Patient Guide: Zilebesiran as Add-on Therapy in Patients With High Cardiovascular Risk and Hypertension Not Adequately Controlled by Standard of Care Antihypertensive Medications (KARDIA-3)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 193 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06272487
Status: ACTIVE_NOT_RECRUITING
Condition: High Cardiovascular Risk, Hypertension
Phase: PHASE2

Where You Can Participate

This study is available at 193 locations across the country.

Top locations include:
  • • Alexander City, Alabama
  • • Daphne, Alabama
  • • Foley, Alabama
  • • And 190 more locations

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Zilebesiran as Add-on Therapy in Patients With High Cardiovascular Risk and Hypertension Not Adequately Controlled by Standard of Care Antihypertensive Medications (KARDIA-3) - Join Clinical Trial NCTNCT06272487

How to Join This Clinical Trial - NCTNCT06272487

Learn how to participate in this PHASE2 trial studying an investigational therapy for High Cardiovascular Risk, Hypertension. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
High Cardiovascular Risk, Hypertension
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06272487 - 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 193 locations. Find a study site near you:

Clinical Research Site

Alexander City, Alabama 35010 - United States

Status: Contact for availability

Clinical Research Site

Daphne, Alabama 36606 - United States

Status: Contact for availability

Clinical Research Site

Foley, Alabama 36535 - United States

Status: Contact for availability

Clinical Research Site

Huntsville, Alabama 35801 - United States

Status: Contact for availability

Clinical Research Site

Huntsville, Alabama 35805 - United States

Status: Contact for availability

Clinical Research Site

Montgomery, Alabama 36117 - United States

Status: Contact for availability

Clinical Research Site

Gilbert, Arizona 85297 - United States

Status: Contact for availability

Clinical Research Site

Phoenix, Arizona 85028 - United States

Status: Contact for availability

Clinical Research Site

Sun City, Arizona 85351 - United States

Status: Contact for availability

Clinical Research Site

Tempe, Arizona 85283 - United States

Status: Contact for availability

And 183 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 clinical trial for High Cardiovascular Risk, Hypertension:

  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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