LivingGLP1
Study S001445

Multicentre, Single-arm, Non-interventional Regulatory Post- Marketing Surveillance (rPMS) Study to Evaluate the Safety and Effectiveness of Saxenda® for Weight Management in Routine Clinical Practice in Taiwan.

Registration

Registration
NCT06283641
Study type
OBSERVATIONAL
Status
COMPLETED
Enrollment
300
Start
2024-04-08
Primary completion
2025-01-13
Lead sponsor
Novo Nordisk A/S
Conditions
Obesity
Interventions
DRUG:Liraglutide
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:U1111-1289-9747

Registered primary outcomes

  • Incidence of adverse events (AEs) by preferred term (PT) [From baseline (week 0) to week 26]

Linked records (2)

Automatic links, confirmed or rejected during screening. A record citing this registration may be a secondary analysis, a commentary or a review that mentions the trial.
RecordTitleYearDesignIdentifiersLink basis
R0002259A multicenter real-world study on the safety and effectiveness of the glucagon-like peptide-1 receptor agonist (liraglutide) in adolescents with obesity in Taiwan.
Chiu CF, Obesity research & clinical practice
2026Nonrandomized studyPMID 42744726DOIcites ClinicalTrials.gov:NCT06283641
R0008690Liraglutide in Adults With Obesity: A Multicentre, Single-Arm, Post-Marketing Surveillance Study in Taiwan.
Tu ST, Endocrinology, diabetes & metabolism
2026Nonrandomized studyPMID 42762462DOIcites ClinicalTrials.gov:NCT06283641