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Jan 6, 2025 · References: FDA approves obecabtagene autoleucel for adults with relapsed or refractory B-cell precursor acute lymphoblastic leukemia. US Food and Drug Administration. …
Nov 12, 2024 · The U.S. Food and Drug Administration (FDA) approved obecabtagene autoleucel (Aucatzyl), a CD19-directed CAR T-cell immunotherapy developed by Autolus Inc., for adults …
The November 2024 FDA approval of obecabtagene autoleucel (obe-cel; Aucatzyl) for adult patients with relapsed or refractory B-cell precursor acute lymphoblastic leukemia (ALL) marks …
Nov 10, 2024 · The Friday approval came ahead of the Nov. 16 target date for an FDA decision. London-based Autolus will market its new therapy under the name Aucatzyl.
Aucatzyl® (obecabtagene autoleucel) – New orphan drug approval On November 8, 2024, the FDA announced the approval of Autolus’ Aucatzyl (obecabtagene autoleucel), for the …
Nov 8, 2024 · The FDA has approved obecabtagene autoleucel (obe-cel; Aucatzyl) for the treatment of adult patients with relapsed or refractory B-cell precursor acute lymphoblastic …
Nov 20, 2024 · Obe-cel, short for obecabtagene autoleucel (Aucatzyl by Autolus Inc.), is a CAR T-cell therapy that was recently FDA-approved on November 8th, 2024, for adults with …
Nov 8, 2024 · AUCATZYL was approved by the FDA for the treatment of adult patients with relapsed or refractory B-cell precursor acute lymphoblastic leukemia on November 08, 2024.
Feb 10, 2025 · On November 8, 2024, the US Food and Drug Administration (FDA) approved obecabtagene autoleucel (AUCATZYL, Autolus Inc) for the treatment of adults with relapsed or …
On November 8, 2024, the FDA approved obecabtagene autoleucel (Aucatzyl, Autolus Inc.) for relapsed or refractory B-cell precursor acute lymphoblastic leukemia.
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