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A Study of Allogeneic Mesenchymal Bone Marrow Cells in Subjects With Ischemic Stroke

Primary Purpose

Ischemic Stroke

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Allogeneic adult mesenchymal bone marrow stem cells
Sponsored by
Stemedica Cell Technologies, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Stroke focused on measuring allogeneic, adult, stem, cells, stroke, ischemic

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Clinical diagnosis of ischemic stroke for longer than 6 months
  • Brain CT/MRI scan at initial diagnosis and at enrollment consistent with ischemic stroke
  • No substantial improvement in neurologic or functional deficits for the 2 months prior to enrollment
  • NIHSS score between 6-20
  • Life expectancy greater than 12 months
  • Prior to treatment patient received standard medical care for the secondary prevention of ischemic stroke
  • Adequate organ function as defined by the following criteria:

Exclusion Criteria:

  • History of uncontrolled seizure disorder
  • History of cancer within the past 5 years.
  • History of cerebral neoplasm
  • Positive for hepatitis B, C or HIV
  • Myocardial infarction withing six months of study entry
  • Findings on baseline CT suggestive of subarachnoid or intracerebral hemorrhage within past 12 months.
  • Allergies to Bovine or Porcine products

Sites / Locations

  • Mercy Gilbert and Chandler Medical Center
  • University of California Irvine Department of Neurology
  • University of California San Diego Division of Neurological Surgery

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Stem cells

Arm Description

All subjects will receive allogeneic adult mesenchymal bone marrow stem cells

Outcomes

Primary Outcome Measures

The primary endpoint will be the safety of treatment with aMBMC during the twelve-month study period.
The primary endpoint will be the safety of treatment with aMBMC during the twelve-month study period as determined by the incidence and severity of adverse events, clinically-significant changes on clinical laboratory tests, vital signs, physical and neurologic examinations.

Secondary Outcome Measures

National Institutes of Health Stroke Scale Score.
The change from the baseline in National Institutes of Health Stroke Scale score will be calculated at 1, 3, 6, 9, 12 months post-treatment, as available:
Mini Mental Status Exam score.
The change from the baseline in Mini Mental Status Exam score will be calculated at 1, 3, 6, 9, 12 months post-treatment, as available.
Barthel Index Score.
The change from the baseline in Barthel Index score at 1, 3, 6, 9, 12 months post-treatment, as available.
The Geriatric Depression Scale Score.
The change from baseline in the Geriatric Depression Scale score at 1, 3, 6, 9, 12 months post-treatment, as available.

Full Information

First Posted
February 10, 2011
Last Updated
November 29, 2018
Sponsor
Stemedica Cell Technologies, Inc.
Collaborators
University of California, San Diego, Mercy Gilbert Medical Center at AZ, Chandler Regional Medical Center at Chandler AZ, UCI Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT01297413
Brief Title
A Study of Allogeneic Mesenchymal Bone Marrow Cells in Subjects With Ischemic Stroke
Official Title
A Phase I/II, Multi-Center, Open-Label Study to Assess the Safety, Tolerability, and Preliminary Efficacy of a Single Intravenous Dose of Allogeneic Mesenchymal Bone Marrow Cells to Subjects With Ischemic Stroke
Study Type
Interventional

2. Study Status

Record Verification Date
November 2018
Overall Recruitment Status
Completed
Study Start Date
February 2011 (undefined)
Primary Completion Date
September 2017 (Actual)
Study Completion Date
November 15, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Stemedica Cell Technologies, Inc.
Collaborators
University of California, San Diego, Mercy Gilbert Medical Center at AZ, Chandler Regional Medical Center at Chandler AZ, UCI Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to assess the safety and tolerability of allogeneic adult mesenchymal bone marrow cells administered intravenously to patients with ischemic stroke.
Detailed Description
Stroke remains a major global healthcare problem. Recent data compiled by the American Heart Association (AHA) for 2008 show that the annual incidence of new or recurrent stroke in the United States is about 780,000, with approximately 600,000 of these strokes being first attacks. Among adults age 20 and older, the estimated prevalence of stroke in 2005 was 5.8 million in the United States, resulting in >150,000 deaths annually, with 4.8 million stroke survivors alive today. Stroke ranks as the country's third leading cause of death, behind only cancer and heart disease. The only approved treatments of acute ischemic stroke involve restoring blood flow to the affected region by using thrombolytics or mechanical devices that physically remove clots. However, the use of thrombolytics is limited due to the therapeutic window of < 3-6 hours post onset of stroke symptoms such that only a small fraction of stroke patients receive this therapy. Following the completion of a stroke, there is little therapy to offer patients to promote recovery other than physical, occupational, and speech therapy. Allogeneic mesenchymal stem cells have been used in a number of clinical trials for different indications demonstrated the safety of allogeneic mesenchymal stem cell treatment. In addition to their ability to differentiate into multiple different cell types that would be contributory to the recovery and repair of the brain by replacing destroyed cells, mesenchymal stem cells also secrete angiogenins, cytokines and trophic factors that can support and stimulate multiple other cell types. The cascade of cellular events following the release of these cytokines and trophic factors would also potentially lead to beneficial effects by restoring blood supply, by rescuing cells at risk, and by stimulating the remaining cell populations to repair and propagate new cells and synaptic connections.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Stroke
Keywords
allogeneic, adult, stem, cells, stroke, ischemic

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
38 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Stem cells
Arm Type
Experimental
Arm Description
All subjects will receive allogeneic adult mesenchymal bone marrow stem cells
Intervention Type
Biological
Intervention Name(s)
Allogeneic adult mesenchymal bone marrow stem cells
Intervention Description
Patients will receive intravenously one dose of 0.5-1.5 million cells per kg of allogeneic adult mesenchymal bone marrow stem cells
Primary Outcome Measure Information:
Title
The primary endpoint will be the safety of treatment with aMBMC during the twelve-month study period.
Description
The primary endpoint will be the safety of treatment with aMBMC during the twelve-month study period as determined by the incidence and severity of adverse events, clinically-significant changes on clinical laboratory tests, vital signs, physical and neurologic examinations.
Time Frame
12 month
Secondary Outcome Measure Information:
Title
National Institutes of Health Stroke Scale Score.
Description
The change from the baseline in National Institutes of Health Stroke Scale score will be calculated at 1, 3, 6, 9, 12 months post-treatment, as available:
Time Frame
12 months
Title
Mini Mental Status Exam score.
Description
The change from the baseline in Mini Mental Status Exam score will be calculated at 1, 3, 6, 9, 12 months post-treatment, as available.
Time Frame
12 month
Title
Barthel Index Score.
Description
The change from the baseline in Barthel Index score at 1, 3, 6, 9, 12 months post-treatment, as available.
Time Frame
12 month
Title
The Geriatric Depression Scale Score.
Description
The change from baseline in the Geriatric Depression Scale score at 1, 3, 6, 9, 12 months post-treatment, as available.
Time Frame
12 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Clinical diagnosis of ischemic stroke for longer than 6 months Brain CT/MRI scan at initial diagnosis and at enrollment consistent with ischemic stroke No substantial improvement in neurologic or functional deficits for the 2 months prior to enrollment NIHSS score between 6-20 Life expectancy greater than 12 months Prior to treatment patient received standard medical care for the secondary prevention of ischemic stroke Adequate organ function as defined by the following criteria: Exclusion Criteria: History of uncontrolled seizure disorder History of cancer within the past 5 years. History of cerebral neoplasm Positive for hepatitis B, C or HIV Myocardial infarction withing six months of study entry Findings on baseline CT suggestive of subarachnoid or intracerebral hemorrhage within past 12 months. Allergies to Bovine or Porcine products
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lev Verkh, PhD
Organizational Affiliation
Stemedica Cell Technologies, Inc.
Official's Role
Study Director
Facility Information:
Facility Name
Mercy Gilbert and Chandler Medical Center
City
Gilbert
State/Province
Arizona
ZIP/Postal Code
85224
Country
United States
Facility Name
University of California Irvine Department of Neurology
City
Orange
State/Province
California
ZIP/Postal Code
92868
Country
United States
Facility Name
University of California San Diego Division of Neurological Surgery
City
San Diego
State/Province
California
ZIP/Postal Code
92123
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
31495331
Citation
Levy ML, Crawford JR, Dib N, Verkh L, Tankovich N, Cramer SC. Phase I/II Study of Safety and Preliminary Efficacy of Intravenous Allogeneic Mesenchymal Stem Cells in Chronic Stroke. Stroke. 2019 Oct;50(10):2835-2841. doi: 10.1161/STROKEAHA.119.026318. Epub 2019 Sep 9.
Results Reference
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A Study of Allogeneic Mesenchymal Bone Marrow Cells in Subjects With Ischemic Stroke

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