Abstract

Among patients with ILD associated with systemic sclerosis, the annual rate of decline in FVC was lower with nintedanib than with placebo; no clinical benefit of nintedanib was observed for other manifestations of systemic sclerosis. The adverse-event profile of nintedanib observed in this trial was similar to that observed in patients with idiopathic pulmonary fibrosis; gastrointestinal adverse events, including diarrhea, were more common with nintedanib than with placebo. (Funded by Boehringer Ingelheim; SENSCIS ClinicalTrials.gov number, NCT02597933.).

Keywords

NintedanibInterstitial lung diseaseMedicineScleroderma (fungus)LungIdiopathic pulmonary fibrosisPathologyInternal medicine

MeSH Terms

AdministrationOralAdultDiarrheaDisease ProgressionDouble-Blind MethodEnzyme InhibitorsFemaleHumansIndolesLung DiseasesInterstitialMaleMiddle AgedProtein-Tyrosine KinasesSclerodermaSystemicVital Capacity

Affiliated Institutions

Related Publications

Publication Info

Year
2019
Type
article
Volume
380
Issue
26
Pages
2518-2528
Citations
1463
Access
Closed

Social Impact

Social media, news, blog, policy document mentions

Citation Metrics

1463
OpenAlex
75
Influential
1285
CrossRef

Cite This

Oliver Distler, Kristin B. Highland, Martina Gahlemann et al. (2019). Nintedanib for Systemic Sclerosis–Associated Interstitial Lung Disease. New England Journal of Medicine , 380 (26) , 2518-2528. https://doi.org/10.1056/nejmoa1903076

Identifiers

DOI
10.1056/nejmoa1903076
PMID
31112379

Data Quality

Data completeness: 90%