Legend Biotech Announces Closing of License Transaction for Certain CAR-T Therapies Targeting DLL3
Jan 03, 2024
Legend Biotech Announces Closing of License Transaction for Certain CAR-T Therapies Targeting DLL3
Jan 03, 2024
Legend Biotech to Participate in the 42nd Annual J.P. Morgan Healthcare Conference
Jan 02, 2024
Legend Biotech Announces Exclusive, Global License Agreement for Certain CAR-T Therapies Targeting DLL3
Nov 13, 2023
Legend Biotech to Showcase Leadership in Multiple Myeloma Treatment at the ASH 2023 Annual Meeting
Nov 02, 2023
Legend Biotech Announces Submission of Supplemental Application to the U.S. FDA for Expanded Use of CARVYKTI® (ciltacabtagene autoleucel)
Jun 06, 2023
Ciltacabtagene Autoleucel (cilta-cel) Reduced Risk of Disease Progression or Death by 74% vs Standard Regimens for Adult Patients with Relapsed and Refractory Multiple Myeloma in CARTITUDE-4 Study
Jun 05, 2023
Legend Biotech Announces Submission to the European Medicines Agency for Expanded Use of CARVYKTI® (ciltacabtagene autoleucel)
May 25, 2023
Legend Biotech to Demonstrate Progress in Advancing Potential Treatment Options for Patients with Multiple Myeloma at ASCO and EHA Annual Meetings
May 16, 2023
Legend Biotech Corporation Announces Pricing of Registered Direct Offering of $350 million of American Depositary Shares
May 08, 2023
Legend Biotech Announces Phase 3 CARTITUDE-4 Study of CARVYKTI®(ciltacabtagene autoleucel) Has Met Its Primary Endpoint in the Treatment of Patients with Relapsed and Refractory Multiple Myeloma
Jan 27, 2023
Legend Biotech Announces Notification of Delinquency from The Nasdaq Stock Market LLC
Jan 10, 2023
Legend Biotech to Participate in the 41st Annual JP Morgan Healthcare Conference
Jan 04, 2023
Legend Biotech Announces Acceptance of Its New Drug Application for Ciltacabtagene Autoleucel (Cilta-Cel) in China
Jan 02, 2023
Legend Biotech Announces FDA Clearance of IND Application for LB2102 in Extensive Stage Small Cell Lung Cancer
Nov 21, 2022
Legend Biotech Shares Updated Data from Comprehensive Cilta-Cel Clinical Development Program at ASH 2022
Nov 03, 2022
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
Sep 27, 2022
Legend Biotech Announces Participation in Upcoming Investor Conferences in August
Aug 19, 2022
Legend Biotech Announces Preliminary Results for the Six-Months Ended June 30, 2022
Aug 05, 2022
Legend Biotech Appoints Three New Directors and Elects New Chairman of the Board
Aug 04, 2022
Legend Biotech Corporation Announces Proposed Public Offering (July 25, 2022)
Jul 25, 2022
Longer-Term Data from CARTITUDE Program Continue to Show Deep and Durable Responses with Ciltacabtagene Autoleucel Across Lines of Therapy in Patients with Multiple Myeloma
Jun 04, 2022
Legend Biotech Announces U.S. FDA Clearance of IND Application for Solid Tumor CAR-T, LB1908 for Relapsed or Refractory Gastric, Esophageal and Pancreatic Cancers
Jun 03, 2022
Legend Biotech Reports First Quarter 2022 Financial Results and Recent Highlights
Jun 01, 2022
Legend Biotech to Host Investors at the 2022 American Society of Clinical Oncology (ASCO) Annual Meeting
May 31, 2022
CARVYKTI® (ciltacabtagene autoleucel) Granted Conditional Approval by the European Commission for the Treatment of Patients with Relapsed and Refractory Multiple Myeloma
May 26, 2022
Legend Biotech to Highlight Continued Progress in the Treatment of Multiple Myeloma with Updated Data from BCMA CAR-T Studies at 2022 ASCO and EHA
May 18, 2022
Legend Biotech Announces Participation in Upcoming Investor Conferences in May
May 06, 2022
Legend Biotech Achieves Milestone Under Collaboration Agreement with Janssen Biotech, Inc. for BCMA CAR-T
Apr 21, 2022
Legend Biotech Announces Appointment of Global Head of Research and Early Development
Apr 01, 2022
CARVYKTI® (ciltacabtagene autoleucel) Receives Positive CHMP Opinion for the Treatment of Patients with Relapsed and Refractory Multiple Myeloma
Mar 25, 2022
Legend Biotech Reports Fourth Quarter and Full Year 2021 Financial Results and Recent Highlights
Mar 18, 2022
CARVYKTI™ (ciltacabtagene autoleucel), BCMA-Directed CAR-T Therapy, Receives U.S. FDA Approval for the Treatment of Adult Patients with Relapsed or Refractory Multiple Myeloma
Feb 28, 2022
Legend Biotech Announces Preliminary Results for the Year Ended December 31, 2021
Feb 18, 2022
Legend Biotech Announces FDA Clinical Hold of its Phase 1 Clinical Trial for LB1901
Feb 15, 2022
Legend Biotech Achieves Milestone Payments in BCMA CAR-T Collaboration with Janssen
Feb 11, 2022
Legend Biotech to Participate in the 40th Annual J.P. Morgan Healthcare Conference
Jan 04, 2022
Legend Biotech Announces Appointment of Dr. Ying Huang to the Board of Directors
Dec 30, 2021
Legend Biotech Corporation Announces Proposed Public Offering (December 14, 2021)
Dec 14, 2021
Two-Year Analysis of CARTITUDE-1 Shows Early, Durable and Deepening Responses of Ciltacabtagene Autoleucel (cilta-cel) in Heavily Pretreated Patients with Multiple Myeloma
Dec 13, 2021
Legend Biotech to Host Hybrid KOL Event Detailing CARTITUDE Data from the 63rd American Society of Hematology (ASH) Annual Meeting
Dec 07, 2021
Legend Biotech Announces Submission of New Drug Application to Japanese Regulatory Authority for BCMA CAR-T Therapy Cilta-cel for the Treatment of Relapsed or Refractory Multiple Myeloma
Dec 06, 2021
Legend Biotech Reports Third Quarter 2021 Financial Results and Recent Highlights
Nov 16, 2021
Legend Biotech Showcases Updated and New Data from Comprehensive BCMA CAR-T, Cilta-Cel, Program and First Preclinical Results for Tri-specific CAR-T at 2021 ASH
Nov 04, 2021
Legend Biotech Begins Phase 1 Clinical Trial in the US to Evaluate Investigational Anti-CD4 CAR-T Therapy for Relapsed or Refractory T-Cell Lymphoma
Sep 13, 2021
Legend Biotech to Participate in the 19th Annual Morgan Stanley Global Healthcare Conference
Aug 30, 2021
Legend Biotech Reports Second Quarter 2021 Financial Results and Recent Highlights
Aug 23, 2021
Legend Biotech Announces New and Updated Data for Investigational BCMA CAR-T Ciltacabtagene Autoleucel (cilta-cel) for the Treatment of Relapsed or Refractory Multiple Myeloma at 2021 ASCO and EHA Meetings
Jun 01, 2021
U.S. Food and Drug Administration Grants BCMA CAR-T Cilta-cel Priority Review for the Treatment for Relapsed/Refractory Multiple Myeloma
May 26, 2021
Legend Biotech Reports First Quarter 2021 Financial Results and Recent Highlights
May 18, 2021
Legend Biotech Reports New and Updated Data from BCMA CAR-T Program at 2021 ASCO and EHA Meetings
May 12, 2021
Legend Biotech Announces Submission of European Marketing Authorisation Application for BCMA CAR-T Therapy Ciltacabtagene Autoleucel (cilta-cel) for the Treatment of Relapsed and/or Refractory Multiple Myeloma
Apr 30, 2021
Legend Biotech Reports Fourth Quarter and Full Year 2020 Financial Results and Business Update
Mar 18, 2021
Legend Biotech Announces Fourth Quarter and Full-Year 2020 Earnings Conference Call
Mar 10, 2021
Legend Biotech Announces Preliminary Results for the Year Ended December 31, 2020
Feb 19, 2021
Legend Biotech Announces BCMA CAR-T Therapy Cilta-cel Accepted for Accelerated Assessment in Europe for the Treatment of Relapsed and/or Refractory Multiple Myeloma
Feb 01, 2021
Legend Biotech Announces Initiation of Rolling Submission of Biologics License Application to U.S. FDA SeekingApproval of BCMA CAR-T Therapy Cilta-cel for the Treatment of Relapsed and/or Refractory Multiple Myeloma
Dec 21, 2020
Legend Biotech to Participate in the 39th Annual J.P. Morgan Healthcare Conference
Dec 15, 2020
Legend Biotech Announces FDA Clearance of the IND for LB1901, an Investigational Autologous AntiCD4 CAR-T Therapy for Relapsed or Refractory T-Cell Lymphoma
Dec 14, 2020
Legend Biotech Announces Phase 1b/2 Study Data of Cilta-cel, an Investigational BCMA CAR-T, Showing Early, Deep, and Durable Responses in Heavily Pretreated Patients with Multiple Myeloma
Dec 05, 2020
Legend Biotech Announces Appointment of Dr. Patrick Casey to the Board of Directors
Dec 03, 2020
Legend Biotech to Host Virtual Investor KOL Event Reviewing Latest CARTITUDE-1 Data from the 62nd American Society of Hematology (ASH) Annual Meeting
Nov 24, 2020
Legend Biotech Announces New Appointment to the Board of Directors and Resignation of Dr. Fangliang Zhang
Nov 23, 2020
Legend Biotech Announces ASH 2020 Data Presentations for Ciltacabtagene Autoleucel (cilta-cel), an Investigational BCMA CAR-T Cell Therapy in Development for Patients with Relapsed and/or Refractory Multiple Myeloma (RRMM)
Nov 05, 2020
Legend Biotech Names Current Chief Financial Officer, Ying Huang, as Interim CEO
Sep 21, 2020
Legend Biotech to Participate in the 18th Annual Morgan Stanley Virtual Global Healthcare Conference
Sep 01, 2020
The China Center for Drug Evaluation, National Medical Products Administration Has Recommended Breakthrough Therapy Designation for ciltacabtagene autoleucel (cilta-cel, LCAR-B38M CAR-T Cells), an Investigational BCMA CAR-T Cell Therapy
Aug 05, 2020
Updated Results from Phase 1b/2 Study of BCMA CAR-T Therapy JNJ-4528 Shows Early, Deep and Durable Responses in Heavily Pretreated Patients with Relapsed or Refractory Multiple Myeloma
May 13, 2020
Legend Biotech and Noile-Immune Biotech Announce Collaborative Research and Licensing Agreement
May 04, 2020
Legend Biotech Raises $150.5 Million in Series A Preferred Financing To Advance its Oncology Pipeline and Platform
Apr 01, 2020
Legend Biotech Announces Milestone Payment Achieved from the LCAR-B38M CAR-T Collaboration with Janssen
Jan 28, 2020
Updated Data from LEGEND-2, a Phase 1/2 Open-label Study of BCMA-Directed CAR-T Cell Therapy LCAR-B38M Show Long-term Responses, Safety Profile, and Complete Response Rate in Treatment of Patients with Advanced Relapsed or Refractory Multiple Myelomama
Dec 09, 2019
Initial Data from Phase 1b/2 Study of BCMA-Directed CAR-T Cell Therapy JNJ-4528 Show Early and High Responses in Advanced Relapsed or Refractory Multiple Myeloma
Dec 07, 2019
U.S. Food and Drug Administration Grants Breakthrough Therapy Designation for
JNJ-68284528, an Investigational BCMA CAR-T Cell Therapy
Dec 06, 2019
Legend Biotech Announces Data Presentations at ASH 2019 for JNJ-68284528 (JNJ-4528)/LCAR-B38M, an Investigational B-Cell Maturation Antigen (BCMA) Chimeric Antigen Receptor (CAR)-T Cell Therapy being Studied in Patients with Relapsed and/or Refractory Multiple Myeloma (RRMM)
Nov 06, 2019
Legend Biotech Announces Milestones Achieved from the LCAR-B38M CAR-T Collaboration with Janssen
Aug 05, 2019
New Data from LEGEND-2 Study of LCAR-B38M BCMA CAR-T Therapy Show High Overall Response in Patients with Advanced Relapsed or Refractory Multiple Myeloma
Apr 15, 2019
European Medicines Agency Grants Janssen PRIME Designation for JNJ-68284528 (LCAR-B38M), an Investigational BCMA CAR-T Therapy Discovered by Legend Biotech
Apr 03, 2019
Legend Biotech Ireland, Ltd. celebrates the official opening of its European headquarters in Dublin, Ireland
Mar 05, 2019
Legend Biotech USA, Inc. joins The American Society for Blood and Marrow Transplantation (ASBMTTM) Corporate Council
Feb 01, 2019
ASH 2018: Updated Data from Phase 1/2 Open-Label Study of BCMA-Directed CAR-T Cell Therapy LCAR-B38M Show Tolerable Safety Profile, High Overall Response and MRD Negative Rate in Treatment of Patients with Advanced Relapsed or Refractory Multiple Myeloma
Dec 03, 2018
Legend Biotech Chairman Frank Zhang awarded 2018 Person of the Year from China Healthcare Summit
Nov 14, 2018
Legend Announces FDA clearance of IND application on CAR-T immuno-cell therapy for the Treatment of Multiple Myeloma
May 30, 2018
Nanjing Legend formally received the permission of a clinical trial granted by the CFDA with respect to LCAR-B38M CAR-T for autologous infusion
Mar 13, 2018
Legend Biotech Announces Closing of Global Strategic LCAR-B38M CAR-T Cell Immunotherapy Collaboration with Janssen
Dec 22, 2017
Legend Biotech Corporation Announces Confidential Submission of Draft Registration Statement for Proposed Initial Public Offering
Aug 26, 2022
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)
Dec 11, 2023
We focus on serious and intractable diseases to help patients around the world.
We are technology agnostic in targeting hematologic malignancies and solid tumors. We are exploring 4 different technologies to help treat disease.
Our leaders bring significant expertise from some of the world’s largest pharma companies.
We are an end-to-end cell therapy company. Our capabilities extend from discovery to commercialization.
We offer a variety of career choices that support the development of novel therapies.
Our pipeline is comprised of investigational agents and innovative technologies in personalized medicine. We are devoted to exploring the potential of cell therapies to treat diseases that are considered intractable and incurable, including hematological malignancies and solid tumors.