Drug intelligence / Profile preview

gemcitabine + cyclophosphamide + doxorubicin + vincristine + prednisone

Development stage
Phase 2
Lead developer
Eli Lilly
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules
Administration
Intravenous, Oral
01

Overview

This is a combination chemotherapy regimen consisting of five drugs: - **Gemcitabine** is a nucleoside analog that inhibits DNA synthesis, leading to cell death. - **Cyclophosphamide** is an alkylating agent that cross-links DNA, preventing cell division and causing apoptosis. - **Doxorubicin** (also known as hydroxydaunorubicin or adriamycin) is an anthracycline antibiotic that intercalates into DNA and inhibits topoisomerase II, resulting in DNA damage and cell death. - **Vincristine** (also called Oncovin) binds to tubulin and inhibits microtubule formation, arresting cells in metaphase during mitosis. - **Prednisone** is a synthetic corticosteroid with anti-inflammatory and immunosuppressive properties; it also induces apoptosis in certain cancer cells. This specific combination does not correspond to a widely recognized named regimen. However, four of these agents—cyclophosphamide, doxorubicin, vincristine, prednisone—form the well-established CHOP regimen for non-Hodgkin lymphoma[5][6]. Gemcitabine has been studied as an additional agent or substitute in various experimental regimens for lymphomas or solid tumors but is not part of standard CHOP-based protocols. The mechanism of action involves multiple pathways targeting rapidly dividing cancer cells through cytotoxicity (chemotherapy) and immune modulation (steroid).

02

Targets

DNA polymerase familyTOP2A (DNA topoisomerase II)GR (Glucocorticoid receptor)RNR (Ribonucleotide reductase)TUBB (Tubulin (alpha and beta subunits))DNA interstrand cross-link

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