ERAS-801 is under clinical development by Erasca and currently in Phase I for Recurrent Glioblastoma Multiforme (GBM). According to GlobalData, Phase I drugs for Recurrent Glioblastoma Multiforme (GBM) have an 87% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how ERAS-801’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.
ERAS-801 overview
ERAS-801 is under development for the treatment of recurrent glioblastoma multiforme and non-small cell lung cancer. It is administered through oral route. The therapeutic candidate is a small molecule which acts by targeting epidermal growth factor receptor (EGFR).
Erasca overview
Erasca is an oncology drug development company that uses its artificial intelligence drug discovery platform to treat and cure cancer. The company is headquartered in San Diego, California, the US.
For a complete picture of ERAS-801’s drug-specific PTSR and LoA scores, buy the report here.
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