Expired Study
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Morrisville, North Carolina 27560


Purpose:

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


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.


NCT ID:

NCT00097240


Primary Contact:

Study Director
Ivor Caro, M.D
Genentech


Backup Contact:

N/A


Location Contact:

Morrisville, North Carolina 27560
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: December 18, 2017

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