Blinatumomab: First Global Approval

被引:69
作者
Sanford, Mark [1 ]
机构
[1] Springer, Auckland 0754, New Zealand
关键词
ACUTE LYMPHOBLASTIC-LEUKEMIA; MINIMAL RESIDUAL DISEASE; CELL LYMPHOMA DLBCL; HIGH RESPONSE RATE; TERM-FOLLOW-UP; ANTIBODY BLINATUMOMAB; B-LINEAGE; FREE SURVIVAL; THERAPY; PHASE-2;
D O I
10.1007/s40265-015-0356-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Blinatumomab (BLINCYTO (TM)) is a novel, bispecific T-cell engaging antibody that binds cluster of differentiation (CD) 19 antigens on blast cells while also binding and activating the CD3/T cell receptor complex, causing cell lysis. The antibody is being developed by Amgen as a treatment for haematological cancers that originate from B cell lines. Blinatumomab was approved by the US FDA in December 2014 for the treatment of adults with Philadelphia chromosome (Ph)-negative relapsed/refractory B-cell precursor acute lymphoblastic leukaemia (BCP-ALL). It is awaiting approval for this indication in the EU and is in phase III development in various countries. This article summarizes the milestones in the development of blinatumomab leading to its first approval for the treatment of Ph-negative BCP-ALL.
引用
收藏
页码:321 / 327
页数:7
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