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COMPLETEDNCT00097240

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

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

Lead sponsor: Genentech, Inc.•1 U.S. locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Genentech, Inc.

Age

All ages

Sex

FEMALE

Healthy Volunteers

No

Inclusion Criteria

•Any patient who has used Raptiva within 6 weeks prior to conception or during her pregnancy may be included in the Registry. Enrollment is based on Raptiva exposure, whether inadvertent or deliberate, in relation to pregnancy. Enrollment should occur as early as possible during the pregnancy and must occur prior to knowledge of pregnancy outcome.

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: August 4, 2010Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment18

Start dateJan 2005

Last updatedAug 4, 2010

Condition

Psoriasis Pregnancy

Locations shown

FOLLOW Raptiva Pregnancy Registry

Morrisville, North Carolina

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: August 4, 2010Data synced to Clareo: May 25, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions