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Table 3 Registered clinical trials of MSC-based therapy in kidney transplantation according to ClinicalTrials.gov

From: Preconditioning is an effective strategy for improving the efficiency of mesenchymal stem cells in kidney transplantation

ClinicalTrials.gov identifier

Aim of study

Enrollment

Phase

Status

NCT03478215

To investigate the safety and effectiveness of dose-escalation MSCs infusion compared to saline-only infusion in kidney transplantation

24

Phase 2

Recruiting

NCT02565459

To test MSCs as a strategy to induce tolerance in kidney transplant recipients

22

Phase 1

Recruiting

NCT02057965

To test the effectiveness of MSCs in combination with everolimus in facilitating tacrolimus withdrawal

70

Phase 2

Recruiting

NCT02492308

To determine the efficacy of autologous SVF derived MSCs in reduction of posttransplant immunosuppressants

120

Phase 1 and 2

Recruiting

NCT02409940

To evaluate the effect of allogeneic or autologous MSCs on immune cell response in kidney transplantation

17

Phase 1

Active but not recruiting

NCT02490020

To clarify the key role of MSCs to reduce AR and DGF after renal transplantation

260

Phase 1

Enrolling by invitation

NCT02561767

To determine the efficacy and safety of allogeneic MSCs in kidney transplantation

120

Phase 1 and 2

Not yet recruiting

NCT02563340

To investigate the efficacy and safety of allogeneic MSCs on chronic AMR after kidney transplantation

60

Phase 1 and 2

Not yet recruiting

NCT02563366

To investigate whether allogeneic MSCs can promote function recovery in patients with poor early graft function after kidney transplantation

120

Phase 1 and 2

Not yet recruiting

NCT03585855

To find out the effectiveness of MSCs in combination with standard therapy against AMR

4

Not applicable

Terminated (safety reason)

NCT00752479

To define the safety and biological/mechanistic effect of MSCs in living-related kidney transplant recipients

4

Phase 1 and 2

Terminated (necessity of major revision of the protocol)

  1. MSCs mesenchymal stem cells, SVF stromal vascular fraction, AR acute rejection, DGF delayed graft function, AMR antibody-mediated rejection