ClinicalTrials.Veeva

Menu

Study Evaluating Rapamune in Patients After Kidney Transplantation

Wyeth logo

Wyeth

Status

Terminated

Conditions

Renal Transplantation

Treatments

Drug: sirolimus

Study type

Observational

Funder types

Industry

Identifiers

NCT00240214
0468E-100875

Details and patient eligibility

About

The purpose of this study is to obtain data on the effectiveness and safety of Rapamune under everyday conditions

Enrollment

500 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients having received a renal allograft from a cadaveric or living donor with low or moderate risk of developing acute rejection episodes.

Exclusion criteria

  • Contraindications according to Summary of the Product Characteristics (SmPC).

Trial design

500 participants in 1 patient group

1
Description:
sirolimus
Treatment:
Drug: sirolimus

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems