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Monday, April 19, 2021

Allogene Gets FDA IND Clearance for Multiple Myeloma Med

 

  • TurboCAR Technology Allows a Programmable Cytokine Signaling to Potentially Control T Cell Exhaustion and Improve Function and Potency of AlloCAR T™ Cells

  • Phase 1 IGNITE Trial Expected to Begin in Mid-2021

  • ALLO-605 is One of Allogene’s Three Strategies to Target BCMA for the Treatment of Patients with Multiple Myeloma

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