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Clinical Trial Summary

The purpose of this study is to assess the antitumor activity, safety, and tolerability of tislelizumab plus investigational agent(s) with or without chemotherapy. This study is structured as a master protocol with separate sub- studies. Sub-study 1 includes participants with non-small cell lung cancer (NSCLC) with high programmed cell death protein ligand-1 (PD-L1) expression (≥ 50%), and Sub-study 2 includes participants with NSCLC with low or negative (PD-L1) expression (< 50%).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05635708
Study type Interventional
Source BeiGene
Contact BeiGene
Phone +1-877-828-5568
Email clinicaltrials@beigene.com
Status Recruiting
Phase Phase 2
Start date March 7, 2023
Completion date July 2025

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