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Topline Data Demonstrate Survival Improvement With Amivantamab-vmjw for NSCLC

The MARIPOSA study evaluated amivantamab-vmjw (Rybrevant; Janssen Pharmaceutical) in combination with lazertinib compared to osimertinib and compared to lazertinib monotherapy in the first-line treatment of EGFR-mutated non–small cell lung cancer.
United States Peter Lebowitz Alexander Spira Virginia Cancer Specialists Research Institute Oncology At Janssen Research Development Janssen Pharmaceutical Companies Of Johnson

First-Line Amivantamab Plus Lazertinib Meets PFS End Point in EGFR+ NSCLC

First-line treatment with the combination of amivantamab and lazertinib resulted in a statistically significant and clinically meaningful improvement in progression-free survival compared with osimertinib in patients with locally advanced or metastatic non–small cell lung cancer harboring EGFR mutations.
United States Alexander Spira Peter Lebowitz Virginia Cancer Specialists Research Institute Lung Cancer Dvanced Or Metastatic Non Small Cell Lung Cancer

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Amivantamab/Chemotherapy ± Lazertinib Improves PFS in Pretreated EGFR+ NSCLC

Amivantamab-vmjw plus carboplatin and pemetrexed, administered with or without lazertinib, significantly improved progression-free survival vs chemotherapy alone in patients with locally advanced or metastatic non–small cell lung cancer with EGFR exon 19 deletions or L858R substitutions after progression on or after osimertinib.
Peter Lebowitz Janssen Research Development Janssen Research Small Cell Lung Cancer Lung Cancer Janssen Research Amp Development

Johnson & Johnson : Janssen Submits Supplemental New Drug Application to the U.S. Food and Drug Administration Seeking Full Approval of BALVERSA® (erdafitinib) for the Treatment of Patients with Locally Advanced or Metastatic Urothelial Carcinoma and Selected Fibroblast Growth Factor Receptor Gene Alterations -Today at 09:18 am

News Release Media Contacts: Suzanne Frost Phone: +1 416-317-0304 Ania DiAntonio ...
Peter Lebowitz Ania Diantonio Drug Administration Astex Pharmaceuticals Administration Seeking Full Approval American Society Of Clinical Oncologyannual Meeting

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