Patient Guide: Efficacy, Safety, and Pharmacokinetics of Vericiguat in Pediatric Participants With Heart Failure Due to Left Ventricular Systolic Dysfunction (MK-1242-036)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 93 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05714085
Status: 🟢 Enrolling Now
Condition: Heart Failure, Left Ventricular Systolic Dysfunction
Phase: PHASE2, PHASE3

Where You Can Participate

This study is available at 93 locations across the country.

Top locations include:
  • • Loma Linda, California
  • • Los Angeles, California
  • • Aurora, Colorado
  • • And 90 more locations

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Efficacy, Safety, and Pharmacokinetics of Vericiguat in Pediatric Participants With Heart Failure Due to Left Ventricular Systolic Dysfunction (MK-1242-036) - Join Clinical Trial NCTNCT05714085

How to Join This Clinical Trial - NCTNCT05714085

Learn how to participate in this PHASE2, PHASE3 trial studying an investigational therapy for Heart Failure, Left Ventricular Systolic Dysfunction. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Heart Failure, Left Ventricular Systolic Dysfunction. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Heart Failure, Left Ventricular Systolic Dysfunction
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2, PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05714085 - 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 93 locations. Find a study site near you:

Clinical Research Site

Loma Linda, California 92354 - United States

Status: RECRUITING

Clinical Research Site

Los Angeles, California 90095 - United States

Status: RECRUITING

Clinical Research Site

Aurora, Colorado 80045 - United States

Status: RECRUITING

Clinical Research Site

Washington, District of Columbia 20010 - United States

Status: RECRUITING

Clinical Research Site

Saint Petersburg, Florida 33701 - United States

Status: RECRUITING

Clinical Research Site

Atlanta, Georgia 30329 - United States

Status: RECRUITING

Clinical Research Site

Ann Arbor, Michigan 48109 - United States

Status: RECRUITING

Clinical Research Site

Saint Louis, Missouri 63110 - United States

Status: RECRUITING

Clinical Research Site

Bronx, New York 10467 - United States

Status: RECRUITING

Clinical Research Site

New York, New York 10032 - United States

Status: RECRUITING

And 83 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2, PHASE3 clinical trial for Heart Failure, Left Ventricular Systolic Dysfunction:

  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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