J&J presents new RYBREVANT lung cancer data at WCLC
Johnson & Johnson shares final overall survival and safety findings for its EGFR-mutated NSCLC therapies.
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Global healthcare company developing medicines and medical technologies
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In short: J&J reported strong Q2 2026 growth, secured FDA approval for its OTTAVA surgical robot, and proposed a $5.5 billion talc settlement.
Johnson & Johnson shares final overall survival and safety findings for its EGFR-mutated NSCLC therapies.
IMAAVY is the first treatment for this rare disease, showing durable hemoglobin responses and fatigue improvement in clinical trials.
The FDA-cleared update enhances AI-powered planning, navigation accuracy, and imaging compatibility for the robotically-assisted bronchoscopy platform.
Taubert led Innovative Medicine to over $60 billion in annual revenue during her 21-year tenure. Cavanaugh succeeds her and joins the Executive Committee on September 1, 2026.
Johnson & Johnson (J&J) has announced that the National Institute for Health and Care Excellence (NICE) has published Final ...
Johnson & Johnson's COPERNICUS Phase 2b results suggest less-frequent dosing may improve EGFR NSCLC care with low side effects.
Johnson & Johnson announced new results from the Phase 2b COPERNICUS study evaluating how subcutaneous RYBREVANT FASPRO (amivantamab and hyaluronidase-lpuj) plus LAZCLUZE (lazertinib), with less...
Sept 15 (Reuters) - Contineum Therapeutics said on Monday an experimental depression drug it developed with Johnson & Johnson failed to meet the main goal...
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