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PROSPECTIVE, OPEN, MULTICENTRIC AND INTERNATIONAL STUDY OF MONITORING THE EFFICACY AND SECURITY OF MYFORTIC (ERL080A) IN RENAL TRANSPLANTATION RECEPTORS.

Not Applicable
Conditions
-Z94
Z94
Registration Number
PER-051-02
Lead Sponsor
OVARTIS BIOSCIENSES PERU S.A.,
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Male and female patients of at least 6 years of age.
2. Recipients of a primary or secondary kidney transplant of cadaveric origin, or from a related or unrelated living donor.
3. Patients currently receiving Neoral in association with MMF and corticosteroids as part of their immunosuppression regimen for at least 3 months prior to evaluation.

Exclusion Criteria

1. Patients with multiple organ transplantation (eg, kidney and pancreas) or with a previous transplant of any other organ other than the kidney (secondary kidney transplant allowed).
2. Evidence of rejection of the graft or treatment of an episode of acute rejection within two months prior to the evaluation.
3. Patients with any known hypersensitivity to Myfortic or other components of the pharmaceutical form (eg, lactose)
Patients with thrombocytopenia (<75,000 / mm2), an absolute neutrophil count <1,500 / mm2 and / or leukopenia (<2,500 / mm2), and / or hemoglobin <6.0 g / dL before recruitment.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<br>Outcome name:Monitoring and recording of all infections, all adverse events and all serious adverse events, regular monitoring of laboratory values of hematology, clinical chemistry and urine analyzes, and regular measurement of vital signs<br>Measure:To evaluate the parameters related to the safety and function of the graft in the recipients of a kidney transplant in maintenance.<br>Timepoints:throughout the study<br>
Secondary Outcome Measures
NameTimeMethod
<br>Outcome name:Acute rejection confirmed by biopsy<br>Chronic rejection<br>loss of the graft<br>graft function<br><br><br>Measure:To determine the efficacy, evaluated as the incidence of episodes of acute rejection and the survival of the graft, in the recipients of a renal transplant in maintenance.<br>Timepoints:according to need<br>
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