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Pregnancy Exposure Registry for Avonex (Interferon Beta-1a)

Multiple Sclerosis Clinical Trial

Official title:
Avonex Pregnancy Exposure Registry

Clinical Trial Summary

The primary objectives of the study were to prospectively record and analyze birth defects and spontaneous fetal losses in women with multiple sclerosis (MS) exposed to Avonex within approximately 1 week of conception or during the first trimester of pregnancy, where the outcome of the pregnancy was unknown prospectively and to prospectively record and analyze pregnancy outcomes in an exploratory fashion of women with MS who stopped therapy, but who may have been exposed to Avonex with approximately 1 week of conception or during the first trimester of pregnancy.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00168714
Study type Observational
Source Biogen
Contact
Status Completed
Phase N/A
Start date February 2004
Completion date September 2011
View Details
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