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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00461825
Other study ID # Afssaps-980654
Secondary ID
Status Completed
Phase Phase 3
First received March 30, 2007
Last updated April 17, 2007
Start date July 1998
Est. completion date February 2007

Study information

Verified date April 2007
Source Poitiers University Hospital
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Interventional

Clinical Trial Summary

We have previously defined factors that predict the long term success of maintenance CsA monotherapy (CsAm) after kidney transplantation : donor age < 40 years, serum creatinine level at the initiation of CsAm £ 125 µmol/L, no rejection episode before CsAm initiation. We have also shown that the 8-year graft survival in 329 selected patients enrolled in maintenance CsA-m was 84 % (Hurault de Ligny et al, Transplantation, 2000 ; 69 : 1327-1332). These results were obtained with an old formulation of cyclosporin, azathioprine, steroid withdrawal over the first year and induction antibody. This prospective randomized multicentre study was designed to clarify whether maintenance Neoral + MMF or Neoral + AZA is better than a CsAm and wether Neoral + MMF is better than Neoral + AZA in low immunological risk cadaveric kidney transplant recipients.


Description:

Between july 1998 and january 2004 selected patients were randomly assigned equally within each centre to receive CsAm or bitherapy with equally CsA + MMF or CsA + AZA.


Recruitment information / eligibility

Status Completed
Enrollment 207
Est. completion date February 2007
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 25 Years and older
Eligibility - Inclusion criteria:

- Primary cadaveric renal transplant with induction therapy, delayed Neoral, MMF and prednisone

- Steroid withdrawal >= 3 months before enrolment

- Bitherapy Neoral + CellCept

- Follow up time since transplantation : 11-24 months

- Recipient age >= 25 years

- Donor age <= 45 years

- Serum creatinine level <= 125 µmol/L and/or calculated creatinine clearance >= 50 ml/mn (CG formula)

- No or only one steroid-sensitive acute rejection episode during the first year post-transplantation

- PRA <= 25 %

- Written informed consent

- Exclusion Criteria:

- Living donor transplantation

- Recipient receiving tacrolimus

- Azathioprine intolerance

- Thrombopenia < 100 000/mm³

- Neutropenia < 1500/mm³

- Hemoglobinemia <= 8g/dl

- On going infection

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Cyclosporin A: C0: 75–125ng/ml-dose adapted in the 3 groups

Group A: CsA + Azathioprine(1 to 2 mg/kg/day)

Group B: CsA + CellCept(500 mg x 2/day)

Group C: CsAm


Locations

Country Name City State
France Caen university Hospital Caen
France Dupuytren University Hospital Limoges
France Poitiers University hospital Poitiers
France Reims University Hospital Reims
France Rouen University Hospital Rouen

Sponsors (1)

Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

References & Publications (2)

Hurault de Ligny B, Toupance O, Lavaud S, Bauwens M, Peyronnet P, Le Meur Y, Ryckelynck JP, Jolly D, Leroux-Robert C, Touchard G. Factors predicting the long-term success of maintenance cyclosporine monotherapy after kidney transplantation. Transplantation. 2000 Apr 15;69(7):1327-32. — View Citation

Touchard G, Hauet T, Cogny Van Weydevelt F, Hurault de Ligny B, Peyronnet P, Lebranchu Y, Toupance O, N'Doye P, Busson M. Maintenance cyclosporin monotherapy after renal transplantation--clinical predictors of long-term outcome. Nephrol Dial Transplant. 1997 Sep;12(9):1956-60. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary to compare maintenance CsAm with dual therapy groups and within dual therapy MMF with AZA for :
Primary The incidence and the delay of occurrence of graft dysfunction episode defined as ³ 20 % increase in serum creatinine level (mean of three results obtained in the same laboratory) and requiring a graft biopsy.
Primary Causes of graft dysfunction episodes diagnosed by graft biopsy.
Primary The incidence of serious infections (HVZ, EBV, HPV genital infection, febrile UTI, pneumonitis...)
Secondary To compare the three treatment groups for the following parameters :
Secondary Incidence of therapeutic failure defined by biopsy proven acute rejection episode or CsA renal toxicity
Secondary Graft function evaluated by serum creatinine level and calculated creatinine clearance (CG formula)
Secondary Adverse events
Secondary Patient and graft survival
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