Feasibility and Safety of Allogeneic Adipose Mesenchymal Stem Cells (aMSCs) Delivery Into Kidney Allografts Procured From Deceased Donors With High Kidney Donor Profile Index (KDPI)

Sponsor
Tambi Jarmi (Other)
Overall Status
Recruiting
CT.gov ID
NCT04388761
Collaborator
(none)
15
1
3
40.1
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Study Details

Study Description

Brief Summary

The purpose of this research is to test an investigational drug called Adipose Mesenchymal Stem Cells (aMSCs) for the treatment of ischemia re-perfusion injury (IRI) in patients that have had a kidney transplant.

Condition or Disease Intervention/Treatment Phase
  • Drug: Allogeneic adipose derived mesenchymal stem cells
Phase 1

Study Design

Study Type:
Interventional
Anticipated Enrollment :
15 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Feasibility and Safety of Allogeneic Adipose Mesenchymal Stem Cells (aMSCs) Delivery Into Kidney Allografts Procured From Deceased Donors With High Kidney Donor Profile Index (KDPI)
Actual Study Start Date :
Sep 28, 2020
Anticipated Primary Completion Date :
Feb 1, 2024
Anticipated Study Completion Date :
Feb 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intra parenchymal injection

5 subjects will receive AMSCs via direct injection into the kidney parenchyma only

Drug: Allogeneic adipose derived mesenchymal stem cells
Injection of Allogeneic adipose derived mesenchymal stem cells into the Kidney allograft

Experimental: Intra-arterial infusion

5 subjects will receive AMSCs via intra-arterial infusion only

Drug: Allogeneic adipose derived mesenchymal stem cells
Injection of Allogeneic adipose derived mesenchymal stem cells into the Kidney allograft

Experimental: Intra parenchymal injection & Intra-arterial infusion

5 subjects will receive AMSCs via direct injection into the kidney parenchyma and intra-arterial infusion

Drug: Allogeneic adipose derived mesenchymal stem cells
Injection of Allogeneic adipose derived mesenchymal stem cells into the Kidney allograft

Outcome Measures

Primary Outcome Measures

  1. Serious Adverse Events (SAEs) [1 year]

    Number of serious adverse events reported. SAEs will include delayed graft function (30 days post-transplant), difficult to control bleeding (intraoperative), sub-scapular kidney hematoma or arteriovenous fistula formation (24 hours postop), and development of stroke, myocardial infarction, or pulmonary embolism (1 year post-transplant).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Male or female kidney transplant candidates age 18 and above.

  • Patient is receiving kidney allograft from deceased donor with KDPI>85%.

  • Ability of subject to give appropriate consent.

  • Females of childbearing potential with agreement to use birth control for six months post-transplant.

  • Approved by the Mayo Clinic Transplant Selection Committee.

  • Signed Authorization for Donation of Anatomical Gifts on file.

Exclusion Criteria:
  • Positive pregnancy test at the time of the kidney offer is called for the potential recipient.

  • Kidney transplant potential recipients with active malignancy (except none melanoma skin malignancies).

  • Patients with previous history of solid organ transplant (Heart, Lung, Intestine, Kidney and/or Pancreas).

  • Patients with previous history of bone marrow transplant.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Mayo Clinic in Florida Jacksonville Florida United States 32224

Sponsors and Collaborators

  • Tambi Jarmi

Investigators

  • Principal Investigator: Tambi Jarmi, MD, Mayo Clinic

Study Documents (Full-Text)

None provided.

More Information

Additional Information:

Publications

None provided.
Responsible Party:
Tambi Jarmi, Principal Investigator, Mayo Clinic
ClinicalTrials.gov Identifier:
NCT04388761
Other Study ID Numbers:
  • 20-000264
First Posted:
May 14, 2020
Last Update Posted:
Oct 14, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
Yes
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 14, 2021