drugset / Trial / NCT03943589

A Study of Imlifidase in Patients With Guillain-Barré Syndrome

NCT03943589

Phase 2 Completed 30 enrolled Hansa Biopharma AB
NaSingle-groupOpen-labelTreatment

Summary

The study participants are patients which have been diagnosed with Guillain-Barré Syndrome (GBS) and are planned to receive treatment with intravenous immunoglobulin (IVIg). IVIg is a standard of care treatment for GBS patients. The patients in this study will be treated with the study medicine imlifidase on day 1, and with IVIg on days 3-7. The purpose of this study is to investigate the safety and effectiveness of imlifidase in patients diagnosed with GBS.

Timeline

Start
2019-11-12
Primary completion
2024-02-27
Completion
2024-02-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Imlifidase Protein / enzyme biologic 0.25 mg/kg Intravenous