drugset / Trial / NCT05981703

A Study Investigating BGB-26808 Alone or in Combination With Tislelizumab in Participants With Advanced Solid Tumors

NCT05981703

Phase 1 Recruiting 217 enrolled BeOne Medicines
RandomizedSequentialOpen-labelTreatment

Summary

This is an open-label, multicenter, and nonrandomized dose escalation and dose expansion study to evaluate BGB-26808 as monotherapy or in combination with tislelizumab in participants with advanced solid tumors. The main purpose of this study is to explore the recommended dosing for BGB-26808.

Timeline

Start
2023-09-21
Primary completion
2027-09-30
Completion
2027-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject BGB-26808 Unknown Oral
Subject Tislelizumab Monoclonal antibody Intravenous