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Assessment and Tracking of Long-term Alefacept (LFA-3/IgG1 Fusion Protein) Safety (ATLAS)

Phase 4
18 Years
Not Enrolling

Thank you

Trial Information

Assessment and Tracking of Long-term Alefacept (LFA-3/IgG1 Fusion Protein) Safety (ATLAS)

There are no study-mandated tests, visits or clinical interventions after the 1st
(enrolling) visit. After the patient is enrolled in the study, they will be contacted every
6 months to complete structured telephone interviews conducted by the ATLAS Study Center.

Inclusion Criteria:

- Psoriasis patients who are prescribed alefacept consistent with product labeling are
eligible for enrollment.

Type of Study:


Study Design:

Observational Model: Cohort, Time Perspective: Prospective

Outcome Measure:

To measure the rates of non-Hodgkin's lymphoma (NHL) and infections that require hospitalization occurring in psoriasis patients treated with alefacept

Outcome Time Frame:

At six month intervals for five years

Safety Issue:


Principal Investigator

Vice President Medical Affairs

Investigator Role:

Study Director

Investigator Affiliation:

Astellas Pharma Global Development


United States: Institutional Review Board

Study ID:




Start Date:

July 2003

Completion Date:

January 2012

Related Keywords:

  • Psoriasis
  • Psoriasis
  • Alefacept
  • AmeviveĀ®
  • Drug exposure
  • Psoriasis



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