Study Evaluating Rapamune in Patients After Kidney Transplantation

NCT00240214 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2008-03-14

No results posted yet for this study

Summary

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

Conditions

  • Renal Transplantation

Interventions

DRUG

sirolimus

Tablet, dosage is determined by trough level

Sponsors & Collaborators

  • Wyeth is now a wholly owned subsidiary of Pfizer

    lead INDUSTRY

Principal Investigators

  • Medical Monitor · Wyeth is now a wholly owned subsidiary of Pfizer

  • Trial Manager · For Germany, [email protected]

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-04-30
Primary Completion
2008-02-29
Completion
2008-02-29

Countries

  • Germany

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00240214 on ClinicalTrials.gov