Zelenectide pevedotin (BT-8009):一种靶向nectin-4治疗膀胱癌的双环肽毒素偶联物。

IF 4.9 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Antonio Cigliola, Valentina Tateo, Michela Ravasi, Giorgia Di Maria, Serena Manzo, Brigida Anna Maiorano, Chiara Mercinelli, Andrea Necchi
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引用次数: 0

摘要

Zelenectide pevedotin (BT8009)是一种针对nectin-4的新型自行车毒素偶联物,旨在克服现有抗nectin-4抗体-药物偶联物如enfortumab vedotin (EV)的局限性。其创新的分子设计增强了肿瘤的穿透性,最大限度地减少了全身毒性,并实现了独立于内化的治疗效果。涉及领域:本综述评估了BT8009的临床前原理和临床数据,重点关注其药代动力学特性、安全性和与EV相比的有效性。本文分析了正在进行的I/II期Duravelo-1试验的主要发现,以及II/III期Duravelo-2试验设计中的挑战及其对未来临床开发的潜在影响。专家意见:BT8009的初步数据显示了一个有趣的临床特征,具有良好的疗效和显著的安全性。然而,正在进行的试验的设计引起了人们的关注,特别是由于使用了过时的控制臂,并且缺乏与电动汽车的直接比较。这些限制可能会延迟其临床应用和监管批准,影响其在竞争日益激烈的治疗领域的定位。尽管如此,如果正在进行和未来的试验证实其有效性和安全性优势,BT8009可能代表着治疗表达nectin-4的实体肿瘤(如尿路上皮癌)的有价值的进步,值得在更强大的比较研究中进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Zelenectide pevedotin (BT-8009): a bicyclic peptide toxin conjugate targeting nectin-4 for the treatment of bladder cancer.

Introduction: Zelenectide pevedotin (BT8009) is a novel Bicycle Toxin Conjugate targeting nectin-4, designed to overcome the limitations of already existing anti-nectin-4 antibody-drug conjugates such as enfortumab vedotin (EV). Its innovative molecular design enhances tumor penetration, minimizes systemic toxicity, and achieves therapeutic efficacy independent from internalization.

Areas covered: This review evaluates the preclinical rationale and clinical data for BT8009, focusing on its pharmacokinetic properties, safety, and efficacy compared to EV. Key findings from the ongoing phase I/II Duravelo-1 trial are analyzed alongside challenges in the design of the phase II/III Duravelo-2 trial and their potential implications for future clinical development.

Expert opinion: Preliminary data on BT8009 reveal an intriguing clinical profile, with promising efficacy and a notable safety profile. However, the design of ongoing trials raises concerns, particularly due to the use of outdated control arms and the lack of direct comparisons to EV. These limitations could delay its clinical adoption and regulatory approval, impacting on its positioning in an increasingly competitive therapeutic landscape. Nonetheless, if ongoing and future trials confirm its efficacy and safety advantages, BT8009 could represent a valuable advancement for the treatment of nectin-4 expressing solid tumors such as urothelial carcinoma, warranting further investigation in more robust comparative studies.

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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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