A Randomized Study of Sativex on Cognitive Function and Mood: Multiple Sclerosis Patients

Jazz Pharmaceuticals

Status and phase: Completed; Phase 4

Conditions: Spasticity; Multiple Sclerosis

Treatments: Drug: Sativex; Drug: Placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT01964547

GWMS1137

Details and patient eligibility

About

A study to compare the change in cognitive performance and psychological status of patients with spasticity due to Multiple Sclerosis when treated with Sativex or placebo, added to existing anti-spasticity therapy over a period of 48 weeks. Secondary objectives were to evaluate the effect of Sativex on mood and spasticity and to assess the safety and tolerability of Sativex.

Full description

Eligible patients entered this 50 week multicenter, double-blind, randomised, placebo-controlled, parallel group study which evaluated the effect of Sativex on cognitive performance. At each scheduled clinic visit, patients were assessed for cognitive performance, mood, severity of spasticity, use of investigational medicinal products and number of visits to a healthcare professional. Primary efficacy comparisons were made between scores recorded during baseline and scores recorded at the end of treatment.

Enrollment: 121 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria (ALL to be fulfilled):

• Patient is willing and able to give informed consent for participation in the study.

• Patient is aged 18 years or above.

• Diagnosed with any disease sub-type of multiple sclerosis.

• Diagnosed with symptomatic spasticity due to multiple sclerosis.

• Patient has at least moderate spasticity in the opinion of the investigator.

• Patient fulfils at least one of the two criteria below. Subject must be either:

  • Currently established on a regular dose of anti-spasticity therapy, or
  • Previously tried and failed anti-spasticity therapy.

• Stable medication regimen for at least four weeks prior to study entry, for all medications which may have an effect on spasticity and/or cognition.

• If the patient is taking disease modifying medication this must be at a stable dose for three months prior to the initial visit.

• Willing and able to comply with all study requirements.

• Willing for his or her name to be notified to the responsible authorities for participation in this study, as applicable.

• Willing to allow his or her primary care practitioner and consultant, if appropriate, to be notified of participation in the study.

Exclusion Criteria (if ANY apply):

• Any history or immediate family of schizophrenia, other psychotic illness, severe personality disorder or other significant psychiatric disorder other than depression associated with their underlying condition.
• Any concomitant disease or disorder (such as poorly controlled epilepsy or seizures) that may influence the patient's level of cognition or mood.
• Currently using or has used cannabis or cannabinoid-based medications within 30 days of study entry and unwilling to abstain for the duration of the study.
• Any known or suspected history of a diagnosed dependence disorder, current heavy alcohol consumption (more than 60g of pure alcohol per day for men, and more than 40g of pure alcohol per day for women), current use of an illicit drug or current non-prescribed use of any prescription drug.
• Any known or suspected hypersensitivity to cannabinoids or any of the excipients of the investigational medicinal products.
• Female patients of child bearing potential and male subjects whose partner is of child bearing potential, unless willing to ensure that they or their partner use effective contraception during the study and for three months thereafter.
• Female patient who is pregnant, lactating or planning pregnancy during the course of the study and for three months thereafter.
• Patients who have received an investigational medicinal product within the 12 weeks prior to the initial visit.
• Any other significant disease or disorder which, in the opinion of the investigator, may either put the patient at risk because of participation in the study may influence the result of the study, or the patient's ability to participate in the study.
• Following a physical examination, the patient has any abnormalities that, in the opinion of the investigator would prevent the patient from safe participation in the study.
• Previously randomised to this study.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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121 participants in 2 patient groups, including a placebo group

Sativex

Active Comparator group

Description:

Contains delta-9-tetrahydrocannabinol (THC), 27 mg/mL:cannabidiol (CBD), 25 mg/mL, in ethanol:propylene glycol (50:50) excipients, with peppermint oil (0.05%) flavouring. Each actuation delivers THC 2.7 mg and CBD 2.5 mg. Dose: 100 µL oromucosal spray to be administered up to a maximum of 12 sprays per day. There was an initial dose-titration period during which patients gradually increased their dose of study drug according to individual response and tolerability.

Treatment:

Drug: Sativex

Placebo

Placebo Comparator group

Description:

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%). Dose: 100 µL oromucosal spray to be administered up to a maximum of 12 sprays per day. There was an initial dose-titration period during which patients gradually increased their dose of study drug according to individual response and tolerability.

Treatment:

Drug: Placebo