
Johnson & Johnson (NYSE: JNJ) has announced that the European Commission (EC) has approved an indication extension for Tecvayli (teclistamab) in combination with daratumumab for adults with relapsed or refractory multiple myeloma (RRMM) who have received at least one prior therapy, introducing the option as early as second line.
The approval is supported by the Phase III MajesTEC-3 trial, which compared subcutaneous teclistamab plus daratumumab against investigator's choice of daratumumab, dexamethasone and either pomalidomide or bortezomib in patients with one to three prior lines of therapy.
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