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

Status: Recruiting
Location: See all (40) locations...
Study Type: Observational
SUMMARY

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®).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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with Alexion C5IT at the time of enrollment, including patients previously treated with Soliris or Ultomiris and withdrawn from treatment.

• Capable of giving signed informed consent, which includes compliance with the protocol requirements and restrictions.

• Participants must have myasthenia gravis historical data, such as MG-ADL and MGFA class, available to be enrolled in the Registry.

Locations
United States
Alabama
Clinical Trial Site
RECRUITING
Birmingham
Arizona
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Scottsdale
California
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Fresno
Clinical Trial Site
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Orange
Clinical Trial Site
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Rancho Mirage
Clinical Trial Site
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Sylmar
Colorado
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Colorado Springs
Clinical Trial Site
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Fort Collins
Connecticut
Clinical Trial Site
RECRUITING
New Haven
Washington, D.c.
Clinical Trial Site
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Washington D.c.
Florida
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Clearwater
Clincal Trial Site
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Gainesville
Clinical Trial Site
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Jacksonville
Clinical Trial Site
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Tampa
Georgia
Clinical Trial Site
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Augusta
Iowa
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Iowa City
Kentucky
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Lexington
Massachusetts
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Boston
Michigan
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Lansing
Missouri
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Columbia
North Carolina
Clinical Trial Site
RECRUITING
Chapel Hill
Clinical Trial Site
RECRUITING
Charlotte
Clinical Trial Site
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Durham
New York
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New Hyde Park
Ohio
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Dayton
Pennsylvania
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Philadelphia
Tennessee
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Chattanooga
Clinical Trial Site
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Knoxville
Texas
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Dallas
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Houston
Vermont
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Burlington
Wisconsin
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Milwaukee
Other Locations
Austria
Clinical Trial Site
RECRUITING
Vienna
Canada
Clinical Trial Site
RECRUITING
Brampton
Clinical Trial Site
RECRUITING
London
Clinical Trial Site
RECRUITING
Montreal
China
Clinical Trial Site
RECRUITING
Chengdu
Germany
Clinical Trial Site
RECRUITING
Hanover
Italy
Clinical Trial Site
RECRUITING
Milan
Clinical Trial Site
RECRUITING
Naples
Contact Information
Primary
Alexion Pharmaceuticals, Inc. (Sponsor)
clinicaltrials@alexion.com
1-855-752-2356
Time Frame
Start Date: 2019-12-02
Estimated Completion Date: 2029-12-31
Participants
Target number of participants: 500
Related Therapeutic Areas
Sponsors
Leads: Alexion Pharmaceuticals, Inc.

This content was sourced from clinicaltrials.gov