Drug intelligence / Profile preview

afatinib + nintedanib

Development stage
Unknown
Lead developer
Boehringer Ingelheim
Modality
Small Molecules
Administration
Oral
01

Overview

A combination of two oral small-molecule tyrosine kinase inhibitors used investigationally together in solid tumors. Afatinib is an irreversible ErbB family blocker that covalently inhibits EGFR (ErbB1), HER2 (ErbB2), and HER4, thereby suppressing signaling across ErbB homo- and heterodimers and downstream proliferation pathways. Nintedanib is a triple angiokinase inhibitor that competitively inhibits VEGFR-1/2/3, PDGFR-α/β, and FGFR-1/2/3, exerting anti-angiogenic and anti-fibrotic effects; it also has activity against additional kinases such as FLT3 and Src family kinases. The combo has been explored in early-phase trials across advanced solid tumors (e.g., establishing MTDs for continuous afatinib plus nintedanib), with limited activity in unselected castration-resistant prostate cancer on sequential schedules. Primary rationale is dual blockade of tumor cell ErbB signaling and tumor microenvironment/angiogenesis pathways.

Brand names
VargatefGiotrif
Other names
nintedanibafatinib
02

Targets

VEGFR (VEGFR family)LYN (LYN proto-oncogene, Src family tyrosine kinase)ERBB2 (Erb-b2 receptor tyrosine kinase 2)FGFR3 (Fibroblast growth factor receptor 3)PDGFRA (Platelet-derived growth factor receptor alpha)ERBB4 (Erb-b2 receptor tyrosine kinase 4)EGFR T790M (Epidermal growth factor receptor T790M mutant)FLT3 (Fms related receptor tyrosine kinase 3)LCK (Proto-oncogene tyrosine-protein kinase Lck)

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