WO2024209429 - T CELLS FOR USE IN TREATING RELAPSED OR REFRACTORY ACUTE MYELOID LEUKEMIA

National phase entry is expected:
Publication Number WO/2024/209429
Publication Date 10.10.2024
International Application No. PCT/IB2024/053367
International Filing Date 05.04.2024
Title **
[English] T CELLS FOR USE IN TREATING RELAPSED OR REFRACTORY ACUTE MYELOID LEUKEMIA
[French] LYMPHOCYTES T DESTINÉS À ÊTRE UTILISÉS DANS LE TRAITEMENT DE LA LEUCÉMIE MYÉLOÏDE AIGUË RÉCIDIVANTE OU RÉFRACTAIRE
Applicants **
TAKEDA PHARMACEUTICAL COMPANY LIMITED 1-1, Doshomachi 4-chome Chuo-ku Osaka-shi, Osaka 541-0045, JP
Inventors
ABIKOFF, Cori c/o Millennium Pharmaceuticals, Inc. 40 Landsdowne Street Cambridge, Massachusetts 02139, US
ATKURI, Kondala c/o Millennium Pharmaceuticals, Inc. 40 Landsdowne Street Cambridge, Massachusetts 02139, US
LIU, Yue c/o Millennium Pharmaceuticals, Inc. 40 Landsdowne Street Cambridge, Massachusetts 02139, US
Priority Data
63/457,937   07.04.2023   US
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Quotation for National Phase entry

Country StagesTotal
China Filing2540
EPO Filing, Examination27858
Japan Filing538
South Korea Filing575
USA Filing, Examination11435
MasterCard Visa

Total: 42946

The term for entry into the National Phase has expired. This quotation is for informational purposes only

Abstract[English] The present disclosure provides, among other things, methods for treating relapsed or refractory acute myeloid leukemia by administering to a subject in need thereof a therapeutically effective amount of an allogeneic composition comprising VDelta1+ (Vδ1+) gamma delta (γδ) T cells such that one or more symptoms or biomarkers is improved after treatment. The present disclosure also provides suitable doses of compositions comprising allogeneic Vδ1+gamma delta (γδ) T cells for administration to a subject suffering from relapsed or refractory AML. In some embodiments, the Vδ1+gamma delta (γδ) T cells are untransduced.[French] La présente divulgation concerne, entre autres, des méthodes de traitement de la leucémie myéloïde aiguë récidivante ou réfractaire par administration à un sujet qui en a besoin d'une quantité thérapeutiquement efficace d'une composition allogénique comprenant des lymphocytes T VDelta1+ (Vδ1+) gamma delta (γδ) de telle sorte qu'un ou plusieurs symptômes ou biomarqueurs sont améliorés après traitement. La présente divulgation concerne également des doses appropriées de compositions comprenant des lymphocytes T allogéniques Vδ1+gamma delta (γδ) pour une administration à un sujet souffrant de LMA récidivante ou réfractaire. Dans certains modes de réalisation, les lymphocytes Vδ1+gamma delta (γδ) sont non transduits.
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