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A First-in-Human (FIH) Study of BG-C137, an Anti-Fibroblast Growth Factor Receptor 2b (FGFR2b) Antibody Drug Conjugate, in Participants With Advanced Solid Tumors

Recruiting · Phase 1 · NCT06625593

Conditions: Advanced Solid Tumor

At a glance

Research payments reported, 2025
$467,543
U.S. investigators named
6
Sites paid
7
Planned or actual enrollment
168

About the trial

Sponsor
BeOne Medicines
Tested
BG-C137 (drug), Anticancer Agents (drug)
Dates
Started 2024-12-09; completion 2026-12-31
Results posted
Not yet

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics (PK), pharmacodynamics, and preliminary antitumor activity of BG-C137 alone and in combination with anticancer agents in participants with advanced solid tumors. The study will be conducted in two phases: Phase 1a (Monotherapy Dose Escalation, and Safety Expansion; Combination Dose Confirmation and Safety Expansion) and Phase 1b (Dose Expansion).

From ClinicalTrials.gov, last updated 2026-07-09. Full record, eligibility and contacts (opens in a new tab)

Industry funding

Beone Medicines USA, Inc. reported $467,543 in research payments for this study in 2025 (34 payments).

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

  • The Board of Regents of the University of Wisconsin System $128,547
  • Ut MD Anderson Cancer Center $91,599
  • Yale Cancer Center $68,813
  • Mayo Clinic Scottsdale $61,418
  • Fred Hutchinson Cancer Center $45,095
  • University of Southern California, Norris Comprehensive Cancer Center $40,394
  • Yale University $31,677

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