Antibody drug conjugates: Development, characterization, and regulatory considerations

被引:13
|
作者
Kommineni, Nagavendra [1 ]
Pandi, Palpandi [1 ]
Chella, Naveen [1 ]
Domb, Abraham J. [2 ]
Khan, Wahid [1 ]
机构
[1] NIPER, Dept Pharmaceut, Hyderabad 500037, Andhra Pradesh, India
[2] Hebrew Univ Jerusalem, Fac Med, Sch Pharm, IL-91120 Jerusalem, Israel
关键词
antibody drug conjugates; cytotoxicity; monoclonal antibody; synthesis; MONOMETHYL AURISTATIN E; TRASTUZUMAB EMTANSINE; POLYMERIC NANOPARTICLES; INOTUZUMAB OZOGAMICIN; GEMTUZUMAB OZOGAMICIN; MONOCLONAL-ANTIBODIES; BRENTUXIMAB VEDOTIN; LINKER STABILITY; TARGETED DRUGS; CANCER-THERAPY;
D O I
10.1002/pat.4789
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Previously, cancer chemotherapy was often accompanied by severe side effects. Antibody drug conjugates (ADCs) were introduced to address this treatment complication. ADCs are a potent category of bioconjugates and immunoconjugates designed as targeted therapy for the treatment of cancer. ADCs are complex molecules composed of an antibody linked via linker chemistry to a cytotoxic payload or drug. Therefore, biologic properties of the cell-surface target antigen are important in designing an effective ADC as an anticancer agent. ADCs have the ability to discriminate between the healthy and diseased tissue, so that healthy cells are less effected and get maximum therapeutic benefit. This review describes the development, characterization, and regulatory consideration of ADCs, and it summarizes the approved products in the market and in clinical trials.
引用
收藏
页码:1177 / 1193
页数:17
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