Remove tag teclistamab
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J&J gets first approval for multiple myeloma bispecific Tecvayli

pharmaphorum

Tecvayli (teclistamab) has been approved by the European Commission for adults with the blood cancer whose disease has progressed have after at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 antibody, said J&J. and 18,3 months, respectively.

FDA 96
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CHMP backs J&Jā€™s myeloma bispecific Tecvayli, ahead of US decision

pharmaphorum

Tecvayli (teclistamab) is an off-the-shelf bispecific antibody targeting both BCMA and CD3 which is also under review at the FDA and if approved will slot into J&J’s myeloma therapy portfolio alongside Darzalex (daratumumab) ā€“ an antibody directed at CD38 ā€“ and BCMA-targeted CAR-T therapy Carvykti (ciltacabtagene autoleucel). .”