Panitumumab
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Panitumumab
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Source | Human |
Target | ? |
Identifiers | |
CAS number | ? |
ATC code | L01 |
Chemical data | |
Formula | ? |
Mol. mass | ? |
Pharmacokinetic data | |
Bioavailability | ? |
Metabolism | ? |
Half life | ∼7.5 days (range: 4-11 days) |
Excretion | ? |
Therapeutic considerations | |
Pregnancy cat. |
? |
Legal status |
℞ Prescription only |
Routes | intravenous |
Panitumumab (ABX-EGF) is a fully human monoclonal antibody targeting the EGF receptor. It received its first licence for clinical use on humans by the FDA, for patients suffering with non-curable colorectal cancer in September 2006. [1] Panitumumab is manufactured by Amgen and marketed as Vectibix in the USA.
The compound works by inhibiting the activation of the EGFR (epidermal growth factor receptor). This results in a halting of a cascade of intracellular signals which would otherwise promote the cell (and cancer cells) to multiply. [2]
As this is a fully human monoclonal antibody, patients run less of a risk of suffering an allergic reaction during its administration (which is via the intravenous route). This is an issue that had caused problems in the use of cetuximab (Erbitux) a drug that has the same mechanism of action but it is an IgG1 chimeric monoclonal antibody. [3]
Panitumumab is a monoclonal antibody of the IgG2 isotype. It is produced by immunization of transgenic mice, that are able to produce human immunoglobulin light and heavy chains. After immunization a specific clone of B cells that produce an antibody against EGFR was selected and immortalized for the generation of the antibody.
[edit] References
- ^ U. S. Food and Drug Administration [1]
- ^ Plunkett, Jack W. (September 30, 2005). Plunkett's Biotech & Genetics Industry Almanac 2006 (in English). Plunkett Research, Ltd.. Retrieved on October 20, 2006.
- ^ (September 1, 2006) Les Cancers Digestifs (in French). Springer. Retrieved on October 20, 2006.
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