Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06829719

TTV-based mAnagement Of Long-term ImmunosuppreSsion in Kidney Transplantation

Personalization of Maintenance Immunosuppression Based on TTV Viral Load to Prevent Long-term Complications in Renal Transplantation

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
300 (estimated)
Sponsor
Hospices Civils de Lyon · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Long-term outcomes in kidney transplantation remain a significant challenge, as complications such as donor-specific antibodies (DSA), antibody-mediated rejection, infections, and cancer increasingly threaten graft and patient survival over time. The development of non-invasive biomarkers to guide the management of therapeutic immunosuppression beyond the first year post-transplantation is therefore a crucial unmet need. Torque Teno Virus (TTV), a non-pathogenic virus with a high prevalence worldwide, has emerged as a promising biomarker in this context. Its replication inversely reflects immune control by T cells, correlating with the depth of therapeutic immunosuppression. Additionally, its slow replication kinetics make TTV DNAemia a useful marker for evaluating patient adherence to immunosuppressive treatments. The TAOIST study tests whether longitudinal monitoring of TTV DNAemia every three months, starting from the second year after transplantation, can guide the personalization of immunosuppressive therapy. The primary endpoint is the time to the first occurrence of complications linked to inadequate immunosuppression, including dnDSA, biopsy-proven rejection, infection, cancer, or graft loss. Secondary objectives include evaluating the acceptability of TTV DNAemia among healthcare professionals and assessing its cost-effectiveness compared to standard care. An ancillary objective examines the link between TTV DNAemia and the immunosuppressant possession ratio (IPR) to explore its potential as a marker of treatment adherence.

Conditions

Interventions

TypeNameDescription
BIOLOGICALTTV DNAemiaEvery 3 months, one sample added at the same time (7mL) of a routine laboratory analysis for TTV DNAemia
OTHEREQ-5D-5L questionnaireCompleted every 6 months and each time a complication of interest occurs
BIOLOGICALBiological testsBiological tests as routine care procedure (creatinine, CNI pre-dose trough level) will be performed every 6 months

Timeline

Start date
2025-04-23
Primary completion
2028-05-01
Completion
2031-02-02
First posted
2025-02-17
Last updated
2025-07-02

Locations

4 sites across 1 country: France

Source: ClinicalTrials.gov record NCT06829719. Inclusion in this directory is not an endorsement.