Pregnancy Exposure Registry for Tysabri®

NCT00472992 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 376

Last updated 2014-08-11

No results posted yet for this study

Summary

The primary objective of the Registry was to evaluate the outcomes of pregnancy in women with Multiple Sclerosis (MS) or Crohn's Disease (CD) who were exposed to TYSABRI® at any time within 90 days prior to first day of Last Menstrual Period (LMP) or during pregnancy.

Conditions

Sponsors & Collaborators

  • Elan Pharmaceuticals

    collaborator INDUSTRY
  • Biogen

    lead INDUSTRY

Principal Investigators

  • Medical Director · Biogen

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-01-31
Primary Completion
2012-07-31
Completion
2012-07-31

Countries

  • United States

Study Locations

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Entities

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 NCT00472992 on ClinicalTrials.gov