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KITE'S CAR T-CELL THERAPY TECARTUS® (BREXUCABTAGENE AUTOLEUCEL) GRANTED EUROPEAN MARKETING AUTHORISATION FOR THE TREATMENT OF RELAPSED OR REFRACTORY ACUTE LYMPHOBLASTIC LEUKAEMIA (r/r ALL)

KITE’S  CAR  T-CELL  THERAPY  TECARTUS®  (BREXUCABTAGENE  AUTOLEUCEL)  GRANTED EUROPEAN MARKETING AUTHORISATION FOR THE TREATMENT OF  RELAPSED  OR  REFRACTORY  ACUTE  LYMPHOBLASTIC  LEUKAEMIA  (r/r ALL)  Approval Marks Kite’. ....

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Gilead Sciences, Inc.: Kite's CAR T-cell Therapy Tecartus Granted European Marketing Authorization for the Treatment of Relapsed or Refractory Acute Lymphoblastic Leukemia (r/r ALL)

Approval Marks Kite's Fourth Indication in Europe for its Two Cell Therapies and First in Leukemia Overall Complete Remission of 71% and a Median Overall Survival of More Than Two Years ....

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U.S. FDA Approves Kite's Tecartus® as the First and Only Car T for Adults With Relapsed or Refractory B-cell Acute Lymphoblastic Leukemia

65% of Patients Achieved Overall Complete Remission with Tecartus High Unmet Need: Fifty Percent of Adult Patients Will Relapse on Currently Available Treatments Approval Marks Kite’s Fourth Indication for its Cell Therapies and First in Leukemia Kite, a Gilead Company today announced the U.S. Food and Drug Administration has granted approval for Tecartus ® for the treatment of adult patients with . ....

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Atopische Dermatitis: Vierte Indikation für Upadacitinib erwartet

Atopische Dermatitis: Vierte Indikation für Upadacitinib erwartet
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