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Recruiting

A Study of the Pharmacokinetic Interaction Between Pirfenidone and BMS-986278 in Healthy Participants - IM027-041

Updated: 29 July, 2019   |   ClinicalTrials.gov

Print Friendly Summary

CONSIDERING THIS TRIAL?
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Use the Study Participant's Guide to navigate the process of participating in a clinical trial. Understand key factors to consider before deciding and get questions to ask your healthcare team.

Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 21-65

    Age Range

  • 1

    Location(s)

  • Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: BMS-986278
Drug: BMS-986278
Experimental: BMS-986278 + Pirfenidone
Drug: BMS-986278 Drug: Pirfenidone
Experimental: Pirfenidone
Drug: Pirfenidone

Key Eligibility Criteria

Inclusion Criteria: - Signed Informed Consent. - Healthy participant, as determined by no clinically significant deviation from normal in medical history, physical examination, ECGs, and clinical laboratory determinations. Exclusion Criteria: - Women of child bearing potentia (WOCBP), pregnant or breastfeeding. - History of significant cardiovascular disease. - Participants who have smoked or used smoking cessation or nicotine containing products within 3 months of the first dose of study. Other protocol defined inclusion/exclusion criteria could apply.

We strongly recommend you contact BMS to report Side Effects (Adverse Events)
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