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Efficacy and Safety of Novel Biologics in Myasthenia Gravis: A prospective cohort study

Efficacy and Safety of Novel Biologics in Myasthenia Gravis: A prospective cohort study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300077188
Enrollment
Unknown
Registered
2023-11-01
Start date
2023-11-01
Completion date
Unknown
Last updated
2023-11-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Myasthenia Gravis

Interventions

Treated with novel biologics:None

Sponsors

The First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 95 Years

Inclusion criteria

Inclusion criteria: 1) Patients with MG = 18 years of age; 2) MGFA Class II-IV; 3) QMG score =6; 4) Not treated or receiving a stable dose of MG treatments.

Exclusion criteria

Exclusion criteria: 1) Have been treated with novel biologics (including rituximab, olfatumumab, eculizumab, efgartigimod, etc.) in the pase 6 months. 2) Had a thymectomy inthe past 3 months. 3) Have been treated with IVIg/plasma exchange in the past month. 4) Suffering from active hepatitis B, or hepatitis C antibody positive, or HIV antibody positive and low CD4 count. 5) Female patients who are pregnant. 6) Suffering from other serious chronic diseases that may affect the evaluation.

Design outcomes

Primary

MeasureTime frame
QMG;

Secondary

MeasureTime frame
MG-ADL;IgG;Cytokine;Deterioration & recurrence rate;Myasthenia gravis related antibodies;

Countries

China

Contacts

Public ContactXiuming Guo

The First Affiliated Hospital of Chongqing Medical University

xmguo813@163.com+86 151 7888 5505

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026