Table 1.
|
|
Inclusion criteria |
Patients contributing to pooled analysis, n |
||||||
---|---|---|---|---|---|---|---|---|---|
Study |
Duration
*
|
Age, y |
HbA
1c
, % |
eGFR, |
PBO |
CANA |
CANA |
Total |
Aged |
mL/min/1.73 m 2 | 100 mg | 300 mg | ≥65 y | ||||||
Monotherapy |
26 weeks |
≥18 to ≤80 |
≥7.0 and ≤10.0 |
≥50 |
192 |
195 |
197 |
584 |
118 |
Add-on to MET |
26 weeks |
≥18 to ≤80 |
≥7.0 and ≤10.5 |
≥55 |
183 |
368 |
367 |
918 |
149 |
Add-on to MET + SU |
26 weeks |
≥18 to ≤80 |
≥7.0 and ≤10.5 |
≥55 |
156 |
157 |
156 |
469 |
85 |
Add-on to MET + PIO |
26 weeks |
≥18 to ≤80 |
≥7.0 and ≤10.5 |
≥55 |
115 |
113 |
114 |
342 |
93 |
Overall total, n | 646 | 833 | 834 | 2,313 | 445 |
eGFR, estimated glomerular filtration rate; PBO, placebo; CANA, canagliflozin; MET, metformin; SU, sulphonylurea; PIO, pioglitazone.
*Assessment time point; mean treatment exposure of 24.2, 24.3, and 23.8 weeks with canagliflozin 100 and 300 mg and placebo, respectively.