Mesenchymal Stromal Cells for Ischemic Stroke
Status: | Not yet recruiting |
---|---|
Conditions: | Peripheral Vascular Disease, Neurology |
Therapuetic Areas: | Cardiology / Vascular Diseases, Neurology |
Healthy: | No |
Age Range: | 18 - 83 |
Updated: | 4/21/2016 |
Start Date: | December 2015 |
End Date: | December 2017 |
Contact: | Chad Tremont, BS |
Email: | Chad.c.tremont@uth.tmc.edu |
Phone: | 713.500.6624 |
SAfety of Mesenchymal Stromal Cells for Ischemic Stroke
The purpose of this study is to determine if mesenchymal stem cells given by IV is feasible
and safe in patients with recent ischemic stroke and to decide the maximum tolerated dose
when given between 3-10 days after an ischemic stroke.
and safe in patients with recent ischemic stroke and to decide the maximum tolerated dose
when given between 3-10 days after an ischemic stroke.
This is a randomized, double-blind, placebo controlled study. . Approximately 48 subjects
will be enrolled in the trial, undergo a real or SHAM MSC IV infusion and will be follow out
to 1 year. There will potentially be 4 Cohorts with the dose escalation at a 3:1
randomization schedule
Objectives:
- The primary hypothesis' are that intravenous administration of allogeneic bone marrow
derived mesenchymal stem cells is feasible and safe in patients with recent ischemic
stroke and to determine the maximum tolerated dose (MTD) of IV MSCs when administered
sub-acutely between 3-10 days following ischemic stroke.
- The secondary hypothesis is that allogeneic MSC transplantation will improve functional
outcome after recent ischemic stroke.
Safety and clinical efficacy points to be evaluated at Day 7 clinic visit, Day 30, Day 60,
Day 90, and Day 180. Primary outcome or Primary endpoint of the study is to define the
safety or harm of the MSCs
will be enrolled in the trial, undergo a real or SHAM MSC IV infusion and will be follow out
to 1 year. There will potentially be 4 Cohorts with the dose escalation at a 3:1
randomization schedule
Objectives:
- The primary hypothesis' are that intravenous administration of allogeneic bone marrow
derived mesenchymal stem cells is feasible and safe in patients with recent ischemic
stroke and to determine the maximum tolerated dose (MTD) of IV MSCs when administered
sub-acutely between 3-10 days following ischemic stroke.
- The secondary hypothesis is that allogeneic MSC transplantation will improve functional
outcome after recent ischemic stroke.
Safety and clinical efficacy points to be evaluated at Day 7 clinic visit, Day 30, Day 60,
Day 90, and Day 180. Primary outcome or Primary endpoint of the study is to define the
safety or harm of the MSCs
Inclusion Criteria:
1. acute ischemic stroke
2. age 18 to 83 years
3. post stroke mRS > 3
4. NIHSS of 7-25
5. Deficits on the total NIHSS can be lower than 7 provided the patients have moderate
aphasia or visual loss (2 on the Best Language or Visual loss NIHSS subcomponent)
*Criteria for mRS not used for this category of subjects
6. Last seen normal st within 3-9 days prior to stroke. Time of onset for wake-up stroke
will be defined as the time the patient woke up with symptoms.
7. stem cell transplantation procedure must be performed between 3-10 days after stroke
symptom onset
Exclusion Criteria:
1. Ischemic stroke, primary hemorrhagic or traumatic lesion of the brain or myocardial
infarction within past 30 days prior to current stroke.
2. Mechanical heart valve
3. Uncontrolled seizure disorder, defined as a seizure within the last 6 months
4. Developmental delay
5. Chronic kidney disease
6. Hepatic disease or altered liver function
7. Pulmonary disease
8. Cancer within 5 years prior to study
9. Prior immunosuppression, including chemotherapy within last 3 years
10. Known HIV
11. Uncorrected coagulopathy or severe anemia
12. Pregnancy
13. Unable to undergo MRI or CT scan
14. Imaging shows clinically significant hemorrhage
We found this trial at
1
site
Houston, Texas 77030
Principal Investigator: Sean Savitz, MD
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