A Phase 2 interventional study of Neramexane mesylate in Nystagmus, Congenital, Nystagmus, Acquired and Multiple Sclerosis, sponsored by Merz Pharmaceuticals GmbH. Terminated at 1 site in United Kingdom. Open to participants aged 18 Years to 81 Years. Per ClinicalTrials.gov, last updated 2010-07-01.
Sponsored by Merz Pharmaceuticals GmbH (part of Merz Pharma) · Phase 2, Interventional, and Treatment
The purpose of this study is to investigate the long-term safety, tolerability and efficacy of neramexane mesylate in the treatment of congenital idiopathic nystagmus (CIN). In addition, a subgroup of multiple sclerosis (MS) patients suffering from acquired nystagmus will be included.
27 studies on the registry are indexed under Nystagmus, Pathologic; 3 are open to participants now.
This study's planned enrollment of 48 is close to the median of 48 across 17 interventional studies indexed under Nystagmus, Pathologic.
Browse Nystagmus, Pathologic studies →Merz Pharmaceuticals GmbH is the lead sponsor of 61 studies on the registry; none are open to participants now.
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Exclusion Criteria:
open-label treatment of 36 months Neramexane mesylate up to 75 mg per day
Long-term safety, Visual acuity
Time frame: Baseline, week 4, month 3, 6, 9, 12, 18, 24, 30, 36 and follow-up
This study is terminated, as verified in Jun 2010. You cannot join it, but the record below documents what was studied.
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Studies of the drug tested here: Neramexane mesylate