Enroll in the Registry

Am I eligible?

You may be eligible if you are:
  • Taking or have taken SUNOSI® (solriamfetol) for the treatment of excessive daytime sleepiness (EDS) associated with narcolepsy or OSA during pregnancy
  • A pregnant woman diagnosed with narcolepsy or OSA
  • A pregnant woman who does not have a diagnosis of narcolepsy or OSA, but who has taken at least one dose of SUNOSI or another wake-promoting medication or stimulant during pregnancy (since the first day of your last menstrual period)

Contact Request Form

Complete this form and a registry team member will contact you with more information about participating in the Registry.

I authorize the SUNOSI Pregnancy Registry to contact me and/or leave a message for me at these numbers or to contact me via email at the address listed below. I agree to the Registry referencing the SUNOSI Pregnancy Registry in messages or emails.

The registry is open from 8:30 am – 5:00 pm ET Monday-Friday

Privacy Statement
Pharmaceutical Product Development, LLC. (PPD) respects your privacy and understands that it is important to you. The information you provide on this form will be used to contact you for the purposes of assessing your eligibility to participate in the SUNOSI® Pregnancy Registry. This information will be held by PPD and not shared with the study sponsor (Axsome Therapeutics, Inc.) or any other third party without your permission. In the event you choose not to enroll, Registry staff will request permission to share your contact information with Axsome Therapeutics, Inc. in order for them to contact you for safety follow up about your pregnancy. If you do not provide permission, and do not enroll in the Registry your contact details will be deleted.