LivingGLP1
Study S002354

A Multicentre, Prospective, Single-arm, Non-interventional Regulatory Post-marketing Surveillance (rPMS) Study to Investigate the Safety and Effectiveness of Wegovy® (Semaglutide) in Patients With Obesity and Patients With Overweight in Routine Clinical Practice in Korea.

Registration

Registration
NCT07018544
Study type
OBSERVATIONAL
Status
ENROLLING_BY_INVITATION
Enrollment
840
Start
2024-11-19
Primary completion
2027-02-28
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity and Overweight
Interventions
OTHER:semaglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1281-9419

Registered primary outcomes

  • Number (incidence) of AEs [From Visit 1 (baseline, 0 week) to Visit 4 (22 weeks < ~ ≤ 30 weeks)]

Linked records (0)

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