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Multicenter Randomized Two-arms Study Evaluating the BK Viral Clearance in Kidney Transplant Recipients With BK Viremia.
Sponsor: University Hospital, Strasbourg, France
Summary
BK virus nephropathy (BKVN), a consequence of the strong immunosuppressive therapy given after kidney transplantation, represents a growing problem in the kidney transplant (KT) setting. In recent cohorts, BKVN concerns up to 10% of kidney transplant recipients and early signs of BK virus (BKV) infection as development of asymptomatic viruria and viremia are even much more frequent (40% and 20% of patients, respectively). In this context, finding strategies to prevent BKV infection or treat patients before the occurrence of BKV nephropathy is challenging. For several years, detection of BKV replication by real-time PCR in urine and/or blood of kidney transplant recipients at early stages of infection allowed adaptation of their therapy. As BKV reactivates essentially in patients with over-immunosuppression, the first step of the treatment is the reduction of immunosuppression. However, reducing immunosuppression (IS) can lead to acute rejection and allograft loss. Other treatments have been proposed (cidofovir, quinolones) but their toxicity profile or their lack of clinical efficacy are now demonstrated. Hence, an efficient and safe strategy against uncontrolled BKV replication is urgently needed. MTor-inhibitors are well known immunosuppressive drugs used in organ transplantation to prevent graft-rejection. They have furthermore anti-viral effects that can be beneficial for prevention of viral infections after transplantation. Recent evidence that inhibition of mTor pathway had an impact on BK infected cells provides additional insight into the observed benefits associated with these drugs. The aim of our study is to evaluate the effect of the mTor inhibitor everolimus on the prevention of severe BKV infection (BKV nephropathy or loss of the allograft) after kidney transplantation compared to the reduction of immunosuppression alone in kidney recipients with BK viremia.
Official title: Multicenter Randomized Two-arms Study Evaluating the BK Viral Clearance in Kidney Transplant Recipients With BK Viremia After Reduction of Immunosuppression Alone vs. Reduction of Immunosuppression and Replacement of Mycophenolate Mofetil by Everolimus
Key Details
Gender
All
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
130
Start Date
2018-01-15
Completion Date
2024-08-01
Last Updated
2026-06-05
Healthy Volunteers
No
Interventions
everolimus
Patients with viremia above 2.8 log of copies/ml will be randomized (ratio 1:1) into either of 2 groups Group 1 : control group : immunosuppression lowering or Group 2 : experimental group : immunosuppression lowering and replacement of mycophenolate acid by everolimus Evolution of BKV viremia and allograft function will be assessed during 2 years after randomization
Locations (15)
CHU - Hôpital Sud
Amiens, France
CHRU d'Angers
Angers, France
CHU - Hôpital de la Cavale Blanche
Bois-Guillaume, France
CHU - Hôpital de la Cavale Blanche
Brest, France
CHU Côte de Nacre
Caen, France
CHU Hôpital Gabriel Montpied
Clermont-Ferrand, France
CHU - Hôpital Dupuytren
Limoges, France
Hôpital Edouard Herriot
Lyon, France
AP-HP Hôpital Necker
Paris, France
AP-HP - Hôpital Georges Pompidou
Paris, France
CHU Poitiers - Hôpital Jean Bernard
Poitiers, France
CHU - Hôpital Maison Blanche
Reims, France
CHU Rennes - Hôpital Pontchaillou
Rennes, France
Les Hôpitaux Universitaires
Strasbourg, France
CHRU - Hôpital Bretonneau
Tours, France