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Study identifier: NCT01435291 Synced from ClinicalTrials.gov · August 04, 2026
● Completed

AADAPT - Analysis of Advagraf Dose Adaptation Post Transplantation

Condition: Renal Transplantation  ·  Sponsor: Centre Hospitalier Universitaire de Nice

PhasePhase 4
Planned participants45
Who can joinAll sexes, 18 Years to 70 Years
Healthy volunteersNo

About this study

A pharmacokinetics and pharmacogenetics study to complement the current knowledge of tacrolimus prolonged release (Advagraf®) in the immediate post-transplantation period and at steady-state (M3 post transplantation) and to improve the optimal dose of Advagraf® based on tacrolimus AUC estimated by two Limited Samples Strategies during the first 3 months after renal transplantation. Data obtained with tacrolimus prolonged release will be compared with those of tacrolimus immediate release (Prograf®)

This description comes directly from the study's public registry record.

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No contact information is available for this study as per the public registry record.

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Locations (4)

Hôpital BicêtreLe Kremlin-Bicêtre, France
CHU de NiceNice, France
CHU de RangueilToulouse, France
CHRU Tours Hôpital BretonneauTours, France

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