drugset / Trial / NCT05123703
A Study to Evaluate Safety and Efficacy of Ocrelizumab in Comparison With Fingolimod in Children and Adolescents With Relapsing-remitting Multiple Sclerosis (RRMS)
RandomizedParallel-groupQuadruple-blindTreatment
Summary
This double-blind, double-dummy study will evaluate the safety and efficacy of ocrelizumab compared with fingolimod in children and adolescents with RRMS aged between 10 and \< 18 years over a flexible duration. The double-blind period will last until after the last participant randomized has completed 24 weeks.
Timeline
- Start
- 2022-05-19
- Primary completion
- 2025-06-09
- Completion
- 2029-09-17
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Fingolimod | Small molecule | 0.25 mg | Oral |
| Comparator | Fingolimod | Small molecule | 0.5 mg | Oral |
| Subject | Ocrelizumab | Monoclonal antibody | 300 mg | Intravenous |
| Subject | Ocrelizumab | Monoclonal antibody | 600 mg | Intravenous |