The objective of the study is to investigate the long-term safety and efficacy of BI 10773 given for 52 weeks as add-on therapy to one oral antidiabetic drug in patients with type 2 diabetes mellitus with insufficient glycaemic control.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
1,162
Number of Patients With Drug Related Adverse Events
Number of Patients With Drug Related Adverse Events after the first drug intake until 7 days after the last treatment administration, up to 383 days
Time frame: After the first drug intake until 7 days after the last treatment administration, up to 383 days
Change From Baseline in HbA1c
Change from baseline in HbA1c after 52 weeks of treatment
Time frame: Baseline and 52 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
BI 10773 high dose tablet once daily
Placebo tablets once daily
1245.52.023 Boehringer Ingelheim Investigational Site
Adachi-ku, Tokyo, Japan
1245.52.048 Boehringer Ingelheim Investigational Site
Aki-gun, Hiroshima, Japan
1245.52.012 Boehringer Ingelheim Investigational Site
Annaka, Gunma, Japan
1245.52.087 Boehringer Ingelheim Investigational Site
Atami, Shizuoka, Japan
1245.52.008 Boehringer Ingelheim Investigational Site
Beppu, Oita, Japan
1245.52.073 Boehringer Ingelheim Investigational Site
Chiyoda-ku, Tokyo, Japan
1245.52.002 Boehringer Ingelheim Investigational Site
Chuo-ku, Tokyo, Japan
1245.52.020 Boehringer Ingelheim Investigational Site
Chuo-ku, Tokyo, Japan
1245.52.021 Boehringer Ingelheim Investigational Site
Chuo-ku, Tokyo, Japan
1245.52.031 Boehringer Ingelheim Investigational Site
Fujisawa, Kanagawa, Japan
...and 77 more locations