A Study of the Safety and Tolerability of GWP42006 in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

66

Participants

Timeline

Start Date

August 31, 2013

Primary Completion Date

December 31, 2013

Study Completion Date

December 31, 2013

Conditions
Epilepsy
Interventions
DRUG

Placebo

Placebo control matched to the oral or intravenous experimental comparator drug

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."

Trial Locations (1)

NG11 6JS

Quotient Clinical, Nottingham

Sponsors
All Listed Sponsors
lead

Jazz Pharmaceuticals

INDUSTRY