Table 1

Baseline demographics and clinical characteristics

DemographicsTotal
(n=443)
Risankizumab (150 mg)
(n=224)
Placebo
(n=219)
Sex, n (%)
 Female224 (55.1)124 (55.4)120 (54.8)
Age (years), mean±SD52.9±12.653.1±12.552.7±12.6
White race, n (%)428 (96.6)218 (97.3)210 (95.9)
Duration of PsA (years), mean±SD8.2±8.38.2±8.28.2±8.3
Presence of dactylitis (LDI >0), n (%)97 (22.0)40 (17.9)57 (26.3)
Presence of enthesitis (LEI >0), n (%)305 (68.8)147 (65.6)158 (72.1)
PASI (in patients with BSA ≥3%), mean±SD8.0±8.47.7±6.78.4±9.9
Tender joint count (68 joints), mean±SD22.6±14.422.8±14.922.3±13.8
Swollen joint count (66 joints), mean±SD13.3±8.913.0±8.713.6±9.0
Body surface area—psoriasis ≥3, n (%)242 (54.6)123 (54.9)119 (54.3)
Number of prior csDMARDs, n (%)
 023 (5.2)12 (5.4)11 (5.0)
 1169 (38.1)88 (39.3)81 (37.0)
 2120 (27.1)60 (26.8)60 (27.4)
 >3131 (29.6)64 (28.6)67 (30.6)
Number of prior bDMARDs, n (%)
 0237 (53.5)119 (53.1)118 (53.9)
 ≥1206 (46.5)105 (46.9)101 (46.1)
Number of prior failed bDMARDs, n (%)
 0269 (60.7)137 (61.2)132 (60.3)
 1136 (30.7)72 (32.1)64 (29.2)
 ≥238 (8.6)15 (6.7)23 (10.5)
Concomitant csDMARD at baseline, n (%)
 Any csDMARD270 (60.9)141 (62.9)129 (58.9)
 Any MTX209 (47.2)110 (49.1)99 (45.2)
  MTX alone191 (43.1)102 (45.5)89 (40.6)
  MTX and other csDMARD18 (4.1)8 (3.6)10 (4.6)
 csDMARD other than MTX61 (13.8)31 (13.8)30 (13.7)
  Any sulfasalazine, without MTX18 (4.1)9 (4.0)9 (4.1)
  Any leflunomide, without MTX27 (6.1)12 (5.4)15 (6.8)
  Any apremilast, without MTX14 (3.2)9 (4.0)5 (2.3)
 None173 (39.1)83 (37.1)90 (41.1)
BMI in kg/m2, n (%)
 BMI <2576 (17.2)38 (17.0)38 (17.4)
 BMI ≥25 to <30136 (30.7)68 (30.4)68 (31.1)
 BMI ≥30231 (52.1)118 (52.7)113 (51.6)
  • bDMARD, biologic disease-modifying antirheumatic drug; BMI, body mass index; BSA, body surface area; csDMARD, conventional synthetic disease-modifying antirheumatic drug; LDI, Leeds Dactylitis Index; LEI, Leeds Enthesitis Index; MTX, methotrexate; PASI, Psoriasis Area and Severity Index; PsA, psoriatic arthritis.