Skip to main content

A Study of Tislelizumab in Combination With Investigational Agents in Participants With Non-Small Cell Lung Cancer

Completed · Phase 2 · NCT05635708

Conditions: Non-small Cell Lung Cancer, Metastatic Non-small Cell Lung Cancer

At a glance

Research payments reported, 2025
$685,268
U.S. investigators named
5
Sites paid
6
Planned or actual enrollment
418

About the trial

Sponsor
BeiGene
Tested
Tislelizumab (drug), BGB-A445 (drug), LBL-007 (drug), Carboplatin (drug), Cisplatin (drug), pemetrexed (drug), Paclitaxel (drug), Nab paclitaxel (drug), BGB-15025 (drug)
Dates
Started 2023-02-10; completion 2026-10-29
Results posted
Not yet

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%).

From ClinicalTrials.gov, last updated 2026-10-30. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Beigene, Ltd. reported $685,268 in research payments for this study in 2025 (114 payments).

Products named: Tevimbra

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.