Study Comparing Tacrolimus Formulations for Preventing Kidney Transplant Rejection in Adults

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What is this study about?

This clinical trial is focused on studying the effectiveness and practicality of two medications, Envarsus and Advagraf, in patients who have received a kidney transplant. Both medications contain the active ingredient tacrolimus, which is used to prevent the body from rejecting a transplanted kidney. The study aims to compare how well these two medications are absorbed by the body and to determine if one is superior to the other in terms of how much of the drug is available in the bloodstream after taking it.

Participants in the study will be adults who have undergone a kidney transplant. The study will involve taking one of the two medications once daily. The trial will last for a period of up to three years, during which various health parameters will be monitored. These include the levels of tacrolimus in the blood, kidney function, and any side effects experienced. The study will also look at how quickly patients reach the desired drug levels in their blood and how stable these levels remain over time.

The purpose of this study is to gather information that could help improve the management of kidney transplant patients by identifying the most effective and convenient medication regimen. By comparing Envarsus and Advagraf, researchers hope to provide valuable insights into which formulation offers better outcomes for patients in terms of drug absorption and overall health after a kidney transplant.

1 joining the study

Upon joining the study, the patient will be randomly assigned to one of two groups. Each group will receive a different formulation of the medication tacrolimus, which is used to prevent organ rejection after a kidney transplant.

2 medication administration

The patient will take the assigned medication once daily. The two formulations being compared are Envarsus and Advagraf. Both are prolonged-release forms of tacrolimus, meaning they release the medication slowly over time.

The specific dosage will depend on the formulation assigned. For Advagraf, available dosages include 5 mg, 0.5 mg, 3 mg, and 1 mg capsules. For Envarsus, available dosages include 0.75 mg, 1 mg, and 4 mg tablets.

3 monitoring and assessments

The patient’s blood levels of tacrolimus will be monitored at various intervals: day 4, day 14, day 28, and week 12 after transplantation. This monitoring helps assess how well the medication is working and its concentration in the body.

The primary goal is to measure the C/D ratio (concentration/dose ratio) at 12 weeks to evaluate the bioavailability of the medication.

4 follow-up evaluations

Additional evaluations will occur at 1, 2, and 3 years post-transplantation. These evaluations will include assessments of kidney function, incidence of rejection episodes, and any adverse reactions to the medication.

The study will also track the patient’s quality of life using a specific questionnaire designed for kidney transplant recipients.

5 study completion

The study is expected to conclude by March 31, 2029. Throughout the study, the patient will continue to receive regular medical care and monitoring to ensure their safety and the effectiveness of the treatment.

Who Can Join the Study?

  • Must provide a signed and dated written informed consent, which means you agree to participate in the study after being informed about it.
  • Must be an adult, which means you are 18 years old or older, whether male or female.
  • Must have kidney problems that require a kidney transplant and be approved to receive either a first or second kidney from a living or deceased donor.
  • Must have a blood type that is compatible with the donor kidney. This means your blood type matches with the donor’s blood type.
  • Must be able to swallow a medication called tacrolimus, which is available in tablet or capsule form.

Who Cannot Join the Study?

  • Patients who are not adults cannot participate. This means only individuals who are 18 years or older are eligible.
  • Patients who have not received a kidney transplant are not eligible. The study is for those who have had a kidney transplant.
  • Patients who are not taking tacrolimus, a medication used to prevent organ rejection, cannot participate.
  • Patients who are part of a vulnerable population, such as those unable to give consent, are not eligible.
  • Patients who are pregnant or breastfeeding cannot participate in the study.
  • Patients with any medical condition that the study doctors believe would make participation unsafe are not eligible.

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Other Sites

Site Name City Country Status
Universitaetsklinikum Regensburg AöR Regensburg Germany
Universitaetsklinikum Aachen AöR Aachen Germany
Charite Research Organisation GmbH Berlin Germany
Ualkufjmwlsymmksiamhy Kinzqhsppqylirogcgzucdk Bnuhpb Gxhv Bochum Germany
Ujoqueasaabvrzsmyaxxg Mssckavv Alt Munster Germany
Kcpxmook dsj Ubxjofcwolrw Mhxnxlib Ado Munich Germany
Uqcwuofbmssyffokvnakd Wrfjctptc Ads Wuerzburg Germany
Umgourpmqa Mqqnawa Cmzxdq Hdqpezzkedkcppkig Hamburg Germany

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Germany Germany
Not recruiting
01.10.2023

Trial locations

Investigated drugs:

Envarsus is a medication used in this trial to help prevent the body from rejecting a transplanted kidney. It is a once-daily oral formulation of tacrolimus, which is an immunosuppressant. The trial aims to assess how well this formulation is absorbed by the body compared to another tacrolimus formulation.

Advagraf is another once-daily oral formulation of tacrolimus used in the trial. Like Envarsus, it is used to prevent kidney transplant rejection by suppressing the immune system. The trial compares the absorption and effectiveness of Advagraf to that of Envarsus in kidney transplant patients.

Transplant Rejection – Transplant rejection occurs when the recipient’s immune system attacks the transplanted organ or tissue, recognizing it as foreign. This immune response can lead to inflammation and damage to the transplanted organ. Rejection can be acute, happening shortly after the transplant, or chronic, developing over a longer period. Symptoms may include fever, pain at the transplant site, and reduced function of the transplanted organ. The severity and progression of rejection can vary, potentially leading to the failure of the transplanted organ if not managed.

Trial ID:
2023-503531-18-00
Protocol code:
TaC:Drop
Trial Phase:
Therapeutic confirmatory (Phase III)

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