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0 0.00151777970511709 0.00325238508239372 0.00628794449262791 0.0110581092801387 0.0130095403295749 0.0169124024284476 0.019731136166522
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CARVYKTI® (ciltacabtagene autoleucel) Approved by the European Commission for Second-line Treatment of Patients with Relapsed and Refractory Multiple Myeloma

Legend Biotech Corporation - American Depositary Shares (LEGN) 
Company Research Source: Business Wire
New indication for this one-time infusion may provide patients with a treatment-free respite as early as first relapse SOMERSET, N.J.--(BUSINESS WIRE)--Legend Biotech Corporation (NASDAQ: LEGN) (Legend Biotech), a global leader in cell therapy, announced today that the European Commission (EC) has granted approval of CARVYKTI® (ciltacabtagene autoleucel, cilta-cel) for the treatment of adult patients with relapsed and refractory multiple myeloma who have received at least one prior line of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent (IMiD), have demonstrated disease progression on the last therapy and are refractory to lenalidomide.“The European Commission’s approval of CARVYKTI has the potential to transform the treatment paradigm for patients battling multiple myeloma by bringing our novel therapy to them earlier in the course of this incurable disease,” said Ying Huang, Ph.D., Chief Executive Officer of Legend Biotech. “This approval is a testamen Show less Read more
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