Table 1

Demographics and baseline disease characteristics, including baseline scores for disease activity assessments (safety population)*

CT-P10
N=102
RTX
N=51
Age (years)49.8±12.651.3±10.9
Sex, no. (%) of patients
 Female88 (86.3)46 (90.2)
 Male14 (13.7)5 (9.8)
Ethnicity, no. (%) of patients
 Caucasian69 (67.6)35 (68.6)
 Asian15 (14.7)9 (17.6)
 Other18 (17.6)7 (13.7)
Height (cm)161.9±8.1162.1±8.7
Weight (kg)71.4±17.772.4±16.0
Body mass index (kg/m2)27.2±6.027.5±5.5
Disease duration (years)11.0±7.810.3±9.1
C reactive protein (mg/dL)1.8±1.72.1±3.0
Erythrocyte sedimentation rate (mm/hour)49.5±24.550.1±26.7
RF positive, no. (%) of patients82 (80.4)40 (78.4)
Anti-CCP positive, no. (%) of patients86 (84.3)43 (84.3)
Swollen joint count (66 joints assessed)16.5±8.214.5±7.0
Tender joint count (68 joints assessed)27.4±14.827.1±14.2
Disease Activity Score in 28 joints
 C reactive protein6.0±0.96.0±0.9
 Erythrocyte sedimentation rate6.8±0.96.7±0.9
Health Assessment Questionnaire Disability Index score1.7±0.71.7±0.7
Prior anti-TNF agents, no. (%) of patients
 188 (86.3)42 (82.4)
 214 (13.7)9 (17.6)
Prior anti-TNF agent status, no. (%) of patients
 Failure93 (91.2)47 (92.2)
 Intolerance9 (8.8)4 (7.8)
Duration of prior TNF-antagonist use (months)18.9±20.323.7±26.7
Prior TNF antagonists used, no. (%) of patients†
 Adalimumab37 (36.3)18 (35.3)
 Certolizumab3 (2.9)2 (3.9)
 Etanercept30 (29.4)19 (37.3)
 Golimumab12 (11.8)3 (5.9)
 Infliximab32 (31.4)19 (37.3)
 Investigational drug‡3 (2.9)1 (2.0)
Weekly dose of MTX at baseline (mg)15.4±4.815.7±4.1
  • *Except where indicated otherwise, values are mean±SD.

  • †Some patients had previously received more than one anti-TNF agent.

  • ‡Refers to any anti-TNF agent given in a prior study.

  • CCP, cyclic citrullinated peptide; MTX, methotrexate; RF, rheumatoid factor; RTX, rituximab; TNF, tumour necrosis factor.