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

PHASE2CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

May 31, 2008

Conditions
Nystagmus, Congenital IdiopathicNystagmus, Acquired
Interventions
DRUG

Neramexane mesylate

2 double-blind, cross-over treatment periods of 7 weeks separated by a wash-out phase, up to 75 mg Neramexane mesylate per day

Trial Locations (1)

LE2 7LX

University of Leicester, Leicester Royal Infirmary, Ophthalmology Group, Leicester

Sponsors
All Listed Sponsors
lead

Merz Pharmaceuticals GmbH

INDUSTRY

NCT00661440 - Efficacy and Safety Study of Neramexane to Treat Congenital and Acquired Nystagmus | Biotech Hunter | Biotech Hunter