Skip to main content
Clinical Trials/NCT02563340
NCT02563340
Unknown
Phase 1

Efficacy and Safety of Bone Marrow-derived Mesenchymal Stem Cells (BM-MSCs) on Chronic Antibody-mediated Rejection (cAMR) After Kidney Transplantation: A Multi-center Perspective Study

First Affiliated Hospital, Sun Yat-Sen University1 site in 1 country60 target enrollmentStarted: November 2015Last updated:

Overview

Phase
Phase 1
Sponsor
First Affiliated Hospital, Sun Yat-Sen University
Enrollment
60
Locations
1
Primary Endpoint
Estimated glomerular filtration rate (eGFR)

Overview

Brief Summary

This study is designed to investigate the efficacy and safety of allogeneic bone marrow-derived mesenchymal stem cells (BM-MSCs) on chronic antibody-mediated rejection (cAMR) after kidney transplantation. Chronic AMR is diagnosed according to Banff criteria 2013 based on renal graft biopsy and donor specific antibodies (DSA) examination. cAMR patients are assigned to MSCs group or control group. Patients in control group are prescribed to current desensitization therapy including at least one of the following treatments: plasmapheresis (PP), intravenous immunoglobulin (IVIG), rituximab or Bortezomib, depending on individual pathological and immunological features (eg. DSA type and titer) of each study subjects. Patients in MSCs group receive additional BM-MSCs therapy besides desensitization treatments as in control group. Allogeneic BM-MSCs (1*10^6/kg) are intravenously administered every two weeks for four consecutive doses. All cAMR patients are followed up for one year. Renal function, DSA level, pathological features, patient/graft survival, and severe adverse events are monitored during the follow-up period. Immunological features of patients in both groups are consecutively examined.

Study Design

Study Type
Interventional
Allocation
Non Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Single (Participant)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • kidney transplantation
  • cAMR diagnosis is determined based on renal graft biopsy and DSA examination
  • Patient is willing and capable of giving written informed consent for study participation and able to participate in the study for 12 months

Exclusion Criteria

  • Combined or multi-organ transplantation
  • Women who are pregnant, intend to become pregnant in the next 1 years, breastfeeding, or have a positive pregnancy test on enrollment or prior to study medication administration
  • Donors or recipients are known hepatitis C antibody-positive or polymerase chain reaction (PCR) positive for hepatitis C
  • Donors or recipients are known hepatitis B surface antigen-positive or PCR positive for hepatitis B
  • Donors or recipients are known human immunodeficiency virus (HIV) infection
  • Patients with active infection
  • Recipients with a history of substance abuse (drugs or alcohol) within the past 6 months, or psychotic disorders that are not capable with adequate study follow- up
  • Patients with severe cardiovascular dysfunction
  • WBC\<3\*10\^9/L or RBC \<5g/dL
  • Highly allergic constitution or having severe history of allergies

Outcomes

Primary Outcomes

Estimated glomerular filtration rate (eGFR)

Time Frame: 12 months

eGFR at month 12 after enrollment

Secondary Outcomes

  • Graft survival rate(12 months)
  • Pathological manifestation(12 months)
  • Donor specific antibody (DSA) level(12 months)
  • Severe adverse events(12 months)
  • Patient survival rate(12 months)

Investigators

Sponsor
First Affiliated Hospital, Sun Yat-Sen University
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Changxi Wang

Director of Organ Transplant Center

First Affiliated Hospital, Sun Yat-Sen University

Study Sites (1)

Loading locations...

Similar Trials

Unknown
Phase 1
Effect of BM-MSCs in DCD Kidney TransplantationKidney TransplantationAcute Kidney Tubular Necrosis
NCT02561767First Affiliated Hospital, Sun Yat-Sen University120
Completed
Phase 1
Treatment of Spinal Cord Injuries With (AutoBM-MSCs)vs (WJ-MSCs).Spinal Cord Injuries
NCT04288934University of Jordan20
Active, not recruiting
Phase 1
Research study aiming at investigating the potential effectiveness and safety of a treatment for chronic advanced heart failure of ischemic origin. The treatment is based on patient own stem cells that will be collected and guided to the cardiac cells lineage before being injected into the heart muscle.Chronic advanced symptomatic heart failure secondary to ischemic cardiomyopathyMedDRA version: 19.0Level: LLTClassification code 10010684Term: Congestive heart failureSystem Organ Class: 100000004849Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14]
EUCTR2011-001117-13-PLCelyad SA240
Active, not recruiting
Phase 1
Research study aiming at investigating the potential effectiveness and safety of a treatment for chronic advanced heart failure of ischemic origin. The treatment is based on patient own stem cells that will be collected and guided to the cardiac cells lineage before being injected into the heart muscle.Chronic advanced symptomatic heart failure secondary to ischemic cardiomyopathyMedDRA version: 17.0Level: LLTClassification code 10010684Term: Congestive heart failureSystem Organ Class: 100000004849Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14]
EUCTR2011-001117-13-IECardio3 BioSciences SA240
Active, not recruiting
Phase 1
Research study aiming at investigating the potential effectiveness and safety of a treatment for chronic advanced heart failure of ischemic origin. The treatment is based on patient own stem cells that will be collected and guided to the cardiac cells lineage before being injected into the heart muscle.Chronic advanced symptomatic heart failure secondary to ischemic cardiomyopathyMedDRA version: 17.1 Level: LLT Classification code 10010684 Term: Congestive heart failure System Organ Class: 100000004849Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14]
EUCTR2011-001117-13-HRCardio3 BioSciences SA240