Condition: Idiopathic Pulmonary Fibrosis · Idiopathic Pulmonary Fibrosis (IPF) · Sponsor: Mannkind Corporation
This trial is a randomized, double-blind, placebo-controlled study evaluating the safety and preliminary efficacy of inhaled Nintedanib Dry Powder Inhalation (DPI) in adults with idiopathic pulmonary fibrosis (IPF). Participants are randomized to receive either 2 mg QID, 4 mg BID, or matching placebo for 12 weeks, followed by a 24-week open-label extension in which all participants receive active treatment. The primary focus is on safety-particularly bronchospasm events, lung function changes (FEV1, FEV1/FVC), and adverse event rates and assessing the effectiveness of nintedanib DPI in treating IPF.
This description comes directly from the study's public registry record.
Wassim Fares, MD, SVP, Therapeutic Area Head, Orphan Lung Disease, MD · 203-796-3407 · wfares@mannkindcorp.com
Always discuss trial participation with your own doctor first.
| Trial Management Group Inc | Windsor, Ontario, Canada | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07679893