Study of Human Central Nervous System Stem Cells (HuCNS-SC) in Patients With Thoracic Spinal Cord Injury
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ClinicalTrials.gov Identifier: NCT01321333 |
Recruitment Status :
Completed
First Posted : March 23, 2011
Last Update Posted : June 18, 2015
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Condition or disease | Intervention/treatment | Phase |
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Thoracic Spinal Cord Injury Spinal Cord Injury Spinal Cord Injury Thoracic Spinal Cord Trauma | Biological: HuCNS-SC cells | Phase 1 Phase 2 |
Study Type : | Interventional (Clinical Trial) |
Actual Enrollment : | 12 participants |
Allocation: | N/A |
Intervention Model: | Single Group Assignment |
Masking: | None (Open Label) |
Primary Purpose: | Treatment |
Official Title: | A Phase I/II Study of the Safety and Preliminary Efficacy of Intramedullary Spinal Cord Transplantation of Human Central Nervous System (CNS) Stem Cells (HuCNS-SC®) in Subjects With Thoracic (T2-T11) Spinal Cord Trauma |
Study Start Date : | March 2011 |
Actual Primary Completion Date : | April 2015 |
Actual Study Completion Date : | April 2015 |

Arm | Intervention/treatment |
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Experimental: HuCNS-SC cells
Single dose intramedullary administration of HuCNS-SC cells
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Biological: HuCNS-SC cells
single dose intramedullary transplantation of HuCNS-SC cells in the thoracic spinal cord
Other Names:
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- Types and frequencies of adverse events and serious adverse events [ Time Frame: One year after transplant ]Analysis of types and frequencies of adverse events one year after transplant.

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Ages Eligible for Study: | 18 Years to 60 Years (Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- T2-T11 thoracic spinal cord injury based on American Spinal Injury Association (ASIA) level determination by the principal investigator (PI)
- T2-T11 thoracic spinal cord injury as assessed by magnetic resonance imaging (MRI) and/or computerized tomography (CT)
- ASIA Impairment Scale (AIS) Grade A, B, or C
- Minimum of six weeks post injury for the initiation of screening
- Must have evidence of preserved conus function
- Must be at stable stage of medical recovery after injury
Exclusion Criteria:
- History of traumatic brain injury without recovery
- Penetrating spinal cord injury
- Evidence of spinal instability or persistent spinal stenosis and/or compression related to initial trauma
- Previous organ, tissue or bone marrow transplantation
- Previous participation in any gene transfer or cell transplant trial
- Current or prior malignancy

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01321333
Canada, Alberta | |
Foothills Medical Center | |
Calgary, Alberta, Canada, T2N-2T9 | |
Canada, Ontario | |
Toronto Western Hospital | |
Toronto, Ontario, Canada | |
Switzerland | |
University Hospital Balgrist- Uniklinik Balgrist, Forschstrasse 340 | |
Zurich, Switzerland, 8008 |
Study Chair: | Stephen Huhn, MD | StemCells, Inc. |
Responsible Party: | StemCells, Inc. |
ClinicalTrials.gov Identifier: | NCT01321333 |
Other Study ID Numbers: |
CL-N02-SC |
First Posted: | March 23, 2011 Key Record Dates |
Last Update Posted: | June 18, 2015 |
Last Verified: | June 2015 |
thoracic spinal cord injury spinal cord injury thoracic sub-acute spinal cord injury human neural stem cells |
stem cells stem cells transplant stem cells transplant spinal cord injury |
Spinal Cord Injuries Wounds and Injuries Thoracic Injuries Spinal Cord Diseases Trauma, Nervous System Aortic Dissection Dissection, Blood Vessel |
Aneurysm Vascular Diseases Cardiovascular Diseases Acute Aortic Syndrome Aortic Diseases Central Nervous System Diseases Nervous System Diseases |