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NCT00359814

Conversion Study to Optimize Immunosuppressive Regimen by Exchange of Azathioprine by Mycophenolatmofetile and Cyclosporine A Dose Reduction for Patients After Heart Transplantation in Lon-Term

Completed NA Last updated 13 February 2009
What this trial tests

NA trial testing Mycophenolatmofetile in Heart Transplantation in 23 participants. Completed in 1 June 2008.

Timeline
1 November 2004
Primary endpoint
1 June 2008
1 June 2008

Quick facts

Lead sponsorHannover Medical School
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment23
Start date1 November 2004
Primary completion1 June 2008
Estimated completion1 June 2008
Sites1 location across Germany

Drugs / interventions tested

Conditions studied

Sponsor

Hannover Medical School

Who can join

Adults 18 to 75, any sex, with Heart Transplantation. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to improve or save renal function by optimizing the immunosuppressive regimen by reducing the Cyclosporine A dose and the exchange of Azathioprine by Mycophenolatmofetile, which is an effective immunosuppressive agent and will minimize the risk of acute rejection episodes.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Heart Transplantation

Currently open trials in the same condition.

Other Hannover Medical School trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00359814.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing