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
| Type | Name | Description |
|---|---|---|
| DRUG | No Intervention | No 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.