 | |
| Monoclonal antibody | |
|---|---|
| Type | Whole antibody |
| Source | Chimeric (mouse/human) |
| Target | EGF receptor |
| Clinical data | |
| Trade names | Erbitux |
| AHFS/Drugs.com | Monograph |
| License data | |
| Pregnancy category |
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| Routes of administration | Intravenous |
| ATC code | |
| Legal status | |
| Legal status | |
| Pharmacokinetic data | |
| Elimination half-life | 114 hrs |
| Identifiers | |
| CAS Number | |
| DrugBank | |
| ChemSpider |
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| UNII | |
| KEGG | |
| ChEMBL | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C6484H10042N1732O2023S36 |
| Molar mass | 145781.92 g·mol−1 |
  (what is this?) (verify) | |
Cetuximab, sold under the brand name Erbitux, is an epidermal growth factor receptor (EGFR) inhibitor medication used for the treatment of metastatic colorectal cancer and head and neck cancer.[2] Cetuximab is a chimeric (mouse/human) monoclonal antibody given by intravenous infusion.[2]
Cetuximab was approved for medical use in the United States in 2004.[4]
- ^ "FDA-sourced list of all drugs with black box warnings (Use Download Full Results and View Query links.)". nctr-crs.fda.gov. FDA. Retrieved 22 October 2023.
- ^ a b c "Erbitux- cetuximab solution". DailyMed. 27 September 2021. Archived from the original on 20 October 2021. Retrieved 2 June 2022.
- ^ "Erbitux EPAR". European Medicines Agency. 17 September 2018. Archived from the original on 14 May 2021. Retrieved 2 June 2022.
- ^ "Drug Approval Package: Erbitux BLA 125084". accessdata.fda.gov. 13 September 2004. Retrieved 17 August 2024.