Complement-targeted therapeutics: Are we there yet, or just getting started?

被引:0
|
作者
Ricklin, Daniel [1 ]
机构
[1] Univ Basel, Dept Pharmaceut Sci, Mol Pharm Grp, Klingelbergstr 50, CH-4056 Basel, Switzerland
基金
瑞士国家科学基金会;
关键词
Complement system; Drug Discovery and Development; Therapeutics; PAROXYSMAL-NOCTURNAL HEMOGLOBINURIA; FACTOR-H POLYMORPHISM; MACULAR DEGENERATION; DOUBLE-BLIND; ECULIZUMAB; DISCOVERY; DISEASE; PHASE-3; SYSTEM; INHIBITION;
D O I
10.1002/eji.202350816
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Therapeutic interventions in the complement system, a key immune-inflammatory mediator and contributor to a broad range of clinical conditions, have long been considered important yet challenging or even unfeasible to achieve. Almost 20 years ago, a spark was lit demonstrating the clinical and commercial viability of complement-targeted therapies. Since then, the field has experienced an impressive expansion of targeted indications and available treatment modalities. Currently, a dozen distinct complement-specific therapeutics covering several intervention points are available in the clinic, benefiting patients suffering from eight disorders, not counting numerous clinical trials and off-label uses. Observing this rapid rise of complement-targeted therapy from obscurity to mainstream with amazement, one might ask whether the peak of this development has now been reached or whether the field will continue marching on to new heights. This review looks at the milestones of complement drug discovery and development achieved so far, surveys the currently approved drug entities and indications, and ventures a glimpse into the future advancements yet to come. After a hesitant start, the number of available therapeutics that target the human complement system has surged from one to a dozen drugs in less than 20 years. Meanwhile, the clinical arsenal encompasses treatment modalities directed to several targets for the therapy of a steadily growing spectrum of complement-related disorders. image
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页数:15
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