drugset / Trial / NCT03277248

Study to Assess the Efficacy and Safety of Ublituximab in Participants With Relapsing Forms of Multiple Sclerosis (RMS)

NCT03277248 ↗

Phase 3 Completed 545 enrolled TG Therapeutics, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study determines the Annualized Relapse Rate (ARR) in participants with RMS after 96 weeks (approximately 2 years) treatment with intravenous (IV) infusion of ublituximab/oral placebo compared to 14 mg oral teriflunomide/IV placebo.

Timeline

Start
2017-08-25
Primary completion
2020-08-04
Completion
2020-11-12

Outcome

Met primary endpoint

registry analysis (superiority test); Ublituximab + Oral Placebo vs Teriflunomide + IV Placebo; p = 0.0022; Rate Ratio (Ublituximab / Teriflunomide) 0.509 (95% CI 0.330 to 0.784); NCT03277248 ↗

Drugs

EvaluationDrugModalityDoseRoute
Comparator Teriflunomide Small molecule 14 mg Oral
Subject Ublituximab Monoclonal antibody 450 mg Intravenous