The
VYEPTI
Pregnancy
Registry

Welcome to the VYEPTI Pregnancy Registry

H. Lundbeck A/S (Lundbeck), the manufacturer of eptinezumab-jjmr (VYEPTI®), is conducting the VYEPTI Pregnancy Registry. This is an observational study in pregnant women diagnosed with migraine and treated with VYEPTI during pregnancy or up to 20 weeks prior to becoming pregnant. The purpose of this study is to collect and process data of pregnant women and their unborn and newborn baby(ies) to assess the use of VYEPTI or other preventive migraine medications in pregnancy. In addition, infant health outcomes will be collected up to the infant's first birthday.

Participation in this study will help Lundbeck to determine if there are any effects of VYEPTI on pregnant women or babies whose mothers were treated with VYEPTI during pregnancy. Results from the registry study will be shared with regulatory agencies (e.g. FDA) and may be added to product labeling to provide Healthcare Providers additional prescribing information.

Who can participate?

Find Out More and Enroll

If you are able and willing to provide consent for the Registry, you may be eligible to participate in either of the two scenarios:

A

You have received VYEPTI any time during your pregnancy or up to 20 weeks prior to becoming pregnant;

or

B

You have taken other preventive medication for migraine during your pregnancy and/or up to 1 week (depending on medication) prior to becoming pregnant. Preventive medications can include, but are not limited to, amitriptyline, venlafaxine, divalproex, topiramate, valproate, atenolol, metoprolol, propranolol, nadolol, timolol, and onabotulinumtoxin A.

The following options are available if you would like to learn more about the Registry or are interested in enrolling in the Registry:

Call

1-855-810-8549


Hours of operation:

Monday - Friday

8:00 a.m. to 5:00 p.m. Eastern Time

Email: vyeptipregnancyregistry@ubc.com

Notify your healthcare provider right away if you become pregnant or plan to become pregnant while on VYEPTI or within 20 weeks of receiving VYEPTI

Who can participate?

For more information about Vyepti, please see the
Full Prescribing Information and Patient Information.