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  2. KRAS - Wikipedia

    en.wikipedia.org/wiki/KRAS

    A phase Ia/Ib dose escalation trial of the oral selective KRAS G12C inhibitor divarasib was published in 2023, where the drug was tested in non-small cell lung cancer, colorectal cancer, and other solid tumors with KRAS G12C mutations. [55] It continues in phase I and II studies for several cancer types as of August 2023. [56] [57] [58] [59]

  3. List of antineoplastic agents - Wikipedia

    en.wikipedia.org/wiki/List_of_antineoplastic_agents

    EGFR inhibitor. Squamous cell head and neck cancer or EGFR-positive and KRAS wild-type metastatic colorectal cancer. Infusion-related reactions, skin reactions, hypomagnesaemia, hypocalcaemia, hypokalaemia, blood clots, interstitial lung disease and aseptic meningitis. Denosumab: SC: RANKL inhibitor.

  4. Sotorasib - Wikipedia

    en.wikipedia.org/wiki/Sotorasib

    [4] [5] It targets a specific mutation, G12C, in the protein K-Ras encoded by gene KRAS which is responsible for various forms of cancer. [7] [8] Sotorasib is an inhibitor of the RAS GTPase family. [4] The most common side effects include diarrhea, musculoskeletal pain, nausea, fatigue, liver damage and cough. [4] [5]

  5. KRAS Inhibitors Market: New Treatments Are Set to Change ...

    lite.aol.com/tech/story/0022/20240930/9248499.htm

    New York, USA, Sept. 30, 2024 (GLOBE NEWSWIRE) -- KRAS Inhibitors Market: New Treatments Are Set to Change Cancer Care | DelveInsight According to DelveInsight’s analysis, the growth of the KRAS Inhibitors market is expected to be mainly driven by increasing incidence, a rise in awareness and access to treatment, and robust pipeline activity for cancer indications in the 7MM.

  6. K-Ras(G12C) inhibitor 6 - Wikipedia

    en.wikipedia.org/wiki/K-Ras(G12C)_inhibitor_6

    K-Ras(G12C) inhibitor 6 is an irreversible inhibitor of oncogenic K-Ras(G12C), subverting the native nucleotide preference to favour GDP over GTP. Its family of inhibitors allosterically control GTP affinity and effector interactions by fitting inside a "pocket", or binding site, of mutant K-Ras. It is the most frequently mutated oncogene. [1]

  7. MEK inhibitor - Wikipedia

    en.wikipedia.org/wiki/MEK_inhibitor

    A MEK inhibitor is a chemical or drug that inhibits the mitogen-activated protein kinase ... and is now in phase III development in KRAS mutation positive NSCLC ...

  8. Panitumumab - Wikipedia

    en.wikipedia.org/wiki/Panitumumab

    Panitumumab was approved by the European Medicines Agency (EMEA) in 2007, and by Health Canada in 2008, for "the treatment of refractory EGFR-expressing metastatic colorectal cancer in patients with non-mutated (wild-type) KRAS". Panitumumab was the first monoclonal antibody to demonstrate the use of KRAS as a predictive biomarker.

  9. Cetuximab - Wikipedia

    en.wikipedia.org/wiki/Cetuximab

    Accordingly, genetic testing to confirm the absence of KRAS mutations (and so the presence of the KRAS wild-type gene), is now clinically routine before the start of treatment with EGFR inhibitors. mCRC patients with wild-type KRAS tumors have been shown to benefit from a response rate of over 60% and a decreased risk for progression of over 40 ...