Study:
Assessment and Tracking of Long-term Alefacept (LFA-3/IgG1 Fusion Protein) Safety (ATLAS)
Rationale:
n/a
Purpose:
Subjects exposed to alefacept are to be enrolled. Subjects will be contacted every 6 months
to gather general health information.
Study Status: Recruiting
Recruiting:
n/a
| Condition |
Intervention |
Phase |
|
Psoriasis |
Drug: Alefacept exposure |
Phase 4 |
Verified by
Astellas Pharma Inc
December, 2011
Sponsored by: Astellas Pharma Inc
Information provided by: Astellas Pharma Inc
ClinicalTrials.gov identifier: NCT00454701
Study Type: Interventional
Study Design: Observational Model: Cohort, Time Perspective: Prospective
Cleveland Clinic Foundation
Cleveland, Ohio 44195
United States
Vice President Medical Affairs., Study Director