Trial Information

Summary: AVONEX® Pregnancy Registry – Are you a pregnant woman with MS who is taking or has taken AVONEX®?

Biogen Idec, the maker of AVONEX®, has set up a pregnancy registry to collect information on pregnancies, and the children of those pregnancies, exposed to AVONEX®

The AVONEX® Pregnancy Registry will collect prospective reports from pregnant women and health care providers. Information provided to the Registry will be collected through telephone interviews with the pregnant woman at 4 to 5 months of pregnancy and 8 to 12 weeks after her estimated due date.

Inclusion criteria:

• Pregnant women who have been exposed to AVONEX® within approximately one week of conception or during the first trimester of pregnancy. (Registry phone representatives will help to determine eligibility.)
• Provide sufficient information to determine that the pregnancy is prospectively registered– meaning the outcome of the pregnancy is unknown. (Registry phone representatives will help to determine eligibility.)
• Provide verbal consent to participate in the Registry.
• Verbally provide contact information for herself, her health care practitioner, and the infant’s health care practitioner (if applicable).

Exclusion criteria:

• Registry phone representatives will help to determine eligibility.

http://www.criver.com/registries

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Trial listings updated: June 1, 2008 at 5:45:20 AM