Phase I trial of the DLL3/CD3 bispecific T-cell engager BI 764532 in DLL3-positive small-cell lung cancer and neuroendocrine carcinomas

Author:

Wermke Martin1,Felip Enriqueta2,Gambardella Valentina3,Kuboki Yasutoshi4,Morgensztern Daniel5,Hamed Zohra Oum’6,Liu Meiruo7,Studeny Matus8,Owonikoko Taofeek K9

Affiliation:

1. Technical University Dresden, Medical Faculty, NCT/UCC Early Clinical Trial Unit, Dresden, Germany

2. Department of Medical Oncology, Vall d'Hebron University Hospital & Vall d'Hebron Institute of Oncology, Barcelona, Spain

3. Department of Medical Oncology, Hospital Clínico Universitario, INCLIVA Biomedical Research Institute, University of Valencia, Valencia, Spain

4. Department of Experimental Therapeutics, National Cancer Center Hospital East, Kashiwa, Chiba, Japan

5. Washington University School of Medicine, St. Louis, MO 63110, USA

6. Boehringer Ingelheim France S.A.S., Reims, France

7. Boehringer Ingelheim Pharmaceuticals Inc, Ridgefield, CT 06877, USA

8. Boehringer Ingelheim International GmbH, Ingelheim, Germany

9. Division of Hematology/Oncology, UPMC Hillman Cancer Center, University of Pittsburgh, PA 15232, USA

Abstract

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.

Funder

Boehringer Ingelheim

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

Reference26 articles.

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