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Home » Topics » Immunotherapy » CAR T

CAR T
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CAR T cell with implanted gene strand
Immuno-oncology

Next-generation CAR EBV T-cell therapy from Atara Biotherapeutics

Dec. 29, 2023
Chimeric antigen receptor (CAR) therapies targeted against CD19 have been widely used for the treatment of B-cell malignancies. However, the down-regulation of CD19 can lead to relapse, and autologous CAR T therapies have limitations that need to be addressed.
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Immuno-oncology

CD22-targeting SC-262 evades immune system and shows promise for B-cell lymphoma

Dec. 20, 2023
It is known that CD19-directed CAR T-cell therapy is useful in the treatment of large B-cell lymphoma, but about 60% of patients relapse after treatment, and about 30% of these are CD19-negative patients with poor survival. Sana Biotechnology Inc. is developing a hypoimmune CD22-directed CAR T-cell therapy, named SC-262, for the potential treatment of large B-cell lymphoma.
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Immuno-oncology

Vittoria’s VIPER-101 CAR T-cell therapy cleared to enter clinic for T-cell lymphoma

Dec. 11, 2023
Vittoria Biotherapeutics Inc. has received FDA clearance of its IND application to initiate a first-in-human phase I trial with VIPER-101, a gene-edited, autologous, chimeric antigen receptor (CAR) T-cell therapy for treatment of patients with relapsed or refractory T-cell lymphoma.
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Immuno-oncology

Chimeric's CHM-2101 gains IND clearance for GI cancers

Oct. 31, 2023
Chimeric Therapeutics Ltd. has received FDA clearance of its IND application for CHM-2101, a first-in-class CDH17 chimeric antigen receptor (CAR) T cell therapy for gastrointestinal (GI) cancers.
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3D illustration demonstrating CAR T therapy
Immuno-oncology

Caribou’s allogeneic anti-CLL-1 CAR T-cell therapy CB-012 cleared to enter clinic for AML

Oct. 19, 2023
Caribou Biosciences Inc. has received FDA clearance of its IND application for CB-012, an allogeneic anti-C-type lectin-like molecule-1 (anti-CLL-1) chimeric antigen receptor (CAR) T-cell therapy. CLL-1 is highly expressed on acute myeloid leukemia (AML) cells and leukemic stem cells, but it is not expressed on hematopoietic stem cells.
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Cancer and blood cells
Immuno-oncology

Cimeio collaborates with Penn on CD45-targeting CAR T-cell therapy for blood and bone marrow cancers

Oct. 17, 2023
Cimeio Therapeutics Inc. has entered into a preclinical research collaboration with a researcher at the University of Pennsylvania (Penn) to research and evaluate a novel universal immunotherapy with potential to treat multiple blood and bone marrow cancers.
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Cancer cells
Immuno-oncology

Sparx and Arovella partner on CLDN18.2-CAR-iNKT cell therapy

Oct. 11, 2023
Sparx Group has formed a strategic alliance with Arovella Therapeutics Ltd. for the development of a CLDN18.2-chimeric antigen receptor (CAR)-invariant natural killer T (iNKT) cell therapy.
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CAR T cells attacking cancer cell
Immuno-oncology

Glycotope and Max Delbrück Center collaborate to explore combined use of Glycotargets and CAR technology

Sep. 26, 2023
Glycotope GmbH and the Max Delbrück Center for Molecular Medicine in the Helmholtz Association have signed an agreement to explore the potential of combining Glycotope’s antibodies against protein/carbohydrate combined glyco-epitopes (Glycotargets) with chimeric antigen receptor (CAR) technology developed by the Max Delbrück Center.
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Cells, DNA illustration
Immuno-oncology

Epitope editing in hematopoietic cells provides CAR T immunotherapy against all types of blood cancer

Sep. 22, 2023
A new method of CAR T-cell immunotherapy developed by researchers at the University of Pennsylvania Perelman School of Medicine could serve as a treatment for most blood cancers. Until now, CAR T-based immunotherapy for hematological malignancies has targeted the antigens CD19 for B cells, CD7 for T cells, BCMA for myeloma, and CD33 for AML.
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CAR T cell attacking cancer cells
Immuno-oncology

Leucid Bio gets MHRA go-ahead for phase I/II study of NKG2D CAR T-cell therapy LEU-011

Sep. 21, 2023
Leucid Bio Ltd. has received approval from the U.K. Medicines and Healthcare products Regulatory Agency (MHRA) to commence a phase I/II trial of LEU-011 for the treatment of adults with relapsed or refractory solid tumors.
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