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European Commission Approves Johnson & Johnson TECVAYLI Combo for Multiple Myeloma

Johnson & Johnson logoJohnson & Johnson
Sig3.02Sen+3.73Env0.00Soc+2.94Gov-0.05

The European Commission approved Johnson & Johnson’s TECVAYLI (teclistamab) plus daratumumab for adults with relapsed or refractory multiple myeloma, based on Phase 3 results showing material improvements in patient outcomes versus existing standards of care. The approval expands J&J’s oncology immunotherapy options in Europe for hematology.

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