Drug intelligence / Profile preview

cetuximab + cisplatin + capecitabine

Development stage
Unknown
Lead developer
Merck KGaA
Modality
DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

Cetuximab is a recombinant chimeric human/mouse IgG1 monoclonal antibody that targets the epidermal growth factor receptor (EGFR), inhibiting its activation and downstream signaling, which leads to inhibition of cell proliferation, survival, and tumor progression. It is primarily used in the treatment of colorectal cancer and squamous cell carcinoma of the head and neck[1][3][4]. Cisplatin is a platinum-based chemotherapy agent that forms DNA crosslinks, leading to apoptosis in rapidly dividing cells; it is widely used for various solid tumors including head and neck, lung, ovarian, bladder, and testicular cancers. Capecitabine is an oral prodrug converted to 5-fluorouracil (5-FU) in vivo; it inhibits thymidylate synthase resulting in impaired DNA synthesis. Capecitabine is indicated for breast cancer, gastric cancer, colorectal cancer (including adjuvant therapy), among others[6]. The combination of these agents may be used as part of chemoradiotherapy regimens for certain advanced or metastatic cancers.

Brand names
ErbituxXeloda
Other names
cetuximab, cisplatin, capecitabineErbitux + cisplatin + Xeloda
02

Targets

TS (Thymidylate synthase)EGFR (Epidermal growth factor receptor)DNA

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