Table 3 |
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|
Clinical activity assessments in the multi dose phase at eight weeks |
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|
Placebo |
MTRX1011A 1.5 mg/kg SC |
MTRX1011A 3.5 mg/kg SC |
MTRX1011A 5.0 mg/kg IV |
|||||
|
baseline |
eight weeks |
baseline |
eight weeks |
baseline |
eight weeks |
baseline |
eight weeks |
|
|
|
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|
ACR20, % patients |
14 |
8 |
33 |
25 |
||||
|
ACR50, % patients |
0 |
0 |
25 |
0 |
||||
|
ACR70, % patients |
0 |
0 |
8 |
0 |
||||
|
DAS-CRP |
5.4 (4.3 to 6.6) |
4.4 (3.2 to 5.9) |
5.7 (4.1 to 6.7) |
5.6 (4.0 to 7.7) |
5.9 (3.7 to 6.8) |
4.6 (2.6 to 6.8) |
6.5 (4.2 to 8.0) |
5.5 (3.2 to 6.8) |
|
CRP, mg/dL |
1.7 (0.03 to 4.0) |
1.1 (0.1 to 3.0) |
0.8 (0.02 to 2.3) |
1.1 (0.02 to 4.2) |
1.1 (0.02 to 7.7) |
1.7 (0.1 to 9.8) |
2.1 (0.1 to 8.2) |
1.1 (0.1 to 3.9) |
|
ESR, mm/hour |
47 (15 to 120) |
36 (8 to 104) |
32 (8 to 60) |
30 (6 to 108) |
39 (0 to 78) |
34 (8 to 58) |
61 (26 to 110) |
51 (29 to 104) |
|
SJC |
7 (0 to 16) |
7 (0 to 19) |
14 (2 to 30) |
18 (2 to 51) |
20 (7 to 52) |
8 (0 to 36) |
26 (3 to 59) |
17 (0 to 30) |
|
TJC |
36 (10 to 53) |
25 (3 to 62) |
42 (12 to 65) |
37 (4 to 67) |
41 (8 to 68) |
18 (0 to 66) |
48 (22 to 65) |
30 (24 to 33) |
|
VAS, |
||||||||
|
Patient, pain |
60 (42 to 77) |
39 (19 to 57) |
57 (17 to 79) |
59 (10 to 89) |
62 (18 to 91) |
54 (14 to 89) |
78 (62 to 90) |
47 (20 to 67) |
|
Patient, overall |
69 (54 to 94) |
43 (18 to 75) |
63 (17 to 98) |
58 (17 to 88) |
70 (40 to 93) |
56 (10 to 87) |
81 (60 to 100) |
52 (25 to 75) |
|
VAS, Physician, global |
60 (26 to 78) |
44 (25 to 63) |
51 (21 to 80) |
52 (12 to 88) |
66 (35 to 100) |
51 (13 to 88) |
58 (45 to 76) |
52 (33 to 73) |
|
|
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|
Data are expressed as group mean, with ranges depicted between parentheses. ACR, American College of Rheumatology; CRP, C-reactive protein; DAS, disease activity score; ESR, erythrocyte sedimentation rate; IV, intravenous; SC, subcutaneous; SJC, swollen joint count; TJC, tender joint count; VAS, visual analog scale. |
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|
Scheerens et al. Arthritis Research & Therapy 2011 13:R177 doi:10.1186/ar3502 |
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