic testing, targeted therapeutics, companion diagnostics, new treatment paradigm and long-term diagnostic products. A&G Pharmaceutical offers clinical and preclinical programs, clinical diagnostic testing, disease recurrence monitoring, and laboratory testing services. The company’s products are used in screening, detection, and treatment of various cancers. A&G Pharmaceutical is headquartered in Columbia, Maryland, the US.

For a complete picture of AG-01’s drug-specific PTSR and LoA scores, buy the report here.

GlobalData

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 its clinical pathway (PTSR), as well as how likely the drug will be approved (LoA). This is based on a proprietary algorithm built from the drugs’ sales forecast, regulatory milestones, cost forecasts, WACC rate and other proprietary data sources found on GlobalData’s Pharmaceutical Intelligence Center.