RTI uses cookies to offer you the best experience online. By clicking “accept” on this website, you opt in and you agree to the use of cookies. If you would like to know more about how RTI uses cookies and how to manage them please view our Privacy Policy here. You can “opt out” or change your mind by visiting: http://optout.aboutads.info/. Click “accept” to agree.
Secukinumab’s time to psoriasis response on patient-reported psoriasis symptoms (ERASURE study)
Gottlieb, A., Gnanasakthy, A., Strober, B., Zhang, J., & Tran, MH. (2014). Secukinumab’s time to psoriasis response on patient-reported psoriasis symptoms (ERASURE study). Journal of the American Academy of Dermatology, 70(5, Suppl. 1), AB189. https://doi.org/10.1016/j.jaad.2014.01.782
Background: Secukinumab (AIN457), a fully human anti–interleukin-17A monoclonal antibody, was evaluated in a phase 3 clinical study at week 12 (vs. placebo) for efficacy and safety in subjects with moderate to severe plaque psoriasis. Time to symptom response was evaluated using the Psoriasis Symptom Diary (PSD), which measures psoriasis-related characteristics subjects have reported as important and relevant to their disease and treatment.