TAIZ -Monocytes for the Induction of Donor Specific Tolerance in Renal Allograft Recipients (Cadaver Kidney)

NCT ID: NCT00223093

Last Updated: 2005-10-28

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE1
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-02-29
• Study Completion Date: 2005-08-31

Brief Summary

Induce tolerance or reduce the amount of immunosuppression after renal transplant patient (receiving cadaver kidney)with so called TAIZ-monocytes

Conditions

Renal Transplantation

Keywords

renal transplantation, TAIZ-moncytes

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Interventions

TAIZ

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Male or female adult patients aged between 18 and 64 years (inclusive). A female of childbearing potential may be enrolled provided she:

• has a negative pregnancy test at Screening and
• is routinely using adequate contraception prior to and during the study and
• agrees not to attempt to become pregnant during the study and
• is not lactating A female of non-childbearing potential will be defined as one who has been postmenopausal for at least one year or has been surgically sterilised.

2. Patients receiving a first renal transplant.

3. Patients who fulfil the criteria to receive an allogeneic renal transplant from a cadaver (according to the Eurotransplant (ET) manual on organ allocation and the Bundesärztekammer allocation criteria).

4. Patients who, after the nature of the study and the disclosure of their data has been explained to them, have freely given Informed Consent in writing.

Exclusion Criteria

1. Patients who have received a renal transplant.

2. Patients who have an active infection at the time of entry into the study (Screening).

3. Recipient and donor pairs who show the following incompatible CMV constellation: the donor is CMV positive and the recipient is CMV negative.

4. Patients and donor who have positive evidence of HIV or have active virus hepatitis B and C.

5. Patients with a history of alcohol and/or drug abuse.

6. Patients who are pregnant women or nursing mothers.

7. Known hypersensitivity or contraindication to one of the immunosuppressives administered during the course of the study: tacrolimus, sirolimus or steroids (prednisolone and methylprednisolone).

8. Patients with a history or present symptoms of autoimmune vasculitis.

9. Detection of >5% HLA antibodies (current values determined during the last three months).

10. Patients with a malignancy or history of malignancy.

11. Patients with renal insufficiency due to a vasculitis.

12. Recipient and donor pairs with complete HLA matching.

13. Patients whose condition requires continuous systemic steroid administration.

14. Patients who are simultaneously participating or plan to participate in any other clinical study.

15. Psychiatric or emotional problems or lack of knowledge of the German language which would invalidate the giving of Informed Consent or limit the ability of the subject to comply with study requirements.

16. Unwillingness or inability to provide Informed Consent or to participate satisfactorily for the entire trial period

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital Schleswig-Holstein

OTHER

Sponsor Role: lead

Principal Investigators

Ulrich Kunzendorf, MD

Role: PRINCIPAL_INVESTIGATOR

University of Schleswig-Holstein, Campus Kiel Department of Nephrolgy

Other Identifiers

006

Identifier Type: -

Identifier Source: org_study_id