A Study Measuring the Effectiveness, Safety, and Tolerability of BMS-986278 in Participants With Lung Fibrosis
Completed · Phase 2 · Has a placebo group
Conditions studied: Pulmonary Fibrosis
In brief
The purpose of this study is to provide an initial evaluation of the effectiveness of BMS-986278 in participants with lung fibrosis, to demonstrate the safety of BMS-986278, and provide information on the drug levels of BMS-986278 in these participants.
Key facts
- Study ID
- NCT04308681
- Run by
- Bristol-Myers Squibb
- People needed
- 403
- Starts
- 2020-07-29
- Expected to finish
- 2023-09-22
- Last updated by the study team
- 2026-02-03
Who can join
Age: 21 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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.
You may not qualify if…
- 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
Where it is running
- Local Institution — Phoenix, Arizona, United States
- Local Institution - 0028 — Los Angeles, California, United States
- Local Institution - 0043 — Stanford, California, United States
- University of Colorado Anschutz Medical Campus-Department of Medicine — Aurora, Colorado, United States
- Local Institution - 0006 — Denver, Colorado, United States
- Local Institution - 0171 — New Haven, Connecticut, United States
- Local Institution - 0035 — Gainesville, Florida, United States
- Local Institution - 0166 — Orlando, Florida, United States
- Local Institution - 0078 — Atlanta, Georgia, United States
- Local Institution - 0031 — Kansas City, Kansas, United States
- Local Institution - 0154 — Baltimore, Maryland, United States
- Local Institution - 0003 — Boston, Massachusetts, United States
- Local Institution - 0030 — Chesterfield, Missouri, United States
- Local Institution - 0036 — St Louis, Missouri, United States
- Local Institution - 0029 — Cincinnati, Ohio, United States
- Local Institution - 0164 — Columbus, Ohio, United States
- Local Institution — Hershey, Pennsylvania, United States
- Local Institution — Nashville, Tennessee, United States
- Local Institution - 0096 — Charlottesville, Virginia, United States
- Local Institution — Falls Church, Virginia, United States
- Local Institution - 0049 — Buenos Aires, Distrito Federal, Argentina
- Local Institution - 0103 — Rosario, Santa Fe Province, Argentina
- Local Institution - 0097 — San Miguel de Tucumán, Tucumán Province, Argentina
- Local Institution - 0115 — Buenos Aires, Argentina
- Local Institution - 0032 — Birmingham, Alabama, United States
Full record on ClinicalTrials.gov
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