BRIEF-Johnson & Johnson Announces Approval Of Subcutaneous Rybrevant®▼ By European Commission

+0.32%

Johnson & Johnson

JNJ

240.40

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Feb 23 (Reuters) - Johnson & Johnson JNJ.N:

SUBCUTANEOUS RYBREVANT®▼ (AMIVANTAMAB) APPROVED BY EUROPEAN COMMISSION FOR EVERY-THREE-WEEK AND EVERY-FOUR-WEEK DOSING FOR PATIENTS WITH ADVANCED EGFR-MUTATED NON-SMALL CELL LUNG CANCER
J&J: SC AMIVANTAMAB IS NOW AUTHORISED FOR USE ACROSS ALL PREVIOUSLY APPROVED INTRAVENOUS (IV) AMIVANTAMAB INDICATIONS-WEBSITE

Further company coverage: JNJ.N

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