Patient Guide: Registry Study to Observe Long-term Safety of Vamorolone (AGAMREE®) in Patients With Duchenne Muscular Dystrophy.

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 25 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06564974
Status: 🟢 Enrolling Now
Condition: Duchenne Muscular Dystrophy
Phase: Not Specified

Where You Can Participate

This study is available at 25 locations across the country.

Top locations include:
  • • Phoenix, Arizona
  • • Little Rock, Arkansas
  • • Los Angeles, California
  • • And 22 more locations

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Registry Study to Observe Long-term Safety of Vamorolone (AGAMREE®) in Patients With Duchenne Muscular Dystrophy. - Join Clinical Trial NCTNCT06564974

How to Join This Clinical Trial - NCTNCT06564974

Learn how to participate in this Not Specified trial studying an investigational therapy for Duchenne Muscular Dystrophy. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Duchenne Muscular Dystrophy
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06564974 - 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 25 locations. Find a study site near you:

Clinical Research Site

Phoenix, Arizona 85016 - United States

Status: RECRUITING

Clinical Research Site

Little Rock, Arkansas 72202 - United States

Status: RECRUITING

Clinical Research Site

Los Angeles, California 90027 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Palo Alto, California 94305 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Sacramento, California 95817 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Gainesville, Florida 32610 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Miami, Florida 33155 - United States

Status: RECRUITING

Clinical Research Site

Orlando, Florida 32827 - United States

Status: RECRUITING

Clinical Research Site

Chicago, Illinois 60611 - United States

Status: RECRUITING

Clinical Research Site

Indianapolis, Indiana 46202 - United States

Status: NOT_YET_RECRUITING

And 15 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Duchenne Muscular Dystrophy:

  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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