Purpose: to evaluate the safety and tolerability of different formulations of an FDA approved medication.

2 periods each 4 nights
11 visits

Participate in a clinical study for the treatment of cardiomyopathy.

This is a clinical study to assess the similarity of 1x 15mg dose versus 3x 5mg dose of mavacamten for the treatment of cardiomyopathy.

This study is to assess how a capsule is processed in the body when given different formulations of an FDA approved medication.

This study has two separate admits each of 4 nights and 5 days & 11 outpatient visits over 4 months.

Reimbursement for study participation will be provided for time and travel of up to $8,750.

This study has been reviewed and approved by an independent ethics committee.

This study requires adults willing to adhere to the contraception requirements for this study.

Call 612-315-6490 to discuss your eligibility today!

Eligibility

Age: 18-60
BMI: 18-32kg/m2
Medication: Any prescription medications within 28 days or OTC medications within 14 days prior to dosing.
Contraception: Willing to adhere to the contraception requirements for this study
Compensation: up to $8,750
Smoking Status: Must not have used any tobacco products within 2 months prior to dose