66
Participants
Start Date
August 31, 2013
Primary Completion Date
December 31, 2013
Study Completion Date
December 31, 2013
Placebo
Placebo control matched to the oral or intravenous experimental comparator drug
GWP42006
"Oral administration of 25 (Group/dose level 1a and 1b), 75 (Group/dose level 2a and 2b), 200 (Group/dose level 3a and 3b) and 400 mg GWP42006 (Group/dose level 4a and 4b), provided as 50 mg/mL GWP42006 solution in sesame oil containing flavourings and sweetener, for dilution on the day of dosing, as required.~Additional intravenous administration of 5 mg GWP42006 and 10 mL Solutol HS 15 solution to Group/dose level 3a and 3b subjects."
Quotient Clinical, Nottingham
Lead Sponsor
Jazz Pharmaceuticals
INDUSTRY