In this study, we will compare BOTOX® versus Zanaflex ® for the treatment of muscle
overactivity in the upper limb following stroke or brain traums. This is a critical step
in the development of local intramuscular treatment for patients with muscle overactivity
following an acute brain lesions, as opposed to the more classic oral treatments.
This study will be a multicenter, randomized, prospective, parallel, double blind study that
enrolls subjects at twelve sites (including Mt. Sinai) throughout the United States and
Europe. The purpose of this study is to evaluate the safety and efficacy of BOTOX® compared
to Zanaflex® in reducing upper limb muscle tone in post-stroke subjects, as well as
evaluating changes in muscle tone-related disability and drug-therapy tolerance. This will
be an 18 week study. Subjects are eligible if they have been medically stable with upper
limb spasticity 6 months after their first stroke. Subjects will be randomized to one of
three treatment groups: Treatment Group I - intramuscular BOTOX® plus oral placebo,
Treatment Group II - intramuscular placebo plus oral Zanaflex®, Treatment Group III -
intramuscular placebo plus oral placebo. The dose of BOTOX® will be at the discretion of
the investigator with a maximum of 500 U per subject. The dose of the Zanaflex® will be
4mg/day to a maximum of 36mg/day. The study anticipates that 150 subjects will be enrolled
to provide sufficient information to answer the primary objective of safety and efficacy of
the study.
Minimum age: 18 Years.
Maximum age: 85 Years.
Gender(s): Both.
Inclusion Criteria:
- Outpatient, male and female subjects, of any race, between 18 and 85 years of age.
- Female subjects of childbearing potential must have a negative urine pregnancy test
result at Visit 1/Screening. (A female is considered of childbearing potential unless
she is postmenopausal or without a uterus and/or both ovaries.)
- Subjects with a history of stroke or traumatic brain injury, more than 90 days prior
to Visit 2/Baseline, that result in disability caused by focal upper limb muscle over
activity, as assessed by the Investigator and characterized by the following:
- A wrist Ashworth tone of +3 or greater as measured on the Modified Ashworth
Scale at Visit 1/Screening and Visit 2/Baseline;
- A minimum measurement of +2 on the Disability Assessment Scale (DAS) for the
principal therapeutic intervention target assessment (hygiene, dressing, pain,
and cosmesis) chosen by the Investigator and the subject or subject’s caregiver
at Visit 1/Screening and Visit 2/baseline.
- Subjects, who, as assessed by the Investigator, clearly understand the intent of the
study and are willing and able to comply with study instructions, complete the entire
study and sign Informed Consent Form.
Exclusion Criteria:
- Female subjects who are pregnant (positive urine pregnancy test at Visit
1/screening), nursing, planning a pregnancy during the study period or female
subjects of childbearing potential who are not using a reliable means of
contraception. Reliable means of contraception. Reliable methods of contraception are
hormonal methods or intrauterine device in use at least 14 days before study drug
administration.
- Subjects with a severe contracture at the wrist (inability to passively move the
joint more than 10 degrees) or a history of tendon transfer in the study limb.
- Subjects who have had a cast of the study limb within two weeks of the Visit
1/Screening or are planning casting of the study limb during the study period.
- Subjects with a diagnosis of Myasthenia Gravis, Eaton-Lambert Syndrome, Amyotrophic
Lateral Sclerosis or any other disease that might interfere with neuromuscular
function.
- Subjects with profound atrophy (as per the Investigator’s assessment) of the muscle
in the target area(s) of injection.
- Subjects with an infection at the injection site or systemic infection (in this case,
postpone study entry until one week following recovery).
- Subjects with diagnosed orthostatic hypotension or subjects that are taking alpha-2
adrenergic agonists (e. g. clonidine).
- Subjects with impaired renal and/or hepatic function.
- Subjects with a known allergy or sensitivity to the study medications or its
components.
- Subjects who are currently taking tizanidine or have taken tizandidine within 14 days
prior to Visit 2/Baseline.
- Subjects who have received previous botulinum toxin injection(s) of any serotype into
the target limb within 4 months of Visit 2/Baseline.
- Subjects who have received phenol or alcohol injections to the study limb.
- Subjects who are currently taking oral gabaergic medications (baclofen, gabapentin,
benzodiazepines) or dantrolone sodium, or have been taking these drugs within 2 weeks
of baseline (Visit 2). Please note that benzodiazepines will be excluded only as
antispasmodic medications but not as hypnotics or anxiolytics on a PRN basis.
- Subjects who have not been on stable doses of their CNS medications (antidepressant,
antianxiety drugs) for at least 2 months prior to Visit 1 (dose regimen must remain
stable throughout the study).
- Subjects who are currently using medication that are contraindicated with the
concomitant use of BOTOX® or Zanaflex®.
- Subjects currently participating in an investigational drug study or who have
participated in an investigational drug study within 30 days of Visit 1/Screening.
- Subjects that in the Investigator’s opinion have a concurrent condition that may put
them at significant risk, may confound the study results, or may interfere
significantly with the conduct of the study.
- Subjects with a history of poor cooperation, non-compliance with medical treatment,
or unreliability.
- Subjects currently receiving anticoagulant therapy and who have an INR > 3. 5