Drug intelligence / Profile preview

cyclophosphamide + fludarabine + plerixafor

Development stage
Unknown
Lead developer
Sanofi
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous, Subcutaneous
01

Overview

This is a combination regimen consisting of three drugs—cyclophosphamide, fludarabine, and plerixafor—used primarily in the context of hematopoietic stem cell mobilization and conditioning for transplantation. Cyclophosphamide is an alkylating agent that crosslinks DNA, leading to cell death; fludarabine is a purine analog that inhibits DNA synthesis; and plerixafor is a small molecule antagonist of the chemokine receptor CXCR4, which disrupts the interaction between stromal-derived factor-1 (SDF-1/CXCL12) and CXCR4 to mobilize hematopoietic stem cells from bone marrow into peripheral blood. This combination may be used as part of preparative regimens for allogeneic or autologous stem cell transplantation in patients with hematological malignancies such as chronic lymphocytic leukemia (CLL), non-Hodgkin lymphoma (NHL), or multiple myeloma. The addition of plerixafor can enhance stem cell yield when standard mobilization strategies are insufficient[1][2][4].

02

Targets

DNA polymerase familyCXCR4 (C-X-C motif chemokine receptor 4)DNARNR (Ribonucleotide reductase)

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