• Janssen files EGFR-targeting antibody amivantamab with EMA pharmatimes
    January 05, 2021
    Janssen, the pharmaceutical division of Johnson & Johnson, has submitted a marketing authorisation application to the European Medicines Agency (EMA) for approval of its epidermal growth factor receptor (EGFR)-targeting bispecific antibody amivantamab.
  • Janssen Submits BLA for Metastatic Lung Cancer Treatment americanpharmaceuticalreview
    December 24, 2020
    The Janssen Pharmaceutical Companies of Johnson & Johnson announced the submission of a Biologics License Application (BLA) to the U.S. Food and Drug Administration (FDA) seeking approval of amivantamab for the treatment of patients with metastatic ...
  • Janssen eyes US approval for EGFR-targeting NSCLC therapy pharmatimes
    December 08, 2020
    Janssen has submitted an application the US Food and Drug Administration (FDA) seeking approval for its non-small cell lung cancer (NSCLC) with epidermal growth factor receptor (EGFR) exon 20 mutations therapy amivantamab.
  • Janssen Announces Phase 1 Results for Amivantamab for Advanced NSCLC americanpharmaceuticalreview
    May 21, 2020
    The Janssen Pharmaceutical Companies of Johnson & Johnson announced results from the Phase 1 CHRYSALIS study.
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