Ampyra for Optic Neuritis in Multiple Sclerosis
Completed · Phase 2/Phase 3 · Has a placebo group
Conditions studied: Multiple Sclerosis, Optic Neuritis
In brief
Fifty subjects will be enrolled in this Phase II, investigator-initiated, randomized and blinded cross-over trial of dalfampridine of 8 weeks duration The study will test the hypothesis that dalfampridine, when administered to subjects with incomplete visual recovery after optic neuritis from MS, will result in symptomatic improvement in visual function. The study will consist of one screening/baseline visit, one visit during treatment with active drug, and one visit on placebo. After the baseline visit, subjects will be randomly assigned to receive study medication or placebo for the first three weeks, followed by a two week wash-out, and then treatment reallocation for the latter three weeks.
Key facts
- Study ID
- NCT01337986
- Run by
- Washington University School of Medicine
- People needed
- 53
- Starts
- 2011-05-01
- Expected to finish
- 2013-12-01
- Last updated by the study team
- 2020-01-30
Who can join
Age: 18 and older, up to 55. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Washington University (John L. Trotter MS Center) — St Louis, Missouri, United States
Full record on ClinicalTrials.gov
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