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Bone Marrow-Derived Mesenchymal Stem Cell Therapy for Chronic Kidney Disease

Primary Purpose

Chronic Kidney Diseases

Status
Active
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Allogeneic adipose-derived mesenchymal stem cells (MSC)
Allogeneic adipose-derived mesenchymal stem cells (MSC)
Sponsored by
LaTonya J. Hickson
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Kidney Diseases

Eligibility Criteria

30 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Age 30-80 years
  2. Estimated glomerular filtration rate (eGFR) 25-55 ml/min/1.73m2

    1. If eGFR 45-55 ml/min/1.73m2, then albumin:creatinine ratio ≥300 mg/g or proteinuria ≥300 mg/day despite maximally tolerated dose of RAAS drugs (e.g. ACE Inhibitors, Angiotensin Receptor Blockers)
    2. If eGFR 25-44 ml/min/1.73m2, must have urine albumin:creatinine ratio ≥30mg/g despite maximally tolerated dose of RAAS drugs (e.g. ACE Inhibitors, Angiotensin Receptor Blockers)
  3. Hemoglobin A1c of ≤ 8% despite maximally tolerated anti-diabetes therapy
  4. Ability to give informed consent

Exclusion Criteria:

  1. Anemia (hemoglobin <9 g/dL)
  2. Body weight >150 kg or BMI >50
  3. Uncontrolled hypertension: sustained systolic blood pressure (SBP) >150 mmHg or diastolic blood pressure (DBP) ≥100 mmHg despite maximal doses of at least 2 different classes of anti-hypertensive medications
  4. Chronic hypotension history: sustained SBP <85 mmHg
  5. Glomerulonephritis not in partial or complete remission for 6 months (or estimated/ measured proteinuria greater than 10 grams/day),
  6. Active glomerulonephritis (glomerular diseases with evidence of active urinary sediment, serology or biopsy findings) including ANCA-associated glomerulonephritis, post-infectious glomerulonephritis, lupus nephritis, amyloidosis, or other monoclonal gammopathy of renal significance
  7. Autosomal dominant or recessive polycystic kidney disease
  8. Nephrotic syndrome defined as proteinuria >3.5 g per 24 hours, plus hypoalbuminemia (serum albumin less than or equal to 2.5 g/L) and edema.
  9. Proteinuria >5 g/day (with or without nephrotic syndrome).
  10. Kidney failure requiring renal replacement therapy (hemodialysis, peritoneal dialysis, or kidney transplantation)
  11. Active immunosuppression therapy (including prednisone greater than or equal to 10 mg daily)
  12. Kidney transplantation history
  13. Solid organ transplantation history
  14. Recent cardiovascular event (myocardial infarction, stroke, congestive heart failure (NYHA class ≥III or ejection fraction ≤30%) within 6 months or uncontrolled cardiac arrhythmias (e.g. ventricular arrhythmia, supraventricular tachycardia and bradyarrhythmia)
  15. History of liver cirrhosis
  16. Chronic obstructive pulmonary disease or asthma requiring daily medication
  17. History of blood clotting disorder (thromboembolism; pulmonary embolism, deep venous thrombosis)
  18. Pregnancy
  19. Unwilling to use contraception for at least 2 months after MSC infusion if sexually active and able to become pregnant or father a child.
  20. Active malignancy
  21. Active infection (e.g. systemic or specific organ involvement such as pneumonia or osteomyelitis)
  22. Recent COVID-19 infection within the last 3 months
  23. History of hepatitis B or C (without cure), or HIV infection
  24. History of allergic reaction to cellular products (ie. blood transfusions, platelets)
  25. Active tobacco use
  26. Illicit drug use and excessive alcohol use
  27. Presence of psychosocial issues (e.g., uncontrolled mental illness, unpredictable childcare or eldercare responsibilities, irregular/ inflexible work schedule) that may interfere with the ability to complete all study procedures
  28. Subjects anticipating prolonged travel or other physical restrictions that would prohibit return for scheduled study visits.
  29. Inability to give informed consent

Sites / Locations

  • Mayo Clinic Florida
  • Mayo Clinic Rochester

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

Dose Arm 1

Dose Arm 2

Arm Description

Subjects with chronic kidney disease will receive allogeneic bone marrow-derived mesenchymal stem cells (MSC) in two intravenous infusions of 100x10^6 cells at time zero and three months

Subjects with chronic kidney disease will receive allogeneic bone marrow-derived mesenchymal stem cells (MSC) single intravenous infusion of 200x10^6 cells

Outcomes

Primary Outcome Measures

Adverse events and/or serious adverse events
Number of adverse events and/or serious adverse events associated with mesenchymal stem cells intervention
Change in eGFR Value
Blood serum estimated glomerular filtration rate (eGFR) reported in milliliters per minute (mL/min)

Secondary Outcome Measures

Full Information

First Posted
May 2, 2022
Last Updated
September 7, 2023
Sponsor
LaTonya J. Hickson
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1. Study Identification

Unique Protocol Identification Number
NCT05362786
Brief Title
Bone Marrow-Derived Mesenchymal Stem Cell Therapy for Chronic Kidney Disease
Official Title
Bone Marrow-Derived Mesenchymal Stem Cell Therapy for Chronic Kidney Disease
Study Type
Interventional

2. Study Status

Record Verification Date
September 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
July 1, 2022 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
LaTonya J. Hickson

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Kidney Diseases

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Interventional Study Model
Sequential Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
14 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dose Arm 1
Arm Type
Experimental
Arm Description
Subjects with chronic kidney disease will receive allogeneic bone marrow-derived mesenchymal stem cells (MSC) in two intravenous infusions of 100x10^6 cells at time zero and three months
Arm Title
Dose Arm 2
Arm Type
Experimental
Arm Description
Subjects with chronic kidney disease will receive allogeneic bone marrow-derived mesenchymal stem cells (MSC) single intravenous infusion of 200x10^6 cells
Intervention Type
Drug
Intervention Name(s)
Allogeneic adipose-derived mesenchymal stem cells (MSC)
Intervention Description
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
Intervention Type
Drug
Intervention Name(s)
Allogeneic adipose-derived mesenchymal stem cells (MSC)
Intervention Description
Single intravenous infusion delivered systemically through a peripheral IV(over 30 minutes to 2 hours) of 200x10^6 cells at day 0
Primary Outcome Measure Information:
Title
Adverse events and/or serious adverse events
Description
Number of adverse events and/or serious adverse events associated with mesenchymal stem cells intervention
Time Frame
15 months
Title
Change in eGFR Value
Description
Blood serum estimated glomerular filtration rate (eGFR) reported in milliliters per minute (mL/min)
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 30-80 years Estimated glomerular filtration rate (eGFR) 25-55 ml/min/1.73m2 If eGFR 45-55 ml/min/1.73m2, then albumin:creatinine ratio ≥300 mg/g or proteinuria ≥300 mg/day despite maximally tolerated dose of RAAS drugs (e.g. ACE Inhibitors, Angiotensin Receptor Blockers) If eGFR 25-44 ml/min/1.73m2, must have urine albumin:creatinine ratio ≥30mg/g despite maximally tolerated dose of RAAS drugs (e.g. ACE Inhibitors, Angiotensin Receptor Blockers) Hemoglobin A1c of ≤ 8% despite maximally tolerated anti-diabetes therapy Ability to give informed consent Exclusion Criteria: Anemia (hemoglobin <9 g/dL) Body weight >150 kg or BMI >50 Uncontrolled hypertension: sustained systolic blood pressure (SBP) >150 mmHg or diastolic blood pressure (DBP) ≥100 mmHg despite maximal doses of at least 2 different classes of anti-hypertensive medications Chronic hypotension history: sustained SBP <85 mmHg Glomerulonephritis not in partial or complete remission for 6 months (or estimated/ measured proteinuria greater than 10 grams/day), Active glomerulonephritis (glomerular diseases with evidence of active urinary sediment, serology or biopsy findings) including ANCA-associated glomerulonephritis, post-infectious glomerulonephritis, lupus nephritis, amyloidosis, or other monoclonal gammopathy of renal significance Autosomal dominant or recessive polycystic kidney disease Nephrotic syndrome defined as proteinuria >3.5 g per 24 hours, plus hypoalbuminemia (serum albumin less than or equal to 2.5 g/L) and edema. Proteinuria >5 g/day (with or without nephrotic syndrome). Kidney failure requiring renal replacement therapy (hemodialysis, peritoneal dialysis, or kidney transplantation) Active immunosuppression therapy (including prednisone greater than or equal to 10 mg daily) Kidney transplantation history Solid organ transplantation history Recent cardiovascular event (myocardial infarction, stroke, congestive heart failure (NYHA class ≥III or ejection fraction ≤30%) within 6 months or uncontrolled cardiac arrhythmias (e.g. ventricular arrhythmia, supraventricular tachycardia and bradyarrhythmia) History of liver cirrhosis Chronic obstructive pulmonary disease or asthma requiring daily medication History of blood clotting disorder (thromboembolism; pulmonary embolism, deep venous thrombosis) Pregnancy Unwilling to use contraception for at least 2 months after MSC infusion if sexually active and able to become pregnant or father a child. Active malignancy Active infection (e.g. systemic or specific organ involvement such as pneumonia or osteomyelitis) Recent COVID-19 infection within the last 3 months History of hepatitis B or C (without cure), or HIV infection History of allergic reaction to cellular products (ie. blood transfusions, platelets) Active tobacco use Illicit drug use and excessive alcohol use Presence of psychosocial issues (e.g., uncontrolled mental illness, unpredictable childcare or eldercare responsibilities, irregular/ inflexible work schedule) that may interfere with the ability to complete all study procedures Subjects anticipating prolonged travel or other physical restrictions that would prohibit return for scheduled study visits. Inability to give informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
LaTonya Hickson, MD
Organizational Affiliation
Mayo Clinic
Official's Role
Principal Investigator
Facility Information:
Facility Name
Mayo Clinic Florida
City
Jacksonville
State/Province
Florida
ZIP/Postal Code
32224
Country
United States
Facility Name
Mayo Clinic Rochester
City
Rochester
State/Province
Minnesota
ZIP/Postal Code
55905
Country
United States

12. IPD Sharing Statement

Links:
URL
https://www.mayo.edu/research/clinical-trials
Description
Mayo Clinic Clinical Trials

Learn more about this trial

Bone Marrow-Derived Mesenchymal Stem Cell Therapy for Chronic Kidney Disease

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