GRN-300 is under clinical development by Greenfire Bio 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 81% phase transition success rate (PTSR) indication benchmark for progressing into Phase II. GlobalData’s report assesses how GRN-300’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.
GRN-300 overview
Greenfire Bio overview
Greenfire Bio (Greenfire) is a clinical-stage biopharmaceutical company developing drugs for treating cancer. Its products include GRN-300: ovarian cancer, triple-negative breast cancer, M-001 melanoma, M-002 glioma, M-003 colorectal cancer, M-004 hepatocellular, MGFB: carcinoma, and PCLX-001 refractory colorectal cancer—acute myeloid leukemia (AML). Greenfire operates through its subsidiaries, Green3Bio and MGFB Bio, which focus on developing the SIK2/3 inhibitor and therapeutic vaccine products. The company leverages an integrated ecosystem of development organizations and internal expertise to accelerate product development. Greenfire is headquartered in Austin, Texas, the US.
For a complete picture of GRN-300’s drug-specific PTSR and LoA scores, buy the report here.
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