drugset / Trial / NCT00624468

Atacicept in Subjects With Optic Neuritis

NCT00624468

Phase 2 Terminated 34 enrolled EMD Serono Merck KGaA, Darmstadt, Germany · collab
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This study was intended to evaluate the efficacy, safety and tolerability of atacicept compared to placebo and to explore the neuroprotective effect of atacicept as assessed by OCT in subjects with ON as CIS. The study was randomized. Study medication was administered via subcutaneous (under the skin) injections.

Timeline

Start
2008-06
Primary completion
2009-09
Completion
2011-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Atacicept Protein / enzyme biologic 150 mg Subcutaneous

Indications