La Commission européenne autorise TECVAYLI®▼ (teclistamab) de Johnson & Johnson associé au daratumumab dans le traitement du myélome multiple récidivant ou réfractaire, offrant ainsi une nouvelle référence thérapeutique potentielle
BEERSE, BELGIQUE, 24 août 2026 (GLOBE NEWSWIRE) -- Johnson & Johnson a annoncé aujourd’hui que la Commission européenne (CE) a approuvé une extension d’indication pour TECVAYLI ® (teclistamab) en association avec le daratumumab pour le traitement des adultes atteints d’un myélome multiple récidivant ou réfractaire (MMR…
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