Patient Guide: Study of Efficacy and Safety of Inclisiran in Asian Participants With Atherosclerotic Cardiovascular Disease (ASCVD) or ASCVD High Risk and Elevated Low Density Lipoprotein Cholesterol (LDL-C)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 45 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04765657
Status: ACTIVE_NOT_RECRUITING
Condition: Hypercholesterolemia
Phase: PHASE3

Where You Can Participate

This study is available at 45 locations across the country.

Top locations include:
  • • Lanzhou, Gansu
  • • Foshan, Guangdong
  • • Guangzhou, Guangdong
  • • And 42 more locations

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Study of Efficacy and Safety of Inclisiran in Asian Participants With Atherosclerotic Cardiovascular Disease (ASCVD) or ASCVD High Risk and Elevated Low Density Lipoprotein Cholesterol (LDL-C) - Join Clinical Trial NCTNCT04765657

How to Join This Clinical Trial - NCTNCT04765657

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
NCTNCT04765657 - 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 45 locations. Find a study site near you:

Clinical Research Site

Lanzhou, Gansu 730030 - China

Status: Contact for availability

Clinical Research Site

Foshan, Guangdong 528000 - China

Status: Contact for availability

Clinical Research Site

Guangzhou, Guangdong 510080 - China

Status: Contact for availability

Clinical Research Site

Baotou, Inner Mongolia 014040 - China

Status: Contact for availability

Clinical Research Site

Hohhot, Inner Mongolia 010017 - China

Status: Contact for availability

Clinical Research Site

Nanjing, Jiangsu 210008 - China

Status: Contact for availability

Clinical Research Site

Nanjing, Jiangsu 211166 - China

Status: Contact for availability

Clinical Research Site

Nantong, Jiangsu 226000 - China

Status: Contact for availability

Clinical Research Site

Suzhou, Jiangsu 215004 - China

Status: Contact for availability

Clinical Research Site

Xuzhou, Jiangsu 221003 - China

Status: Contact for availability

And 35 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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