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. 2021 Dec 20;6:27–36. doi: 10.1016/j.jdin.2021.11.001

Table I.

Baseline demographics and characteristics

Characteristic Placebo (n = 90) Upadacitinib 15 mg (n = 91) Upadacitinib 30 mg (n = 91)
Female, n (%) 16 (17.8) 23 (25.3) 22 (24.2)
Age (y), mean (SD) 36.3 (12.6) 35.9 (13.2) 34.7 (12.7)
Age group (y), n (%)
 Adolescents (<18) 9 (10.0) 10 (11.0) 10 (11.0)
 Adults (≥18) 81 (90.0) 81 (89.0) 81 (89.0)
Weight (kg), mean (SD) 67.6 (12.8) 65.1 (14.2) 66.2 (14.4)
BSA (%), mean (SD) 62.0 (20.5) 61.7 (23.7) 66.7 (21.2)
Disease duration since diagnosis (y), mean (SD) 24.7 (14.4) 23.0 (14.3) 20.7 (14.1)
hs-CRP (mg/L), mean (SD) 3.1 (6.4) 2.3 (3.8) 3.9 (8.8)
vIGA-AD, n (%)
 Moderate (score < 4) 47 (52.2) 47 (51.6) 48 (52.7)
 Severe (score = 4) 43 (47.8) 44 (48.4) 43 (47.3)
EASI, mean (SD) 34.4 (13.0) 34.2 (14.1) 36.1 (14.5)
Worst Pruritus NRS, mean (SD) 6.8 (1.3) 6.7 (1.4) 7.0 (1.4)
Medical history, n (%)
 Asthma 34 (37.8) 29 (31.9) 28 (30.8)
 Rhinitis allergic 58 (64.4) 45 (49.5) 45 (19.5)
 Conjunctivitis allergic 11 (12.2) 8 (8.8) 12 (13.2)

BSA, Body surface area; EASI, Eczema Area and Severity Index; hs-CRP, high-sensitivity C-reactive protein; NRS, numerical rating scale; vIGA-AD, validated Investigator's Global Assessment for Atopic Dermatitis.