21 November 2024 - Authorisation is based on results from the Phase 3 CARTITUDE-4 (MMY3002) study, which showed treatment with Carvykti reduced the risk of disease progression or death by 74 per cent compared to standard of care.
Johnson & Johnson announced today that Health Canada has issued a Notice of Compliance for Carvykti (ciltacabtagene autoleucel) for the treatment of adult patients with multiple myeloma who have received one to three prior lines of therapy, including a proteasome inhibitor and an immunomodulatory agent, and who are refractory to lenalidomide.