IAM-1363 is under clinical development by Iambic Therapeutics 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 IAM-1363’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.
IAM-1363 overview
IAM-H1 is under development for the treatment of HER2-driven solid tumors including colorectal cancer, non-small cell lung cancer, bladder cancer, breast cancer. The therapeutic candidate acts by targeting human epidermal growth factor receptor 2 (HER2) and HER2 mutants. It is administered through oral route as capsules. It is being developed based on NeuralPLexer technology, a artificial intelligence (AI)-driven drug-discovery platform.
Iambic Therapeutics overview
Iambic Therapeutics is a biotechnology company developing therapeutics from AI drug discovery platform used to treat solid tumor diseases. The company is headquartered in San Diego, California, the US.
For a complete picture of IAM-1363’s drug-specific PTSR and LoA scores, buy the report here.
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