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Mesenchymal Stem Cells
Autologous, Adipose derived Mesenchymal Stem Cells for Spinal Cord Injury (CELLTOP Trial)
Phase 1
Waitlist Available
Led By Wenchun Qu, MD, PhD
Research Sponsored by Allan Dietz, Ph.D.
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline, 96 weeks
Awards & highlights
CELLTOP Trial Summary
This trial is testing whether it's safe to give patients with spinal cord injuries mesenchymal stem cells derived from fat tissue. All subjects will receive this experimental treatment, which is not approved by the FDA.
Eligible Conditions
- Spinal Cord Injury
- Paralysis
CELLTOP Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline, 96 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline, 96 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Acute Coryza
Secondary outcome measures
Change in Aspartate Aminotransferase (AST)
Change in Blood Urea Nitrogen (BUN)
Change in Carbon Dioxide
+18 moreCELLTOP Trial Design
1Treatment groups
Experimental Treatment
Group I: Phase IExperimental Treatment1 Intervention
Patients will receive a single dose of 100 million autologous, adipose derived mesenchymal stem cells. The cells are isolated from patient's adipose tissue and expanded for intrathecal delivery.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Autologous, Adipose derived Mesenchymal Stem Cells
2017
Completed Phase 1
~10
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Who is running the clinical trial?
Allan Dietz, Ph.D.Lead Sponsor
Allan DietzLead Sponsor
Mohamad BydonLead Sponsor
Frequently Asked Questions
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