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Pan-KRAS inhibitor

A single inhibitor for all KRAS mutations

The recent design of mutation-selective KRAS inhibitors has led to US Food and Drug Administration approval of two inhibitors of KRAS(G12C), sotorasib and adagrasib. A study published in Nature reports the development of a first-in-class pan-KRAS-selective inhibitor. Here we comment on the current status of KRAS-targeting approaches.

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Fig. 1: Classes of KRAS inhibitors.

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Correspondence to Ryan B. Corcoran.

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Competing interests

R.B.C. has received consulting or speaking fees from Abbvie, Amgen, Array Biopharma/Pfizer, Asana Biosciences, Astex Pharmaceuticals, Astellas, Avidity Biosciences, BMS, C4 Therapeutics, Chugai, Cogent Biosciences, Daiichi-Sankyo Elicio, Erasca, Fog Pharma, Genentech, Guardant Health, Ipsen, Kinnate Biopharma, LOXO, Merrimack, Mirati Therapeutics, Natera, Navire, Nested Therapeutics, N-of-one/Qiagen, Novartis, nRichDx, Remix Therapeutics, Revolution Medicines, Roche, Syndax, Tango Therapeutics, Taiho and Theonys; holds equity in Avidity Biosciences, C4 Therapeutics, Cogent Biosciences, Erasca, Kinnate Biopharma, Interline Therapeutics, Nested Therapeutics, nRichDx, Remix Therapeutics, Revolution Medicines and Theonys; is a co-founder, equity holder and board member of Alterome Therapeutics and Sidewinder Therapeutics; and has received research funding from Asana, AstraZeneca, Invitae, Lilly, Novartis and Pfizer.

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Corcoran, R.B. A single inhibitor for all KRAS mutations. Nat Cancer 4, 1060–1062 (2023). https://doi.org/10.1038/s43018-023-00615-x

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