“…(Goodman et al, 1984) The topical use of CL has been a well-established and effective primary therapy for the management of lymphoid malignancies, including MF, since the 1950s. (Gilmore et al, 2020, Kim, 2003, Lessin et al, 2013 A 0•016% CL gel formulation was purposely developed to treat MF, and in 2013 was approved by the U.S. Food and Drug Administration for the topical treatment of stage IA and IB MF in patients who received prior skin-directed therapy, (Helsinn Birex Pharmaceuticals Ltd, 2013, Talpur et al, 2014 based on results of a phase II trial. (Lessin et al, 2013, Talpur et al, 2014, Trautinger et al, 2017 Additionally, CL gel has been registered in Israel since 2016 in the same US indication, (Denis et al, 2019) and was approved by the European Medicines Agency in 2017…”