作者
Marcus Maurer,Ana Giménez‐Arnau,Gordon Sussman,Martin Metz,Diane R. Baker,Andrea Bauer,Jonathan A. Bernstein,Randolf Brehler,Chia‐Yu Chu,Wen‐Hung Chung,I V Danilycheva,Clive Grattan,Jacques Hébert,Constance H. Katelaris,Michaël Makris,Raisa Meshkova,Sinisa Savic,Rodney Sinclair,Karl Sitz,Petra Staubach,Bettina Wedi,Juergen Loeffler,Avantika Barve,Kenneth Kobayashi,Eva Hua,Thomas Severin,Reinhold Janocha
摘要
In the majority of patients with chronic spontaneous urticaria, most currently available therapies do not result in complete symptom control. Ligelizumab is a next-generation high-affinity humanized monoclonal anti-IgE antibody. Data are limited regarding the dose–response relationship of ligelizumab and the efficacy and safety of ligelizumab as compared with omalizumab and placebo in patients who have moderate-to-severe chronic spontaneous urticaria that is inadequately controlled with H1-antihistamines at approved or increased doses, alone or in combination with H2-antihistamines or leukotriene-receptor antagonists.