drugset / Trial / NCT02398461

An Intravenous Infusion Study of rHIgM22 in Patients With Multiple Sclerosis Immediately Following a Relapse

NCT02398461 ↗

Phase 1 Completed 27 enrolled Acorda Therapeutics PRA Health Sciences · collab
RandomizedSingle-groupQuadruple-blindTreatment

Summary

This is a Phase 1, multi-center, double-blind, randomized, placebo-controlled, dose-escalation study in subjects with relapsing Multiple Sclerosis (MS). The primary outcome will be the safety and tolerability of a single dose of rHIgM22 in relapsing MS subjects.

Timeline

Start
2015-04
Primary completion
2017-09
Completion
2017-09-21

Drugs

EvaluationDrugModalityDoseRoute
Subject rHIgM22 Protein / enzyme biologic 0.5 mg/kg Intravenous
Subject rHIgM22 Protein / enzyme biologic 2 mg/kg Intravenous

Indications