Patient Guide: Evaluating Long-term Safety of Efgartigimod Administered Intravenously and Efgartigimod PH20 Administered Subcutaneously in Children With Generalized Myasthenia Gravis

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 12 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05374590
Status: ENROLLING_BY_INVITATION
Condition: Generalized Myasthenia Gravis
Phase: PHASE2, PHASE3

Where You Can Participate

This study is available at 12 locations across the country.

Top locations include:
  • • Chicago, Illinois
  • • Charlottesville, Virginia
  • • Edegem,
  • • And 9 more locations

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Evaluating Long-term Safety of Efgartigimod Administered Intravenously and Efgartigimod PH20 Administered Subcutaneously in Children With Generalized Myasthenia Gravis - Join Clinical Trial NCTNCT05374590

How to Join This Clinical Trial - NCTNCT05374590

Learn how to participate in this PHASE2, PHASE3 trial studying an investigational therapy for Generalized Myasthenia Gravis. Current status: ENROLLING_BY_INVITATION.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Generalized Myasthenia Gravis
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2, PHASE3 - Large-scale efficacy study
Enrollment Status
ENROLLING_BY_INVITATION
Study Identifier
NCTNCT05374590 - 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 12 locations. Find a study site near you:

Clinical Research Site

Chicago, Illinois 60611 - United States

Status: Contact for availability

Clinical Research Site

Charlottesville, Virginia 22903 - United States

Status: Contact for availability

Clinical Research Site

Edegem, 2650 - Belgium

Status: Contact for availability

Clinical Research Site

Marseille, 13005 - France

Status: Contact for availability

Clinical Research Site

Essen, 45147 - Germany

Status: Contact for availability

Clinical Research Site

Leiden, 2333 ZA - Netherlands

Status: Contact for availability

Clinical Research Site

Gdańsk, 80-211 - Poland

Status: Contact for availability

Clinical Research Site

Katowice, 40-123 - Poland

Status: Contact for availability

Clinical Research Site

Warszawa, 02-097 - Poland

Status: Contact for availability

Clinical Research Site

Valencia, 46026 - Spain

Status: Contact for availability

And 2 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, PHASE3 clinical trial for Generalized Myasthenia Gravis:

  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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