[HTML][HTML] Pirfenidone safety and adverse event management in idiopathic pulmonary fibrosis
LH Lancaster, JA de Andrade, JD Zibrak… - European respiratory …, 2017 - Eur Respiratory Soc
Pirfenidone is one of two approved therapies for the treatment of idiopathic pulmonary
fibrosis (IPF). Randomised controlled clinical trials and subsequent post hoc analyses have …
fibrosis (IPF). Randomised controlled clinical trials and subsequent post hoc analyses have …
[HTML][HTML] Bench-to-bedside: Translational development landscape of biotechnology in healthcare
C Liao, S Xiao, X Wang - Health Sciences Review, 2023 - Elsevier
Biotechnology is a rapidly evolving field that has the potential to transform the way we
diagnose and treat diseases and is changing the landscape of healthcare. Great endeavors …
diagnose and treat diseases and is changing the landscape of healthcare. Great endeavors …
[HTML][HTML] A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis
TE King Jr, WZ Bradford… - New England journal …, 2014 - Mass Medical Soc
Background In two of three phase 3 trials, pirfenidone, an oral antifibrotic therapy, reduced
disease progression, as measured by the decline in forced vital capacity (FVC) or vital …
disease progression, as measured by the decline in forced vital capacity (FVC) or vital …
Effect of pirfenidone on mortality: pooled analyses and meta-analyses of clinical trials in idiopathic pulmonary fibrosis
Background In clinical trials of idiopathic pulmonary fibrosis, rates of all-cause mortality are
low. Thus prospective mortality trials are logistically very challenging, justifying the use of …
low. Thus prospective mortality trials are logistically very challenging, justifying the use of …
Incidence and prevalence of idiopathic pulmonary fibrosis in US adults 18–64 years old
G Raghu, SY Chen, Q Hou, WS Yeh… - European Respiratory …, 2016 - Eur Respiratory Soc
We sought to present the epidemiology of idiopathic pulmonary fibrosis (IPF) in adults 18–64
years old in the USA. From adults aged 18–64 years in a large administrative claims data in …
years old in the USA. From adults aged 18–64 years in a large administrative claims data in …
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
KR Flaherty, KK Brown, AU Wells… - BMJ open …, 2017 - bmjopenrespres.bmj.com
600 patients aged≥ 18 years will be randomised in a 1: 1 ratio to nintedanib or placebo.
Patients with diagnosis of IPF will be excluded. The study population will be enriched with …
Patients with diagnosis of IPF will be excluded. The study population will be enriched with …
Clinical effectiveness of antifibrotic medications for idiopathic pulmonary fibrosis
TM Dempsey, LR Sangaralingham, X Yao… - American journal of …, 2019 - atsjournals.org
Rationale: Since their approval, there has been no real-world or randomized trial evidence
evaluating the effect of the antifibrotic medications pirfenidone and nintedanib on clinically …
evaluating the effect of the antifibrotic medications pirfenidone and nintedanib on clinically …
Acute exacerbation of idiopathic pulmonary fibrosis: shifting the paradigm
CJ Ryerson, V Cottin, KK Brown… - European Respiratory …, 2015 - Eur Respiratory Soc
The goal of this review is to summarise the clinical features, management, and prognosis of
acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF). AE-IPF has previously been …
acute exacerbations of idiopathic pulmonary fibrosis (AE-IPF). AE-IPF has previously been …
Antifibrotic therapy for fibrotic lung disease beyond idiopathic pulmonary fibrosis
BF Collins, G Raghu - European Respiratory Review, 2019 - Eur Respiratory Soc
Two antifibrotic medications (nintedanib and pirfenidone) were recommended
(conditionally) for the treatment of patients with idiopathic pulmonary fibrosis (IPF) in the …
(conditionally) for the treatment of patients with idiopathic pulmonary fibrosis (IPF) in the …
Idiopathic pulmonary fibrosis: effects and optimal management of comorbidities
CS King, SD Nathan - The Lancet Respiratory Medicine, 2017 - thelancet.com
Despite the development of pharmacological therapies that are effective in slowing the
progression of idiopathic pulmonary fibrosis (IPF), it remains a debilitating and lethal …
progression of idiopathic pulmonary fibrosis (IPF), it remains a debilitating and lethal …