An Observational Study of the Use and Safety of Raptiva During Pregnancy (FOLLOW) - NCT00097240-27560 (Clinical Trial 122585)
Permalink: http://www.ClinicalConnection.com/exp/ExpandedPatientViewStudy122585.aspx
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Morrisville |
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NC |
| Zip Code: |
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27560 |
| Conditions: |
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Psoriasis - Pregnancy |
| Purpose: |
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The Raptiva Pregnancy Registry is a prospective observational study established to obtain
data on pregnancy outcomes of women who are exposed to Raptiva.
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| Study summary: |
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| Criteria: |
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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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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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January 31, 2010 |
Modifications to
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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Clinical trials are medical research studies designed to test the safety and/or
effectiveness of new drugs, devices, or treatments in humans. These studies are
conducted worldwide for a range of conditions and illnesses. Learn more about
clinical research and participating in a study at
About Clinical Trials.
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