Table 3 |
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|
Secondary endpoints in patients with inflammatory osteoarthritis of the knee who received open-label adalimumab |
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|
Baseline |
4 weeks |
8 weeks |
12 weeksa |
22 weeksb |
|
|
|
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|
Patient global |
60.6 (22.0) |
49.7 (22.1)** |
37.4 (22.6)* |
36.1 (21.9)* |
44.4 (22.5) |
|
Physician global |
69.7 (12.7) |
44.6 (17.8)* |
34.5 (16.9)* |
40.7 (22.0)* |
40.1 (25.3) |
|
Activity impairment |
6.30 (1.17) |
5.70 (1.53) |
4.90 (1.59)** |
5.10 (2.00)* |
5.19 (1.80) |
|
Sleep impairment |
2.90 (0.64) |
2.35 (0.81) |
2.10 (0.72)** |
2.05 (0.89)** |
2.50 (0.73) |
|
Target joint tenderness |
1.75 (0.44) |
1.00 (0.73) |
0.95 (0.69)** |
0.95 (0.94)** |
0.81 (75) |
|
Target joint swelling |
2.15 (0.37) |
1.45 (0.89)** |
1.00 (1.03)* |
1.15 (1.14)** |
0.75 (0.77) |
|
|
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|
Mean (standard deviation) values for secondary endpoints over 22 weeks in 20 patients with inflammatory osteoarthritis of the knee who received open-label adalimumab for 12 weeks. aWeek 12 data versus baseline according to paired t test using last-observation-carried-forward data. bWeek 22 data are based on 16 patients who attended for assessment. *P < 0.0001, **P < 0.05. |
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|
Maksymowych et al. Arthritis Research & Therapy 2012 14:R206 doi:10.1186/ar4044 |
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