Clinical Trials Directory

Trials / Completed

CompletedNCT01656343

Belatacept and Risk of Post-transplant Lymphoproliferative Disorder in US Renal Transplant Recipients

Belatacept and Risk of PTLD in US Renal Transplant Recipients

Status
Completed
Phase
Study type
Observational
Enrollment
775 (actual)
Sponsor
Bristol-Myers Squibb · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

* To estimate the incidence rates of post-transplant lymphoproliferative disorder (PTLD) in adult, EBV seropositive, kidney alone transplant recipients treated with belatacept at the time of transplantation * To estimate the incidence rates of PTLD in adult, EBV seropositive, kidney alone transplant recipients treated with calcineurin inhibitors (CNI)-based regimens at the time of transplantation * To compare the PTLD incidence rates in adult, EBV seropositive, kidney alone transplant recipients treated with belatacept to the rates in adult, EBV seropositive, kidney alone transplant recipients treated with CNI-based regimens at the time of transplantation

Conditions

Interventions

TypeNameDescription
DRUGCalcineurin inhibitors (CNI)No Intervention
DRUGBelataceptNo Intervention

Timeline

Start date
2011-10-31
Primary completion
2019-08-05
Completion
2019-08-05
First posted
2012-08-03
Last updated
2022-07-22

Source: ClinicalTrials.gov record NCT01656343. Inclusion in this directory is not an endorsement.

Belatacept and Risk of Post-transplant Lymphoproliferative Disorder in US Renal Transplant Recipients (NCT01656343) · Clinical Trials Directory