An Observational Study of the Use and Safety of Raptiva During Pregnancy (FOLLOW)

Completed

• Conditions: Psoriasis; Pregnancy

• Registration Number: NCT00097240
• Lead Sponsor: Genentech, Inc.

Brief Summary

The Raptiva Pregnancy Registry was a prospective observational study established to obtain data on pregnancy outcomes of women who were exposed to Raptiva.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2004-11-19
• Study First Submitted QC: 2004-11-19
• Study First Posted: 2004-11-22
• Study Start: 2005-01
• Study Completion: 2009-09
• Status Verified: 2010-08
• Last Update Submitted: 2010-08-02
• Last Update Posted: 2010-08-04

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 18

Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Trial Locations

Locations (1)

FOLLOW Raptiva Pregnancy Registry; 🇺🇸 Morrisville, North Carolina, United States