Viewing Study NCT00260208



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Last Modification Date: 2024-10-26 @ 9:21 AM
Study NCT ID: NCT00260208
Status: TERMINATED
Last Update Posted: 2011-12-06
First Post: 2005-11-30

Brief Title: Liver Fibrosis in Patients Transplanted for Hepatitis C Receiving Either Cyclosporine Microemulsion or Tacrolimus
Sponsor: Novartis Pharmaceuticals
Organization: Novartis

Study Overview

Official Title: A Multicenter Randomized Open-label Study to Compare the Development of Liver Fibrosis at 12 Months After Transplantation for Hepatitis C Cirrhosis in Patients Receiving Either Cyclosporine Microemulsion or Tacrolimus
Status: TERMINATED
Status Verified Date: 2011-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Study was prematurely terminated due to poor recruitment
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Following a transplant for hepatitis C cirrhosis the infection comes back in 70-90 of cases and over time causes fibrosis and eventually cirrhosis of the new liver The aim of this study was to see if the frequency of liver fibrosis was different with cyclosporine microemulsion than tacrolimus
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