154
Participants
Start Date
April 30, 2012
Primary Completion Date
April 30, 2013
Study Completion Date
April 30, 2013
AFQ056
"AFQ056 will be supplied as oral modified release tablets in 25 mg, 50 mg, 100 mg, 150 mg, and 200 mg.~Patients will be randomized in two groups by amantadine status.~* Group 1: Patients are not permitted to take amantadine within 2 weeks prior to the BL1 visit.~* Group 2: Patients must be on a stable and well tolerated dose of amantadine for at least 4 weeks prior to BL1 and must maintain the stable dose of amantadine during the remainder of the study.)"
Placebo
Placebo for AFQ056 will be supplied as oral tablets.
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Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY