Pharmacokinetic Study of Adoport® (Tacrolimus) in Patients With de Novo Kidney Transplantation

NCT ID: NCT03076151

Last Updated: 2025-07-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 30 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2018-02-12
• Study Completion Date: 2019-07-31

Brief Summary

Tacrolimus is a calcineurin inhibitor widely used for the prevention of allograft rejection in solid organ and bone marrow transplantation. It is characterized by a narrow therapeutic index and large inter-individual pharmacokinetic variability. Adoport® is an immediate-release formulation of tacrolimus, to be administered twice daily. Because of a narrow therapeutic window and a better correlation between pre-dose level and effects than between dose and effect, therapeutic drug monitoring (TDM) based on trough whole blood tacrolimus concentrations is recommended for Adoport®. TDM helps to minimize the risk of acute rejection and the occurrence of adverse effects (mainly nephrotoxicity and, to a lesser extent, neurotoxicity).

As reported in a consensus document from a consortium of European experts on tacrolimus TDM, the interdose area-under-the curve (AUC0-12h) is expected to be the best marker of tacrolimus exposure. However, tacrolimus monitoring based on full AUC0-12h is difficult to set up in routine, due to clinical constraints and the necessity of multiple samples. Calculation of the AUC0-12h using Bayesian estimation and a limited sampling strategy, i.e. a few blood samples collected during the early phase post-dose would represent an elegant solution, as already done for other tacrolimus formulations.

Furthermore, the pharmacokinetics (PK) of tacrolimus is influenced by a single nucleotide polymorphism within intron 3 of cytochrome P450 3A5 (CYP3A5). Patients who carry at least one CYP3A5*1 allele are considered to be CYP3A5 expressors (about 12% of the Caucasian population, Hapmap project) and thus require a 1.5 to 2-fold higher starting dose than CYP3A5*3/*3 carriers to reach the predefined target exposure early after transplantation. Although this polymorphism showed no impact on the performance of the Bayesian estimators previously developed for other tacrolimus formulation, the patient status for CYP3A5*3 will be considered in this pharmacokinetic study as a potential covariate in, or confounding factor of, the PK model. Specifically, owing to a 12% frequency in the White European population, about 4 patients carriers of the CYP3A5*1 allele are expected in this study; the performance of the PK model and Bayesian estimator developed will be specifically evaluated in this subgroup.

Conditions

Transplantation; Kidney; Pharmacokinetic

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: OTHER
• Blinding Strategy: NONE

Study Groups

Tacrolimus monohydrate (ADOPORT®)

patients with de novo Kidney Transplantation under Tacrolimus (ADOPORT®) treatment.

Group Type: EXPERIMENTAL

Tacrolimus monohydrate (ADOPORT®)

Intervention Type: DRUG

Pharmacokinetic of Tracrolimus (ADOPORT®) on 9 blood sampling by kinetics on 4 kinetics

Interventions

Tacrolimus monohydrate (ADOPORT®)

Pharmacokinetic of Tracrolimus (ADOPORT®) on 9 blood sampling by kinetics on 4 kinetics

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Subject's written informed consent of the study

2. Male and female (>= 18 years)

3. Recipients of a first kidney allograft

4. Patients transplanted for less than 7 days at enrolment

5. Patients affiliated to a social security system

Exclusion Criteria

1. Patients presenting any contraindication to tacrolimus according to the summary of product characteristics of Adoport®

2. Patient presenting anti-HLA antibodies against the graft in pre-transplantation (DSA)

3. Recipients of any transplanted organ other than the kidney

4. Pregnant (positive BHCG test) or lactating women

5. Women without any method of contraception, except for women with no childbearing potential (according to the guidelines of the working group, Clinical Trial Facilitation Group, related to contraception and pregnancy test in clinical trials)

6. Patients participating in any other interventional clinical study at inclusion as well as during the whole course of the current study

7. Patient under judicial protection

8. Patients incapable of understanding the purposes and risks of the study, who cannot give written informed consent, or who are unwilling to comply with the study protocol

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University Hospital, Limoges

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Pierre Marquet, MD

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Limoges

Locations

Amiens Picardie University Hospital

Amiens, , France

Limoges University Hospital

Limoges, , France

Poitiers University Hospital

Poitiers, , France

CHU de ROUEN

Rouen, , France

Tours University Hospital

Tours, , France

Countries

France

References

Marquet P, Destere A, Monchaud C, Rerolle JP, Buchler M, Mazouz H, Etienne I, Thierry A, Picard N, Woillard JB, Debord J. Clinical Pharmacokinetics and Bayesian Estimators for the Individual Dose Adjustment of a Generic Formulation of Tacrolimus in Adult Kidney Transplant Recipients. Clin Pharmacokinet. 2021 May;60(5):611-622. doi: 10.1007/s40262-020-00959-y. Epub 2020 Nov 24.

Reference Type: RESULT

PMID: 33230714 (View on PubMed)

Other Identifiers

I16009 (IMPAKT)

Identifier Type: -

Identifier Source: org_study_id