drugset / Trial / NCT02306811

Efficacy and Safety of Vatelizumab in Patients Who Completed Treatment in Study DRI13839

NCT02306811 ↗

Phase 2 Terminated 62 enrolled Genzyme, a Sanofi Company
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Primary Objective: To assess the long-term safety of vatelizumab in MS patients Secondary Objective: To assess the long-term efficacy of vatelizumab

Timeline

Start
2015-02
Primary completion
2016-04
Completion
2016-07

Outcome

Outcome not reported

Stopped: “Study discontinued based on planned interim analysis of the primary endpoint. Not linked to any safety concern.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Vatelizumab Monoclonal antibody — Intravenous