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

NCT00097240 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 18

Last updated 2010-08-04

No results posted yet for this study

Summary

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

Conditions

Sponsors & Collaborators

  • Genentech, Inc.

    lead INDUSTRY

Principal Investigators

  • Ivor Caro, M.D · Genentech, Inc.

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-01-31
Completion
2009-09-30

Countries

  • United States

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00097240 on ClinicalTrials.gov