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Cocktail Probe Substrates + BMS-986419 for Healthy Subjects
Phase 1
Waitlist Available
Research Sponsored by Bristol-Myers Squibb
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 28 days after last dose
Awards & highlights
Study Summary
This trial tests the effects of a drug on 6 common medicines in healthy people.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 28 days after last dose
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 28 days after last dose
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Secondary outcome measures
Area under the plasma concentration-time curve from time zero extrapolated to infinite time (AUC(INF))
Area under the plasma concentration-time curve from time zero to time of the last quantifiable concentration (AUC(0-T))
Columbia-Suicide Severity Rating Scale (C-SSRS)
+8 moreTrial Design
1Treatment groups
Experimental Treatment
Group I: Cocktail Probe Substrates + BMS-986419Experimental Treatment7 Interventions
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Fexofenadine
2016
Completed Phase 4
~950
BMS-986419
2023
Completed Phase 1
~30
Caffeine
2014
Completed Phase 3
~2980
Bupropion
2011
Completed Phase 4
~3310
Omeprazole
2006
Completed Phase 4
~940
Flurbiprofen
2022
Completed Phase 4
~870
Midazolam
2018
Completed Phase 4
~1910
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Logistics
Participation is compensated
You will be compensated for participating in this trial.
Who is running the clinical trial?
Bristol-Myers SquibbLead Sponsor
2,650 Previous Clinical Trials
4,130,810 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:Research Study Groups:
This trial has the following groups:- Group 1: Cocktail Probe Substrates + BMS-986419
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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