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Immunoadsorption Therapy in Managing NMDAR Antibodies Encephalitis
Sponsor: Assistance Publique - Hôpitaux de Paris
Summary
The purpose of the study is to assess the efficacy of immunoadsorption therapy (IA) on improving the neurological status of severe pediatric anti-NMDAR encephalitis patients.
Official title: Prospective Assessment of Efficacy of Immunoadsorption Therapy in Managing Childhood NMDA-Receptor (NMDAR) Antibodies Encephalitis
Key Details
Gender
All
Age Range
Any - 18 Years
Study Type
INTERVENTIONAL
Enrollment
20
Start Date
2021-06-23
Completion Date
2026-06
Last Updated
2023-07-13
Healthy Volunteers
No
Conditions
Interventions
IA session
10 IA sessions performed in 28 days maximum, using TherasorbTM adsorbers which contain sheep derived polyvalent antihuman-immunoglobulin coupled to SepharoseTM CL-4B.
Rituximab
Concomitantly, Rituximab will be given each week for 4 weeks (one injection by week +/- 3 days): * at least 1 day before each IA session * the last injection will occur after the last session IA (minimum one day after)
Locations (1)
Hôpital Necker Enfants-Malades
Paris, France