Back to resultsA Study of Sativex® for Relief of Spasticity in Subjects With Multiple Sclerosis.
Primary Purpose
Spasticity, Multiple Sclerosis
Status
Completed
Phase
Phase 3
Locations
United Kingdom
Study Type
Interventional
Intervention
Sativex®
Placebo
Sponsored by
About this trial
This is an interventional supportive care trial for Spasticity focused on measuring Spasticity, Multiple Sclerosis
Eligibility Criteria
Inclusion Criteria:
- Willing and able to give informed consent.
- Male or female, aged 18 years or above.
- Stable disease for at least three months prior to study entry, in the opinion of the investigator.
- Diagnosed with MS whose spasticity was not wholly relieved with the therapy at the time of study entry.
- Significant spasticity in at least two muscle groups defined as a score of two or more on the Ashworth Scale for each muscle group.
- Stable dose of current anti-spasticity medication for at least 30 days prior to study entry.
- Willing to maintain a stable dose of anti-spasticity medication and level of physiotherapy for the duration of the study.
- Clinically acceptable laboratory results at Visit 2.
- Willing, if female and of child bearing potential or male subjects with a partner of child bearing potential, to ensure that effective contraception was used during the study and for three months thereafter.
- No cannabinoid use (cannabis, Marinol® or Nabilone) for at least seven days before Visit 1 and were willing to abstain from any use of cannabis during the study.
- Able (in the investigators opinion) and willing to comply with all study requirements.
- Willing for the Home Office to be notified of his or her participation in the study (applicable to the UK centres only).
- Willing to allow his or her GP and consultant, if appropriate, to be notified of participation in the study.
Exclusion Criteria:
- History of schizophrenia, other psychotic illness, severe personality disorder or other significant psychiatric disorder other than depression associated with their underlying condition.
- Known history of alcohol or substance abuse.
- Severe cardiovascular disorder, such as ischaemic heart disease, arrhythmias, poorly controlled hypertension or severe heart failure.
- History of epilepsy.
- Female subject who was pregnant, lactating or planning pregnancy during the course of the study.
- Significant renal or hepatic impairment.
- Scheduled elective surgery or other procedures requiring general anaesthesia during the study.
- Subject who was terminally ill or was inappropriate for placebo medication.
- Any other significant disease or disorder which, in the opinion of the investigator, either put the subject at risk because of participation in the study, or influenced the result of the study, or the subject's ability to participate in the study.
- Regular levodopa (Sinemet®, Sinemet Plus®, Levodopa, L-dopa, Madopar®, Benserazide) therapy within seven days of study entry.
- Male subject receiving sildenafil (Viagra®) and unwilling to stop medication for the duration of the study.
- Subjects who were taking fentanyl (Durogesic®, Actiq®)
- Subjects who were taking antiarrhythmic medications.
- Known or suspected hypersensitivity to cannabinoids or any of the excipients of the study medications.
- Known or suspected adverse reaction to cannabinoids.
- Planned travel outside the UK during the study (applicable to the UK centres only).
- Donation of blood during the study.
- Subjects who had participated in another research study in the 12 weeks prior to study entry.
- Subjects previously randomised into this study.
Sites / Locations
- Royal Berkshire Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Sativex
Placebo
Arm Description
Outcomes
Primary Outcome Measures
Assessment of Change From Baseline in the Mean Spasticity 0-10 Numerical Rating Scale Score.
The spasticity Numerical Rating Scale was completed at the same time each day, i.e. bedtime in the evening. The patient was asked "on a scale of '0 to 10', please indicate the number that best describes your average spasticity in the last 24 hours" where 0 = no spasticity and 10 = worst ever spasticity. For the analysis, end of treatment was defined as the mean of the last seven days in the study or the last three days if the subject withdrew due to worsening spasticity or lack of efficacy. A negative value indicates an improvement in spasticity score from baseline.
Secondary Outcome Measures
Change From Baseline in Mean Ashworth Scale Score at the End of Treatment
The mean Ashworth Scale score across muscle groups was calculated using only those muscle groups with a score of greater than or equal to two at baseline. All 20 muscle groups were assessed for spasticity (using a 1-5 scale): 1= no increase in muscle tone to 5= passive movement is difficult and affected part is rigid in flexion or extension. The score for all 20 muscle groups were added to give a total score out of 100; minimum score was 20. A decrease in score indicates an improvement in condition.
Change From Baseline in Mean Spasm Frequency Score at the End of Treatment
Each day subjects recorded in their diary the frequency of their spasms using the following scoring system: 0 = no spasms, 1 = one or fewer spasms per day, 2 = between one and five spasms per day, 3 = six to nine spasms per day, 4 = ten or more spasms per day or continuous contraction. For the analysis, end of treatment was defined as the mean of the last seven days in the study or the last three days if the subject withdrew due to worsening spasticity or lack of efficacy.
Change From Baseline in Mean Motricity Index Score for the Arms
Arm - 3 movements were pinch grip, elbow flexion and shoulder abduction. The total arm score was the addition of the score for the 3 arm movements. One point was then added to give a maximum score of 100; minimum was 1 point. Where both arms were assessed, the average of the two limbs scores was used as the assessment score; otherwise the affected limb total score was used. An increase in score indicates an improvement in condition..
Patient's Global Impression of Change in Condition at the End of Treatment
A 7-point Likert-type scale was used, with the question: 'Please assess the change in your condition since entry into the study using the scale below' with the markers "very much improved, much improved, slightly improved, no change, slightly worse, much worse or very much worse". At Visit 2 (Baseline) patients wrote a brief description of their condition which was used at end of treatment to aid their memory regarding their symptoms at study start. For each of above markers the number of participants were reported.
Incidence of Adverse Events as a Measure of Subject Safety
The number of subjects who reported an adverse event during the course of the study is presented.
Change From Baseline in Mean Motricity Index Score for the Legs
Ankle dorsiflexion, knee extension and hip flexion were assessed and scored to give a maximum of 100%. The Motricity Index score (scale 1-100) was recorded for limbs that had an associated Ashworth Scale score, which was greater than or equal to two at baseline.
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT00711646
Brief Title
A Study of Sativex® for Relief of Spasticity in Subjects With Multiple Sclerosis.
Official Title
A Double Blind, Randomised, Parallel Group Study to Assess the Efficacy, Safety and Tolerability of Cannabis Based Medicine 1:1 THC:CBD Compared With Placebo for the Treatment of Spasticity in Patients With Multiple Sclerosis.
Study Type
Interventional
2. Study Status
Record Verification Date
April 2023
Overall Recruitment Status
Completed
Study Start Date
June 2002 (undefined)
Primary Completion Date
March 2004 (Actual)
Study Completion Date
March 2004 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Jazz Pharmaceuticals
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this study is to evaluate the efficacy, safety and tolerability of Sativex® in subjects diagnosed with MS and spasticity.
Detailed Description
This was an eight week (two weeks baseline, six weeks treatment), multicentre, double blind, randomised, placebo controlled parallel group study to evaluate the efficacy, safety and tolerability of Sativex® in subjects diagnosed with MS and spasticity. Subjects were screened to determine eligibility and completed a two week baseline period. Subjects then returned to the site for assessment, randomisation and dose introduction. Visits occurred at the end of treatment week two and at the end of the study (treatment week six) or withdrawal.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Spasticity, Multiple Sclerosis
Keywords
Spasticity, Multiple Sclerosis
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
189 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Sativex
Arm Type
Experimental
Arm Title
Placebo
Arm Type
Placebo Comparator
Intervention Type
Drug
Intervention Name(s)
Sativex®
Other Intervention Name(s)
GW-1000-02
Intervention Description
containing THC (27 mg/ml):CBD (25 mg/ml), in ethanol:propylene glycol (50:50) excipients, with peppermint oil (0.05%) flavouring. Maximum permitted dose was eight actuations in any three hour period and 24 actuations (THC 65 mg: CBD 60 mg) in 24 hours
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
GW-4001-01
Intervention Description
containing peppermint oil, 0.05% (v/v), quinoline yellow, 0.005% (w/v), sunset yellow, 0.0025% (w/v), in ethanol:propylene glycol (50:50) excipient.
Primary Outcome Measure Information:
Title
Assessment of Change From Baseline in the Mean Spasticity 0-10 Numerical Rating Scale Score.
Description
The spasticity Numerical Rating Scale was completed at the same time each day, i.e. bedtime in the evening. The patient was asked "on a scale of '0 to 10', please indicate the number that best describes your average spasticity in the last 24 hours" where 0 = no spasticity and 10 = worst ever spasticity. For the analysis, end of treatment was defined as the mean of the last seven days in the study or the last three days if the subject withdrew due to worsening spasticity or lack of efficacy. A negative value indicates an improvement in spasticity score from baseline.
Time Frame
0-52 days
Secondary Outcome Measure Information:
Title
Change From Baseline in Mean Ashworth Scale Score at the End of Treatment
Description
The mean Ashworth Scale score across muscle groups was calculated using only those muscle groups with a score of greater than or equal to two at baseline. All 20 muscle groups were assessed for spasticity (using a 1-5 scale): 1= no increase in muscle tone to 5= passive movement is difficult and affected part is rigid in flexion or extension. The score for all 20 muscle groups were added to give a total score out of 100; minimum score was 20. A decrease in score indicates an improvement in condition.
Time Frame
Days 0 - 52
Title
Change From Baseline in Mean Spasm Frequency Score at the End of Treatment
Description
Each day subjects recorded in their diary the frequency of their spasms using the following scoring system: 0 = no spasms, 1 = one or fewer spasms per day, 2 = between one and five spasms per day, 3 = six to nine spasms per day, 4 = ten or more spasms per day or continuous contraction. For the analysis, end of treatment was defined as the mean of the last seven days in the study or the last three days if the subject withdrew due to worsening spasticity or lack of efficacy.
Time Frame
Days 0 - 52
Title
Change From Baseline in Mean Motricity Index Score for the Arms
Description
Arm - 3 movements were pinch grip, elbow flexion and shoulder abduction. The total arm score was the addition of the score for the 3 arm movements. One point was then added to give a maximum score of 100; minimum was 1 point. Where both arms were assessed, the average of the two limbs scores was used as the assessment score; otherwise the affected limb total score was used. An increase in score indicates an improvement in condition..
Time Frame
Day 7 and 52
Title
Patient's Global Impression of Change in Condition at the End of Treatment
Description
A 7-point Likert-type scale was used, with the question: 'Please assess the change in your condition since entry into the study using the scale below' with the markers "very much improved, much improved, slightly improved, no change, slightly worse, much worse or very much worse". At Visit 2 (Baseline) patients wrote a brief description of their condition which was used at end of treatment to aid their memory regarding their symptoms at study start. For each of above markers the number of participants were reported.
Time Frame
Day 52
Title
Incidence of Adverse Events as a Measure of Subject Safety
Description
The number of subjects who reported an adverse event during the course of the study is presented.
Time Frame
Day 0-52
Title
Change From Baseline in Mean Motricity Index Score for the Legs
Description
Ankle dorsiflexion, knee extension and hip flexion were assessed and scored to give a maximum of 100%. The Motricity Index score (scale 1-100) was recorded for limbs that had an associated Ashworth Scale score, which was greater than or equal to two at baseline.
Time Frame
Day 7 and Day 52
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Willing and able to give informed consent.
Male or female, aged 18 years or above.
Stable disease for at least three months prior to study entry, in the opinion of the investigator.
Diagnosed with MS whose spasticity was not wholly relieved with the therapy at the time of study entry.
Significant spasticity in at least two muscle groups defined as a score of two or more on the Ashworth Scale for each muscle group.
Stable dose of current anti-spasticity medication for at least 30 days prior to study entry.
Willing to maintain a stable dose of anti-spasticity medication and level of physiotherapy for the duration of the study.
Clinically acceptable laboratory results at Visit 2.
Willing, if female and of child bearing potential or male subjects with a partner of child bearing potential, to ensure that effective contraception was used during the study and for three months thereafter.
No cannabinoid use (cannabis, Marinol® or Nabilone) for at least seven days before Visit 1 and were willing to abstain from any use of cannabis during the study.
Able (in the investigators opinion) and willing to comply with all study requirements.
Willing for the Home Office to be notified of his or her participation in the study (applicable to the UK centres only).
Willing to allow his or her GP and consultant, if appropriate, to be notified of participation in the study.
Exclusion Criteria:
History of schizophrenia, other psychotic illness, severe personality disorder or other significant psychiatric disorder other than depression associated with their underlying condition.
Known history of alcohol or substance abuse.
Severe cardiovascular disorder, such as ischaemic heart disease, arrhythmias, poorly controlled hypertension or severe heart failure.
History of epilepsy.
Female subject who was pregnant, lactating or planning pregnancy during the course of the study.
Significant renal or hepatic impairment.
Scheduled elective surgery or other procedures requiring general anaesthesia during the study.
Subject who was terminally ill or was inappropriate for placebo medication.
Any other significant disease or disorder which, in the opinion of the investigator, either put the subject at risk because of participation in the study, or influenced the result of the study, or the subject's ability to participate in the study.
Regular levodopa (Sinemet®, Sinemet Plus®, Levodopa, L-dopa, Madopar®, Benserazide) therapy within seven days of study entry.
Male subject receiving sildenafil (Viagra®) and unwilling to stop medication for the duration of the study.
Subjects who were taking fentanyl (Durogesic®, Actiq®)
Subjects who were taking antiarrhythmic medications.
Known or suspected hypersensitivity to cannabinoids or any of the excipients of the study medications.
Known or suspected adverse reaction to cannabinoids.
Planned travel outside the UK during the study (applicable to the UK centres only).
Donation of blood during the study.
Subjects who had participated in another research study in the 12 weeks prior to study entry.
Subjects previously randomised into this study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christine Collin, MB BS MRCP FRCP
Organizational Affiliation
Royal Berkshire Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Berkshire Hospital
City
Reading
State/Province
Oxfordshire
ZIP/Postal Code
RG1 5AN
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
17355549
Citation
Collin C, Davies P, Mutiboko IK, Ratcliffe S; Sativex Spasticity in MS Study Group. Randomized controlled trial of cannabis-based medicine in spasticity caused by multiple sclerosis. Eur J Neurol. 2007 Mar;14(3):290-6. doi: 10.1111/j.1468-1331.2006.01639.x.
Results Reference
result
PubMed Identifier
25475413
Citation
Di Marzo V, Centonze D. Placebo effects in a multiple sclerosis spasticity enriched clinical trial with the oromucosal cannabinoid spray (THC/CBD): dimension and possible causes. CNS Neurosci Ther. 2015 Mar;21(3):215-21. doi: 10.1111/cns.12358. Epub 2014 Dec 4.
Results Reference
derived
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A Study of Sativex® for Relief of Spasticity in Subjects With Multiple Sclerosis.
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