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A Study of BMS-986484 Alone and Combination Therapy in Participants With Advanced Solid Tumors

Active, not recruiting · Phase 1 · NCT06544655

Conditions: Advanced Solid Tumors

At a glance

Research payments reported, 2025
$8,016
U.S. investigators named
3
Sites paid
3
Planned or actual enrollment
213

About the trial

Sponsor
Bristol-Myers Squibb
Tested
BMS-986484 (drug), Nivolumab (biological), Oxaliplatin (drug), Capecitabine (drug), Fluorouracil (drug), Calcium folinate (drug)
Dates
Started 2024-10-10; completion 2027-10-14
Results posted
Not yet

The purpose of this study is to assess the safety and tolerability of BMS-986484 administered alone, in combination with nivolumab in participants with advanced/metastatic solid tumors including non-small cell lung cancer (NSCLC), microsatellite stable (MSS) colorectal carcinoma (CRC), pancreatic ductal adenocarcinoma (PDAC), gastric/gastroesophageal junction adenocarcinoma (G/GEJC), and squamous cell carcinoma of the head and neck (SCCHN).

From ClinicalTrials.gov, last updated 2026-04-17. Full record, eligibility and contacts (opens in a new tab)

Industry funding

E.r. Squibb & Sons, L.l.c. reported $8,016 in research payments for this study in 2025 (3 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

  • Usc Norris Comprehensive Cancer Center $2,960
  • The University of Arizona Cancer Center - North $2,561
  • Next Oncology $2,495

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