Clinical data | |
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Trade names | Tarceva |
Other names | Erlotinib hydrochloride |
AHFS/Drugs.com | Monograph |
MedlinePlus | a605008 |
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Pregnancy category | |
Routes of administration | By mouth |
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Pharmacokinetic data | |
Bioavailability | 59% |
Protein binding | 95% |
Metabolism | Liver (mainly CYP3A4, less CYP1A2) |
Elimination half-life | 36.2 hrs (median) |
Excretion | >98% as metabolites, of which >90% via feces, 9% via urine |
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CompTox Dashboard (EPA) | |
ECHA InfoCard | 100.216.020 |
Chemical and physical data | |
Formula | C22H23N3O4 |
Molar mass | 393.443 g·mol−1 |
3D model (JSmol) | |
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Erlotinib, sold under the brand name Tarceva among others, is a medication used to treat non-small cell lung cancer (NSCLC) and pancreatic cancer.[4] Specifically it is used for NSCLC with mutations in the epidermal growth factor receptor (EGFR) — either an exon 19 deletion (del19) or exon 21 (L858R) substitution mutation — which has spread to other parts of the body.[4] It is taken by mouth.[4]
Common side effects include rash, diarrhea, muscle pain, joint pain, and cough.[4][3] Serious side effects may include lung problems, kidney problems, liver failure, gastrointestinal perforation, stroke, and corneal ulceration.[4] Use in pregnancy may harm the baby.[4] It is a receptor tyrosine kinase inhibitor, which acts on the epidermal growth factor receptor (EGFR).[4]
Erlotinib was approved for medical use in the United States in 2004.[5][4][3] It is on the World Health Organization's List of Essential Medicines.[6]