Skip to main content

Table 4 Response criteria: SF-36 scores at baseline and at study assessment time points

From: Efficacy and safety of the human anti-IL-1beta monoclonal antibody canakinumab in rheumatoid arthritis: results of a 12-week, phase II, dose-finding study

Variable

Canakinumab 150 mg SC q4wk, n = 71

Canakinumab 300 mg SC q2wk, n = 64

Canakinumab 300 mg SC q2wk + 600 mg IV loading dose, n = 69

Placebo, n = 70

Mean SF-36 physical component summary score

Baseline, mean (SD)

27.19 (7.092)

28.57 (7.497)

26.29 (6.080)

27.48 (6.616)

Week 2, mean (SD)

29.70 (7.944)

28.94 (7.503)

27.86 (6.441)

29.58 (8.438)

Week 4, mean (SD)

30.40 (8.400)

30.87 (8.608)

28.91 (8.445)

29.94 (8.413)

Week 8, mean (SD)

31.48 (9.833)

31.32 (8.230)

28.89 (7.322)

29.44 (8.569)

Week 12, mean (SD)

32.92 (9.922)

31.62 (8.752)

30.33 (7.129)

30.17 (9.221)

Mean SF-36 mental component summary score

Baseline, mean (SD)

44.38 (12.891)

43.40 (11.325)

41.61(10.845)

44.64(12.779)

Week 2, mean (SD)

45.94 (12.518)

46.02 (11.083)

42.37 (10.585)

45.09 (12.834)

Week 4, mean (SD)

46.61 (12.469)

46.14 (12.008)

43.85 (11.433)

46.16 (12.835)

Week 8, mean (SD)

47.41 (12.228)

46.22 (12.762)

44.09 (11.849)

45.82 (12.032)

Week 12, mean (SD)

48.44 (12.421)

46.74 (11.595)

43.05 (11.958)

44.99 (12.294)

  1. Abbreviations: IV, intravenous; q2wk, every 2 weeks; q4wk, every 4 weeks; SC, subcutaneous; SF-36, Short Form-36; SD, standard deviation