作者
Sandrine Vendeville,Franck Amblard,Leda Bassit,Leonid N. Beigelman,Lawrence M. Blatt,Xiaohong Chen,Loke Ming Chou,Dieudonné Buh Kum,Sushmita Chanda,Jérôme Deval,Xuesong Geng,Kusum Gupta,Andreas Jekle,Jing Wang,Xiaojuan Hu,Hyunsoon Kang,Cheng Liu,Jyanwei Liu,David C. McGowan,Dinah Misner,Pierre Raboisson,Abel Acosta Sanchez,V. N. Serebryany,Antitsa Stoycheva,Julian Symons,Hua Tan,Hannah Vanrusselt,Caroline Williams,Michael J. Welch,Liangliang Zhang,Qingling Zhang,Yafeng Zhang,Raymond F. Schinazi,David B. Smith,Yannick Debing
摘要
Chronic hepatitis B (CHB) represents a significant unmet medical need with few options beyond lifelong treatment with nucleoside analogues, which rarely leads to a functional cure. Novel agents that reduce levels of HBV DNA, RNA and other viral antigens could lead to better treatment outcomes. The capsid assembly modulator (CAM) class of compounds represents an important modality for chronic suppression and to improve functional cure rates, either alone or in combination.