drugset / Trial / NCT01803867

An Intravenous Infusion Study of rHIgM22 in Patients With Multiple Sclerosis

NCT01803867 ↗

Phase 1 Completed 72 enrolled Acorda Therapeutics PRA Health Sciences · collab
RandomizedSingle-groupQuadruple-blindTreatment

Summary

This is a Phase I, multi-center, double-blind, randomized, placebo-controlled, dose-escalation study designed to evaluate safety, tolerability, pharmacokinetics, and immunogenicity of single intravenous (IV) administrations of rHIgM22 in patients with all clinical presentations of MS.

Timeline

Start
2013-03
Primary completion
2014-10
Completion
2015-01

Drugs

EvaluationDrugModalityDoseRoute
Comparator rHIgM22 Protein / enzyme biologic — Intravenous

Indications