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) |