Idiopathic Pulmonary Fibrosis Clinical Trial
Official title:
It's Not JUST Idiopathic Pulmonary Fibrosis Study
Study of progression of fibrosis in ILD
The overall aims of this study are - Identify biomarkers and gene expression profiles that determine progressive fibrotic lung disease regardless of aetiology - To prospectively assess biomarkers which predict progressive fibrosis in patients with fibrosing lung disease of alternate aetiology, including RA-UIP, Asbestosis, Chronic Hypersensitivity Pneumonitis and Unclassifiable fibrotic lung disease - Investigate genetic associations and epigenetic modifications which affect fibrotic disease severity and progression - Prospectively evaluate longitudinal disease behaviour in patients with non IPF-fibrotic lung diseases with a view to developing composite clinical end-points for subsequent use in intervention studies in patients ;
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|---|---|---|---|
| Active, not recruiting |
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Phase 2 | |
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Phase 2 | |
| Recruiting |
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||
| Completed |
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| Not yet recruiting |
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Phase 2 | |
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Phase 1/Phase 2 | |
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Phase 1 | |
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Phase 2/Phase 3 |