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Study of Human Central Nervous System (CNS) Stem Cell Transplantation in Cervical Spinal Cord Injury

S

StemCells, Inc

Status and phase

Terminated
Phase 2

Conditions

Spine Injury
Cervical Spinal Cord Injury
Cervical Spine Injury

Treatments

Drug: HuCNS-SC cells

Study type

Interventional

Funder types

Industry

Identifiers

NCT02163876
CL-SCI-201

Details and patient eligibility

About

This study will evaluate the safety and efficacy of human central nervous system stem cell transplantation into patients with traumatic injury in the cervical region of the spinal cord.

Enrollment

31 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male or female subjects age 18 to 60 years.
  • Traumatic cervical spinal cord injury (cSCI) with C5-C7 motor levels according to the International Standards for Neurological Classification of Spinal Cord Injury (ISNCSCI) as determined by the Investigator.
  • American Spinal Injury Association Impairment Scale (AIS) Grades B or C
  • Minimum of 12 weeks post-injury prior to Screening

Exclusion criteria

  • History of penetrating SCI.
  • MRI evidence of complete spinal cord interruption .
  • Evidence of spinal instability, stenosis and/or persistent cord compression related to the initial trauma.
  • Prior participation in another investigational study within 90 days prior to Screening.
  • Previous organ, tissue, bone marrow transplantation, or gene transfer
  • History of malignancy (except non-melanoma skin cancers) that require(d) radiation and/or chemotherapy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

31 participants in 2 patient groups

HuCNS-SC cells
Experimental group
Description:
Intramedullary transplantation of HuCNS-SC cells in the cervical spine
Treatment:
Drug: HuCNS-SC cells
non-surgery arm
No Intervention group
Description:
non-surgery arm

Trial contacts and locations

14

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Data sourced from clinicaltrials.gov

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