drugset / Trial / NCT00661440

Efficacy and Safety Study of Neramexane to Treat Congenital and Acquired Nystagmus

NCT00661440 ↗

Phase 2 Completed 48 enrolled Merz Pharmaceuticals GmbH
RandomizedCrossoverDouble-blindTreatment

Summary

The purpose of this study is to investigate the safety and efficacy of neramexane mesylate in the treatment of congenital idiopathic nystagmus (CIN) in comparison to placebo. In addition, a subgroup of multiple sclerosis (MS) patients suffering from acquired nystagmus will be included; this subgroup will be analyzed in an exploratory manner only.

Timeline

Start
2008-05
Primary completion
—
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject Neramexane Small molecule 75 mg —

Indications