Study summary
An antifibrotic pill slowed lung function decline in limited scleroderma too
49.1ml/year lung capacity decline, vs 74.5 with placebo
What was tested
Nintedanib, an antifibrotic pill approved for idiopathic pulmonary fibrosis, against placebo, in people with limited cutaneous systemic sclerosis and lung disease.
What they found
- Lung capacity declined 49.1 ml a year vs 74.5 ml with placebo.
- The benefit continued in the open-label extension.
What it means
Shows the lung benefit applies across scleroderma subtypes.
Last reviewed 2026-11-15 by the Find a Trial editorial team.
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