MSC for Occlusive Disease of the Kidney

This study is currently recruiting participants.
Verified May 2013 by Mayo Clinic
Sponsor:
Information provided by (Responsible Party):
Stephen C. Textor, M.D., Mayo Clinic
ClinicalTrials.gov Identifier:
NCT01840540
First received: April 23, 2013
Last updated: May 8, 2013
Last verified: May 2013

April 23, 2013
May 8, 2013
April 2013
April 2014   (final data collection date for primary outcome measure)
Renal blood flow and function in the treated kidneys. [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
Individual kidney blood flow, measured by multidetector CT contrast transit times, will be measured before and after MSC infusion.
Renal blood flow and function in the treated kidneys. [ Time Frame: 2 years ] [ Designated as safety issue: Yes ]
Individual kidney blood flow, function and structure will be evaluated before and after MSC infusion. Toxicity data will be determined at each dose level.
Complete list of historical versions of study NCT01840540 on ClinicalTrials.gov Archive Site
Level of kidney function. [ Time Frame: 2 years ] [ Designated as safety issue: No ]
Level of kidney function will be assessed as glomerular filtration rate by iothalamate clearance. Tissue oxygenation within each kidney will be measured by Blood Oxygen Level Dependent (BOLD) magnetic resonance.
Level of kidney function and blood pressure. [ Time Frame: 2 years ] [ Designated as safety issue: No ]
Measure of glomerular filtration rate and oscillometrics blood pressure after 3 months.
Blood pressure levels. [ Time Frame: 2 years ] [ Designated as safety issue: No ]
Blood pressure will be assessed by oscillometric measurement.
Not Provided
 
MSC for Occlusive Disease of the Kidney
Phase I Study of Autologous Mesenchymal Stem Cells in the Treatment of Atherosclerotic Renal Artery Stenosis

To determine the safety and toxicity of intra-arterial infused autologous adipose derived mesenchymal stromal (stem) cells in patients with vascular occlusive disease of the kidney.

Not Provided
Interventional
Phase 1
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
  • Atherosclerotic Renal Artery Stenosis
  • Ischemic Nephropathy
  • Repair of Renal Microvasculature
Drug: Arterial infusion of autologous mesenchymal stem cells
Experimental: Arterial infusion of autologous mesenchymal stem cells
Patients will undergo a subcutaneous fat biopsy for expansion of mesenchymal stromal (stem) cells (MSC) in the Human Cell Therapy Laboratory. Patients will be admitted to the inpatient Clinical Research Unit of the Mayo Clinic Center for 3 days prior to treatment, for pre-infusion tests. Renal angiography will be performed to deliver a single intra-arterial dose of MSC's into one affected kidney. Patients will be observed for 24 hours for acute adverse events. Patients will have remote visits at 1 week, 4 weeks,8 weeks, and 6 months. At 3 months, patients will return for repeat evaluation of kidney function, blood flow and structural alterations within the clinical research unit at St. Mary's Hospital, Rochester, Minnesota. Thereafter, health assessment and blood draws will be repeated at 12 and 24 months with urinary cytology and MRI.  
Intervention: Drug: Arterial infusion of autologous mesenchymal stem cells
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
15
April 2017
April 2014   (final data collection date for primary outcome measure)

4.1 Inclusion Criteria

  1. Are between ages 40 and 80 years old.
  2. Advanced vascular occlusive disease (atherosclerosis) affecting one or both kidneys: defined as a) loss of parenchymal volume and renal blood flow (measured by MDCT as previously described (17) and/or duplex ultrasound velocity above 300 cm/sec to the affected kidney to be infused with MSC's.
  3. Have serum creatinine below 2.5 mg/dL
  4. Have no-contraindications to angiography: severe contrast allergy
  5. Have no contraindications to MR evaluations: e.g. pacemaker or magnetically active metal fragments, claustrophobia
  6. Ability to comply with protocol
  7. Competent and able to provide written informed consent

4.2 Exclusion Criteria

  1. Advanced CKD: Stage 5 (two kidney eGFR < 15 ml/min/1.73 m2) contralateral renal artery occlusion/stenosis above 75% or ESRD requiring dialysis
  2. Clinically significant abnormalities on laboratory examination, including Bilirubin (> 2 x normal), platelets (<100 thousand), potassium (>5.5 mEq/L), and sodium (<130 mEq/L), ALT or AST more than 2 x normal, Prothrombin time (INR>1.4), Hemoglobin <10.0 g/dL.
  3. Clinically significant medical conditions within the six months before administration of MSCs: e.g. myocardial infarction, active angina, congestive heart failure) that would, in the opinion of the investigators, compromise the safety of the patient.
  4. Specific exclusions:

    1. Clinical history of deep vein thrombosis within three months of MSC administration
    2. Uncontrolled hypertension (Systolic BP >180 mmHg despite therapy)
    3. Active infection
    4. Reduced ejection fraction (below 30%)
    5. Evidence of hepatitis B,C, or HIV
    6. Diabetes treated with insulin and/or glucose lowering agents
    7. Anemia (Hgb<10 g/dL)
    8. Regular use of potentially renotoxic drugs, e.g. non-steroidal anti-inflammatory agents (NSAID's): (>2 x weekly)
  5. History of cancer including melanoma (with the exception of localized skin cancers)
  6. Investigational drug exposure within thirty (30) days of baseline
  7. Beck's depression score above 16
  8. Pregnant or breast feeding.
  9. History of clinically significant auto-immunity or any previous example of fat-directed autoimmunity
Both
40 Years to 80 Years
No
Contact: Stephen C. Textor, MD stextor@mayo.edu
Contact: Beverly K. Tietje, Associates 507-255-0401 tietje.beverly@mayo.edu
United States
 
NCT01840540
12-009298
No
Stephen C. Textor, M.D., Mayo Clinic
Mayo Clinic
Not Provided
Principal Investigator: Stephen Textor, MD Mayo Clinic
Mayo Clinic
May 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP