A Study to Evaluate the Safety of Exposure to Wegovy During Pregnancy
NCT05503927 · Enrolling by invitation
Last updated 2026-07-27This clinical trial is testing the safety of the medication Wegovy in pregnant individuals who are overweight or obese to see how it may affect their babies.
Status Enrolling by invitation Only people invited by the researchers can join.
Type Observational
Participants 2,701 people Planned (estimated).
Who can join Ages 15–50 · female only
Timeline Started 2020-02 · est. completion 2027-08
Where 2 sites · United States
What this study is testing ClinicalTrials.gov NCT05503927 ↗
Description as written by the study sponsor.
This is an observational cohort study using administrative insurance claims data. The aim of this non-interventional study (NIS) is to compare maternal, fetal and infant outcomes of women exposed to Wegovy during pregnancy to a reference population not exposed to Wegovy, so that participants and healthcare providers can make informed treatment decisions.
Treatments tested
- No Intervention Other
This is a non-interventional study, therefore no intervention is used.
| Main thing measured | Number of Infants with Major Congenital Malformation (MCM) |
|---|---|
| Sponsor | Novo Nordisk A/S |
| Conditions studied | Pregnancy, Obesity, Overweight |
| GLP-1 drugs | semaglutide |
Full protocol, eligibility, and contacts on ClinicalTrials.gov NCT05503927 ↗