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Study to Evaluate Adverse Events, and Change in Disease Activity, When Intravenously (IV) Infused With Livmoniplimab in Combination With IV Infused Budigalimab in Adult Participants With Hepatocellular Carcinoma (HCC)

Active, not recruiting · Phase 2 · NCT05822752

Conditions: Hepatocellular Carcinoma

At a glance

Research payments reported, 2025
$282,470
U.S. investigators named
10
Sites paid
10
Planned or actual enrollment
130

About the trial

Sponsor
AbbVie
Tested
Budigalimab (drug), Livmoniplimab (drug), Lenvatinib (drug), Sorafenib (drug)
Dates
Started 2023-09-21; completion 2026-11
Results posted
Not yet

Hepatocellular carcinoma (HCC) is a common cancer worldwide and a leading cause of cancer-related death. The majority of participants first presenting with HCC have advanced unresectable or metastatic disease. The purpose of this study is to evaluate the optimized dose, adverse events, and efficacy of livmoniplimab in combination with budigalimab. Livmoniplimab is an investigational drug being developed for the treatment of HCC. There are 3 treatment arms in this study and participants will be randomized in a 1:1:1 ratio. Participants will either receive livmoniplimab (at different doses) in combination with budigalimab (another investigational drug), lenvatinib, or sorafenib. Approximate…

From ClinicalTrials.gov, last updated 2025-08-14. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $282,470 in research payments for this study in 2025 (47 payments).

Products named: Venclexta

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.