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Study Investigating Rapamune For Post-Marketing Surveillance

Kidney Transplantation Clinical Trial

Official title:
Post Marketing Surveillance Study To Observe Safety And Efficacy Of Rapamune

Clinical Trial Summary

To provide safety and effectiveness information for Rapamune during the post-marketing period as required by Korea Food and Drug Administration (KFDA) regulations in order to identify any potential drug related treatment factors in the Korean population, such as:

1. Unknown adverse reactions, especially serious adverse reactions

2. To assess the incidence of adverse reactions under the routine drug uses

3. Factors that may affect the safety of the drug (e.g., proteinuria)

4. Factors that may affect the effectiveness of the drug

Clinical Trial Description

All patients who receive Rapamune for certain period of time should be included as far as patients consent to participate ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00484094
Study type Observational
Source Pfizer
Contact
Status Completed
Phase N/A
Start date July 2011
Completion date June 2015
View Details
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