This trial is conducted in Asia. The aim of this study is to investigate the safety profile of liraglutide (Victoza®) under normal conditions of use in Korean subjects with type 2 diabetes mellitus.
Study Type
OBSERVATIONAL
Enrollment
64
Administered either alone or in combination therapy according to the package insert (PI). Self-administered once daily, at any time subcutaneously (s.c., under the skin) in the abdomen, thigh or upper arm).
Novo Nordisk Investigational Site
Pyungchon-Dong 896, Dongan-Gu, South Korea
Novo Nordisk Investigational Site
Seoul, South Korea
Novo Nordisk Investigational Site
Seoul, South Korea
Novo Nordisk Investigational Site
Seoul, South Korea
The incidence of SADRs (Serious Adverse Drug Reactions)
Time frame: Up to 6 months
HbA1c (Glycosylated haemoglobin) change
Time frame: Month 0, month 6
Percentage of subjects reaching the target of HbA1c below 7.0%
Time frame: Month 6
Change in body weight
Time frame: Month 0, month 6
Number of SAEs/ ADRs (Serious Adverse Events/Adverse Drug Reactions)
Time frame: Up to 6 months
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Novo Nordisk Investigational Site
Ulsan, South Korea
Novo Nordisk Investigational Site
Ulsan, South Korea
Novo Nordisk Investigational Site
Wŏnju, South Korea