HomeTrialNCT05503927
🔬NCT05503927ENROLLING BY INVITATION

A Study to Evaluate the Safety of Exposure to Wegovy During Pregnancy

Study Summary

This is an observational, retrospective, 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.

Interventions / Drugs
View on ClinicalTrials.gov ↗
Study Details
Enrollment1139 participants
Primary Completion
Lead SponsorNovo Nordisk A/S
Data Retrieved2026-04-11 02:55:47.366886+00:00
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