Biosimilars in inflammatory bowel disease: A review of post-marketing experience

被引:15
作者
Deiana, Simona [1 ]
Gabbani, Tommaso [1 ]
Annese, Vito [1 ]
机构
[1] AOU Careggi Univ Hosp, Div Gastroenterol, I-50139 Florence, Italy
关键词
Adalimumab biosimilar; CTP-13; ZRC-3197; Infliximab biosimilars; Biologic drugs; CROHNS-DISEASE; INNOVATOR INFLIXIMAB; COMBINATION THERAPY; CLINICAL-EXPERIENCE; ULCERATIVE-COLITIS; PARALLEL-GROUP; DOUBLE-BLIND; CT-P13; EFFICACY; SAFETY;
D O I
10.3748/wjg.v23.i2.197
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Biologic compounds are obtained from living organisms or cell cultures by means of biotechnology methods. A similar biologic drug, commonly called biosimilar, is a product copied by a native approved biologic drug whose license has expired. Biosimilar drugs usually are marketed at a lower price and provide important financial savings for public healthcare systems. Some differences between biosimilars and original biologic drugs might exist but they are acceptable if they fall within defined "boundaries of tolerance": differences in some features between the two molecules are considered important only if clinical relevant. Considering that the efficacy of the innovator biologic drug has already been established, the clinical studies required for approval of a biosimilar could be reduced compared with those required for the approval of the originator. In this review, real life data available in inflammatory bowel disease patients treated with biosimilars are reported, documenting in general satisfactory outcomes, sustained efficacy and no sign of increased immunogenicity, although, further controlled data are awaited.
引用
收藏
页码:197 / 203
页数:7
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