Drug intelligence / Profile preview

cyclosporine + cytarabine + daunorubicin + gemtuzumab ozogamicin

Development stage
Preclinical
Lead developer
Pfizer
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous, Oral, Subcutaneous, Intrathecal
01

Overview

This is a combination regimen consisting of four drugs: - **Cyclosporine** is an immunosuppressant that inhibits calcineurin, thereby suppressing T-cell activation and cytokine production. - **Cytarabine** is a nucleoside analog antimetabolite that inhibits DNA synthesis, primarily used in the treatment of acute myeloid leukemia (AML) and other hematologic malignancies. - **Daunorubicin** is an anthracycline antibiotic with antimitotic and cytotoxic activity. It intercalates into DNA, inhibits topoisomerase II, generates free radicals, and disrupts nucleic acid synthesis[1][3][5][7]. - **Gemtuzumab ozogamicin** is an antibody-drug conjugate composed of a humanized anti-CD33 monoclonal antibody linked to calicheamicin (a cytotoxic agent). It targets CD33-positive leukemic cells in AML; after binding to CD33 on the cell surface, it delivers calicheamicin intracellularly to induce double-stranded DNA breaks and apoptosis[6][8][10]. This combination may be used as part of investigational or intensive induction regimens for certain subtypes of acute myeloid leukemia (AML), particularly those expressing CD33.

02

Targets

CN (Calcineurin)DNA polymerase familyCD33 (Myeloid cell surface antigen CD33)TOP2A (DNA topoisomerase II)

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