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A First-in-Human Study of BGB-C354 Alone and in Combination With Tislelizumab in Participants With Advanced Solid Tumors

Completed · Phase 1 · NCT06422520

Conditions: Advanced Solid Tumor

At a glance

Research payments reported, 2025
$891,392
U.S. investigators named
5
Sites paid
5
Planned or actual enrollment
63

About the trial

Sponsor
BeOne Medicines
Tested
BGB-C354 (drug), Tislelizumab (drug)
Dates
Started 2024-07-08; completion 2026-05-15
Results posted
Not yet

This is a first-in-human, Phase 1a/1b study to evaluate the safety, tolerability, pharmacokinetics, and preliminary antitumor activity of BGB-C354 alone and in combination with tislelizumab in participants with advanced solid tumors. Study details include: * The study will be conducted in 2 phases: Phase 1a (Monotherapy Dose Escalation and Safety Expansion) and Phase 1b (Dose Expansion). * The visit frequency will be approximately every 21 days during study treatment. Maximum treatment duration will be up to two years. * The study duration is estimated to be approximately 5 years.

From ClinicalTrials.gov, last updated 2026-06-08. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Beone Medicines USA, Inc. reported $891,392 in research payments for this study in 2025 (87 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

  • Ut MD Anderson Cancer Center $300,127
  • Next Oncology $297,603
  • Florida Cancer Specialist (scri) - Fort Myers $212,083
  • Washington University $60,630
  • Dana Farber Mass General Brigham Cancer Care Inc $20,949

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