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RECRUITINGOBSERVATIONAL

Registry of Participants With Generalized Myasthenia Gravis Treated With Alexion C5 Inhibition Therapies (C5ITs)

Long-Term, Observational, Global Registry of Patients With Generalized Myasthenia Gravis Who Have Received Treatment With Complement C5 Inhibition Therapies (C5ITs)

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Long-term, multicenter, multinational, observational, registry of patients with gMG that is designed to collect data on clinical outcomes and safety in patients prescribed Alexion C5 inhibitor therapies (C5IT) such as eculizumab (Soliris®) and ravulizumab (Ultomiris®).

Who May Be Eligible (Plain English)

Who May Qualify: 1. Participants with a diagnosis of gMG who are treated with Alexion C5IT at the time of enrollment, including patients previously treated with Soliris or Ultomiris and withdrawn from treatment. 2. Capable of giving signed willing to sign a consent form, which includes compliance with the protocol requirements and restrictions. 3. Participants must have myasthenia gravis historical data, such as MG-ADL and MGFA class, available to be enrolled in the Registry. Who Should NOT Join This Trial: 1\. Participants currently enrolled in an Alexion-sponsored interventional clinical study for treatment of gMG cannot be enrolled in the Alexion gMG Registry while enrolled/participating in the clinical study for gMG therapy. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: 1. Participants with a diagnosis of gMG who are treated with Alexion C5IT at the time of enrollment, including patients previously treated with Soliris or Ultomiris and withdrawn from treatment. 2. Capable of giving signed informed consent, which includes compliance with the protocol requirements and restrictions. 3. Participants must have myasthenia gravis historical data, such as MG-ADL and MGFA class, available to be enrolled in the Registry. Exclusion Criteria: 1\. Participants currently enrolled in an Alexion-sponsored interventional clinical study for treatment of gMG cannot be enrolled in the Alexion gMG Registry while enrolled/participating in the clinical study for gMG therapy.

Locations (20)

Clinical Trial Site
Birmingham, Alabama, United States
Clinical Trial Site
Scottsdale, Arizona, United States
Clinical Trial Site
Fresno, California, United States
Clinical Trial Site
Orange, California, United States
Clinical Trial Site
Rancho Mirage, California, United States
Clinical Trial Site
Sylmar, California, United States
Clinical Trial Site
Colorado Springs, Colorado, United States
Clinical Trial Site
Fort Collins, Colorado, United States
Clinical Trial Site
New Haven, Connecticut, United States
Clinical Trial Site
Washington D.C., District of Columbia, United States
Clinical Trial Site
Clearwater, Florida, United States
Clincal Trial Site
Gainesville, Florida, United States
Clinical Trial Site
Jacksonville, Florida, United States
Clinical Trial Site
Tampa, Florida, United States
Clinical Trial Site
Augusta, Georgia, United States
Clinical Trial Site
Iowa City, Iowa, United States
Clinical Trial Site
Lexington, Kentucky, United States
Clinical Trial Site
Boston, Massachusetts, United States
Clinical Trial Site
Lansing, Michigan, United States
Clinical Trial Site
Columbia, Missouri, United States