Drug intelligence / Profile preview

cladribine + cytarabine + granulocyte colony stimulating factor

Development stage
Phase 3
Lead developer
Johnson & Johnson
Modality
Small Molecules, Recombinant Proteins and Enzymes
Administration
Intravenous, Subcutaneous
01

Overview

This is a combination chemotherapy regimen consisting of cladribine (a purine nucleoside analog), cytarabine (an antimetabolite), and granulocyte colony stimulating factor (G-CSF, a hematopoietic growth factor). The combination is primarily used in the treatment of relapsed or refractory acute myeloid leukemia (R/R AML). Cladribine inhibits DNA synthesis by incorporating into DNA and causing strand breaks. Cytarabine also inhibits DNA synthesis by acting as an antimetabolite. G-CSF stimulates the production of neutrophils and may sensitize leukemic cells to chemotherapy while supporting recovery from myelosuppression. This regimen has demonstrated significant efficacy in R/R AML with high remission rates and manageable toxicity profiles[1][5][6].

Other names
cladribine + cytarabine + G-CSFCLAGCLAG regimen
02

Targets

DNA polymerase familyCSF3R (Granulocyte colony-stimulating factor receptor)

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