Secukinumab for moderate-to-severe palmoplantar pustular psoriasis: Results of the 2PRECISE study Ulrich Mrowietz, MD, Hervé Bachelez, MD, PhD, A. David Burden, MD, Michael Rissler, PhD, Christian Sieder, PhD, Roberto Orsenigo, MD, Kamel Chaouche-Teyara, PhD Journal of the American Academy of Dermatology Volume 80, Issue 5, Pages 1344-1352 (May 2019) DOI: 10.1016/j.jaad.2019.01.066 Copyright © 2019 American Academy of Dermatology, Inc. Terms and Conditions
Fig 1 2PRECISE study design and patient disposition. This was a phase 3b multicenter, randomized, double-blind, placebo-controlled, parallel-group study. AE, Adverse event; TP2, treatment period 2. Journal of the American Academy of Dermatology 2019 80, 1344-1352DOI: (10.1016/j.jaad.2019.01.066) Copyright © 2019 American Academy of Dermatology, Inc. Terms and Conditions
Fig 2 Proportion of subjects (full analysis set 1, all patients, last observation carried forward) achieving a 75% improvement from baseline in the Palmoplantar Psoriasis Area Severity Index score (PPPASI75) through week 16. The primary end point was not met, but clinical benefit was observed with secukinumab, 300 mg, with 26.6% of subjects achieving PPPASI75 at week 16. Journal of the American Academy of Dermatology 2019 80, 1344-1352DOI: (10.1016/j.jaad.2019.01.066) Copyright © 2019 American Academy of Dermatology, Inc. Terms and Conditions
Fig 3 Improvements in the rate of achievement of a 75% improvement from baseline in the Palmoplantar Psoriasis Area Severity Index (PPPASI75) with secukinumab were observed to continue to week 52. Journal of the American Academy of Dermatology 2019 80, 1344-1352DOI: (10.1016/j.jaad.2019.01.066) Copyright © 2019 American Academy of Dermatology, Inc. Terms and Conditions