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. 2019 Dec 9;47(2):114–120. doi: 10.1111/1346-8138.15173

Table 2.

Baseline patient characteristics, extent of exposure to delgocitinib ointment and concomitant use of topical corticosteroids

  QBA4‐2 (n = 352) Pooled safety population (n = 506)
Age (years) 33.0 (11.1) 32.6 (10.8)
Sex, n (%)
Men 223 (63.4) 318 (62.8)
Women 129 (36.6) 188 (37.2)
Duration of AD (years) 23.9 (12.2) 24.2 (11.7)
mEASI score 8.8 (4.9) 10.5 (5.6)
IGA score, n (%)
0 (clear), 1 (almost clear) 0 2 (0.4)
2 (mild) 110 (31.3) 115 (22.7)
3 (moderate) 215 (61.1) 304 (60.1)
4 (severe) 27 (7.7) 85 (16.8)
Pruritus NRS score 4.7 (2.0) 4.8 (2.0)
Percentage of BSA affected by AD 19.6 (6.9) 21.1 (7.6)
Exposure to delgocitinib ointment
Exposure duration (days) 286.7 (118.4) 251.3 (114.5)
Amount of drug applied (g) 1360.8 (869.7) 1238.6 (786.7)
Amount of drug applied per day (g) 4.8 (2.2) 5.1 (2.3)
Patients who used topical corticosteroids, n (%) 224 (63.6) 288 (56.9)

Data are displayed as mean (SD) unless otherwise indicated. The pooled safety population includes all patients in QBA4‐2 and patients who received delgocitinib ointment in QBA4‐1. AD, atopic dermatitis; BSA, body surface area; IGA, Investigator’s Global Assessment; mEASI, modified Eczema Area and Severity Index; NRS, Numeric Rating Scale.