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
Registered primary outcomes
- Incidence of Adverse Events (AEs) by preferred term [baseline (Visit1, 0 week) to 26 weeks]
Linked records (0)
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