Johnson & Johnson Announced Saturday, Earlier Use Of CARVYKTI Demonstrated Lasting Treatment-Free Remissions At 2.5 Years In Patients With Relapsed Or Refractory Multiple Myeloma

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Johnson & Johnson

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Johnson & Johnson (NYSE:JNJ) announced today updated results from the Phase 3 CARTITUDE-4 study supporting durable treatment-free remissions as early as second line treatment with CARVYKTI® (ciltacabtagene autoleucel; cilta-cel). In 80 percent of as-treated patients with relapsed or refractory multiple myeloma (RRMM) and standard-risk cytogenetics who were treated with CARVYKTI® as early as first relapse, the disease did not progress and no further treatment was required at 2.5 years (30 months).1 These results add to the body of clinical and real-world experience established across more than 9,000 patients treated with CARVYKTI® globally.

Follow-up data from CARTITUDE-4 show at least 80 percent of as-treated standard-risk patients remained progression and treatment-free following a single infusion as early as second line

Data suggest stronger immune fitness in earlier lines may be associated with longer progression free survival

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