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A Study to Evaluate Whether Participants With Melanoma Prefer Subcutaneous vs Intravenous Administration of Nivolumab and Nivolumab + Relatlimab Fixed-dose Combinations

Active, not recruiting · Phase 2 · NCT06101134

Conditions: Melanoma

At a glance

Research payments reported, 2025
$122,889
U.S. investigators named
6
Sites paid
6
Planned or actual enrollment
100

About the trial

Sponsor
Bristol-Myers Squibb
Tested
relatlimab+nivolumab (drug), relatlimab+nivolumab+rHuPH20 (drug), nivolumab (drug), nivolumab+rHuPH20 (drug)
Dates
Started 2023-11-06; completion 2026-12-21
Results posted
Yes

The purpose of this study is to assess the patient's preference for nivolumab subcutaneous (SC) or nivolumab + relatlimab fixed-dose combination (FDC) SC and provide patient experience data by route of administration. This study will also generate safety data which will further characterize the safety profile of patients switching the route of administration from intravenous (IV) to SC.

From ClinicalTrials.gov, last updated 2026-09-14. Full record, eligibility and contacts (opens in a new tab)

Industry funding

E.r. Squibb & Sons, L.l.c. reported $122,889 in research payments for this study in 2025 (6 payments).

Products named: Sotyktu

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.