FDA Approves Rybrevant (amivantamab-vmjw) Plus Lazcluze (lazertinib) for Patients with EGFR-Mutated Advanced Lung cancer
FDA approves Rybrevant (amivantamab-vmjw) plus Lazcluze (lazertinib) for first-line treatment of EGFR-mutated advanced NSCLC, marking a significant development for patients with unmet needs.
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Highlighted Terms
NCT05908734TagrissoLazcluze (lazertinib)NCT02609776LazcluzeJohnson & JohnsonNCT04988295non-small cell lung cancer (NSCLC)NCT04606381NCT05498428NCT05488314Rybrevant (amivantamab-vmjw)EGFR-mutant NSCLCNCT04538664NCT05388669NCT04487080National Comprehensive Cancer Network (NCCN)non-small cell lung cancer (NSCLC)Food and Drug Administration (FDA)U.S. Food and Drug Administration (FDA)RybrevantNCT05663866NCT04077463
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Lazcluze, Rybrevant Approval a 'Big Deal' for EGFR-Mutant NSCLC - Cure Today
Lazcluze plus Rybrevant approved for EGFR-mutant NSCLC, showing 23.7 months median progression-free survival vs. 16.6 months for Tagrisso. Combination offers improved outcomes but with more side effects and requires IV administration. Future research aims to identify optimal patient subsets and develop better drugs.
FDA Approves Rybrevant (amivantamab-vmjw) Plus Lazcluze (lazertinib) for Patients with EGFR-Mutated Advanced Lung cancer
FDA approves Rybrevant (amivantamab-vmjw) plus Lazcluze (lazertinib) for first-line treatment of EGFR-mutated advanced NSCLC, marking a significant development for patients with unmet needs.