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Research Article

Validation of an LC–MS/MS method for the determination of sotorasib, a KRASG12C inhibitor, in human plasma

    Philip Wong

    Amgen Research, Translational Safety & Bioanalytical Sciences, Thousand Oaks, CA 91320, USA

    ,
    Anna Akrami

    Amgen Research, Translational Safety & Bioanalytical Sciences, Thousand Oaks, CA 91320, USA

    ,
    Brett Houk

    Amgen Research, Clinical Pharmacology Modeling & Simulation, Thousand Oaks, CA 91320, USA

    ,
    Irene Vuu

    Amgen Research, Clinical Pharmacology Modeling & Simulation, Thousand Oaks, CA 91320, USA

    &
    Christopher A James

    *Author for correspondence: Tel.: +1 805 447 1771;

    E-mail Address: cajames@amgen.com

    Amgen Research, Translational Safety & Bioanalytical Sciences, Thousand Oaks, CA 91320, USA

    Published Online:https://doi.org/10.4155/bio-2022-0173

    Background: Sotorasib (AMG 510) is a first-in-class KRASG12C inhibitor that received accelerated US FDA approval in 2021 for the treatment of patients with KRASG12C-mutated locally advanced or metastatic non-small-cell lung cancer. Method: An LC–MS/MS method was developed and validated for the determination of sotorasib in human plasma to support clinical development studies. Samples were prepared using protein precipitation and analyzed by LC–MS/MS using gradient elution with a calibration standard curve range of 10.0–10,000 ng/ml. Stable isotope labeled [13C, D3]-sotorasib was used as an internal standard. Results & conclusion: The method fully met FDA guidelines for all validation parameters, including precision, accuracy, selectivity, matrix effect, recovery and stability and has been extensively used to support multiple clinical studies.

    Papers of special note have been highlighted as: • of interest; •• of considerable interest

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