Encephalitis Clinical Trials

Find Encephalitis Clinical Trials Near You

Medium-term Effects of Treatments in Autoimmune Encephalitis (META): a Real-life, Observational Prospective Study

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Observational
SUMMARY

Autoimmune encephalitides are severe neurological disorders requiring urgent treatment, even though there is no standard guideline by lack of empirical evidence. Commonly used treatments are divided into so-called first-line (steroids, intravenous immunoglobulins, plasma exchanges) and second-line (rituximab, cyclophosphamide, tocilizumab, others), and may be used in association or sequentially. There is no standard practice, and initial treatment protocol may consist in first-line alone, first-line with rituximab, or first-line with dual immunosuppression (rituximab and cyclophosphamide). Absence of clear response to initial treatment in the first 4 to 6 weeks may indicate undertreatment and is generally followed by treatment escalation, mostly to dual immunosuppression. However, as the frequency of non-responders to initial treatment is unknown, it is still unclear whether dual immunosuppression should be offered to all patients from inception.

Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:

• Adult or child patient with encephalitis defined as anti-GAD, NMDAR, LGI1, CASPR2, IgLON5 or GFAP

• Untreated or with a decision to treat within the previous 30 days.

Locations
Other Locations
France
Hospices Civil de Lyon
RECRUITING
Bron
Contact Information
Primary
Bastien Pr JOUBERT
bastien.joubert@chu-lyon.fr
04 78 86 17 89
Backup
Géraldine PICARD
geraldine.picard@chu-lyon.fr
04.72.35.58.42
Time Frame
Start Date: 2024-09-01
Estimated Completion Date: 2027-03-01
Participants
Target number of participants: 200
Treatments
group 1 : Patients with NMDAR encephalitis
Patients with untreated anti-NMDAR encephalitis or with a decision to treat within the previous 30 days
group 2 : Patients with GAD encephalitis
Patients with untreated anti-GAD encephalitis or with a decision to treat within the previous 30 days
group 3 : Patients with LGI1 encephalitis
Patients with untreated anti-LGI1 encephalitis or with a decision to treat within the previous 30 days
group 4 : Patients with IgLON5 encephalitis
Patients with untreated anti-IgLON5 encephalitis or with a decision to treat within the previous 30 days
group 5 : Patients with GFAP encephalitis
Patients with untreated anti-GFAP encephalitis or with a decision to treat within the previous 30 days
group 6 : Patients with CASPR2 encephalitis
Patients with untreated anti-CASPR2 encephalitis or with a decision to treat within the previous 30 days
Related Therapeutic Areas
Sponsors
Leads: Hospices Civils de Lyon

This content was sourced from clinicaltrials.gov