This trial is conducted in Japan. The aim of this trial is to investigate the safety and efficacy of biphasic insulin aspart (BIAsp) 50 (NN-X14Mix50) compared with biphasic human insulin (BHI) 50 in subjects with type 2 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
83
Administered subcutaneously (s.c., under the skin) twice daily for 24 weeks. Injected immediately before breakfast and dinner
Administered subcutaneously (s.c., under the skin) twice daily for 24 weeks. Injected 30 minutes before breakfast and dinner
Novo Nordisk Investigational Site
Tokyo, Japan
Glycosylated haemoglobin A1c (HbA1c)
Occurrence of adverse event(s)
Blood glucose
Incidence of hypoglycaemic episodes
Change from baseline in insulin antibodies
Insulin doses
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.