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efficacy and tolerability of mycophenolate mofetil in patients with relapsing autoimmune encephalitis

efficacy and tolerability of mycophenolate mofetil in patients with relapsing autoimmune encephalitis

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100044362
Enrollment
Unknown
Registered
2021-03-17
Start date
2021-03-12
Completion date
Unknown
Last updated
2021-09-07

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

Conditions

Autoimmune Encephalitis

Interventions

Control:Routine first-line immunotherapy
test group:mycophenolate mofetil

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Aged 18-80 years, male or female. (2) one or more of the 8 core clinical manifestations: mental disorders, memory loss, language disorders, seizures, motor disorders, disturbance of consciousness, autonomic nerve dysfunction or central hypoventilation; (3) autoimmune encephalitis antibodies detected in cerebrospinal fluid [CBA method: (anti-NMDARGABAB-R and LGI1/CASPR2 antibody)]. (4) reasonable exclusion of other diseases. (5) AIE relapse for one time or more.

Exclusion criteria

Exclusion criteria: (1) Patients with (HIV) infection of human immunodeficiency virus, brain abscess, viral disease, brain malaria, brain tumor or non-communicable central nervous system disease (such as acute demyelinating encephalomyelitis (ADEM); (2) patients with central nervous system infection of viruses, bacteria, fungi, parasites or Mycobacterium tuberculosis (TB). (3) Encephalopathy secondary to septicemia or systemic inflammatory response syndrome; (4) patients diagnosed with epilepsy, brain trauma and/or other neurological diseases before the onset of encephalitis. (5) other autoimmune encephalitis patients with positive serum and/or CSF laboratory tests: a-amino 3-hydroxy-5-hydroxy-5-methyl-4-isoxazolyl-propionate (AMPA) receptor antibody encephalitis, glutamic acid decarboxylase (GAD) antibody encephalitis; (6) patients lacking key clinical data; (7) pregnant or breastfeeding patients. (8) patients with contraindications using MMF, such as severe infection, etc.

Design outcomes

Primary

MeasureTime frame
cognitive function and inflammatory factor;

Countries

China

Contacts

Public ContactZhen Hong

West China Hospital, Sichuan University

hongzhengoog@aliyun.com+86 18980605818

Outcome results

None listed

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