Table 1. Clinical trials exploring anti-fibrotic drugs' role in cHP therapy.
Agent | Registration No. | Study design | Population | Aims | Primary end point | State |
---|---|---|---|---|---|---|
Nintedanib | NCT02999178 (INBUILD) | Phase III, randomized, double blind, placebo-controlled | Fibrosing ILDs | Efficacy and safety | Annual rate of FVC decline | Completed, published results |
Pirfenidone | NCT02496182 | Phase II/III, placebo-controlled, open-label, proof of concept | cHP | Efficacy and safety | FVC over 52 weeks | Completed, published results |
Pirfenidone | EudraCT 2014–000861-32 DRKS00009822 (RELIEF) | Phase II, randomized, double blind, placebo-controlled | cHP | Efficacy and safety | Absolute change in % FVC from baseline to week 48 | Completed |
Pirfenidone | NCT02958917 | Phase II, randomized, double blind, placebo-controlled | cHP | Efficacy and Safety | Mean change in % FVC from baseline to week 52 | Ongoing |
cHP: chronic hypersensitivity pneumonitis; ILDs: interstitial lung diseases; FVC: forced vital capacity.