Drug intelligence / Profile preview

KITE-222

Development stage
Preclinical
Lead developer
Kite Pharma
Modality
Peripheral Blood HSCs → Hematopoietic Stem Cells → Adult Stem Cells → Stem Cell Therapies → Cell Therapies, CAR-T Cells → Engineered T Cells → Adoptive Cell Transfer → Cell Therapies, Bone Marrow HSCs → Hematopoietic Stem Cells → Adult Stem Cells → Stem Cell Therapies → Cell Therapies
Administration
Intravenous
01

Overview

KITE-222 is an investigational autologous chimeric antigen receptor (CAR) T-cell therapy developed by Kite, a Gilead Company. It is engineered to express a CAR that specifically targets C-type lectin-like molecule-1 (CLL-1), also known as C-type lectin domain family 12 member A. CLL-1 is expressed on malignant cells in up to 90% of patients with acute myeloid leukemia (AML) and is restricted to lineage-committed myeloid cells, sparing healthy hematopoietic stem cells. Preclinical studies have shown robust antigen-specific function and the ability of these CAR T cells to clear AML cells in aggressive tumor models. KITE-222 has received FDA Orphan Drug Designation for AML and is currently being evaluated in Phase 1 clinical trials for relapsed/refractory AML[1][4][6]. The therapy uses an engineered autologous cell therapy platform and is administered intravenously.

02

Targets

CLEC12A

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