GIM-531 is under clinical development by Georgiamune and currently in Phase II for Metastatic Melanoma. According to GlobalData, Phase II drugs for Metastatic Melanoma have a 36% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how GIM-531’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.
GIM-531 overview
GIM-531 is under development for the treatment of solid tumors which include metastatic cutaneous melanoma. The drug candidate acts by targeting regulatory T cell (Treg). It is administered through oral route.
Georgiamune overview
Georgiamune is a biotechnology company that develops immuno therapies for the treatment of cancer and autoimmune diseases. The company is headquartered in Gaithersburg, Maryland, the US.
For a complete picture of GIM-531’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.
