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First Tacrolimus Dose Trough Level is Better Than CYP3A5 Genotyping in Tacrolimus Dose Prediction

C

Chulalongkorn University

Status

Unknown

Conditions

Kidney Transplantation Recipients

Treatments

Drug: Tacrolimus C12

Study type

Observational

Funder types

Other

Identifiers

NCT02356146
IRB225/56

Details and patient eligibility

About

Tacrolimus dose highly varies among Asian kidney transplant recipients. This can be explained by variety of CYP3A5 expression. CYP3A5 genotyping is highly recommended for patients receiving tacrolimus. Here, we assessed the tacrolimus dose prediction by comparing CYP3A5 expression and tacrolimus dosage using tacrolimus concentration after single dose administration prior to kidney transplantation.

Plasma tacrolimus trough level was measured at 12 hours after first dose of 0.1 mg/kg of tacrolimus (TacC12), orally administered in 51 new kidney transplant recipients. Patients with CYP3A5 inhibitor/inducer co-medications were excluded. Genotyping for CYP3A5 expression were carried out by RT-PCR. The dosages of tacrolimus at post-operative day 7 and dosage which provided stable therapeutic levels in post-operative month 1 to 3 (C0 5-8 ng/mL) were recorded.

The genotyping, TacC12, and target tacrolimus dosage have good correlations.

Enrollment

60 estimated patients

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All KT recipients

Exclusion criteria

  • Recipient who not receiving tacrolimus

Trial design

60 participants in 1 patient group

All KT recipient
Treatment:
Drug: Tacrolimus C12

Trial contacts and locations

1

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Central trial contact

Natavudh Townamchai, MD

Data sourced from clinicaltrials.gov

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