Patient Guide: A Double-blind Study Evaluating the Efficacy, Safety, and Tolerability of Zorevunersen in Patients With Dravet Syndrome

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 41 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06872125
Status: 🟢 Enrolling Now
Condition: Dravet Syndrome
Phase: PHASE3

Where You Can Participate

This study is available at 41 locations across the country.

Top locations include:
  • • Phoenix, Arizona
  • • Little Rock, Arkansas
  • • Los Angeles, California
  • • And 38 more locations

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A Double-blind Study Evaluating the Efficacy, Safety, and Tolerability of Zorevunersen in Patients With Dravet Syndrome - Join Clinical Trial NCTNCT06872125

How to Join This Clinical Trial - NCTNCT06872125

Learn how to participate in this PHASE3 trial studying an investigational therapy for Dravet Syndrome. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Dravet Syndrome
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06872125 - 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 41 locations. Find a study site near you:

Clinical Research Site

Phoenix, Arizona 85016 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Little Rock, Arkansas 72202 - United States

Status: RECRUITING

Clinical Research Site

Los Angeles, California 90048 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Orange, California 92868 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

San Francisco, California 94158 - United States

Status: RECRUITING

Clinical Research Site

Aurora, Colorado 80045 - United States

Status: RECRUITING

Clinical Research Site

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

Status: NOT_YET_RECRUITING

Clinical Research Site

Jacksonville, Florida 32207 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Miami, Florida 33155 - United States

Status: RECRUITING

Clinical Research Site

Orlando, Florida 32804 - United States

Status: NOT_YET_RECRUITING

And 31 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 Dravet Syndrome:

  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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