Patient Guide: Study to Evaluate Safety, Tolerability and Efficacy of Inclisiran in Children With Homozygous Familial Hypercholesterolemia

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 15 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06597006
Status: 🟢 Enrolling Now
Condition: Familial Hypercholesterolemia - Homozygous
Phase: PHASE3

Where You Can Participate

This study is available at 15 locations across the country.

Top locations include:
  • • San Francisco, California
  • • San Francisco, California
  • • Washington D.C., District of Columbia
  • • And 12 more locations

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Study to Evaluate Safety, Tolerability and Efficacy of Inclisiran in Children With Homozygous Familial Hypercholesterolemia - Join Clinical Trial NCTNCT06597006

How to Join This Clinical Trial - NCTNCT06597006

Learn how to participate in this PHASE3 trial studying an investigational therapy for Familial Hypercholesterolemia - Homozygous. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Familial Hypercholesterolemia - Homozygous
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06597006 - 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 15 locations. Find a study site near you:

Clinical Research Site

San Francisco, California 94143 - United States

Status: RECRUITING

Clinical Research Site

San Francisco, California 94143 - United States

Status: RECRUITING

Clinical Research Site

Washington D.C., District of Columbia 20010 - United States

Status: RECRUITING

Clinical Research Site

St Louis, Missouri 63110 - United States

Status: RECRUITING

Clinical Research Site

Vienna, 1090 - Austria

Status: RECRUITING

Clinical Research Site

Beijing, 100029 - China

Status: RECRUITING

Clinical Research Site

Ioannina, 455 00 - Greece

Status: RECRUITING

Clinical Research Site

Kota Bharu, Kelantan 16150 - Malaysia

Status: RECRUITING

Clinical Research Site

Amsterdam, North Holland 1105 AZ - Netherlands

Status: RECRUITING

Clinical Research Site

Bloemfontein, Free State 9301 - South Africa

Status: RECRUITING

And 5 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 Familial Hypercholesterolemia - Homozygous:

  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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