“…The most common serious TEAEs included squamous cell carcinoma of the skin. Of note, an increased incidence of non-melanoma skin cancers in patients with AD has been reported in the literature [24][25][26]. [14,19] (N = 7); NCT01859988 [20] (N = 296); NCT01385657 [14,19] (N = 12); NCT01548404 [14] (N = 51); NCT01639040 [14] (N = 17); NCT02260986 [10] (N = 581); NCT01979016 [18] (N = 44); NCT02210780 [15] (N = 168); NCT02277743 [12] (N = 353); NCT02407756 [16] (N = 5); NCT02395133 [22] (N = 415); NCT02277769 [12] (N = 402); NCT02755649 [11] (N = 313); NCT02647086 [17] (N = 13) b These patients completed the treatment and end-of-study periods c Includes reasons of relocation, desire for pregnancy, did not want to discontinue treatment for 12 weeks, work/school conflict, and personal reasons not specified d Includes patients withdrawn from the study, both those receiving treatment at the time of withdrawal and those not receiving treatment during the safety follow-up period e Includes the following dupilumab doses in the parent study: 75 mg qw, 100 mg q4w, 150 mg qw, 200 mg q2w, 200 mg qw, 300 mg q8w, 300 mg q4w, 2 mg/kg, 4 mg/kg f These patients had screen failed in the parent study because the enrollment target was met, but they were permitted to enter the OLE Dupilumab showed substantial and sustained improvement in AD signs and symptoms from the baseline of the parent study, with continued incremental improvement beyond 52 weeks of treatment.…”