drugset / Trial / NCT05505877

Phase I/IIa Study of BR790 in Combination With Tislelizumab in Adult Subjects With Advanced Solid Tumors

NCT05505877

Phase 1/2 Unknown 160 enrolled Shanghai Gopherwood Biotech Co., Ltd.
Non-randomizedSequentialOpen-labelTreatment

Summary

This study is a Phase I/IIa, multi-center, open-label study of BR790 in combination with Tislelizumab with a dose escalation part followed by a dose expansion part in adult subjects with advanced solid tumors. These treatment to characterize the safety, tolerability, PK, PD and preliminary antitumor activity. The study treatment will be administered until the subject experiences unacceptable toxicity, progressive disease, and/or has treatment discontinued at the discretion of the Investigator or the subject, or due to withdrawal of consent.

Timeline

Start
2022-09-10
Primary completion
2024-10-31
Completion
2024-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject BR790 Unknown Oral
Subject Tislelizumab Monoclonal antibody Intravenous

Indications