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Epcoritamab: First Approval
被引:15
|作者:
Frampton, James E.
[1
]
机构:
[1] Springer Nat, Private Bag 65901, Auckland 0754, New Zealand
来源:
关键词:
LARGE B-CELL;
RITUXIMAB PLUS LENALIDOMIDE;
NON-HODGKIN-LYMPHOMA;
SUBCUTANEOUS EPCORITAMAB;
OPEN-LABEL;
TRIAL;
COMBINATION;
MONOTHERAPY;
SAFETY;
R-2;
D O I:
10.1007/s40265-023-01930-4
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Epcoritamab (epcoritamab-bysp; Epkinly & TRADE;; Tepkinly(& REG;)) is a subcutaneously administered CD3xCD20 T-cell-engaging bispecific antibody being co-developed by Genmab and AbbVie for the treatment of mature B-cell non-Hodgkin lymphoma subtypes (B-NHLs), including diffuse large B-cell lymphoma (DLBCL). Epcoritamab received its first (conditional) approval on 19 May 2023, in the USA, for the treatment of adult patients with relapsed or refractory (R/R) DLBCL, not otherwise specified, including DLBCL arising from indolent lymphoma, and high-grade B-cell lymphoma after & GE; 2 lines of systemic therapy. Elsewhere, epcoritamab has received a positive opinion in the EU as a monotherapy for the treatment of adults with R/R DLBCL after & GE; 2 lines of systemic therapy, and is currently under regulatory review in Japan for the treatment of adults with R/R large B-cell lymphoma after & GE; 2 lines of systemic therapy. Clinical development of epcoritamab as monotherapy and in combination with standard of care agents for the treatment of mature B-NHLs is ongoing globally. This article summarizes the milestones in the development of epcoritamab leading to this first approval for R/R DLBCL.
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页码:1331 / 1340
页数:10
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