Cerebral Palsy, Cerebrovascular Accident, Cervical Spinal Cord Injury, Multiple Sclerosis, Spasticity, Traumatic Brain Injury
Conditions
Keywords
Stroke, Traumatic Brain Injury, Monoplegia, Hemiplegia, Upper limb, Multiple Sclerosis, Cerebral Palsy, Cervical Spinal Cord Injury
Brief summary
Phase 2/3, randomized, double-blind, placebo-controlled, single-treatment, multicenter trial assessing the efficacy and safety of MYOBLOC for the treatment of upper limb spasticity in adults followed by an open-label extension safety trial.
Detailed description
Phase 2, randomized, double-blind, placebo-controlled, single-treatment, multicenter trial will compare the efficacy and safety of two doses of MYOBLOC (10,000 Units and 15,000 Units) versus volume-matched placebo in the treatment of upper limb spasticity in adults. An interim analysis will evaluate all available safety and efficacy data from the Phase 2 double-blind trial in order to recommend which dose will be evaluated in subsequent Phase 3 trial. The Phase 3, randomized, double-blind, placebo-controlled, single-treatment, multicenter trial will compare the efficacy and safety of MYOBLOC versus placebo in the treatment of upper limb spasticity in adults. Subjects who complete either the Phase 2 or Phase 3 trial will continue into an open-label extension part of the study where each will receive 4 separate treatments of MYOBLOC (15,000-20,000 Units) \ 13 week apart for upper limb spasticity.
Interventions
DRUGPhase 2; Low Dose MYOBLOC (10,000 Units)
Intramuscular injections on Day 1
Intramuscular injections on Day 1
DRUGPhase 2; Placebo
Intramuscular injections on Day 1
DRUGPhase 3; MYOBLOC
Intramuscular injections on Day 1
DRUGPhase 3; Placebo
Intramuscular injections on Day 1
Sponsors
Solstice Neurosciences, LLC, a subsidiary of MDD US Operations, LLC
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Masking description
No other parties are masked in the clinical trial.
Intervention model description
A Phase 2/3, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Single-Treatment Efficacy and Safety Study of MYOBLOC in the Treatment of Adult Upper Limb Spasticity Followed by an Open-Label Extension, Multiple-Treatment in Safety Study of MYOBLOC
Eligibility
Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No
Inclusion criteria
1. Able to understand the potential risks and benefits, the study requirements, and provide written informed consent before enrollment into the study; or if unable, the subject's Legally Authorized Representative (LAR) may provide written informed consent. 2. Male or female ≥18 to maximum of 80 years of age, inclusive. 3. Upper limb spasticity due to stroke, or traumatic brain injury, or spinal cord injury that occurred ≥ 6 months prior to randomization. Eligible subjects may have upper limb monoplegia or hemiplegia. Subjects with cerebral palsy are eligible for study enrollment. 4. Modified Ashworth Scale (MAS) scores of ≥2 in at least two muscle groups inclusive of the elbow, wrist, and finger flexors at screening and baseline. 5. In the Investigator's opinion, the subject will be available and able to comply with the study requirements for at least 1 year, based on the subject's overall health and disease prognosis. 6. In the Investigator's opinion, the subject will be willing and able to comply with all requirements of the protocol, including completion of study questionnaires. A caregiver may be designated to assist with the physical completion of questionnaires/scales.
Exclusion criteria
1. Quadriplegia/tetraplegia, or triplegia with both upper limbs affected. 2. Uncontrolled epilepsy or any type of seizure disorder with a seizure(s) within the previous year. 3. Neuromuscular disorders including, but not limited to, amyotrophic lateral sclerosis (ALS), primary lateral sclerosis (PLS), multiple sclerosis (MS), myasthenia gravis, or muscular dystrophy. 4. History of major joint contracture(s), in which, based on the Investigator's assessment, the contracture(s) significantly contributes to joint immobility in the affected upper limb. 5. Unresolved fracture(s) in the affected upper limb. 6. Severe atrophy in the affected upper limb. 7. Known hypersensitivity to botulinum toxins type A or B or to any MYOBLOC solution components. 8. Concomitant use or exposure within 5 half-lives of randomization of the following: aminoglycoside antibiotics, curare-like agents, or other agents that may interfere with neuromuscular function. 9. Treatment with a neurolytic agent (e.g., phenol, alcohol blocks) to the affected upper limb within 1 year before randomization. 10. Presence of a spinal stimulator or intrathecal baclofen pump that has not been turned off within 30 days prior to screening. 11. Changes to treatment regimen or any new treatment with oral antispasmodics and/or muscle relaxants within 30 days prior to randomization. 12. Initiation of physical and/or occupational therapy \<30 days before randomization. Subjects receiving physical and/or occupational therapy ≥30 days before randomization must be willing to maintain their therapy regimen through Week 4 of the Double-Blind Period. 13. Prior botulinum toxin type A (BoNT/A) or B (BoNT/B) treatment in the affected upper limb within 24 weeks before screening. Prior BoNT/A or BoNT/B treatment in areas other than the affected upper limb is not exclusionary but must have occurred at least 12 weeks before screening. Prior toxin exposure must have been well tolerated and without any significant long-term side effects in the case of repeated prior exposure. 14. Subjects should not receive nor have any plans to receive any botulinum toxin treatment, other than the study drug (MYOBLOC), from the time that informed consent is obtained until participation in the study is complete. 15. Severe dysphagia (i.e., inability to swallow liquids, solids or both without choking or medical intervention), or dysphagia with a history of aspiration pneumonia, within 6 months before screening. 16. Prior surgery to treat spasticity in the affected upper limb (i.e., tendon lengthening or tendon transfer). 17. Any anticipated or scheduled surgery during the study period, with the exception of dermatological procedures performed under local anesthesia for the purposes of removing precancerous and cancerous lesions. 18. Major surgery within 30 days before screening. 19. Pregnancy or breastfeeding. 20. Females of childbearing potential must agree to practice a medically acceptable method of contraception (e.g., intrauterine device, hormonal contraception started at least one full cycle before study enrollment, or barrier method in conjunction with spermicide) for the duration of the study (including 2 months after study completion). For the purposes of this study, all females are considered to be of childbearing potential unless they are confirmed by the Investigator to be post-menopausal (at least 1 year since last menses and laboratory test confirmation), biologically sterile, or surgically sterile (e.g., hysterectomy with bilateral oophorectomy, tubal ligation). 21. History of drug or alcohol abuse within 6 months before screening. 22. Obstructive pulmonary disease with forced expiratory volume in 1 second (FEV1)/forced vital capacity (FVC) \<70%. 23. Slow vital capacity (SVC) \<60% of predicted. 24. Chronic or current use of inhaled corticosteroids. 25. Ventilator dependence (i.e., 24-hour ventilator dependence when intubated, or due to a failure to wean the subject from the ventilator while hospitalized in the intensive care unit or respiratory care center). Subjects who use oxygen on an as-needed basis or during sleeping hours only via a nasal cannula are eligible for the study. 26. Infection at the planned sites of injection. 27. Treatment with an investigational drug, device, or biological agent within 30 days before screening or while participating in this study. 28. Malignancy diagnosed 3 months before screening. 29. Has one or more screening clinical laboratory test values outside the reference range that, in the opinion of the Investigator, are clinically significant, or any of the following : * Serum creatinine \>1.5 times the upper limit of normal (ULN); * Serum total bilirubin \> 1.5 times ULN; * Serum alanine aminotransferase or aspartate aminotransferase \>2 times ULN. 30. Has any of the following cardiac findings at screening: * Abnormal ECG that is, in the Investigator's opinion/evaluation, clinically significant; * PR interval \>220 ms; * QRS interval \>130 ms; * QTcF interval \>450 ms (for men), or \>470 ms (for women) (QT corrected using Fridericia's method); * Second-or third-degree atrioventricular block; * Any rhythm, other than sinus rhythm, that is interpreted or assessed by the Investigator to be clinically significant. 31. Any other medical illness, condition, or clinical finding that, in the opinion of the Investigator and/or the Sponsor, would put the subject at undue risk.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The Change From Baseline in Modified Ashworth Scale (MAS) Score for Tone of the Primary Target Muscle Group (PTMG) Selected for Treatment at Week 4 Post-injection. | Baseline and Week 4 | The Modified Ashworth Scale (MAS) is an internationally accepted and validated instrument used to measure resistance during passive soft-tissue stretching. Resistance will be measured and recorded using a 6-point scale ranging from 0 (no increase in muscle tone) to 4 (affected part\[s\] rigid in flexion or extension). The post-injection MAS score is subtracted from the baseline MAS score to yield the change from baseline MAS score. A change from baseline MAS score \<0 represents a better outcome. |
| The Clinical Global Impression of Change (CGI-C) Score in Functional Ability at Week 4 Post-injection. | Week 4 | The Clinical Global Impression of Change (CGI-C) scale is a single item clinician assessment of how much the patient's functional ability has improved, worsened or has not changed relative to the patient's baseline state prior to treatment (injection). The CGI-C is rated on a 7-point Likert scale from 1 to 7, where 1 = "Very much improved", 2 = "Much improved", 3 = "Minimally improved", 4 = "No change", 5 = "Minimally worse", 6 = "Much worse", and 7 = "Very much worse". A CGI-C score \<4 represents a better outcome. |
Countries
Hungary, Poland, United States
Contacts
STUDY_DIRECTORJoseph T Hull, PhD
Solstice Neurosciences, LLC, a subsidiary of MDD US Operations, LLC
Participant flow
Recruitment details
The study was conducted at 10 sites located in the United States (4), Poland (6), and Hungary (1).
Pre-assignment details
Participants were enrolled into the Phase 2 portion of study only. After participants completed the Double-Blind Phase (DBP; Treatment 1) of study, they can receive up to 4 treatments of MYOBLOC in the Open-Label Extension (OLE; Treatments 2-5). Since the Phase 2 portion of study did not complete target enrollment, there were no participants enrolled into the Phase 3 portion of study, which also included DBP portion followed by an OLE portion of study.
Baseline characteristics
| Characteristic | — |
|---|---|
| Age, Categorical <=18 years | 0 Participants |
| Age, Categorical >=65 years | 7 Participants |
| Age, Categorical Between 18 and 65 years | 25 Participants |
| Age, Continuous | 52.7 years STANDARD_DEVIATION 12.17 |
| Ethnicity (NIH/OMB) Hispanic or Latino | 0 Participants |
| Ethnicity (NIH/OMB) Not Hispanic or Latino | 7 Participants |
| Ethnicity (NIH/OMB) Unknown or Not Reported | 0 Participants |
| Primary Target Muscle Group (PTMG) Elbow Flexors | 18 Participants |
| Primary Target Muscle Group (PTMG) Finger Flexors | 3 Participants |
| Primary Target Muscle Group (PTMG) Wrist Flexors | 1 Participants |
| Race (NIH/OMB) American Indian or Alaska Native | 1 Participants |
| Race (NIH/OMB) Asian | 0 Participants |
| Race (NIH/OMB) Black or African American | 1 Participants |
| Race (NIH/OMB) More than one race | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 0 Participants |
| Race (NIH/OMB) White | 11 Participants |
| Region of Enrollment Hungary | 1 participants |
| Region of Enrollment Poland | 7 participants |
| Region of Enrollment United States | 4 participants |
| Sex: Female, Male Female | 5 Participants |
| Sex: Female, Male Male | 7 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk | EG002 affected / at risk | EG003 affected / at risk |
|---|---|---|---|---|
| deaths Total, all-cause mortality | 0 / 10 | 0 / 11 | 0 / 11 | 0 / 24 |
| other Total, other adverse events | 4 / 10 | 3 / 11 | 2 / 11 | 5 / 24 |
| serious Total, serious adverse events | 0 / 10 | 0 / 11 | 1 / 11 | 0 / 24 |
Outcome results
None listed