Skip to content

Mycophenolate Mofetil Treatment of Neuromyelitis Optica in Chinese Patients (MONICA)

Mycophenolate Mofetil Treatment of Neuromyelitis Optica in Chinese Patients (MONICA)

Status
Recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPB-16007730
Enrollment
Unknown
Registered
2016-01-09
Start date
2016-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Neuromyelitis optica

Interventions

Case series:Mycophenolate Mofetil

Sponsors

The third affiliated hospital,Sun Yat-sen university
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: (1) 2006 NMO diagnostic criteria or NMOSD criteria; (2) serum NMO-IgG(+) (HEK 293 cells transfection method); (3) aged 18-65 years old, men and women; (4) relapse frequency: two or more attacks in the prior two years, one or more in the recent one year; (5) EDSS less than 7.0, and at least one eye visual acuity of 20/100; (6) written informed consent signed.

Exclusion criteria

Exclusion criteria: (1) using other immunosuppressants, such as cyclophosphamide, cyclosporin A,azathioprine, methotrexate; (2) with concomitant diseases: transaminase 2 times more than normal ceiling; The WBC <4*10^9/L, HGB <80 g/L, PLT <100*10^9/L; (3) with severe cardiovascular, liver, kidney and other important organs and blood, endocrine system diseases; (4) with immunodeficiency, with uncontrolled infections and active gastrointestinal diseases (such as stomach ulcers, etc.); (5) women of childbearing agewith postive urine pregnancy test, lactatin; (6) being allergic to mycophenolate mofetil and prednisone.

Design outcomes

Primary

MeasureTime frame
annual relapse rate;

Countries

China

Contacts

Public ContactQiu Wei
qw9406@gmail.com+86 15899968330

Outcome results

None listed

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