Tacrolimus Formulation and Glucose Metabolism After Kidney Transplantation (TAGLUMET Trial)

Posttransplant Diabetes Mellitus Clinical Trial

— TAGLUMET  

Official title:

Conversion to Extended-release MeltDose® Tacrolimus After Kidney Transplantation - Impact on Glucose Metabolism and Lipid Profile

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT05396898
• Other study ID #: TAGLUMET
• Status: Completed
• Phase: Phase 4
• Start date: December 16, 2020
• Est. completion date: December 30, 2023

Study information

• Verified date: February 2024
• Source: University Hospital Tuebingen
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Posttransplantation diabetes mellitus after kidney transplantation mediated by tacrolimus is mainly dependent on dose and peak plasma concentration. To substantiate the potential benefits on glucose metabolism and lipid profile of LCP-tacrolimus compared to standard twice-daily tacrolimus after kidney transplantation, a prospective randomized intraindividual cross-over conversion trial with a comprehensive assessment of glucose metabolism and lipid profile is performed. Primary endpoint is the difference in insulin secretion between treatments, as the principal parameter affected by tacrolimus peak concentrations.

Aim of the study is, to assess glucose metabolism under different tacrolimus formulations (LCP-tacrolimus and twice-daily tacrolimus).

Description:

Posttransplantation diabetes mellitus (PTDM) is an increasing problem in solid organ transplantation with profound impact on patient and allograft survival. One major contributing factor for the development of PTDM is choice of immunosuppression. Calcineurin inhibitors (CNIs), especially tacrolimus display a substantial diabetogenic potential but remain a cornerstone in maintenance immunosuppression for prevention of rejection and allograft loss. The diabetogenic effect of tacrolimus is mediated predominantly via disturbance of beta-cell function and impaired insulin secretion. There is growing evidence that this effect is dependent on dose and peak plasma concentrations. Once-dailyLCP-tacrolimus has been shown to have lower peak concentrations than twicedaily tacrolimus with comparable efficacy and safety.

LCP-tacrolimus has been shown to improve triglyceride levels, compared to twicedaily tacrolimus. In this study, no effect on the incidence of PTDM was observed, however assessed only by fasting plasma glucose, HbA1c and antidiabetic treatment. As 1/3 of patients with diabetes are solely diagnosed via oral glucose tolerance test, this approach is insufficient for proper evaluation of glucose metabolism, including prediabetes as the principal risk factor.

From pathophysiologic understanding blood lipids and glucose metabolism are strongly associated, as hypertriglyceridemia correlates with insulin resistance. In combination with the lower peak concentrations, it can be hypothesized that LCP-tacrolimus results in better glucose metabolism after kidney transplantation, compared to twicedaily tacrolimus Better understanding of glucose metabolism under different tacrolimus formulations would address a key component of long-term cardiovascular risk and patient outcome after kidney transplantation.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 44
• Est. completion date: December 30, 2023
• Est. primary completion date: August 4, 2023
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Stable adult kidney transplant recipients on maintenance immunosuppression, >=12 months after kidney transplantation; stable is defined as no need for diagnostic and therapeutic interventions (e.g. kidney biopsy)

• Tacrolimus-based immunosuppression in combination with mycophenolic acid or azathioprine and maintenance prednisolone (<= 5 mg/q.d.) for at least 3 months

• Must be >= 18 years at the time of signing the informed consent

• Understand and voluntarily sign an informed consent document prior to any study related assessments/procedures.

• Able to adhere to the study visit schedule and other protocol requirements.

• Subject (male or female) is willing to use highly effective methods during the study treatment (adequate: combined hormonal contraception associated with inhibition of ovulation, progestogen-only hormonal contraception associated with inhibition of ovulation, intrauterine device, intrauterine hormone-releasing system, bilateral tubal occlusion, vasectomized partner, sexual abstinence).

• Females of childbearing potential (FCBP) must agree to pregnancy testing within 7 days from 1st dosing of IMP

• To abstain from breastfeeding during study participation and 28 days after study drug discontinuation.

• All subjects must agree not to share medication

Exclusion Criteria:

• patients with known diabetes mellitus or PTDM, or HbA1c>=6.5%

• fasting plasma glucose on examination day (visit 1) of >= 126 mg/dl (7,0 mmol/l)

• patients with combined transplantation (e.g. liver-kidney, pancreas-kidney, etc.)

• patients with acute infection at time of baseline visit

• patients with known non-adherence

• patients with rejection therapy or increased dosis of corticosteroids for other reasons within 3 months prior to inclusion.

• Women during pregnancy and lactation.

• History of hypersensitivity to the investigational medicinal product or to any drug with similar chemical structure or to any excipient present in the pharmaceutical form of the investigational medicinal product.

• Participation in other interventional clinical trials (inclusive of the Follow-up period)

Related Conditions & MeSH terms

• Diabetes Mellitus
• Posttransplant Diabetes Mellitus

Intervention

Drug:
• LCP-tacrolimus
Prophylaxis of transplant rejection in liver and kidney allograft recipients
• twice-daily tacrolimus
Prophylaxis of transplant rejection in liver, kidney or heart allograft recipients

Locations

Country	Name	City	State
Germany	University Hospital Tuebingen	Tuebingen

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital Tuebingen

Country where clinical trial is conducted

Germany, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Difference in insulin secretion	The Difference in insulin secretion is determined by ratio AUC insulin / AUC glucose during OGTT at timepoints 16 and 32 weeks after randomization in intraindividual treatment crossover.	16 and 32 weeks
Secondary	Differences in parameters of glucose metabolism: fasting plasma glucose	Assessment of fasting plasma glucose determined in [mg/dl].	16 and 32 weeks
Secondary	Differences in parameters of glucose metabolism: OGTT	Assessment of 2h glucose in an extended oral glucose tolerance test (OGTT) determined in [mg/dl].	16 and 32 weeks
Secondary	Differences in parameters of glucose metabolism: insulin sensitivity	Assessment of insulin sensitivity determined in [µmol/l].	16 and 32 weeks
Secondary	Differences in blood lipid levels	Assessment of blood lipid levels determined in [mg/dl].	16 and 32 weeks
Secondary	Allograft function: eGFR	Assessment of eGFR (estimated glomerular filtration rate) determined in [ml/min].	16 and 32 weeks
Secondary	Allograft function: urinary albumin excretion	Assessment of urinary albumin excretion determined in [g/dl].	16 and 32 weeks
Secondary	Drug concentration/dose ratio	Assessment of Drug concentration/dose ratio (C/D Ratio) is determined by; Tacrolimus level [ng/ml] related to the dose of tacrolimus taken orally the previous day [mg]: C/D Ratio [ng/ml x 1/mg].	16 and 32 weeks