Table 1

Demographic and other baseline characteristics (ITT population)*

Characteristics, mean (SD) unless otherwise specifiedOKZ every 2 weeks
N=143
OKZ every 4 weeks
N=142
PBO
N=143
Age (years)52.0 (11.8)49.1 (12.1)52.7 (11.3)
Female (%)81.183.183.9
Duration of RA (years)8.7 (8.0)7.3 (7.0)8.4 (7.8)
MTX dose (mg)†16.1 (3.4)16.3 (3.4)16.1 (3.7)
Duration of prior MTX use (weeks)201.5 (232.1)157.4 (165.6)210.1 (208.2)
Glucocorticoid use, n (%)52 (36.4)‡50 (35.2)‡41 (28.7)‡
Prednisone dose or equivalent (mg)7.6 (6.0)6.1 (2.3)6.6 (2.4)
Prior exposure to TNF inhibitors, n (%)004 (2.8)
BMI (kg/m2)26.6 (5.1)26.4 (5.5)26.9 (5.0)
RF+ (≥15 IU/mL), n (%)115 (80.4)122 (85.9)127 (88.8)
Anti-CCP+ (>10 IU/mL), n (%)110 (76.9)115 (81.0)117 (81.8)
CRP (mg/L)§23.5 (23.1)22.7 (22.7)25.8 (28.7)
TJC¶24.4 (11.4)22.2 (10.3)24.0 (11.3)
SJC¶14.8 (6.5)14.5 (6.7)14.6 (6.9)
DAS28-CRP6.0 (0.7)5.9 (0.7)6.0 (0.8)
CDAI score (0–76)40.5 (9.8)38.7 (9.4)40.4 (10.5)
HAQ-DI score1.74 (0.47)1.64 (0.50)1.78 (0.49)
PtGA (VAS) (mm)70.4 (16.0)68.5 (14.5)69.6 (15.9)
Pain (VAS) (mm)70.2 (16.3)67.4 (18.5)68.3 (17.6)
PGA (VAS) (mm)70.5 (13.9)66.4 (14.2)68.0 (14.3)
  • Pain: patient assessment of pain.

  • *All patients with exception of one were Caucasian.

  • †100% patients were on MTX.

  • ‡P=0.33 (χ2 test).

  • §Upper limit of normal: >6 mg/L.

  • ¶Joint counts were assessed based on 66–68 joint counts.

  • anti-CCP+, anticyclic citrullinated peptide positivity; BMI, body mass index; CDAI, Clinical Disease Activity Index; CRP, C reactive protein; DAS28-CRP, Disease Activity Score 28 based on C reactive protein; HAQ-DI, Health Assessment Questionnaire Disability Index; ITT, intention-to-treat; MTX, methotrexate; N, number of subjects; OKZ, olokizumab; PBO, placebo; PGA, Physician Global Assessment of Disease Activity; PtGA, Patient Global Assessment of Disease Activity; RA, rheumatoid arthritis; RF+, rheumatoid factor positivity; SJC, swollen joint count; TJC, tender joint count; TNF, tumour necrosis factor; VAS, Visual Analogue Scale.