Patient Guide: A Study of EPX-100 (Clemizole Hydrochloride) in Participants 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 46 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04462770
Status: 🟢 Enrolling Now
Condition: Dravet Syndrome
Phase: PHASE3

Where You Can Participate

This study is available at 46 locations across the country.

Top locations include:
  • • Los Angeles, California
  • • Orange, California
  • • San Francisco, California
  • • And 43 more locations

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A Study of EPX-100 (Clemizole Hydrochloride) in Participants With Dravet Syndrome - Join Clinical Trial NCTNCT04462770

How to Join This Clinical Trial - NCTNCT04462770

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
NCTNCT04462770 - 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 46 locations. Find a study site near you:

Clinical Research Site

Los Angeles, California 90027 - United States

Status: TERMINATED

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

New Haven, Connecticut 06510 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Wilmington, Delaware 19803 - United States

Status: RECRUITING

Clinical Research Site

Kissimmee, Florida 34746 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Winter Park, Florida 32789 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Atlanta, Georgia 30328 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Chicago, Illinois 60611 - United States

Status: WITHDRAWN

Clinical Research Site

Louisville, Kentucky 40202 - United States

Status: NOT_YET_RECRUITING

And 36 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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