Spinocerebellar Ataxias
Conditions
Brief summary
The purpose of the clinical trial is to study the therapeutic efficacy and safety of Stemchymal® infusions for polyglutamine spinocerebellar ataxia treatment by a randomized, double-blind, placebo-controlled study design. Eligible subjects will receive Stemchymal® through intravenous infusion.
Interventions
BIOLOGICALStemchymal
Patients will receive Stemchymal® through intravenous infusion
BIOLOGICALPlacebo
Patients will receive Placebo through intravenous infusion
Sponsors
Steminent US, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)
Eligibility
Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
1. Subjects are with genotypically confirmed SCA3. 2. Subjects' SARA scores are in the range of 5 to15. 3. Subjects are between 20 and 70 years of age. 4. Subjects who have signed informed consent. 5. Female subjects of child-bearing potential who are capable of conception must be post-menopausal (one year or greater without menses), surgically incapable of childbearing, or practicing effective methods of birth control. 6. Male subjects must be practicing a medically accepted form of contraception during the study period. Abstinence is an acceptable method of contraception.
Exclusion criteria
1. Subjects who have been enrolled in any kind of cell therapy within six months prior to screening visit (Visit 1). 2. Female subjects who have a positive pregnancy test result. 3. Subjects who have had severe vital organ diseases, including but not limited to cardiac (e.g., heart failure), liver (e.g., acute hepatic failure or chronic liver cirrhosis), lung (e.g., respiratory failure) and renal (e.g., hemodialysis or peritoneal dialysis) diseases, within six months prior to screening visit (Visit 1). 4. Subjects with immunological disorders (e.g., systemic lupus erythematosus), within six months prior to screening visit (Visit 1). 5. Subjects with other neurological disorders (e.g., Alzheimer's disease), within six months prior to screening visit (Visit 1). 6. Subjects who had received chemotherapy/radiotherapy within five years prior to screening visit (Visit 1). 7. Subjects with any history of malignant tumors. 8. Subjects with dementia or other psychiatric illnesses, including but not limited to disabling depression, bipolar disorder, schizophrenia. 9. Subjects with a Beck Depression Inventory Second Edition (BDI-II) score of over 20 points. 10. Subjects not suitable for this clinical trial according to investigator's judgment.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change of Scale for the Assessment and Rating of Ataxia (SARA) scores from baseline (week 0) at 6 months (week 24). | 6 months |
Outcome results
None listed