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The Idiopathic Pulmonary Fibrosis (IPF) cohort in this protocol is now closed. The study is only enrolling patients onto the Progressive Fibrotic Interstitial Lung Disease (PF-ILD) cohort.

Active, Not Recruiting

A Study Measuring the Effectiveness, Safety, and Tolerability of BMS-986278 in Participants With Lung Fibrosis - IM027-040

Updated: 14 March, 2023   |   ClinicalTrials.gov

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Trial Details

  • Phase 2

    Phase

  • Gender(s)

  • 21+

    Age Range

  • Active, Not Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: IPF Dose 1 + Post Treatment Follow-up or OTE
Drug: BMS-986278
Experimental: IPF Dose 2 + Post Treatment Follow-up or OTE
Drug: BMS-986278
Placebo Comparator: IPF Placebo + Post Treatment Follow-up or OTE
Other: BMS-986278 Placebo
Experimental: PF-ILD Dose 1 + Post Treatment Follow-up or OTE
Drug: BMS-986278
Experimental: PF-ILD Dose 2 + Post Treatment Follow-up or OTE
Drug: BMS-986278
Placebo Comparator: PF-ILD Placebo + Post Treatment Follow-up or OTE
Other: BMS-986278 Placebo

Key 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

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Side Effects (Adverse Events) and other reportable events are defined here
Report Side Effects (Adverse Events) or Product Quality Complaints: Medical Information

Have questions? Live support is available 24/7 - Call 855-907-3286 or email clinical.trials@bms.com

Have questions? Live support is available 24/7 -
Call 855-907-3286 or email clinical.trials@bms.com