drugset / Trial / NCT05494762

Safety, Pharmacokinetics, and Antitumor Activity of BGB-B167 Alone and in Combination With Tislelizumab (BGB-A317) in Participants With Advanced Solid Tumors

NCT05494762

Phase 1 Terminated 55 enrolled BeiGene
Non-randomizedSequentialOpen-labelTreatment

Summary

This study will evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of BGB-B167 monotherapy and in combination with tislelizumab (BGB-A317) in participants with select advanced solid tumors.

Timeline

Start
2022-08-25
Primary completion
2025-02-24
Completion
2025-02-24

Drugs

EvaluationDrugModalityDoseRoute
Subject BGB-B167 Unknown Intravenous
Subject Tislelizumab Monoclonal antibody Intravenous

Indications