Recruiting

XR Tacrolimus

Sponsor:

Loyola University

Code:

NCT04917718

Conditions

Chronic Kidney Diseases

Heart Transplant

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Interventions

Conversion from IR Tacrolimus to XR Tacrolimus

Study Details

Brief summary:

Immediate release (IR) tacrolimus peaks in the first two hours after administration. These peak levels are influenced by CYP3A5 expression with expressors requiring higher total daily doses with higher peak levels compared to non-expressors. Tacrolimus XR (Envarsus) is a once daily formulation with delayed absorption and lower peak levels while maintaining similar trough levels as seen with IR tacrolimus. A randomized trial of conversion from IR tacrolimus to tacrolimus XR in kidney transplant recipients have shown similar efficacy and adverse events between the two groups but no improvement in estimated GFR. However, urinary biomarkers of acute kidney injury associated with changes in tacrolimus dosing may be more sensitive then serum creatinine. The objective of this study is to assess renal tubular injury in heart transplant recipients who are converted from immediate release to tacrolimus XR. The hypothesis is that the delayed absorption and lower peak levels of tacrolimus XR will lead to less tubular injury and improved renal function without increased risk to the heart allograft.

Conditions

Chronic Kidney Diseases

Heart Transplant

Study ID

NCT04917718

Start date

Aug 16, 2021

Status verified date

Apr, 2022

Completion date

Dec 31, 2024

Anticipated

Primary completion date

Dec 31, 2024

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 70+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Stable, heart-only transplant recipient within 10 years of transplantation
  • 18 -80 years old
  • Currently taking IR Tacrolimus
  • Baseline eGFR> 30mL/min/1.73m2

Exclusion Criteria:

  • Multiple organ transplant recipients
  • Less than 18 years old
  • Greater than 80 years old
  • Heart-only transplants recipients with active malignancy, rejection, or greater than 10 years from transplantation

Study Design

Enrollment

42 participants

Anticipated

Intervention Model

Single group

Primary purpose

Other

Interventions and Outcome Measures

Arms

experimental: Extended Release Tacrolimus

All participants who consent to the study will be in this group.

Interventions

Conversion from IR Tacrolimus to XR Tacrolimus

All participants will be consented to the study on IR Tacrolimus. After their baseline visit, they will be converted to XR Tacrolimus

Primary outcome measure

  • Urinary neutrophil gelatinase-associated lipocalin (NGAL) [ Time Frame: 4 weeks ]

Central Contacts and Locations

Central contacts

Locations

Loyola University Medical Center

Recruiting

Maywood, Illinois, United States, 60153

More Information

Sponsor

Loyola University

Last update posted

Apr 13, 2022

Last verified

Apr, 2022

Keywords

  • Immediate Release Tacrolimus
  • Extended Release Tacrolimus
  • IR Tacrolimus
  • XR Tacrolimus
  • Renal Tubular Injury
  • Heart Transplant Recipient
  • Chronic Kidney Disease

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-09. This information was provided to ClinicalTrials.gov by Loyola University on 2022-04-13.