Mesenchymal Stem Cell Transplantation in the Treatment of Chronic Allograft Nephropathy

Phase 1

• Conditions: Kidney Transplant; Chronic Allograft Nephropathy
• Interventions: Biological: mesenchymal stem cell

• Registration Number: NCT00659620
• Lead Sponsor: Fuzhou General Hospital

Brief Summary

Mesenchymal Stem Cell (MSC) have been shown to have immunosuppressive and repairing properties. the investigators will infuse expanded MSC into patients who develop Chronic Allograft Nephropathy. The purpose of this study is to find out MSC is more effective in preventing organ rejection and maintaining kidney function.

Detailed Description

Kidney transplantation is a common procedure in hospitals, but organ rejection and chronic nephrotoxicity are potential problems for the patient. Approximately ninety percent of the protocol biopsies of renal allografts, performed at 18 months post transplantation, show histological lesions of chronic calcineurin nephrotoxicity. Mesenchymal Stem Cell (MSC) has been shown to have immunosuppressive and repairing properties. Some patient in this study will also receive two infusions of expanded MSC. This study will evaluate the safety and effectiveness of MSC infusions in patients .

This study will last 2 years. Participants will be randomly assigned to receive either the full immunosuppressive therapy and MSC infusions (Group 1) or immunosuppressive therapy alone (Group 2). Patients will undergo MSC infusions at the start of the study on Day 0. One year post- infusions, patients will be evaluated. At Months 12 participants will undergo kidney biopsies. Blood collection will occur at regular intervals, Serum creatinine and the estimated creatinine clearance will be monthly recorded. The transplanted kidney function will be evaluated.

Study Timeline

• Status Verified: 2008-04
• Study First Submitted: 2008-04-14
• Study First Submitted QC: 2008-04-14
• Last Update Submitted: 2008-04-14
• Study First Posted: 2008-04-16
• Last Update Posted: 2008-04-16
• Study Start: 2008-05
• Primary Completion: 2008-05
• Study Completion: 2010-05

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

• Recipients of a renal allograft, Male and female patients age 18 to 60 years of age.
• Ability to provide written informed consent.
• The serum creatinine form 176umol/L(2mg/ml) to 440umol/L(5mg/ml)
• Renal biopsy Criteria: chronic allograft nephropathy (Banff I-II).
• Immunosuppressant:CNI and MMF and Sirolimus
• Written informed consent, compliant with local regulations.

Exclusion Criteria

• Recipients with leucopenia (WBC < 3000/mm³), thrombocytopenia (Thr < 100.000/mm³),or hyperlipidemia (Tot Chol > 300 mg/dl or Triglycerides > 300 mg/dl).
• Recipients of multiple organs.
• Pregnant women.
• Previous history of malignancy
• Active infection including hepatitis B, hepatitis C, HIV, or TB as determined by a positive skin test or clinical presentation, or under treatment for suspected TB.
• Evidence of cardiovascular disease, existing congestive cardiac failure on physical exam and/or acute coronary syndrome in past 6 months.
• Inadequate compliance to treatment.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
1	mesenchymal stem cell	transplantation of mesenchymal stem cell

Primary Outcome Measures

Name	Time	Method
Creatinine and creatinine clearance rate	5

Secondary Outcome Measures

Name	Time	Method
Patient and graft survival [ Time Frame: At 1 years post-transplant ].	5
The proportion of renal biopsy after 12 months	2
The incidence of infectious complications	5
Incidence of adverse events associated with MSC and immunosuppression	5

Trial Locations

Locations (1)

Fuzhou General Hospital; 🇨🇳 Fuzhou, Fujian, China