Viewing Study NCT00282217



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Last Modification Date: 2024-10-26 @ 9:22 AM
Study NCT ID: NCT00282217
Status: COMPLETED
Last Update Posted: 2007-03-22
First Post: 2006-01-24

Brief Title: Study Evaluating Sirolimus in the Treatment of Kidney Transplant
Sponsor: Wyeth is now a wholly owned subsidiary of Pfizer
Organization: Wyeth is now a wholly owned subsidiary of Pfizer

Study Overview

Official Title: Sirolimus in the Treatment of Histological Defined Chronic Allograft Nephropathy
Status: COMPLETED
Status Verified Date: 2007-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The aim of this study is to test whether withdrawal of calcineurin inhibitors followed by treatment with sirolimus may improve renal function in renal transplant recipients with chronic allograft nephropathy
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None