Drug intelligence / Profile preview

mitomycin + tamoxifen

Development stage
Unknown
Lead developer
Kyowa Kirin
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Intravenous, Oral
01

Overview

Mitomycin + tamoxifen is a combination of two pharmaceutical agents used primarily in the treatment of breast cancer. Mitomycin is an antineoplastic antibiotic that acts as an alkylating agent, cross-linking DNA strands and inhibiting DNA synthesis, leading to cell death. Tamoxifen is a selective estrogen receptor modulator (SERM) that competitively inhibits estrogen binding to its receptor, thereby blocking the growth-promoting effects of estrogen on breast cancer cells. This combination has been studied as part of adjuvant chemoendocrine therapy for stage II, estrogen receptor-positive breast cancer and other malignancies. However, clinical studies have reported increased risks when these drugs are combined—specifically higher incidences of anemia, thrombocytopenia, and hemolytic uremic syndrome (HUS), which can be fatal[1][2]. The use of this combination should be carefully monitored due to these potential toxic interactions.

Other names
mitomycin and tamoxifenmitomycin C plus tamoxifen
02

Targets

DNAESR1 (ERα)

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