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Year

Apr 22, 2024

CARVYKTI® (ciltacabtagene autoleucel) Approved by the European Commission for Second-line Treatment of Patients with Relapsed and Refractory Multiple Myeloma

Apr 11, 2024

Legend Biotech to Host Investor Conference Call on First Quarter 2024 Results

Apr 05, 2024

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

Mar 19, 2024

Legend Biotech Announces Publication of Inaugural Environmental, Social and Governance (ESG) Report

Mar 15, 2024

CARVYKTI® (ciltacabtagene autoleucel) Receives Recommendation from the U.S. FDA Oncologic Drugs Advisory Committee for Earlier Treatment of Patients with Relapsed/Refractory Multiple Myeloma

Mar 11, 2024

Legend Biotech Reports Fourth Quarter and Full Year 2023 Results and Recent Highlights

Feb 23, 2024

Legend Biotech Announces Positive CHMP Opinion for CARVYKTI® (ciltacabtagene autoleucel) for the Treatment of Patients with Relapsed and Lenalidomide Refractory Multiple Myeloma in Earlier Lines of Therapy

Feb 13, 2024

Legend Biotech to Host Investor Conference Call on Fourth Quarter and Full Year 2023 Results

Jan 03, 2024

Legend Biotech Announces Closing of License Transaction for Certain CAR-T Therapies Targeting DLL3

Jan 02, 2024

Legend Biotech to Participate in the 42nd Annual J.P. Morgan Healthcare Conference

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