强生(JNJ.US)宣布EGFR/c-MET双抗“埃万妥单抗”在国内获批一项新适应症

Core Viewpoint - Johnson & Johnson's Amivantamab has received approval for a new indication in China for the treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with specific EGFR mutations [1][2] Group 1: Drug Approval Details - Amivantamab is now approved in combination with Lenzatinib for first-line treatment of NSCLC patients with EGFR 19 exon deletions or L858R mutations [1] - This marks the third indication for Amivantamab in China, following its initial approval for EGFRex20ins mutation NSCLC in February 2025 and a subsequent approval for use with chemotherapy in April 2025 [2] Group 2: Global Approval History - Amivantamab was first granted accelerated approval in the United States in May 2021 [2] - To date, Amivantamab has received a total of four indications globally for the treatment of non-small cell lung cancer [2]