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Janssen Marks First Approval Worldwide for TECVAYLI?(teclistamab) with EC Authorisation of First-in-Class Bispecific Antibody for the Treatment of Patients with Multiple Myeloma

Teclistamab, an off-the-shelf (ready to use) subcutaneously administered therapy, induced deep and rapid responses in triple-class exposed patients with relapsed and refractory multiple myeloma1 The
United States Jenni Mildon Williamn Hait Maria Victoria Mateos Peter Lebowitz Edmond Chan

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Janssen Receives Positive CHMP Opinion for Novel Bispecific Antibody TECVAYLI (teclistamab) for the Treatment of Patients with Relapsed and Refractory Multiple Myeloma (RRMM)

Teclistamab is the first T-cell redirecting bispecific antibody to receive a positive CHMP opinion for adults with RRMM and highlights Janssen's commitment to innovation in multiple myeloma The
United States Jenni Mildon Edmond Chan Mbch Peter Lebowitz None Of The Janssen Pharmaceutical Companies American Society Of Clinical Oncology

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