(a) PROs endpoints from the BREEZE-AD1, AD2, AD4, and AD7: Proportion of patients treated with baricitinib 4 mg achieving ≥4-point improvement in Itch NRS from baseline at W16 compared to placebo. Abbreviations: PBO, placebo; NRS, Numeric Rating Scale; W16, week 16; bari, baricitinib. * In BREEZE-AD4 and AD7, baricitinib was administered in association with topical corticosteroid as for protocol. (b) PROs endpoints from the BREEZE-AD1, AD2, AD4, and AD7: Change from Baseline to W16 in the Dermatology Life Quality Index (DLQI) in patients treated with baricitinib 4 mg compared to placebo. Abbreviations: PBO, placebo; DLQI, Dermatology Life Quality Index; W16, week 16; bari, baricitinib. * In BREEZE-AD4 and AD7, baricitinib was administered in association with topical corticosteroid as for protocol. (c) PROs endpoints from the BREEZE-AD1, AD2, AD4, and AD7: Change from Baseline to W16 in the in ADSS Item 2 in patients treated with baricitinib 4 mg compared to placebo. Abbreviations: PBO, placebo; ADSS, Atopic Dermatitis Symptom Score; W16, week 16; bari, baricitinib. * In BREEZE-AD 4 and AD7, baricitinib was administered in association with topical corticosteroid as for protocol.