Avutometinib potassium is under clinical development by Verastem and currently in Phase II for Human Epidermal Growth Factor Receptor 2 Negative Breast Cancer (HER2- Breast Cancer). According to GlobalData, Phase II drugs for Human Epidermal Growth Factor Receptor 2 Negative Breast Cancer (HER2- Breast Cancer) have a 49% phase transition success rate (PTSR) indication benchmark for progressing into Phase III. GlobalData’s report assesses how Avutometinib potassium’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.
Avutometinib potassium overview
Verastem overview
Verastem is a late-stage development biopharmaceutical company that develops and commercializes new medicines to treat cancer. The company’s pipeline products include avutometinib and defactinib combinations that treat low-grade serous ovarian cancer, non-small cell lung cancer, pancreatic cancer, colorectal cancer and melanoma, among others. Its avutometinib is an orally available small molecule rapidly accelerated fibrosarcoma/mitogen-activated protein kinase (RAF/MEK) clamp that inhibits the renal artery stenosis (RAS) sarcoma (RAS)/RAF/MEK, ERK mitogen-activated pathway kinase pathway which is involved in cell proliferation, migration, transformation and survival of tumor cells. Verastem’s defactinib is a selective focal adhesion kinase-1 (FAK) inhibitor monotherapy that targets solid tumors. The company operates through its subsidiaries in the US and Germany. Verastem is headquartered in Needham, Massachusetts, the US.
For a complete picture of Avutometinib potassium’s drug-specific PTSR and LoA scores, buy the report here.
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