PT  - JOURNAL ARTICLE
AU  - Kevin R Flaherty
AU  - Kevin K Brown
AU  - Athol U Wells
AU  - Emmanuelle Clerisme-Beaty
AU  - Harold R Collard
AU  - Vincent Cottin
AU  - Anand Devaraj
AU  - Yoshikazu Inoue
AU  - Florence Le Maulf
AU  - Luca Richeldi
AU  - Hendrik Schmidt
AU  - Simon Walsh
AU  - William Mezzanotte
AU  - Rozsa Schlenker-Herceg
TI  - 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
AID  - 10.1136/bmjresp-2017-000212
DP  - 2017 Sep 01
TA  - BMJ Open Respiratory Research
PG  - e000212
VI  - 4
IP  - 1
4099  - http://bmjopenrespres.bmj.com/content/4/1/e000212.short
4100  - http://bmjopenrespres.bmj.com/content/4/1/e000212.full
SO  - BMJ Open Resp Res2017 Sep 01; 4
AB  - 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 two-thirds having a usual interstitial pneumonia-like pattern on HRCT. The primary endpoint is the annual rate of decline in forced vital capacity over 52 weeks. The main secondary endpoints are the absolute change from baseline in King’s Brief Interstitial Lung Disease Questionnaire total score, time to first acute interstitial lung disease exacerbation or death and time to all-cause mortality over 52 weeks.Ethics and dissemination The trial is conducted in accordance with the Declaration of Helsinki, the International Conference on Harmonisation Tripartite Guideline for Good Clinical Practice (GCP) and Japanese GCP regulations.Trial registration number NCT02999178.