LivingGLP1
Study S001513

A Multi-centre, Prospective, Open-label, Single-arm, Non-interventional, Regulatory Post Marketing Surveillance (rPMS) Study of Xultophy® (Insulin Degludec / Liraglutide) to Evaluate Safety and Effectiveness in Patients With Type 2 Diabetes Mellitus in Routine Clinical Practice in Korea

Registration

Registration
NCT04952779
Study type
OBSERVATIONAL
Status
COMPLETED
Enrollment
750
Start
2021-06-02
Primary completion
2024-12-15
Lead sponsor
Novo Nordisk A/S
Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG:Xultophy® (insulin degludec/liraglutide)
Results posted
FALSE
Individual participant data sharing
YES
Secondary identifiers
OTHER:1111-1211-7084

Registered primary outcomes

  • Incidence of Adverse Events (AEs) by preferred term [baseline (Visit1, 0 week) to 26 weeks]

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