医学
耐受性
肿瘤科
细胞
神经内分泌肿瘤
T细胞
内科学
癌症研究
肺癌
免疫系统
免疫学
不利影响
生物
遗传学
作者
Martin Wermke,Enriqueta Felip,Valentina Gambardella,Yasutoshi Kuboki,Daniel Morgensztern,Zohra Oum’ Hamed,Meiruo Liu,Matus Studeny,Taofeek K. Owonikoko
出处
期刊:Future Oncology
[Future Medicine]
日期:2022-07-11
卷期号:18 (24): 2639-2649
被引量:28
标识
DOI:10.2217/fon-2022-0196
摘要
Poorly differentiated neuroendocrine carcinomas such as small-cell lung cancer (SCLC) have poor survival and high relapse rates. DLL3 is found on these carcinomas and has become a target of increasing interest in recent years. The bispecific DLL3/CD3 T-cell engager BI 764532 has been shown to induce complete tumor regression in a human T cell-engrafted mouse model. Here, we describe the study design of a first-in-human, phase I, multicenter, open-label, non-randomized, dose-escalation study in patients with SCLC or other DLL3-positive neuroendocrine carcinomas. The study will determine the maximum tolerated dose and evaluate safety, tolerability, pharmacokinetics and preliminary efficacy of BI 764532 monotherapy.
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