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Trials / Completed

CompletedNCT01386359

Evaluating Nulojix (Belatacept) Long-Term Safety in Transplant

Evaluating Nulojix Long-Term Safety in Transplant

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

Summary

To describe how Nulojix (belatacept) is used and to determine how often Post-Transplant Lymphoproliferative Disorder (PTLD), Central Nervous System (CNS) PTLD and Progressive Multifocal Leukoencephalopathy (PML), rare and serious complications of transplant treatment, occur in patients taking Nulojix (belatacept) in a real-world setting.

Detailed description

Time Perspective: Prospective for the majority of patients who are enrolled at the time they begin Nulojix (belatacept) treatment. Retrospective for any patients receiving Nulojix (belatacept) prior to enrollment into ENLiST Registry

Conditions

Interventions

TypeNameDescription
DRUGNo InterventionNo Intervention. Subjects are previously treated with Nulojix (belatacept)

Timeline

Start date
2012-02-29
Primary completion
2019-04-30
Completion
2019-04-30
First posted
2011-07-01
Last updated
2022-06-06

Locations

36 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01386359. Inclusion in this directory is not an endorsement.

Evaluating Nulojix (Belatacept) Long-Term Safety in Transplant (NCT01386359) · Clinical Trials Directory