Status and phase
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About
In total 20 subjects will be enrolled at one participating site -UMC Ljubljana. The 20 subjects will be treated with placebo and NBMI 300 mg in a cross-over design. In case of subject drop-outs, additional subjects may be enrolled as decided by the Sponsor, to allow for expected number of evaluable subjects in each group.
Full description
· The study's primary objective is: To explore the efficacy of 28 days NBMI treatment on motor and non-motor symptoms and heath related quality of life in patients with Progressive Supranuclear Palsy or Multiple Systems Atrophy disease.
The study's secondary objectives are:
The study's exploratory aims are:
Enrollment
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Inclusion criteria
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Interventional model
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20 participants in 2 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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