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First-In-Human Study of Monoclonal Antibody BMS-986218 by Itself and in Combination With Nivolumab in Participants With Advanced Solid Tumors

Terminated · Phase 1, Phase 2 · NCT03110107

Conditions: Advanced Cancer

At a glance

Research payments reported, 2025
$2,000
U.S. investigators named
1
Sites paid
1
Planned or actual enrollment
376

About the trial

Sponsor
Bristol-Myers Squibb
Tested
Ipilimumab (biological), BMS-986218 (biological), Nivolumab (biological)
Dates
Started 2017-05-04; completion 2024-04-04
Results posted
Yes

The purpose of this study is to determine whether BMS-986218 both by itself and in combination with Nivolumab is safe and tolerable in the treatment of advanced solid tumors.

From ClinicalTrials.gov, last updated 2025-04-24. Full record, eligibility and contacts (opens in a new tab)

Industry funding

E.r. Squibb & Sons, L.l.c. reported $2,000 in research payments for this study in 2025 (1 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

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