This randomized, double-blind, placebo-controlled, parallel group study will evaluate the pharmacodynamics and pharmacokinetics of RO5508887 in healthy volunteers. Subjects will be randomized in cohorts to receive single oral doses of either RO5508887 or placebo. In-unit period is 6 days.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
DOUBLE
Enrollment
42
Unnamed facility
Glendale, California, United States
Plasma levels of amyloid biomarkers
Time frame: Pre-dose and up to fullow up, 8-12 days post dose
Cerebral spinal fluid levels of amyloid biomarkers
Time frame: Pre-dose and up to 30 hours post-dose
Safety: Incidence of adverse events
Time frame: approximately 6 months
Pharmacokinetics: Plasma and cerebral spinal fluid concentrations of RO5508887 (and metabolites)
Time frame: Pre-dose and up to 72 hours post-dose
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