A randomised, placebo-controlled study of omipalisib (PI3K/mTOR) in idiopathic pulmonary fibrosis

PT Lukey, SA Harrison, S Yang, Y Man… - European …, 2019 - Eur Respiratory Soc
Phosphatidylinositol 3-kinases (PI3Ks) and mammalian target of rapamycin (mTOR) play a
role in the pathogenesis of idiopathic pulmonary fibrosis (IPF). Omipalisib (GSK2126458) is …

Exploration of a potent PI3 kinase/mTOR inhibitor as a novel anti-fibrotic agent in IPF

PF Mercer, HV Woodcock, JD Eley, M Platé… - Thorax, 2016 - thorax.bmj.com
Rationale Idiopathic pulmonary fibrosis (IPF) is the most rapidly progressive and fatal of all
fibrotic conditions with no curative therapies. Common pathomechanisms between IPF and …

[HTML][HTML] Targeting PI3K/AKT signaling for treatment of idiopathic pulmonary fibrosis

J Wang, K Hu, X Cai, B Yang, Q He, J Wang… - … Pharmaceutica Sinica B, 2022 - Elsevier
Idiopathic pulmonary fibrosis (IPF) is a chronic progressive fibrotic interstitial pneumonia
with unknown causes. The incidence rate increases year by year and the prognosis is poor …

CC-90001, a c-Jun N-terminal kinase (JNK) inhibitor, in patients with pulmonary fibrosis: design of a phase 2, randomised, placebo-controlled trial

Z Popmihajlov, DJ Sutherland… - BMJ Open …, 2022 - bmjopenrespres.bmj.com
Introduction Idiopathic pulmonary fibrosis (IPF) is a progressive and often fatal interstitial
lung disease (ILD); other ILDs have a progressive, fibrotic phenotype (PF-ILD). Antifibrotic …

[HTML][HTML] Pharmacotherapy and adjunctive treatment for idiopathic pulmonary fibrosis (IPF)

S Saito, A Alkhatib, JK Kolls, Y Kondoh… - Journal of thoracic …, 2019 - ncbi.nlm.nih.gov
Idiopathic pulmonary fibrosis (IPF) is an advancing and fatal lung disease with increasing
incidence and prevalence. Nintedanib and pirfenidone were approved by the FDA for the …

Evaluation of pirfenidone and nintedanib in a human lung model of fibrogenesis

KM Roach, E Castells, K Dixon, S Mason… - Frontiers in …, 2021 - frontiersin.org
Introduction: Idiopathic pulmonary fibrosis (IPF) is a progressive, fatal lung disease with a
poor prognosis and increasing incidence. Pirfenidone and nintedanib are the only approved …

Use of animal models in IPF research

R Carrington, S Jordan, SC Pitchford… - Pulmonary pharmacology …, 2018 - Elsevier
Idiopathic pulmonary fibrosis (IPF) is a fatal interstitial lung disease with a poor prognosis
and limited treatment options. Many compounds have shown efficacy in preclinical models …

Anti-fibrotic effects of pirfenidone and rapamycin in primary IPF fibroblasts and human alveolar epithelial cells

M Molina-Molina, C Machahua-Huamani… - BMC pulmonary …, 2018 - Springer
Background Pirfenidone, a pleiotropic anti-fibrotic treatment, has been shown to slow down
disease progression of idiopathic pulmonary fibrosis (IPF), a fatal and devastating lung …

[HTML][HTML] Efficacy of a tyrosine kinase inhibitor in idiopathic pulmonary fibrosis

L Richeldi, U Costabel, M Selman… - … England Journal of …, 2011 - Mass Medical Soc
Background Idiopathic pulmonary fibrosis is a progressive lung disease with a high mortality
rate. Because the signaling pathways activated by several tyrosine kinase receptors have …

The JAK2 pathway is activated in idiopathic pulmonary fibrosis

J Milara, G Hernandez, B Ballester, A Morell, I Roger… - Respiratory …, 2018 - Springer
Background Idiopathic pulmonary fibrosis (IPF) is the most rapidly progressive and fatal
fibrotic disorder, with no curative therapies. The signal transducer and activator of …