drugset / Trial / NCT05503264

A Study to Evaluate the Efficacy, Safety, Pharmacokinetics (PK), and Pharmacodynamics (PD) of Satralizumab in Participants With Anti-N-methyl-D-aspartic Acid Receptor (NMDAR) or Anti-leucine-rich Glioma-inactivated 1 (LGI1) Encephalitis

NCT05503264

Phase 3 Active not recruiting 122 enrolled Hoffmann-La Roche Chugai Pharmaceutical · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to assess the efficacy, safety, PK, and PD of satralizumab in participants with NMDAR and LGI1 encephalitis.

Timeline

Start
2022-09-27
Primary completion
2026-12-16
Completion
2028-12-14

Drugs

EvaluationDrugModalityDoseRoute
Subject Satralizumab Monoclonal antibody Subcutaneous