Skip to main content

A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of Relatlimab Plus Nivolumab in Pediatric and Young Adults With Hodgkin and Non-Hodgkin Lymphoma

Terminated · Phase 1, Phase 2 · NCT05255601

Conditions: Lymphoma, Non-Hodgkin, Hodgkin Disease

At a glance

Research payments reported, 2025
$123,572
U.S. investigators named
11
Sites paid
11
Planned or actual enrollment
5

About the trial

Sponsor
Bristol-Myers Squibb
Tested
Relatlimab (drug), Nivolumab (drug)
Dates
Started 2022-09-13; completion 2025-12-03
Results posted
Yes

The purpose of this study is to assess the safety, tolerability, drug levels, and preliminary efficacy of relatlimab plus nivolumab in pediatric and young adult participants with recurrent or refractory classical Hodgkin lymphoma and non-Hodgkin lymphoma.

From ClinicalTrials.gov, last updated 2026-06-26. Full record, eligibility and contacts (opens in a new tab)

Industry funding

E.r. Squibb & Sons, L.l.c. reported $123,572 in research payments for this study in 2025 (11 payments).

Products named: Opdualag, Opdivo

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.