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Sotorasib - Wikipedia
https://en.wikipedia.org/wiki/Sotorasib
WEBSotorasib, sold under the brand names Lumakras and Lumykras, is an anti-cancer medication used to treat non-small-cell lung cancer. It targets a specific mutation, G12C, in the protein K-Ras encoded by gene KRAS which is responsible for various forms of cancer. Sotorasib is an inhibitor of the RAS GTPase family.
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Sotorasib is First KRAS Inhibitor Approved by FDA - NCI
https://www.cancer.gov/news-events/cancer-currents-blog/2021/fda-sotorasib-lung-cancer-kras
WEBJun 25, 2021 · FDA has approved the first KRAS-blocking drug, called sotorasib (Lumakras). The approval, which covers the use of sotorasib for some patients with advanced lung cancer, was based on the results of the CodeBreak100 trial. It also sets the stage for additional KRAS inhibitors already in development, researchers said.
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Sotorasib for Lung Cancers with KRAS p.G12C Mutation | NEJM
https://www.nejm.org/doi/full/10.1056/NEJMoa2103695
WEBJun 4, 2021 · Sotorasib showed anticancer activity in patients with KRAS p.G12C–mutated advanced solid tumors in a phase 1 study, and particularly promising anticancer activity was observed in a subgroup of...
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Sotorasib Uses, Side Effects & Warnings - Drugs.com
https://www.drugs.com/mtm/sotorasib.html
WEBSep 11, 2023 · Sotorasib is used in adults to treat non-small cell lung cancer who have already been treated with at least one other cancer medicine. Sotorasib is given when the cancer has progressed or has spread to other parts of the body or when surgery is not an option. Your doctor will make sure you have the correct tumor type to be treated with …
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Sotorasib - NCI - National Cancer Institute
https://www.cancer.gov/about-cancer/treatment/drugs/sotorasib
WEBSotorasib is approved to treat: Non-small cell lung cancer (NSCLC) that has spread and has a KRAS p.G12C mutation. It is used in adults who have received at least one other systemic therapy. Sotorasib is approved under FDA’s Accelerated Approval Program.
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FDA grants accelerated approval to sotorasib for KRAS G12C …
https://www.fda.gov/drugs/resources-information-approved-drugs/fda-grants-accelerated-approval-sotorasib-kras-g12c-mutated-nsclc
WEBOn May 28, 2021, the Food and Drug Administration granted accelerated approval to sotorasib (Lumakras™, Amgen, Inc.), a RAS GTPase family inhibitor, for adult patients with KRAS G12C ‑ mutated...
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KRASG12C Inhibition with Sotorasib in Advanced Solid Tumors
https://www.nejm.org/doi/full/10.1056/NEJMoa1917239
WEBSep 20, 2020 · Sotorasib is a small molecule that selectively and irreversibly targets KRAS G12C. Methods. We conducted a phase 1 trial of sotorasib in patients with advanced solid tumors harboring the KRAS...
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FDA Approves First Targeted Therapy for Lung Cancer Mutation …
https://www.fda.gov/news-events/press-announcements/fda-approves-first-targeted-therapy-lung-cancer-mutation-previously-considered-resistant-drug
WEBMay 28, 2021. Today, the U.S. Food and Drug Administration approved Lumakras (sotorasib) as the first treatment for adult patients with non-small cell lung cancer whose tumors have a specific...
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FDA Approves LUMAKRAS™ (Sotorasib), The First And Only ... - Amgen
https://www.amgen.com/newsroom/press-releases/2021/05/fda-approves-lumakras-sotorasib-the-first-and-only-targeted-treatment-for-patients-with-kras-g12cmutated-locally-advanced-or-metastatic-nonsmall-cell-lung-cancer
WEBTHOUSAND OAKS, Calif., May 28, 2021 /PRNewswire/ -- Amgen (NASDAQ: AMGN) today announced that the U.S. Food and Drug Administration (FDA) has approved LUMAKRAS ™ (sotorasib) for the treatment of adult patients with KRAS G12C-mutated locally advanced or metastatic non-small cell lung cancer (NSCLC), as determined by an FDA-approved …
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FDA Approval Summary: Sotorasib for KRAS G12C Mutated …
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9012672/
WEBApr 4, 2022 · On May 28, 2021, the U.S. Food and Drug Administration (FDA) granted accelerated approval to sotorasib (Lumakras™, Amgen) for the treatment of adults with advanced non-small cell lung cancer (NSCLC) with a Kirsten rat sarcoma proto-oncogene (KRAS) G12C mutation who have received at least one prior systemic therapy.
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