Study to Assess the Safety and Effects of Autologous Adipose-Derived Stromal Cells Delivered Into Patients With Multiple Sclerosis
Study Details
Study Description
Brief Summary
The intent of this clinical study is to answer the questions:
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Is the proposed treatment safe
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Is treatment effective in improving the disease pathology of patients with Multiple Sclerosis and clinical outcomes?
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
N/A |
Detailed Description
This will be an open-label, non-randomized multi-center patient sponsored study of Adipose-Derived Stromal Cells (ASC) implantation performed intrathecally and intravenously. ASCs will be derived from the patient's adipose-derived tissue. Liposuction using local anesthesia and syringe collection will be performed to collect the adipose tissue specimen for subsequent processing to isolate the stem cells.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Adipose SVF IV Infusion IV Infusion of Autologous Adipose Derived Stromal Vascular Fraction Intervention: Intravenous Infusion |
Procedure: Harvesting and Implantation of SVF
The cell therapy in this study is composed of stem cells derived from a patient's own adipose tissue that are harvested by liposuction using tumescent technique and isolated in the laboratory. The Adipose SVF will be delivered via intravenous injection.
|
Outcome Measures
Primary Outcome Measures
- Clinical improvement in disability score compared to baseline [3 months]
- Number of patients with adverse events [up to 6 months]
The safety of adipose-derived stem cell injection will be evaluated by assessment of the frequency and nature of adverse events occurring during the study injection and up to the 6-month period following treatment.
- Clinical improvement in disability score compared to baseline [6 months]
Secondary Outcome Measures
- MS disease activity measured by the number of Gd-enhancing brain MRI lesions [3 months]
- Reduced number of relapses or freedom from progression of disease [3 months]
- Reduced number of relapses or freedom from progression of disease [6 months]
- MS disease activity measured by the number of Gd-enhancing brain MRI lesions [6 months]
Eligibility Criteria
Criteria
Inclusion Criteria:
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Males and Females between Age 18 and 80 years.
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Duration of disease: >5 years
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Failure to respond or intolerance to the currently available Multiple Sclerosis (MS) immunomodulatory treatments (ie interferons, Copaxone, immunosuppression): the lack of response to these treatments will be determined/defined by either an increase (deterioration) of at least one degree in the Expanded Disability Status Scale (EDSS) score during the last year or the appearance of at least two major relapses of MS during the same period of time (under treatment) or intolerance to these agents.
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Up to date on all age and gender appropriate cancer screening per American Cancer Society .
Exclusion Criteria:
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Females who are pregnant or nursing or females of childbearing potential who are unwilling to maintain contraceptive therapy for the duration of the study
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Life expectancy < 6 months due to concomitant illnesses.
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Exposure to any investigational drug or procedure within 1 month prior to study entry or enrolled in a concurrent study that may confound results of this study.
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Active infectious disease. For patients who have tested positive, an expert will be consulted as to patient eligibility based on the patient's infectious status
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Any illness which, in the Investigator's judgment, will interfere with the patient's ability to comply with the protocol, compromise patient safety, or interfere with the interpretation of the study results
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Patients on chronic immunosuppressive transplant therapy
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Systolic blood pressure (supine) ≤90 mmHg;
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Resting heart rate > 100 bpm;
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Active clinical infection.
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Cerebrovascular accident within 6 months prior to study entry
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Known drug or alcohol dependence or any other factors which will interfere with the study conduct or interpretation of the results or who in the opinion of the investigator are not suitable to participate.
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History of cancer (other than non-melanoma skin cancer or in-situ cervical cancer) in the last five years.
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Unwilling and/or not able to give written informed consent.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Ageless Regenerative Institute LLC | Aventura | Florida | United States | 33180 |
Sponsors and Collaborators
- Ageless Regenerative Institute
Investigators
- Principal Investigator: Sharon McQuillan, MD, Ageless Regenerative Institute
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- AD-US-MS-001