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Johnson & Johnson : CARVYKTI®▼ (ciltacabtagene autoleucel; cilta-cel) is the first BCMA-targeted treatment approved by the European Commission for patients with relapsed and refractory multiple myeloma who have received at least one prior line of therapy

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FDA Approves Cilta-Cel for Treatment of Relapsed, Refractory Multiple Myeloma

The indication is for adult patients with multiple myeloma who are refractory to lenalidomide and have previously received at least 1 line of therapy. ....

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Legend Biotech Reports Second Quarter 2023 Results and Recent Highlights

Legend Biotech Reports Second Quarter 2023 Results and Recent Highlights
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Legend Biotech Announces Submission of Supplemental Application to the U.S. FDA for Expanded Use of CARVYKTI® (ciltacabtagene autoleucel)

The application is supported by the Phase 3 CARTITUDE-4 study, which showed significant improvement in primary endpoint of progression-free survival compared to standard regimens

CARTITUDE-4 is the. | June 6, 2023 ....

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Legend Biotech (LEGN) Announces Submission of Supplemental Application to the U.S. FDA for Expanded Use of CARVYKTI

Legend Biotech (LEGN) Announces Submission of Supplemental Application to the U.S. FDA for Expanded Use of CARVYKTI
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