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J&J gets first approval for multiple myeloma bispecific Tecvayli

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Johnson & Johnson has its first worldwide regulatory approval ā€“ in the EU ā€“ for Tecvayli, one of two much-anticipated bispecific antibodies the drugmaker has developed for patients with multiple myeloma. Tecvayli previously scored a priority medicines (PRiME) designation from the EMA and a breakthrough-therapy tag from the FDA.

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

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The EMA’s human medicines committee has recommended approval of Johnson & Johnson’s Tecvayli as a fourth-line therapy for multiple myeloma , joining a growing group of BCMA-targeted therapies for the blood cancer. The post CHMP backs J&J’s myeloma bispecific Tecvayli, ahead of US decision appeared first on.