drugset / Trial / NCT03864185
The Evaluation of Efficacy and Safety of Rituximab in Refractory CIDP Patients With IgG4 Autoantibodies
Phase 2
Completed
25 enrolled
Nagoya University
Japan Agency for Medical Research and Development · collabZenyaku Kogyo Co., Ltd. · collab
RandomizedParallel-groupQuadruple-blindTreatment
Summary
To evaluate the efficacy and safety of rituximab (genetical recombination) intravenously administered to CIDP patients with positive or negative IgG4 autoantibody.
Timeline
- Start
- 2019-03-28
- Primary completion
- 2021-05-27
- Completion
- 2021-05-27
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Rituximab | Monoclonal antibody | 375 mg/m2 | Intravenous |