A Safety, Efficacy and Tolerability Study of Sativex for the Treatment of Spasticity in Children Aged 8 to 18 Years

PHASE3CompletedINTERVENTIONAL
Enrollment

72

Participants

Timeline

Start Date

December 31, 2013

Primary Completion Date

September 30, 2016

Study Completion Date

March 31, 2017

Conditions
Cerebral Palsy
Interventions
DRUG

Sativex

Oromucosal spray containing THC (27 mg/mL):CBD (25 mg/mL), in ethanol: propylene glycol (50:50) excipients, with peppermint oil (0.05%) flavouring. Each 100 μL spray delivered THC 2.7 mg and CBD 2.5 mg. The maximum number of daily sprays was 12.

DRUG

Placebo

Oromucosal spray containing ethanol: propylene glycol(50:50) excipients, with peppermint oil (0.05%) flavouring and colourings FD\&C Yellow No.5 (E102 tartrazine) (0.0260%), FD\&C Yellow No.6 (E110 sunset yellow) (0.0038%), FD\&C Red No. 40 (E129 Allura red AC) (0.00330%) and FD\&C Blue No.1 (E133 Brilliant blue FCF) (0.00058%). Each 100 μL spray administered to the sub-lingual or oral mucosa delivered the colourants plus excipients. The maximum daily dose was 12 sprays per day.

Trial Locations (14)

Unknown

Center 14, Prague

Center 7, Tel Aviv

Center 8, Tel Litwinsky

Center 2, Bristol

Center 6, Cambridge

Center 10, Exeter

Center 13, Glasgow

Center 3, Liverpool

Center 1, London

Center 5, London

Center 12, Norwich

Center 9, Nottingham

Center 11, Salisbury

Center 4, Sheffield

Sponsors
All Listed Sponsors
lead

Jazz Pharmaceuticals

INDUSTRY