Table 1. Study designs.
NCT number | Study | Study objective | Study design | Duration/endpoint | No. of patients randomized | Treatments |
---|---|---|---|---|---|---|
NCT00463567 | INHANCE (49) | Efficacy/safety in target population in stage 2 of the study | Multicenter, randomized, double-blind, double-dummy, placebo-controlled, adaptive, seamless, parallel-group study | 26 weeks/trough FEV1 at week 12, indacaterol 150 and/or 300 µg vs. placebo | 1,683 | Indacaterol 150 µg once daily; |
Indacaterol 300 µg once daily; | ||||||
Tiotropium 18 µg open-label once daily; | ||||||
Placebo | ||||||
NCT00677807 | INDORSE (50) | Safety/tolerability/efficacy | Multicenter, randomized, double-blind, placebo-controlled, adaptive, seamless parallel-group study | 26 weeks extension of B2335S/safety profile over 52 weeks | 415 | Indacaterol 150 µg once daily; |
Indacaterol 300 µg once daily; | ||||||
Placebo | ||||||
NCT00567996 | INLIGHT-2 (51) | Efficacy/safety | Multicenter, randomized, double-blind, double- dummy, placebo-controlled, parallel-group study | 26 weeks/trough FEV1 at week 12, indacaterol 150 µg vs. placebo | 1,002 | Indacaterol 150 µg once daily; |
Salmeterol 50 µg twice daily; | ||||||
Placebo | ||||||
NCT00624286 | INLIGHT-1 (52) | Efficacy/safety | Multicenter, randomized, double-blind, placebo-controlled, parallel-group study | 12 weeks/trough FEV1 at week 12, indacaterol 150 µg vs. placebo | 416 | Indacaterol 150 µg once daily; |
Placebo | ||||||
NCT00821093 | INSIST (53) | Efficacy/safety | Multicenter, randomized, parallel-group, double-blind, double dummy study | 12 weeks/FEV1 AUC5 min-11 h 45 min at week 12, indacaterol 150 µg vs. salmeterol 50 µg | 1,123 | Indacaterol 150 µg once daily; |
Salmeterol 50 µg twice daily | ||||||
NCT00900731 | INTENSITY (54) | Efficacy/safety | Multicenter, randomized, parallel-group, blinded, double-dummy study | 12 weeks/trough FEV1 at week 12, indacaterol 150 µg vs. tiotropium 18 µg (non inferiority) | 1,598 | Indacaterol 150 µg once daily; |
Tiotropium 18 µg once daily | ||||||
NCT00846586 | INTRUST-1 (55) | Efficacy/safety | Randomized, double blind | 12 weeks/FEV1 AUC5 min-8 h at week 12, indacaterol 150 µg plus tiotropium 18 µg vs. tiotropium 18 µg | 1,134 | Indacaterol 150 µg once daily plus tiotropium 18 µg once daily; |
Tiotropium 18 µg once daily plus placebo | ||||||
NCT00877383 | INTRUST-2 (55) | Efficacy/safety | Randomized, double-blind | 12 weeks FEV1 AUC5 min-8 h at week 12, indacaterol 150 µg plus tiotropium 18 µg vs. tiotropium 18 µg | 1,142 | Indacaterol 150 µg once daily plus tiotropium 18 µg once daily; |
Tiotropium 18 µg once daily plus placebo | ||||||
NCT00794157 | B1302 (56) | Efficacy/safety/tolerability | Multicenter, randomized, double-blind, placebo-controlled, parallel-group study | 12 weeks/trough FEV1 at week 12, indacaterol 150 and/or 300 µg vs. placebo | 347 | Indacaterol 150 µg once daily; |
Indacaterol 300 µg once daily; | ||||||
Placebo | ||||||
NCT00792805 | B2333 (57) | Efficacy/safety | Multinational, multicenter, randomized, double-blind, placebo-controlled, parallel-group study | 26 weeks/trough FEV1 at week 12, indacaterol 150 and/or 300 µg vs. placebo | 563 | Indacaterol 150 µg once daily; |
Indacaterol 300 µg once daily; | ||||||
Placebo |
AUC, area under the curve; FEV1, forced expiratory volume in 1 sec.