Cigliola Antonio, Tateo Valentina, Michela Ravasi, Di Maria Giorgia, Manzo Serena, Mercinelli Brigida Anna, Maiorano Chiara, Necchi Andrea
Department of Medical Oncology, IRCCS Ospedale San Raffaele, Milan, Italy.
Vita-Salute San Raffaele University, Milan, Italy.
Expert Opin Investig Drugs. 2025 May 22. doi: 10.1080/13543784.2025.2510669.
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.
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.
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 However, the design of ongoing trials raises concerns, particularly due to the use of outdated control arms and the lack of direct comparisons to EV.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.
泽连奈肽佩沃多汀(BT8009)是一种新型的靶向nectin-4的双环毒素偶联物,旨在克服现有抗nectin-4抗体药物偶联物(如恩杂鲁胺佩沃多汀(EV))的局限性。其创新的分子设计增强了肿瘤渗透能力,将全身毒性降至最低,并实现了不依赖内化作用的治疗效果。
本综述评估了BT8009的临床前理论依据和临床数据,重点关注其与EV相比的药代动力学特性、安全性和疗效。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。
关于BT8009的初步数据显示出引人关注的临床特征,疗效有望且安全性显著。然而,正在进行的试验设计引发了担忧,特别是由于使用了过时的对照组且缺乏与EV的直接比较。这些局限性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中的定位。尽管如此,如果正在进行的和未来的试验证实其疗效和安全性优势,BT8009可能代表着治疗表达nectin-4的实体瘤(如尿路上皮癌)的一项有价值的进展,值得在更有力的比较研究中进一步探究。