Patient Guide: A Study to Evaluate the Efficacy and Safety of Enlicitide Decanoate (MK-0616, Oral PCSK9 Inhibitor) Compared With Ezetimibe or Bempedoic Acid or Ezetimibe and Bempedoic Acid in Adults With Hypercholesterolemia (MK-0616-018) CORALreef AddOn

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 35 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06450366
Status: ACTIVE_NOT_RECRUITING
Condition: Hypercholesterolemia
Phase: PHASE3

Where You Can Participate

This study is available at 35 locations across the country.

Top locations include:
  • • Lincoln, California
  • • Flossmoor, Illinois
  • • Louisville, Kentucky
  • • And 32 more locations

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A Study to Evaluate the Efficacy and Safety of Enlicitide Decanoate (MK-0616, Oral PCSK9 Inhibitor) Compared With Ezetimibe or Bempedoic Acid or Ezetimibe and Bempedoic Acid in Adults With Hypercholesterolemia (MK-0616-018) CORALreef AddOn - Join Clinical Trial NCTNCT06450366

How to Join This Clinical Trial - NCTNCT06450366

Learn how to participate in this PHASE3 trial studying an investigational therapy for Hypercholesterolemia. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Hypercholesterolemia
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06450366 - 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 35 locations. Find a study site near you:

Clinical Research Site

Lincoln, California 95648 - United States

Status: Contact for availability

Clinical Research Site

Flossmoor, Illinois 60422 - United States

Status: Contact for availability

Clinical Research Site

Louisville, Kentucky 40213 - United States

Status: Contact for availability

Clinical Research Site

Rockville, Maryland 20854 - United States

Status: Contact for availability

Clinical Research Site

Gulfport, Mississippi 39503 - United States

Status: Contact for availability

Clinical Research Site

Fort Mill, South Carolina 29707 - United States

Status: Contact for availability

Clinical Research Site

Renton, Washington 98057 - United States

Status: Contact for availability

Clinical Research Site

Mar del Plata, Buenos Aires B7600FZO - Argentina

Status: Contact for availability

Clinical Research Site

Buenos Aires, Caba C1061AAS - Argentina

Status: Contact for availability

Clinical Research Site

Rosario, Santa Fe S2000DEJ - Argentina

Status: Contact for availability

And 25 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Hypercholesterolemia:

  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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