Home > Dermatology > AAD 2018 > Late-breakers > Behcet’s syndrome and hidradenitis suppurativa

Behcet’s syndrome and hidradenitis suppurativa

Presented By
Dr Yusuf Yazici, New York University School of Medicine, USA; Prof. Evangelos Giamarellos-Bourboulis, University of Athens Medical School, Greece
AAD 2018
Apremilast effective in Behcet's Syndrome The oral phosphodiesterase (PDE)4 inhibitor apremilast displayed a significant effect on ulcers and ulcer pain associated with Behcet´s syndrome in the RELIEF trial [16]. Behcet's syndrome is a rare, chronic, multi-system inflammatory disorder characterised by oral and genital ulcers, skin lesions, uveitis, arthritis, with vascular, central nervous system, and gastrointestinal involvement. A key symptom occurring in nearly all patients is painful recurrent oral ulcers that can be disabling and have a substantial effect on QoL: there are currently no effective treatment options for them. The oral PDE4 inhibitor apremilast modulates inflammatory mediators and has demonstrated efficacy in a Phase 2 Behcet's syndrome study. These preliminary data were the reason for a Phase 3 trial with apremilast. In the RELIEF study, a total of 207 patients were randomised to apremilast (30 mg twice daily) or placebo. A...

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