Nintedanib (Vargatef)
Not FDA approved for an antineoplastic indication at this time.
Mechanism of action
From the NCI Drug Dictionary: An orally bioavailable, indolinone-derived, receptor tyrosine kinase (RTK) inhibitor with potential antiangiogenic and antineoplastic activities. Multitargeted tyrosine kinase inhibitor BIBF 1120 selectively binds to and inhibits vascular endothelial growth factor receptor (VEGFR), fibroblast growth factor receptor (FGFR) and platelet-derived growth factor receptor (PDGFR) tyrosine kinases, which may result in the induction of endothelial cell apoptosis; a reduction in tumor vasculature; and the inhibition of tumor cell proliferation and migration. In addition, this agent also inhibits members of the Src family of tyrosine kinases, including Src, Lck, Lyn, and FLT-3 (fms-like tyrosine kinase 3).[1][2][3]
Diseases for which it is established
Diseases for which it is used
Patient drug information
- Nintedanib (Vargatef) package insert[4]
- Nintedanib (Vargatef) patient drug information (UpToDate)[5]
History of changes in EMA indication
- 2014-11-21: Initial marketing authorization as Vargatef.
- Uncertain date: Nintedanib (Vargatef) is indicated in combination with docetaxel for the treatment of adult patients with locally advanced, metastatic or locally recurrent non-small cell lung cancer (NSCLC) of adenocarcinoma tumour histology after first line chemotherapy.
Also known as
- Code name: BIBF 1120
- Brand names: Cyendiv, Idofnib, Nifev, Nindanib, Nintena, Nintenib, Nintib, Ofev, Vargatef