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An inhibitor of mutant EGFRs
Aflutinib is an inhibitor of mutant EGFRs.1 It is selective for EGFRL858R, EGFRG719X, EGFRL858R, EGFRL861A, and EGFRT790M mutant EGFRs over wild-type EGFR. Aflutinib (10 and 30 mg/kg) reduces tumor growth in an EGFRL858R and EGFRT790M-expressing LU1868 non-small cell lung cancer (NSCLC) patient-derived xenograft (PDX) mouse model.
1.Shi, Y., Zhang, S., Hu, X., et al.Safety, clinical activity, and pharmacokinetics of alflutinib (AST2818) in patients with advanced NSCLC with EGFR T790M mutationJ. Thorac. Oncol.15(6)1015-1026(2020)
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