Allogene Therapeutics (ALLO) Granted IND Clearance from FDA for ALLO-605
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Allogene Therapeutics Receives IND Clearance from the U.S. Food and Drug Administration for ALLO-605, the First TurboCAR™ Candidate, for the Treatment of Patients with Relapsed/Refractory Multiple M
April 19, 2021 8:30 AM EDTTurboCAR Technology Allows a Programmable Cytokine Signaling to Potentially Control T Cell Exhaustion and Improve Function and Potency of AlloCAR TÂ CellsPhase 1 IGNITE Trial Expected to Begin in Mid-2021ALLO-605 is One of Allogenes Three Strategies to Target BCMA for the Treatment of Patients with Multiple Myeloma
SOUTH SAN FRANCISCO, Calif., April 19, 2021 (GLOBE NEWSWIRE) -- Allogene Therapeutics, Inc. (Nasdaq: ALLO), a clinical-stage biotechnology company pioneering the development of allogeneic CAR T (AlloCAR T) therapies for cancer today announced that the U.S. Food & Drug Administration (FDA) has cleared an... More
