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Unknown
MYK-224 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 52 days
Awards & highlights
Study Summary
This trial will study the effect of combining itraconazole or verapamil with MYK-224, to see if it changes the drug levels of MYK-224 in healthy people.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 52 days
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 52 days
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary 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 the time of the last quantifiable concentration (AUC[0-T])
Maximum observed plasma concentration (Cmax)
Secondary outcome measures
Apparent terminal plasma half-life (T-HALF)
Apparent total body clearance (CLT/F)
Measurement of left ventricle stroke volume (LVSV)
+12 moreTrial Design
3Treatment groups
Experimental Treatment
Group I: Arm 3: MYK-224 + VerapamilExperimental Treatment2 Interventions
Group II: Arm 2: MYK-224 + ItraconazoleExperimental Treatment2 Interventions
Group III: Arm 1: MYK-224Experimental Treatment1 Intervention
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
MYK-224
2023
Completed Phase 1
~90
Itraconazole
2017
Completed Phase 2
~780
Verapamil
2006
Completed Phase 4
~2290
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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
2,640 Previous Clinical Trials
4,129,419 Total Patients Enrolled
Frequently Asked Questions
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