Investigational therapies targeting the granulocyte macrophage colony-stimulating factor receptor-α in rheumatoid arthritis: focus on mavrilimumab

被引:30
作者
Cook, Andrew D. [1 ]
Hamilton, John A. [1 ]
机构
[1] Univ Melbourne, Royal Melbourne Hosp, Dept Med, Parkville, Vic 3050, Australia
关键词
granulocyte macrophage colony-stimulating factor receptor; mavrilimumab; rheumatoid arthritis; GM-CSF RECEPTOR; COLLAGEN-INDUCED ARTHRITIS; HUMAN MONOCLONAL-ANTIBODY; RANDOMIZED PHASE IIB; DOUBLE-BLIND; EFFECTOR PHASE; KEY MEDIATOR; CELL; CYTOKINES; SAFETY;
D O I
10.1177/1759720X17752036
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Mavrilimumab (formerly CAM-3001) is a high-affinity, immunoglobulin G4 monoclonal antibody (mAb) against the granulocyte macrophage colony-stimulating factor (GM-CSF) receptor-alpha chain. Phase I and II trials in patients with rheumatoid arthritis (RA) treated with mavrilimumab have shown encouraging results with respect to both safety and efficacy. No significant adverse events have so far been noted. The trials have demonstrated significant clinical benefit, meeting primary endpoints. Furthermore, for RA patients treated with mavrilimumab, who were tumour necrosis factor (TNF) inhibitor-inadequate responders, there are encouraging preliminary data indicating benefit and identifying potential biomarkers predictive of patients likely to find benefit. Here, we review the clinical trial data for mavrilimumab and discuss its potential as a treatment for RA in light of the competitive landscape in which it resides.
引用
收藏
页码:29 / 38
页数:10
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