Placebo | 50mg | 100mg | 200mg | |
---|---|---|---|---|
(n=72) | (n=72) | (n=70) | (n=69) | |
12 weeks | ||||
ACR20, NRI1, % | 29 | 67*** | 66*** | 73** |
ACR50, NRI, % | 11 | 35** | 37*** | 44*** |
ACR70, NRI, % | 3 | 8 | 19** | 13* |
DAS28(CRP), LOCF3, mean change from BL2 | −1.0 | −1.8*** | −2.0*** | −2.3*** |
CDAI4 mean change from BL, LOCF | −12 | −21*** | −24*** | −25*** |
24 weeks | ||||
ACR20, NRI, % | n/a | 57 | 79 | 67 |
ACR50, NRI, % | n/a | 33 | 39 | 45 |
ACR70, NRI, % | n/a | 19 | 26 | 25 |
DAS28(CRP), LOCF, mean change from BL | n/a | −2.0 | −2.6 | −2.6 |
CDAI mean change from BL, LOCF | n/a | −22 | −30 | −28 |
*p<0.05 vs. placebo; **p<0.01 vs. placebo; ***p<0.001 vs. placebo. ACR scores based on ITT analysis. 1Non-responder imputation. 2Baseline. 3Last observation carried forward. 4Clinical Disease Activity Index.