A Study Measuring the Effectiveness, Safety, and Tolerability of BMS-986278 in Participants With Lung Fibrosis
Pulmonary Fibrosis
About this trial
This is an interventional treatment trial for Pulmonary Fibrosis focused on measuring Idiopathic pulmonary fibrosis, Progressive Fibrotic Interstitial Lung Disease, Idiopathic interstitial pneumonia, Fibrotic interstitial pneumonia, Fibrotic interstitial lung disease, Fibrosing interstitial lung disease, Interstitial lung disease
Eligibility Criteria
Inclusion Criteria:
For the idiopathic pulmonary fibrosis (IPF) Cohort
- Diagnosis of IPF within 7 years of screening
- Female and males ≥ 40 years of age
For the progressive fibrotic interstitial lung disease (PF-ILD) Cohort
- Evidence of progressive ILD within the 24 months before screening
- Female and male ≥ 21 years of age.
Exclusion Criteria:
- Women of childbearing potential (WOCBP)
- Active Smokers
- Current malignancy or previous malignancy up to 5 years prior to screening
- History of allergy to BMS-986278 or related compounds
Other protocol-defined inclusion/exclusion criteria apply
Sites / Locations
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- University of Colorado Anschutz Medical Campus-Department of Medicine
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- Central Florida Pulmonary Group-Research
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- Hopital Europeen Georges Pompidou
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Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Experimental
Experimental
Placebo Comparator
Experimental
Experimental
Placebo Comparator
IPF Dose 1 + Post Treatment Follow-up or OTE
IPF Dose 2 + Post Treatment Follow-up or OTE
IPF Placebo + Post Treatment Follow-up or OTE
PF-ILD Dose 1 + Post Treatment Follow-up or OTE
PF-ILD Dose 2 + Post Treatment Follow-up or OTE
PF-ILD Placebo + Post Treatment Follow-up or OTE
IPF (Idiopathic Pulmonary Fibrosis) OTE (Optional Treatment Extension)
PF-ILD (Progressive Fibrotic Interstitial Lung Disease)