Patient Guide: A Study to Evaluate Mavacamten Impact on Myocardial Structure in Participants With Symptomatic Obstructive Hypertrophic Cardiomyopathy

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 23 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06112743
Status: ACTIVE_NOT_RECRUITING
Condition: Cardiomyopathy, Hypertrophic
Phase: PHASE4

Where You Can Participate

This study is available at 23 locations across the country.

Top locations include:
  • • West Hollywood, California
  • • Atlanta, Georgia
  • • Boston, Massachusetts
  • • And 20 more locations

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A Study to Evaluate Mavacamten Impact on Myocardial Structure in Participants With Symptomatic Obstructive Hypertrophic Cardiomyopathy - Join Clinical Trial NCTNCT06112743

How to Join This Clinical Trial - NCTNCT06112743

Learn how to participate in this PHASE4 trial studying an investigational therapy for Cardiomyopathy, Hypertrophic. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Cardiomyopathy, Hypertrophic. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Cardiomyopathy, Hypertrophic
Treatment Being Tested
Investigational treatment
Study Phase
PHASE4 - Research study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06112743 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 23 locations. Find a study site near you:

Clinical Research Site

West Hollywood, California 90048-1804 - United States

Status: Contact for availability

Clinical Research Site

Atlanta, Georgia 30309 - United States

Status: Contact for availability

Clinical Research Site

Boston, Massachusetts 02114 - United States

Status: Contact for availability

Clinical Research Site

Cleveland, Ohio 44106 - United States

Status: Contact for availability

Clinical Research Site

Pittsburgh, Pennsylvania 15212-4756 - United States

Status: Contact for availability

Clinical Research Site

Houston, Texas 77030 - United States

Status: Contact for availability

Clinical Research Site

Murray, Utah 84107-5701 - United States

Status: Contact for availability

Clinical Research Site

Ciudad Autónoma de Buenos Aires, Buenos Aires 1093 - Argentina

Status: Contact for availability

Clinical Research Site

Ciudad Autónoma de Buenos Aires, Buenos Aires C1428ART - Argentina

Status: Contact for availability

Clinical Research Site

Pilar, Buenos Aires B1629ODT - Argentina

Status: Contact for availability

And 13 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE4 clinical trial for Cardiomyopathy, Hypertrophic:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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