Assessment and Tracking of Long-term Alefacept Safety

NCT00454701 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 1897

Last updated 2013-12-11

No results posted yet for this study

Summary

Subjects exposed to alefacept are to be enrolled. Subjects will be contacted every 6 months to gather general health information.

Conditions

Interventions

DRUG

Alefacept exposure

Observational

Sponsors & Collaborators

  • Astellas Pharma Inc

    lead INDUSTRY

Principal Investigators

  • Vice President Medical Affairs · Astellas Pharma Global Development

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2003-06-30
Primary Completion
2012-02-29
Completion
2012-02-29

Countries

  • United States
  • Canada

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00454701 on ClinicalTrials.gov