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Recruiting

An Investigational Study to Evaluate the Effects of Experimental Medication BMS-986256 in Healthy Participants - IM026-002

Updated: 25 September, 2018   |   ClinicalTrials.gov

Print Friendly Summary

CONSIDERING THIS TRIAL?
Print this page and the trial guide to help you talk with your doctor.
Use the Study Participants 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)

  • 18-55

    Age Range

  • 1

    Location(s)

  • Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Multiple Dose
Drug: BMS-986256 Other: Placebo
Experimental: Sequential Dose
Other: Placebo Drug: BMS-986256
Experimental: Single Dose
Other: Placebo Drug: BMS-986256

Key Eligibility Criteria

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Weight ≥ 50 kg and body mass index (BMI) between 18.0 and 32.0 kg/m2 inclusive at screening - Participants must not be current users (within 6 months before screening) of tobacco or tobacco- or nicotine-containing products; they must also be willing to refrain from using any of these products during their participation in the study - A negative QuantiFERON®-TB Gold test result at screening or documentation of a negative result within 3 months before screening Exclusion Criteria: - Previous participation in the current study or previous exposure within 6 weeks before study drug administration for non-biologics and 12 weeks before study drug administration for biologics - Inability to tolerate oral medication - Inability to tolerate venipuncture, or inadequate venous access Other protocol defined inclusion/exclusion criteria could apply

Have questions? Call 855-907-3286 or Email Us

Have questions?
Call 855-907-3286 or Email Us