CD38单克隆抗体felzartamab治疗晚期抗体介导的排斥反应:一项II期药物评估。

IF 4.1 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Katharina A Mayer, Klemens Budde, Martina Schatzl, Eva Schrezenmeier, Matthias Diebold, Bernd Jilma, Georg A Böhmig
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引用次数: 0

摘要

Felzartamab是一种新型的全人CD38单克隆抗体,目前正在开发用于治疗肾移植后抗体介导的排斥反应(AMR)。涵盖领域:本综述侧重于非zartamab治疗AMR和其他免疫介导肾病的II期临床试验。具体来说,它讨论了药物的作用机制,目前的临床开发阶段,潜在的未来应用和监管状况。专家意见:CD38是一种表达于浆细胞和免疫细胞(包括自然杀伤细胞(NK细胞))表面的激活标记物。在最近的一项II期随机、安慰剂对照临床试验中,felzartamab在肾移植后AMR患者中显示出可接受的安全性和副作用。疗效结果显示潜在的治疗益处,包括形态和分子AMR活性的显著降低。鉴于先前AMR治疗的临床试验结果好坏参半,针对抗体分泌浆细胞和先天效应细胞(如CD38+ NK细胞)的新方法可能提供一种有希望的新治疗策略。Felzartamab也正在研究用于治疗其他抗体介导的肾脏疾病,如狼疮肾炎、原发性膜性肾病和IgA肾病。如果证明有效,它将扩大肾移植排斥反应和原发性肾脏疾病的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CD38 monoclonal antibody felzartamab for late antibody-mediated rejection: a phase II drug evaluation.

Introduction: Felzartamab is a novel, fully human CD38 monoclonal antibody, currently in development for the treatment of antibody-mediated rejection (AMR) following kidney transplantation.

Areas covered: This review focuses on current phase II trials of felzartamab in AMR and other immune-mediated kidney diseases. Specifically, it discusses the drug's mechanism of action, current phase of clinical development, potential future applications and regulatory status.

Expert opinion: CD38 is an activation marker expressed on the surface of plasma cells and immune cells, including natural killer cells (NK cells) cells. In a recent phase II randomized, placebo-controlled clinical trial, felzartamab demonstrated an acceptable safety and side-effect profile in patients with AMR after kidney transplantation. Efficacy outcomes suggested potential therapeutic benefits, including significant reductions in morphologic and molecular AMR activity. Given the mixed results of previous clinical trials for AMR treatments, the novel approach of targeting both antibody-secreting plasma cells and innate effector cells such as CD38+ NK cells may offer a promising new therapeutic strategy. Felzartamab is also being investigated for the treatment of other antibody-mediated kidney diseases, such as lupus nephritis, primary membranous nephropathy and IgA nephropathy. If proven effective, it could expand the therapeutic options for kidney transplant rejection and primary kidney diseases.

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来源期刊
CiteScore
10.00
自引率
0.00%
发文量
71
审稿时长
6-12 weeks
期刊介绍: Expert Opinion on Investigational Drugs (ISSN 1354-3784 [print], 1744-7658 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on drugs in preclinical and early stage clinical development, providing expert opinion on the scope for future development. The Editors welcome: Reviews covering preclinical through to Phase II data on drugs or drug classes for specific indications, and their potential impact on future treatment strategies Drug Evaluations reviewing the clinical and pharmacological data on a particular drug Original Research papers reporting the results of clinical investigations on agents that are in Phase I and II clinical trials The audience consists of scientists, managers and decision-makers in the pharmaceutical industry, and others closely involved in R&D.
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