The purpose of this study is to assess the safety and tolerability of intravenously delivered mesenchymal steml cells (MSC) in one of two fixed dosing regimens at two time points in patients with chronic kidney disease.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
14
Two intravenous infusions delivered systemically through a peripheral IV(over 30 minutes to 2 hours) of 100x10\^6 cells at day 0 and day 84
Single intravenous infusion delivered systemically through a peripheral IV(over 30 minutes to 2 hours) of 200x10\^6 cells at day 0
Mayo Clinic Florida
Jacksonville, Florida, United States
Mayo Clinic Rochester
Rochester, Minnesota, United States
Adverse events and/or serious adverse events
Number of adverse events and/or serious adverse events associated with mesenchymal stem cells intervention
Time frame: 15 months
Change in eGFR Value
Blood serum estimated glomerular filtration rate (eGFR) reported in milliliters per minute (mL/min)
Time frame: 6 months
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