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NCT06700616Active, not recruiting

A Study in Patients With Myasthenia Gravis in China

A Multicenter, Prospective Cohort Study in Patients With Myasthenia Gravis in China

Source: ClinicalTrials.gov · Last updated 18 Sept 2026

Brief summary (registry, in English)

This study is a multi-center, prospective cohort study designed to characterize current clinical practice, clinical and patient-reported outcomes (PROs), disease prognosis, treatment patterns and healthcare resource utilization for Chinese patients with myasthenia gravis (MG). This study will enroll patients with MG as diagnosed by physician. Approximately 1,200 MG patients are intended to be recruited from approximately 40 sites across majority of regions in China. The clinical and PROs included MGFA class, MGFA PIS, MG-ADL (Activities of Daily Living), QMG (Quantitative MG score), MG QOL-15R, EQ-5D etc. All MG patients enrolled will be followed up every 6 months until end of 2027.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
1199 (actual)
First submitted
30 Sept 2024
Start date
26 Sept 2024
Primary completion date
30 Dec 2027
Lead sponsor
AstraZeneca
NCT number
NCT06700616

What you commit to

  • Study type: Observational
  • Participants enrolled: 1199
  • From 26 Sept 2024 to the primary completion date, 30 Dec 2027
  • 20 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • Patients aged ≥18 years with ocular myasthenia gravis (MGFA class I) lasting for more than 2 years;

Other

  • Patients who are currently participating in an interventional clinical trial cannot be enrolled in this study.

Who the study is looking for

  • This study will enroll patients of all ages who are diagnosed with MG of all MGFA classifications by physicians.
  • Patients must have the following data to be enrolled in this study:
    • MGFA classification
    • MG-ADL score
  • MG patients or their legal guardians/representatives are able to sign the Informed Consent Form (ICF).

Age in the registry: 0 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (20)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Research Site
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BeijingChinaUnknown status
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ChengduChinaUnknown status
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FuzhouChinaUnknown status
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GuangzhouChinaUnknown status
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GuiyangChinaUnknown status
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HarbinChinaUnknown status
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HebeiChinaUnknown status
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HenanChinaUnknown status
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Inner MongoliaChinaUnknown status
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JiangsuChinaUnknown status
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LanzhouChinaUnknown status
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NanningChinaUnknown status
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QingdaoChinaUnknown status
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TaiyuanChinaUnknown status
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TianjinChinaUnknown status
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ÜrümqiChinaUnknown status
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WenzhouChinaUnknown status
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WuhanChinaUnknown status
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Xi'anChinaUnknown status
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YinchuanChinaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.