drugset / Trial / NCT00642902

A Phase 2 Study of Atacicept in Subjects With Relapsing Multiple Sclerosis (ATAMS)

NCT00642902

Phase 2 Terminated 255 enrolled EMD Serono
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To evaluate the safety and tolerability of atacicept and to explore if atacicept reduces central nervous system inflammation in subjects with relapsing multiple sclerosis (RMS) as assessed by frequent magnetic resonance imaging (MRI). This study is randomised. Study medication is administered via subcutaneous (under the skin) injections.

Timeline

Start
2008-04
Primary completion
2009-09
Completion
2009-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Atacicept Protein / enzyme biologic 25 mg Subcutaneous
Subject Atacicept Protein / enzyme biologic 75 mg Subcutaneous
Subject Atacicept Protein / enzyme biologic 150 mg Subcutaneous

Indications