Clin2
NCT07877103Likely a fitNot yet recruiting

Individualized tacrolimus dosing based on time of day

End-Stage Renal Disease

Part of Kidney & urinary, Women’s health & pregnancy clinical trials.

This study tests whether giving tacrolimus at a time of day matched to each patient's body clock can improve safety and effectiveness after a kidney transplant. It may help recipients maintain stable drug levels with fewer side effects.

Summary written for real people, not researchers, by Clin2.

Phase
Phase 4
Enrollment
100 people
Ages
18 years to 70 years
Study type
Interventional

Who can take part

  • You are between 18 and 70 years old
  • You had your first kidney transplant, either from a living or deceased donor
  • You are more than 3 months after the transplant and your kidney function is stable
  • You take a standard combination of three anti-rejection drugs, including tacrolimus, mycophenolate, and a steroid
  • Your tacrolimus dose and blood levels have been stable and you are not currently being treated for rejection
  • You are not pregnant or planning pregnancy and do not have active infections or severe stomach issues

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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