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Legend Biotech (LEGN) Announces FDA Grants BCMA CAR-T Cilta-cel Priority Review for the Treatment for Relapsed/Refractory Multiple Myeloma
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U.S. Food and Drug Administration Grants BCMA CAR-T Cilta-cel Priority Review for the Treatment for Relapsed/Refractory Multiple Myeloma
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Legend Biotech Reports New and Updated Data from BCMA CAR-T Program at 2021 ASCO and EHA Meetings
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Legend Biotech (LEGN) Announces Submission of European MAA for BCMA CAR-T Therapy Ciltacabtagene Autoleucel for Treatment of R/R Multiple Myeloma
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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 Multipl
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Janssen Submits Marketing Authorisation Application to the European Medicines Agency Seeking Approval of BCMA CAR-T Therapy Ciltacabtagene Autoleucel (cilta-cel) for the Treatment of Relapsed and/or R
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Legend Biotech Announces Fourth Quarter and Full-Year 2020 Earnings Conference Call
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Legend Biotech Announces Preliminary Results for the Year Ended December 31, 2020
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Janssen Announces CAR-T Therapy Ciltacabtagene Autoleucel (Cilta-cel) Accepted for Accelerated Assessment in Europe for the Treatment of Patients with Heavily Pretreated Multiple Myeloma
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Legend Biotech (LEGN) Announces BCMA CAR-T Therapy Cilta-cel Accepted for Accelerated Assessment in Europe for the Treatment of R/R Multiple Myeloma
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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
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Legend Biotech (LEGN) Announces Initiation of Rolling Submission of BLA to U.S. FDA Seeking Approval of BCMA CAR-T Therapy Cilta-cel for Treatment of R/R Multiple Myeloma
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Legend Biotech Announces Initiation of Rolling Submission of Biologics License Application to U.S. FDA Seeking Approval of BCMA CAR-T Therapy Cilta-cel for the Treatment of Relapsed and/or Refractory
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Janssen Initiates Rolling Submission of a Biologics License Application to U.S. FDA for BCMA CAR-T Therapy Ciltacabtagene Autoleucel (cilta-cel) for the Treatment of Relapsed and/or Refractory Multipl
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Legend Biotech to Participate in the 39th Annual J.P. Morgan Healthcare Conference
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Legend Biotech Added to the NASDAQ Biotechnology Index
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Annual Changes to the Nasdaq Biotechnology Index
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Early, Deep, Durable Responses of Ciltacabtagene Autoleucel (cilta-cel) Observed in Phase 1b/2 CARTITUDE-1 Study Show Potential of BCMA CAR-T in Treatment of Heavily Pretreated Patients with Multiple
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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
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Early, Deep, Durable Responses of Ciltacabtagene Autoleucel (cilta-cel) Observed in Phase 1b/2 CARTITUDE-1 Study Show Potential of BCMA CAR-T in Treatment of Heavily Pretreated Patients with Multiple
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Legend Biotech Announces Appointment of Dr. Patrick Casey to the Board of Directors
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Legend Biotech to Host Virtual Investor KOL Event Reviewing Latest CARTITUDE-1 Data from the 62nd American Society of Hematology (ASH) Annual Meeting
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Legend Biotech (LEGN) Announces Ye Wang Appointed Chairwoman of the Board, Ying Huang Named CEO
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Legend Biotech Announces Leadership Transition
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Legend Biotech Announces Leadership Transition
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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 M
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Top FDA Official, Amy Abernethy, to Keynote Veeva R&D and Quality Summit Online
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BeiGene Appoints Corsee Sanders, Ph.D. to its Board of Directors
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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 Inv

