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

Recruiting · Phase 1 · NCT05981703

Conditions: Advanced Solid Tumor, Solid Tumor

At a glance

Research payments reported, 2025
$1.9M
U.S. investigators named
5
Sites paid
9
Planned or actual enrollment
337

About the trial

Sponsor
BeOne Medicines
Tested
BGB-26808 (drug), Tislelizumab (drug), Chemotherapy (drug)
Dates
Started 2023-09-21; completion 2029-02-28
Results posted
Not yet

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.

From ClinicalTrials.gov, last updated 2026-09-28. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Beigene, Ltd. reported $1.9M in research payments for this study in 2025 (86 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.