Drug intelligence / Profile preview

erlotinib + chemotherapy

Development stage
Unknown
Lead developer
Genentech
Modality
Nucleic Acid-Directed Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Classical Binding Small Molecules → Small Molecules
Administration
Intravenous, Oral
01

Overview

Erlotinib is a small molecule tyrosine kinase inhibitor that targets the epidermal growth factor receptor (EGFR). It works by reversibly binding to the ATP-binding site of EGFR, thereby inhibiting its kinase activity and blocking downstream signaling pathways involved in cell proliferation and survival. Erlotinib is primarily indicated for the treatment of metastatic non-small cell lung cancer (NSCLC) with specific EGFR mutations (exon 19 deletions or exon 21 L858R substitution mutations), as well as for advanced pancreatic cancer in combination with gemcitabine. When used with chemotherapy, erlotinib is specifically approved in combination with gemcitabine for pancreatic cancer; it is not recommended for use alongside platinum-based chemotherapies[1][3][5][7].

Brand names
Tarceva
Other names
erlotinib plus chemotherapyerlotinib beyond progressionerlotinib and chemotherapy
02

Targets

EGFR (Epidermal growth factor receptor)JAK2 V617F (Janus kinase 2 V617F mutant)ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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