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Recruiting

A Study to Assess the Effects on the Single-Dose Drug Levels of Mavacamten in Healthy Participants - CV027-1052

Updated: 23 May, 2023   |   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 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)

  • 18-60

    Age Range

  • 3

    Location(s)

  • Recruiting

Treatment Options

Study Arms
ASSIGNED INTERVENTION
Experimental: Sequence 1
Drug: Mavacamten Capsule 1 Drug: Mavacamten Capsule 3 Drug: Mavacamten Capsule 2
Experimental: Sequence 2
Drug: Mavacamten Capsule 1 Drug: Mavacamten Capsule 3 Drug: Mavacamten Capsule 2
Experimental: Sequence 3
Drug: Mavacamten Capsule 1 Drug: Mavacamten Capsule 3 Drug: Mavacamten Capsule 2
Experimental: Sequence 4
Drug: Mavacamten Capsule 3 Drug: Mavacamten Capsule 2 Drug: Mavacamten Capsule 1
Experimental: Sequence 5
Drug: Mavacamten Capsule 1 Drug: Mavacamten Capsule 3 Drug: Mavacamten Capsule 2
Experimental: Sequence 6
Drug: Mavacamten Capsule 1 Drug: Mavacamten Capsule 3 Drug: Mavacamten Capsule 2

Key Eligibility Criteria

Inclusion Criteria: - Body mass index between 18 and 32 kilograms/meter squared (kg/m^2) inclusive, at the screening visit. - Healthy, as determined by physical examination, vital signs, electrocardiograms (ECGs), and clinical laboratory assessments (including hematology, chemistry, and urinalysis) within the normal range at the screening visit and/or on Day -1. - Cytochrome P450 (CYP) 2C19 normal, rapid, or ultrarapid metabolizer, as determined by genotyping during screening. Exclusion Criteria: - Any significant acute or chronic medical illness. - Current or history of clinically significant cardiac condition, including but not limited to arrhythmia, left ventricular systolic dysfunction, coronary heart disease; current, history, or family history of hypertrophic cardiomyopathy; or evidence of prior myocardial infarction based on ECGs. - CYP2C19 poor (*2/*2, *3/*3, or *2/*3) or intermediate (*1/*2, *1/*3, *2/*17) metabolizer, as determined by genotyping during screening. - Use of CYP2C19 and CYP3A4 inducers or inhibitors within 28 days of study intervention administration. Note: Other protocol-defined inclusion/exclusion criteria apply.

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