Cargando…
Inhibition of mast cells: a novel mechanism by which nintedanib may elicit anti-fibrotic effects
BACKGROUND: Idiopathic pulmonary fibrosis (IPF) is a chronic and progressive lung disease which presents a grave prognosis for diagnosed patients. Nintedanib (a triple tyrosine kinase inhibitor) and pirfenidone (unclear mechanism of action) are the only approved therapies for IPF, but have limited e...
Autores principales: | Overed-Sayer, Catherine, Miranda, Elena, Dunmore, Rebecca, Liarte Marin, Elena, Beloki, Lorea, Rassl, Doris, Parfrey, Helen, Carruthers, Alan, Chahboub, Amina, Koch, Sofia, Güler-Gane, Gülin, Kuziora, Michael, Lewis, Arthur, Murray, Lynne, May, Richard, Clarke, Deborah |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7476277/ https://www.ncbi.nlm.nih.gov/pubmed/32709610 http://dx.doi.org/10.1136/thoraxjnl-2019-214000 |
Ejemplares similares
-
Clinical use of nintedanib in patients with idiopathic pulmonary fibrosis
por: Hajari Case, Amy, et al.
Publicado: (2017) -
Nintedanib in patients with idiopathic pulmonary fibrosis and preserved lung volume
por: Kolb, Martin, et al.
Publicado: (2017) -
Investigating the effects of nintedanib on biomarkers of extracellular matrix turnover in patients with IPF: design of the randomised placebo-controlled INMARK®trial
por: Maher, Toby M, et al.
Publicado: (2018) -
Safety and survival data in patients with idiopathic pulmonary fibrosis treated with nintedanib: pooled data from six clinical trials
por: Lancaster, Lisa, et al.
Publicado: (2019) -
Design of the PF-ILD trial: a double-blind, randomised, placebo-controlled phase III trial of nintedanib in patients with progressive fibrosing interstitial lung disease
por: Flaherty, Kevin R, et al.
Publicado: (2017)