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Articles published by Legend Biotech Corporation
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Legend Biotech to Highlight Leadership in CAR-T Cell Therapy for Patients with Multiple Myeloma at ASCO and EHA
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CARVYKTI® (ciltacabtagene autoleucel) Approved by the European Commission for Second-line Treatment of Patients with Relapsed and Refractory Multiple Myeloma
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Legend Biotech to Host Investor Conference Call on First Quarter 2024 Results
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Legend Biotech’s CARVYKTI® (ciltacabtagene autoleucel) Becomes the First and Only BCMA-Targeted CAR-T Cell Therapy Approved by the FDA for Second-Line Treatment of Multiple Myeloma
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Legend Biotech Announces Publication of Inaugural Environmental, Social and Governance (ESG) Report
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CARVYKTI® (ciltacabtagene autoleucel) Receives Recommendation from the U.S. FDA Oncologic Drugs Advisory Committee for Earlier Treatment of Patients with Relapsed/Refractory Multiple Myeloma
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Legend Biotech Reports Fourth Quarter and Full Year 2023 Results and Recent Highlights
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Legend Biotech to Host Investor Conference Call on Fourth Quarter and Full Year 2023 Results
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Legend Biotech to Participate in the 42nd Annual J.P. Morgan Healthcare Conference
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Patient-Reported Outcomes from the CARTITUDE-4 Study Showed Clinically Meaningful Improvements in Health-Related Quality of Life and Reductions in Multiple Myeloma Symptoms Following Treatment with CARVYKTI® (ciltacabtagene autoleucel)
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Legend Biotech Reports Third Quarter 2023 Results and Recent Highlights
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Legend Biotech Announces Exclusive, Global License Agreement for Certain CAR-T Therapies Targeting DLL3
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Legend Biotech to Host Investor Conference Call on Third-Quarter Results
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Legend Biotech to Showcase Leadership in Multiple Myeloma Treatment at the ASH 2023 Annual Meeting
November 02, 2023
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Legend Biotech Reports Second Quarter 2023 Results and Recent Highlights
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Legend Biotech to Host Investor Conference Call on Second-Quarter Results
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Legend Biotech Announces Submission of Supplemental Application to the U.S. FDA for Expanded Use of CARVYKTI® (ciltacabtagene autoleucel)
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Legend Biotech Announces Submission to the European Medicines Agency for Expanded Use of CARVYKTI® (ciltacabtagene autoleucel)
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Legend Biotech Reports First Quarter 2023 Results and Recent Highlights
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Legend Biotech to Demonstrate Progress in Advancing Potential Treatment Options for Patients with Multiple Myeloma at ASCO and EHA Annual Meetings
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Legend Biotech Announces Participation in Upcoming Investor Conference
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Legend Biotech Shares Updated Data from Comprehensive Cilta-Cel Clinical Development Program at ASH 2022
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CARVYKTI™ (ciltacabtagene autoleucel) Receives Approval from Japan’s Ministry of Health, Labour and Welfare (MHLW) for the Treatment of Patients with Relapsed or Refractory Multiple Myeloma
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Legend Biotech Announces Preliminary Results for the Six-Months Ended June 30, 2022
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