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)

NCT05123703

Phase 3 Active not recruiting 188 enrolled Hoffmann-La Roche PPD Development, LP · collab
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

EvaluationDrugModalityDoseRoute
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