Rybrevant

Chemical Nameamivantamab-vmjw
Dosage FormInjection (intravenous; 350 mg/7 mL)
Drug ClassMonoclonal antibodies
SystemRespiratory
CompanyJanssen Biotech
Approval Year2021

Indication

  • For the treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 20 insertion mutations, as detected by an FDA-approved test, whose disease has progressed on or after platinum-based chemotherapy
Last updated on 4/11/2022

More on this drug: Clinical Trials

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Document TitleYearSource
Rybrevant (amivantamab-vmjw) Prescribing Information.2021Janssen Biotech, Inc., Horsham, PA
Document TitleYearSource
CHMP assessment report: Rybrevant. 2021EMA