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    The FDA granted accelerated approval to teclistamab-cqyv for treatment of certain patients of myeloma. The indication applies to use of teclistamab-cqyv (Tecvayli, Janssen Biotech) for adults with relapsed or refractory multiple myeloma who received at least four prior lines of therapy, including a proteasome inhibitor, an immunomodulatory agent and an anti-CD38 monoclonal antibody.

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    • FDA APPROVED: Tecvayli for advanced multiple myeloma. https://t.co/NzJmV44AzD #Tecvayli #myeloma #HemOnc #OncAlert #MedEd @JanssenUS @US_FDA