Anakinra for refractory pustular psoriasis: A phase II, open-label, dose-escalation trial - 30/11/22
, Dominique C. Pichard, MD b, Daniella M. Schwartz, MD c, Michelle O'Brien, RN, BSN b, Matthew Masciocchi, BSc d, Julie Thompson, BSN b, H. Nida Sen, MD e, Seth M. Steinberg, PhD f, Sandra A. Mitchell, PhD, CRNP g, Adriana A. de Jesus, MD, PhD h, Timothy H. McCalmont, MD a, i, Amit Dey, MD j, Rachel K. Rosenstein, MD, PhD b, Zuoming Deng, PhD k, Raphaela Goldbach-Mansky, MD, MHS h, Nehal N. Mehta, MD j, Edward W. Cowen, MD, MHSc b| Funding sources: This work was supported by the intramural programs of the National Institute of Arthritis and Musculoskeletal and Skin Diseases, United States, National Cancer Institute, United States, National Heart, Lung and Blood Institute, United States and National Institute of Allergy and Infectious Disease, United States. Study drug was provided through a Clinical Trials Agreement between the National Cancer Institute and SOBI. Haley Naik is supported by the National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS K23 AR074531). |
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| IRB approval status: Reviewed and approved by the National Cancer Institute and National Institutes of Health Institutional Review Boards; IRB # 13-C-0071/13-AR-0071. |
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| Key words: acrodermatitis of Hallopeau; anakinra; autoinflammation; inflammatory arthritis; pustular psoriasis; Sneddon-Wilkinson disease. |
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| Reprints not available from the authors. |
Vol 87 - N° 6
P. 1380-1383 - décembre 2022 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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