ClinicalTrials.gg
Not yet recruitingNCT07203664Updated Oct 2, 2025

Use of Tacrolimus and MTOR Inhibitors With Anticipatory Therapy vs. Tacrolimus and Mycophenolic Acid With Universal Prophylaxis in Renal Recipients at High Risk of Posttransplant Cytomegalovirus.

A Phase 4 interventional study of steroids, tacrolimus and mTOR inhibitors and steroids, tacrolimus and mycophenolic acid. in Evaluate the Effectiveness of CMV Prevention Strategies in Kidney Transplant Recipients, sponsored by Hospital Universitario La Paz. Not yet recruiting at 1 site in Spain. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-10-02.

Sponsored by Hospital Universitario La Paz · Phase 4, Interventional, and Other

Phase
Phase 4
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The overall objective of this project is to optimise preventive treatment of CMV infection/disease in renal transplant recipients at increased risk of CMV post-transplantation. The specific objectives are: (1) To compare the incidence of CMV infection/disease at 6 months post-transplant in Ig G CMV positive (R+CMV) recipients receiving induction treatment with thymoglobulin and one of the two maintenance immunosuppressive treatment regimens used in routine clinical practice : tacrolimus and MTOR inhibitors (group 1) or tacrolimus and mycophenolic acid (group 2); (2) To monitor CMV-specific cellular immunity before transplantation, at 15, 30 and 90 days post-transplantation. For this purpose, an exploratory phase 4 clinical trial has been designed in which will select 30 R+CMV patients receiving renal transplantation with induction treatment with thymoglobulin. After signing informed consent, patients will be randomised to receive one of the two immunosuppression regimens indicated above. The patients in group 1 will receive early therapy as a CMV prevention strategy and patients in group 2 will receive universal prophylaxis for 3 months. Follow-up visits to will be conducted according to the usual protocol and clinical and virological variables will be collected. In addition, blood samples will be collected for the assessment of CMV-specific cellular immunity before and after transplantation. The primary endpoint is the presence of CMV infection/disease post-renal transplantation at 6 months. Secondary variables include renal function, acute rejection, patient and graft survival and the occurrence of surgical or haematological complications.

Read the detailed description

HYPOTHESIS The use of immunosuppressive maintenance therapy including mTOR inhibitors versus the use of mycophenolic acid in kidney transplant patients with an increased risk of post-transplant CMV disease (R+CMV receiving induction with thymoglobulin) will allow optimisation of the preventive treatment of these patients, presenting a similar incidence of post-transplant CMV disease in both groups and better maintenance of CMV-specific cellular immunity post-transplant.

OBJECTIVES General Objective: To improve the preventive treatment of CMV disease in renal transplant patients at increased risk.

Main Objectives: (1) To compare the incidence of CMV disease at 6 months post-renal transplant in Ig G CMV-positive recipients receiving induction treatment with thymoglobulin and maintenance treatment with tacrolimus and mTOR inhibitors (group 1) with CMV prevention strategy of anticipatory therapy or tacrolimus and mycophenolic acid (group 2) with CMV prevention strategy with universal prophylaxis. (2) Monitor CMV-specific cellular immune response before transplantation and at 15, 30 and 90 days post-transplantation in each of the two treatment groups using Quantiferon-CMV.

Secondary Objectives: (3) To compare between the two groups the incidence of CMV infection, delayed initial graft function, acute rejection diagnosed by renal biopsy, renal function and patient and graft survival in the first 6 months post-transplant. (4) To compare between the two groups the presence of surgical (lymphocele requiring intervention) or haematological (neutropenia) complications in the first 6 months post-transplantation.

STUDY DESIGN Phase IV, exploratory, randomised, open-label, single-centre, exploratory clinical trial to evaluate the effectiveness of CMV prevention strategies comparing early therapy vs. universal prophylaxis in Ig G CMV-positive kidney transplant recipients treated with thymoglobulin receiving tacrolimus and mTOR inhibitors (group 1) vs. tacrolimus and mycophenolic acid (group 2).

Patients who meet the inclusion criteria and who sign the informed consent form the day before transplant surgery (pre-transplant day) will have a blood sample taken for CMV-specific cellular immunity analysis using quantiferon CMV and will be randomised into two groups on the day of renal transplant surgery (day 0).

a) Group 1: Will receive, as a CMV prevention strategy, early therapy, and as maintenance immunosuppressive treatment steroids, tacrolimus and mTOR inhibitors. b) Group 2: Will receive, as a CMV prevention strategy, universal prophylaxis, and as maintenance immunosuppressive therapy steroids, tacrolimus and mycophenolic acid. A randomisation list will be generated using SAS 9.4. software, in order to achieve a balanced randomisation in the treatment groups. The ratio will be 1:1 for each group and stratified by sex.

Definition of the groups: Group 1: Will receive early therapy, as a prevention strategy, which consists of starting antiviral treatment with valganciclovir (900 mg/12 hours, adjusted to renal function, according to the technical data sheet) when CMV viral replication is detected in blood above 1,000 copies/ml and treatment will be suspended when the viral load is negative in two consecutive controls.

Group 2: will receive universal prophylaxis with valganciclovir (900 mg/24 hours, adjusted to renal function, according to technical data sheet) during the first 3 months post-transplant, as a CMV prevention strategy.

All patients will receive immunosuppressive induction treatment with thymoglobulin (at least 1 dose and a maximum of 5 doses) and immunosuppressive maintenance treatment with tacrolimus + mTOR inhibitors (patients in group 1) or tacrolimus + mycophenolic acid (patients in group 2) following the guidelines of the technical file and the centre's usual protocols.

Follow-up visits will be performed at 15, 30, 90, 120, 120, 150 and 180 days post-transplant where clinical, analytical, virological (CMV viral loads by PCR in whole blood) and immunological (analysis of CMV-specific cellular immunity by CMV quantiferon) data of the patients will be evaluated. Data on the presence or absence of CMV infection or disease at each visit, concomitant medication changes and adverse events will also be collected.

02

Conditions studied

  • Evaluate the Effectiveness of CMV Prevention Strategies in Kidney Transplant Recipients
03

In context

Lead sponsor

Hospital Universitario La Paz is the lead sponsor of 56 studies on the registry; 20 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18 years or more.
  • Positive pre-transplant Ig G CMV serology.
  • Receive induction treatment with thymoglobulin (between 1 and 5 doses).
  • Agree to participate in the study by signing the form.

Exclusion criteria

Exclusion Criteria:

  • Patients with negative pre-transplant Ig G CMV serology.
  • -infected patients.
  • Patients receiving induction therapy with basiliximab.
  • Patients who cannot comply with the follow-up protocol.
  • Patients who cannot receive iMTOR as initial maintenance therapy, such as patients with chronic kidney disease secondary to hepatorenal polycystic kidney disease and patients who are expected to undergo complex vascular surgery.
  • Patients who for any reason should not be included in the study according to the evaluation of the research team.
Terms in these criteria, in plain language(3)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Immunosuppression

A weakened immune system. It can come from an illness, such as HIV or some blood cancers, or from medicines that turn the immune system down, for example after an organ transplant or for an autoimmune disease; steroids at higher doses count.

Read whether the line is about a condition or about medicines, and which medicines and doses it means.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

05

Study design

Phase
Phase 4
Primary purpose
Other
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    mTOR inhibitors

    Preemptive therapy will be administered as a preventive strategy, consisting of initiating antiviral treatment with valganciclovir (900 mg every 12 hours, adjusted according to renal function as per the technical data sheet) when CMV viral replication in blood exceeds 1,000 copies/ml. Treatment will be discontinued once viral load becomes undetectable in two consecutive tests

    Combination Product: steroids, tacrolimus and mTOR inhibitors

  • Active comparator
    Universal prophylaxis

    As a preventive strategy against CMV, the patient will receive universal prophylaxis, and for maintenance immunosuppressive treatment, steroids, tacrolimus, and mycophenolic acid will be administered.

    Combination Product: steroids, tacrolimus and mycophenolic acid.

Interventions

  • Combination productsteroids, tacrolimus and mTOR inhibitors

    Drug pages: Steroids · Tacrolimus · mTOR inhibitors

    Patients receive immunosuppressive induction treatment with thymoglobulin (at least 1 dose and maximum of 5 doses) and immunosuppressive maintenance treatment with tacrolimus + mTOR inhibitors. Preemptive therapy will be administered as a preventive strategy, consisting of initiating antiviral treatment with valganciclovir (900 mg every 12 hours, adjusted according to renal function as per the technical data sheet) when CMV viral replication in blood exceeds 1,000 copies/ml. Treatment will be discontinued once viral load becomes undetectable in two consecutive tests.

  • Combination productsteroids, tacrolimus and mycophenolic acid.

    Patients will receive immunosuppressive induction treatment with thymoglobulin (at least 1 dose and a maximum of 5 doses) and tacrolimus + mycophenolic acid following the guidelines of the technical file and the centre's usual protocols.

06

What researchers measure

Primary outcomes

  1. CMV disease incidence

    To compare the incidence of CMV disease at 6 months post-renal transplantation in Ig G CMV-positive recipients receiving induction treatment with thymoglobulin and maintenance treatment with tacrolimus and mTOR inhibitors (group 1) with CMV prevention strategy of early therapy or tacrolimus and mycophenolic acid (group 2) with CMV prevention strategy with universal prophylaxis.

    Time frame: 6 months after renal transplant

  2. Monitor CMV-specific cellular immune response prior to transplantation

    Monitor CMV-specific cell-mediated immune response before transplantation and at 15, 30 and 90 days post-transplantation in each of the two treatment groups using Quantiferon-CMV.

    Time frame: 4 months

Secondary outcomes

  1. To compare between the two groups the incidence of CMV infection, delayed initial graft function, acute rejection diagnosed by renal biopsy, renal function and patient and graft survival

    To compare between the two groups the incidence of CMV infection, delayed initial graft function, acute rejection diagnosed by renal biopsy, renal function and patient and graft survival in the first 6 months post-transplantation.

    Time frame: 6 months

  2. To compare the presence of surgical (lymphocele requiring intervention) or haematological (neutropenia) complications

    To compare between the two groups the presence of surgical (lymphocele requiring intervention) or haematological (neutropenia) complications in the first 6 months post-transplantation.

    Time frame: 6 months

07

Study locations

1 site
  • Hospital Universitario La Paz, Pº de la Castellana, 261 (Servicio de Nefrologia)
    Madrid, Madrid 28046, Spain
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Start is estimated for Oct 2025; primary completion for Dec 2026, 14 months later.

How these figures are worked out, and which studies are left out of them.

Registered
Sep 9, 2025
First posted
Oct 2, 2025
StartEst.
Oct 30, 2025
Primary completionEst.
Dec 31, 2026
CompletionEst.
Dec 31, 2026
Last update
Oct 2, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Oct 2, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07203664
Lead sponsor
Hospital Universitario La Paz
Responsible party
María Ovidia López Oliva (Dra., Hospital Universitario La Paz) — Principal investigator
First posted
Oct 2, 2025
Start date
Oct 30, 2025 (estimated)
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Oct 2, 2025

Study contacts

María O. López Oliva, Dra
Contact
mlopezo@salud.madrid.org
+34 91 727 70 00

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Oct 2025. You cannot join it, but the record below documents what was studied.

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Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

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Studies of the drugs tested here: Steroids · Tacrolimus · mTOR inhibitors

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