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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 Myeloma

Key Takeaway: 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 Myeloma

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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 Myeloma.
Last updated: Apr 19, 2021