Spinal Cord Injury Clinical Trial
Official title:
PhaseⅠ/ⅡTrial of Autologous Bone Marrow Derived Mesenchymal Stem Cells to Patients With Spinal Cord Injury.
The study is a phase I/II trial designed to establish the safety and efficacy of intravenous combined with intrathecal administration of autologous bone marrow derived mesenchymal stem cells to patients with spinal cord injury.
Spinal cord injury (SCI) is a traumatic disorder resulting in a functional deficit that
usually leads to severe and permanent paralysis. Pharmacological and rehabilitation
therapies to SCI get limited effect. Another promising therapeutic approaches for SCI is
cellular transplantation. Cell types used in SCI therapy include Schwann cells, olfactory
ensheathing cells and adult stem cells, such as neural stem cells, umbilical cord blood
derived cells, mesenchymal stem cells (MSCs) or induced pluripotent stem cells. There are
not yet conclusive evidences on which types of glial or adult stem cells are most effective
in SCI treatment.
MSC have been shown to promote anatomical and functional recovery in animal models of SCI by
promoting tissue sparing ,axonal regeneration, and remyelination. Therapeutic effects of
MSCs are primarily due to the secretion of soluble factors and the provision of
extracellular matrix that provide protection and support repair. MSC are attractive
candidates for transplantation into human patients because they can be easily harvested,
expanded and banked, or derived directly from the patient allowing for autologous
transplantation, obviating the need for immune suppression.
The clinical translation of cellular transplantation strategies requires a safe and
efficient means of cellular delivery. In animal models of SCI, the most common delivery is
direct injection into the injury site, which allows a defined number of cells to be
delivered, but risks further injuring the cord. Less invasive methods for cell delivery have
been investigated, including intravascular delivery (intravenous (IV) and intra-arterial)
and delivery into the cerebrospinal fluid (intrathecal). These minimally-invasive techniques
decrease the risk to the patient and allow delivery of multiple cell doses. Maybe
intrathecal administration is superior to IV delivery, cell engraftment and tissue sparing
were significantly better after intrathecal delivery, but more researches are needed for get
conclusion.
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Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
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