Last updated: 11/03/2018 13:56:15
A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study to evaluate the Efficacy and Safety of GSK1358820 (Botulinum Toxin Type A) in Chinese Subjects with post-stroke upper limb spasticityN/A
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A Multicenter, Double-Blind, Randomized, Placebo-Controlled Study to evaluate the Efficacy and Safety of GSK1358820 (Botulinum Toxin Type A) in Chinese Subjects with post-stroke upper limb spasticity
Trial description: This trial is a multicenter, double-blind, randomized, placebo-controlled study to compare GSK1358820 (Botulinum Toxin Type A, also known as "OnabotulinumtoxinA" or "Botox") with placebo on the efficacy and safety of treatment in poststroke subjects with focal wrist, finger and in some cases, thumb spasticity. Approximately 168 subjects will be enrolled. Subjects will receive a single treatment session of intramuscular GSK1358820 (Botulinum Toxin Type A, also known as "OnabotulinumtoxinA" or "Botox") ‘200U or 240U (if thumb spasticity is present)’ or placebo in a randomization ratio of 1:1. The subjects will be observed until 12 weeks post injection. Outcome measures include changes from baseline at every post injection visit as measured on the Modified Ashworth Scale (MAS), Disability Assessment Scale (DAS) and Global Assessment Scale. The primary efficacy endpoint is the change from baseline at week 6 for wrist flexor muscle tone as measured on the Modified Ashworth Scale. Safety parameters will also be measured including adverse events, vital signs (pulse and blood pressure) and clinical laboratory tests (haematology, serum chemistry and urinanalysis).
Primary purpose:
Treatment
Trial design:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Allocation:
Randomized
Primary outcomes:
Change from Baseline at Week 6 for wrist flexor muscle tone as measured on the Modified Ashworth Scale (MAS)
Timeframe: Baseline (Day 0) and Week 6
Secondary outcomes:
Area under the curve (AUC) for the change from Baseline at Weeks 6 and 12 for MAS wrist score
Timeframe: Baseline (Day 0), Week 6, and Week 12
Change from Baseline at Weeks 1, 4, 8, and 12 for wrist flexor muscle tone as measured on the MAS
Timeframe: Baseline (Day 0) and Weeks 1, 4, 8, and 12
Number of participants classified as wrist treatment responders at all post-injection visits
Timeframe: Weeks 1, 4, 6, 8, and 12
Change from Baseline at Weeks 1, 4, 6, 8, and 12 for finger flexor muscle tone as measured on the MAS
Timeframe: Baseline (Day 0) and Weeks 1, 4, 6, 8, and 12
Change from Baseline at Weeks 1, 4, 6, 8 and 12 for thumb flexor muscle tone as measured on the MAS
Timeframe: Baseline (Day 0) and Weeks 1, 4, 6, 8, and 12
Change from Baseline at Weeks 1, 4, 6, 8, and 12 for principal measure as assessed on the Disability Assessment Scale (DAS)
Timeframe: Baseline (Day 0) and Weeks 1, 4, 6, 8, and 12
Global Assessment Scale (GAS) score as evaluated by the physician at the indicated time points
Timeframe: Weeks 1, 4, 6, 8, and 12
GAS score as evaluated by the care giver or the participants at the indicated time points
Timeframe: Weeks 1, 4, 6, 8, and 12
Interventions:
Enrollment:
170
Primary completion date:
2011-24-06
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Not applicable
Medical condition
Cerebrovascular Accident
Product
OnabotulinumtoxinA
Collaborators
GSK
Study date(s)
April 2010 to June 2011
Type
Interventional
Phase
3
Participation criteria
Sex
Female & Male
Age
18 - 75 years
Accepts healthy volunteers
No
- Subjects eligible for enrolment in the study must meet all of the following criteria:
- 1. Subjects with upper limb spasticity who are at least 6 months post stroke and present with spasticity of both the wrist and fingers in the study limb.
- Subjects meeting any of the following criteria must not be enrolled in the study:
- 1. Presence of fixed contracture of the study limb (absence of passive range of motion).
Inclusion and exclusion criteria
Inclusion criteria:
- Subjects eligible for enrolment in the study must meet all of the following criteria: 1. Subjects with upper limb spasticity who are at least 6 months post stroke and present with spasticity of both the wrist and fingers in the study limb. 2. Wrist flexor muscle tone of 3 or greater and finger flexor muscle tone of 2 or greater as measured on MAS (0 to 4). 3. At least one functional disability item (i.e., hygiene, dressing, pain, or cosmesis) with a rating of 2 or greater on DAS (0 to 3). 4. If using oral anti-spasticity medications, must be stable for at least 1 month prior to study enrolment 5. If using physical therapy, must be stable for at least 1 month prior to study enrolment. 6. Male or female 18 to 75 years old at the time of informed consent. 7. >=40kg in weight. 8. QTc criteria: (either QTcb or QTcf, machine or manual overread, males or females); include the following details as appropriate: QTc<450 millisecond (msec) or <480msec for subjects with Bundle Branch Block-values based on either single electrocardiogram (ECG) values or triplicate ECG averaged QTc values obtained over a brief recording period. 9. Liver function tests: aspartate aminotransferase (AST) and alanine aminotransferase (ALT) <2xULN; alkaline phosphatase and bilirubin ≤1.5xULN (isolated bilirubin >1.5ULN is acceptable if bilirubin is fractionated and direct bilirubin <35%). 10. In the opinion of the investigator, subject must clearly understand the intent of the study and be willing and able to comply with study instructions and complete the entire study. 11. Informed consent has been obtained.
Exclusion criteria:
- Subjects meeting any of the following criteria must not be enrolled in the study: 1. Presence of fixed contracture of the study limb (absence of passive range of motion). 2. Profound atrophy of muscles to be injected (in the investigators opinion). 3. Infection or dermatological condition at the injection sites. 4. Significant inflammation in the study limb limiting joint movement. 5. History of or planned treatment for spasticity with phenol or alcohol block in the study limb. 6. History of or planned surgical intervention for spasticity of the study limb. 7. History (within 3 months of qualification) of or planned (during study period) casting of the study limb. 8. Participation in another clinical study currently, or within the 30 days immediately prior to enrolment. 9. Previous or current botulinum toxin therapy of any serotype. 10. Planned or anticipated initiation of new antispasticity medications during the clinical study. 11. Any medical condition that may put the subject at increased risk with exposure to GSK1358820, including diagnosed myasthenia gravis, Eaton-Lambert syndrome, amyotrophic lateral sclerosis, or any other disorder that might have interfered with neuromuscular function. 12. Concurrent use of aminoglycoside antibiotics or other agents that might interfere with neuromuscular function. A full list of prohibited medications that interfere with neuromuscular transmission is provided as Appendix 1. 13. Current treatment for spasticity with an intrathecal baclofen. 14. Females who are pregnant, nursing, or planning a pregnancy during the study period, or females of childbearing potential, not using a reliable means of contraception. 15. Known allergy or sensitivity to study medication or its components. 16. Bedridden subjects. 17. Unstable liver disease (as defined by the presence of ascites, encephalopathy, coagulopathy, hypoalbuminaemia, esophageal or gastric varices or persistent jaundice), cirrhosis, known biliary abnormalities (with the exception of Gilbert's syndrome or asymptomatic gallstones). 18. Presence of clinically unstable severe cardiovascular, renal or respiratory disease. 19. Investigator's opinion that the subject has a concurrent condition(s) that may put the subject at significant risk, may confound the study results, or may interfere significantly with the conduct of the study.
Trial location(s)
Showing 1 - 6 of 13 Results
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Results posted on ClinicalTrials.gov
Recruitment status
Study complete
Actual primary completion date
2011-24-06
Actual study completion date
2011-24-06
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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