Overview

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

Status:
Completed
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
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.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Merz Pharmaceuticals GmbH
Criteria
Inclusion Criteria:

- patients with congenital idiopathic nystagmus or acquired nystagmus subsequent to
multiple sclerosis

- male or female outpatients

- aged between 18 and 80 years (inclusive) at screening

Exclusion Criteria:

- patients with evidence of neurologic disorders other than CIN such as congenital
nystagmus due to albinism or retinal diseases and/or acquired nystagmus (exemption:
secondary to MS)