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A Phase 3, randomized, double-blind, parallel group, placebo controlled multicenter study to evaluate the efficacy and safety of two doses of GLPG1690 in addition to local standard of care for minimum 52 weeks in subjects with idiopathic pulmonary fibrosis.
Details
Age
Adult
Type of Study
Treatment
Location
University of Colorado Hospital
Principal Investigator
Joyce Lee, MD
Study ID
Protocol Number: 18-2534
More information available at ClinicalTrials.gov: NCT03711162
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