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BI-1808 as a Single Agent and With Pembrolizumab (KEYTRUDA® ) in Treatment of Advanced Malignancies(Keynote-D20)

연구 개요

The goal of this first in human clinical trial is to test BI-1808 administered as single agent and in combination with pembrolizumab in subjects with advanced malignancies whose disease has progressed after standard therapy. The main questions it aims to answer are: * how safe and tolerable is BI-1808 * what is maximum tolerated or administrated dose * to determine recommended dose for further clinical trials. Participants will receive infusions of BI-1808 alone or combination with pembrolizumab every 3 weeks. For the purpose of this study, subjects with advanced malignancies includes subjects with advanced solid tumors and subjects with T-cell lymphoma (TCL),

스폰서
협력: 머크(MSD)
적응증
Advanced Malignancies, Ovarian Cancer, T-cell Lymphoma, Melanoma
중재
BI-1808, Pembrolizumab (KEYTRUDA® ) 25 Mg/mL Solution for Injection
목표 등록
176
시작일
2021-01-25
완료(예정)
2028-01-15

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