What is the TEGSEDI-PRG Pregnancy Observational Study

The TEGSEDI-PRG pregnancy observational study was developed by Akcea Therapeutics, Inc. to follow patients who have taken at least one dose of TEGSEDI® (inotersen) during their pregnancy (or patients who became pregnant within 25 weeks of taking TEGSEDI). The purpose of this study is to learn more about the health of pregnant women who are taking or have not taken TEGSEDI and the health of their babies.

Pregnant women with the polyneuropathy of hereditary transthyretin-mediated amyloidosis (hATTR-PN), who have not taken TEGSEDI, are also eligible for this observational pregnancy study.

Your participation in this study will help Akcea Therapeutics Inc. to gather more information that could help women in the future and their doctors make more informed decisions.

Please notify your HCP if you have become pregnant or plan to become pregnant while taking TEGSEDI®.

Find Out More and Enroll

You are eligible to participate in either of the two scenarios outlined below:

You have taken at least 1 dose of TEGSEDI during your pregnancy or within 25 weeks of becoming pregnant;


You have the polyneuropathy of hereditary transthyretin-mediated amyloidosis (hATTR-PN) and you are pregnant.

Within US:


Hours of Operation:

Monday - Friday

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

Email: TegsediPregnancy@UBC.com

Report a Pregnancy

Live Outside the US?

Email us at: TegsediPregnancy@UBC.com

to find out if you are eligible for this study.

Note: By providing your personal information via this website, you consent to a member of our Pregnancy Coordinating Center contacting you directly as follow-up to your report. Your personal information will not be used or shared for any other purpose.