drugset / Trial / NCT01194570

A Study of Ocrelizumab in Participants With Primary Progressive Multiple Sclerosis

NCT01194570 ↗

Phase 3 Completed 735 enrolled Hoffmann-La Roche
RandomizedParallel-groupDouble-blindTreatment

Summary

This randomized, parallel group, double-blind, placebo controlled study will evaluate the efficacy and safety of ocrelizumab in participants with primary progressive multiple sclerosis. Eligible participants will be randomized 2 : 1 to receive either ocrelizumab or placebo.

Timeline

Start
2011-03-02
Primary completion
2015-07-23
Completion
2022-12-31

Outcome

Met primary endpoint

paper 32.9% with ocrelizumab versus 39.3% with placebo (hazard ratio, 0.76; 95% confidence interval [CI], 0.59 to 0.98; P=0.03). PMID 28002688 ↗

release “In a separate PPMS study (ORATORIO), OCREVUS significantly reduced the risk of confirmed disability progression sustained for at least 12 weeks (primary endpoint)” gene.com ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ocrelizumab Monoclonal antibody 600 mg Intravenous