Viewing Study NCT00097240



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Study NCT ID: NCT00097240
Status: COMPLETED
Last Update Posted: 2010-08-04
First Post: 2004-11-19

Brief Title: An Observational Study of the Use and Safety of Raptiva During Pregnancy FOLLOW
Sponsor: Genentech Inc
Organization: Genentech Inc

Study Overview

Official Title: The Raptiva Pregnancy Registry An Observational Study of the Use and Safety of Raptiva Efalizumab During Pregnancy
Status: COMPLETED
Status Verified Date: 2010-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: FOLLOW
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: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None