Patient Guide: Long-term Safety and Tolerability of Inclisiran in Participants With HeFH or HoFH Who Have Completed the Adolescent ORION-16 or ORION-13 Studies

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 51 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05682378
Status: ACTIVE_NOT_RECRUITING
Condition: Heterozygous or Homozygous Familial Hypercholesterolemia
Phase: PHASE3

Where You Can Participate

This study is available at 51 locations across the country.

Top locations include:
  • • Boca Raton, Florida
  • • New York, New York
  • • Cincinnati, Ohio
  • • And 48 more locations

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Long-term Safety and Tolerability of Inclisiran in Participants With HeFH or HoFH Who Have Completed the Adolescent ORION-16 or ORION-13 Studies - Join Clinical Trial NCTNCT05682378

How to Join This Clinical Trial - NCTNCT05682378

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

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Heterozygous or Homozygous Familial Hypercholesterolemia
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05682378 - 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 51 locations. Find a study site near you:

Clinical Research Site

Boca Raton, Florida 33434 - United States

Status: Contact for availability

Clinical Research Site

New York, New York 10029 - United States

Status: Contact for availability

Clinical Research Site

Cincinnati, Ohio 45229-3039 - United States

Status: Contact for availability

Clinical Research Site

Pittsburgh, Pennsylvania 15224 - United States

Status: Contact for availability

Clinical Research Site

Salt Lake, Utah 84113 - United States

Status: Contact for availability

Clinical Research Site

Ciudad de Formosa, Formosa P3600 - Argentina

Status: Contact for availability

Clinical Research Site

Fortaleza, Ceara 60430275 - Brazil

Status: Contact for availability

Clinical Research Site

Sao Paulo, SP 04023-900 - Brazil

Status: Contact for availability

Clinical Research Site

Sao Paulo, SP 05403 000 - Brazil

Status: Contact for availability

Clinical Research Site

Quebec, G1V 4W2 - Canada

Status: Contact for availability

And 41 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 Heterozygous or Homozygous Familial 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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