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Not Yet Recruiting

A Study to Compare the Taste and Levels in Blood Plasma of BMS-986165 When Taken as Different Formulations by Healthy Adult Participants - IM011-113

Updated: 7 August, 2020   |   ClinicalTrials.gov

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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.
Print this page IM011-113
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Trial Details

  • Phase 1

    Phase

  • Gender(s)

  • 18-55

    Age Range

  • Not Yet Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Treatment Group 1
Drug: BMS-986165 Tablet formulation 1 Drug: BMS-986165 Tablet formulation 2
Experimental: Treatment Group 10
Drug: BMS-986165 Tablet formulation 1 Drug: BMS-986165 Tablet formulation 2
Experimental: Treatment Group 2
Drug: BMS-986165 Tablet formulation 2 Drug: BMS-986165 Tablet formulation 1
Experimental: Treatment Group 3
Drug: BMS-986165 Tablet formulation 2 Drug: BMS-986165 Tablet formulation 1
Experimental: Treatment Group 4
Drug: BMS-986165 Tablet formulation 1 Drug: BMS-986165 Tablet formulation 2
Experimental: Treatment Group 5
Drug: BMS-986165 Tablet formulation 1 Drug: BMS-986165 Tablet formulation 2
Experimental: Treatment Group 6
Drug: BMS-986165 Tablet formulation 1 Drug: BMS-986165 Tablet formulation 2
Experimental: Treatment Group 7
Drug: BMS-986165 Tablet formulation 1 Drug: BMS-986165 Tablet formulation 2
Experimental: Treatment Group 8
Drug: BMS-986165 Tablet formulation 1 Drug: BMS-986165 Tablet formulation 2
Experimental: Treatment Group 9
Drug: BMS-986165 Tablet formulation 1 Drug: BMS-986165 Tablet formulation 2

Key Eligibility Criteria

For more information regarding Bristol-Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: - Healthy participants, as determined by no clinically significant deviation from normal in medical history, physical examination, ECGs, and clinical laboratory determinations in the opinion of the investigator - Women and men must agree to follow specific methods of contraception, if applicable Exclusion Criteria: - Any significant acute or chronic medical condition that presents a potential risk to the participant and/or may compromise the objectives of the study, including a history of/or active liver disease - Inability to tolerate oral medication - History of allergy to BMS-986165 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

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