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Phase 1a/1b First-in-Human Study of BG-C9074 Alone and in Combination With Other Anticancer Therapies in Patients With Advanced Solid Tumors

Recruiting · Phase 1 · NCT06233942

Conditions: Advanced Solid Tumor

At a glance

Research payments reported, 2025
$957,579
U.S. investigators named
5
Sites paid
5
Planned or actual enrollment
308

About the trial

Sponsor
BeOne Medicines
Tested
BG-C9074 (drug), Tislelizumab (drug), Bevacizumab (drug)
Dates
Started 2024-04-12; completion 2028-05-15
Results posted
Not yet

This is a first-in-human, dose finding and dose expansion study to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-C9074 alone and in combination with other anticancer therapies in patients with advanced solid tumors.

From ClinicalTrials.gov, last updated 2026-09-16. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Beone Medicines Ltd. reported $957,579 in research payments for this study in 2025 (252 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

  • Florida Cancer Specialist (scri) - Fort Myers $369,055
  • University of Colorado Cancer Center $229,951
  • University of Southern California, Norris Comprehensive Cancer Center $153,677
  • The Ohio State University Dba: Comprehensive Canc $124,158
  • The Johns Hopkins University $80,738

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