医学
贝里穆马布
单克隆抗体
生物仿制药
伊克泽珠单抗
卡那努马布
食品药品监督管理局
帕尼单抗
阿达木单抗
药理学
药物开发
抗体
药品
病毒学
免疫学
西妥昔单抗
内科学
塞库金单抗
类风湿性关节炎
阿纳基纳
B细胞
疾病
B细胞激活因子
银屑病性关节炎
作者
Aaron Nelson,Eugen Dhimolea,Janice M. Reichert
摘要
Fully human monoclonal antibodies (mAbs) are a promising and rapidly growing category of targeted therapeutic agents. The first such agents were developed during the 1980s, but none achieved clinical or commercial success. Advances in technology to generate the molecules for study - in particular, transgenic mice and yeast or phage display - renewed interest in the development of human mAbs during the 1990s. In 2002, adalimumab became the first human mAb to be approved by the US Food and Drug Administration (FDA). Since then, an additional six human mAbs have received FDA approval: panitumumab, golimumab, canakinumab, ustekinumab, ofatumumab and denosumab. In addition, 3 candidates (raxibacumab, belimumab and ipilimumab) are currently under review by the FDA, 7 are in Phase III studies and 81 are in either Phase I or II studies. Here, we analyse data on 147 human mAbs that have entered clinical study to highlight trends in their development and approval, which may help inform future studies of this class of therapeutic agents.
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