| Outcome Measures: |
Primary: The incidence of SADRs (Serious Adverse Drug Reactions), Up to 6 months | Secondary: HbA1c (Glycosylated haemoglobin) change, Month 0, month 6|Percentage of subjects reaching the target of HbA1c below 7.0%, Month 6|Change in body weight, Month 0, month 6|Number of SAEs/ ADRs (Serious Adverse Events/Adverse Drug Reactions), Up to 6 months
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| Locations: |
Novo Nordisk Investigational Site, Pyungchon-Dong 896, Dongan-Gu, 431-796, Korea, Republic of|Novo Nordisk Investigational Site, Seoul, 02447, Korea, Republic of|Novo Nordisk Investigational Site, Seoul, 03080, Korea, Republic of|Novo Nordisk Investigational Site, Seoul, 150-950, Korea, Republic of|Novo Nordisk Investigational Site, Ulsan, 44455, Korea, Republic of|Novo Nordisk Investigational Site, Ulsan, 682-060, Korea, Republic of|Novo Nordisk Investigational Site, Wonju, 220-701, Korea, Republic of
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