The YORVIPATH Pregnancy Safety Study is designed to learn more about how taking YORVIPATH during pregnancy may affect:
This is an observational study, meaning you and your baby will continue to receive routine medical care from your own doctors. No extra visits, tests, or procedures are required.
By joining this study, you may help doctors and researchers better understand the safety of YORVIPATH. Your contribution could guide future care for pregnant women and their babies. Participation is voluntary.
You may also be eligible to receive compensation after each successful data collection timepoint.
You may be eligible if you:
During pregnancy:
At delivery:
During your baby's first year:
At each time point, you'll share basic information and confirm your contact details.
Your personal and medical information will remain confidential. All identifying details will be removed before data is used for research.
YORVIPATH is an FDA-approved treatment for hypoparathyroidism in adults. However, there is not enough information yet to establish the safety of Yorvipath in pregnancy. This registry helps gather important information about its use during and after pregnancy to better understand effects on mothers and babies. For more information on YORVIPATH please refer to the prescribing information that comes with your medication.
To find out if you are eligible to join the Pregnancy Safety Study: call 877-229-2184, M-F, 8-8 ET or email us at: Yorvipathpregnancy@ubc.com. To report a pregnancy click here.