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A Study to Assess the Dose, Adverse Events, and Change in Disease Activity of Livmoniplimab as an Intravenous (IV) Solution in Combination With Budigalimab as an IV Solution in Adult Participants With Hepatocellular Carcinoma (HCC)

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NCT06109272 · readout ≤ 1,502 d

Sponsored by AbbVie (industry) · ABBV — their whole pipeline →.

Phase
Phase 2/3
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
660estimated
Sites
37
Countries
France, Italy, Puerto Rico +3

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-01-11actualWhen the study began enrolling
Primary completionSep 2030estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionSep 2030estimatedThe whole study's end, after follow-up
First posted2023-10-31actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2025-08-15actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Hepatocellular Carcinoma

Interventions

  • Drug: Livmoniplimab — also filed as ABBV-151
  • Drug: Budigalimab — also filed as ABBV-181
  • Drug: Durvalumab
  • Drug: Atezolizumab
  • Drug: Bevacizumab
  • Drug: Tremelimumab

Primary outcomes

what the primary-completion date above is the date OF
Stage 1: Best Overall Response (BOR) per Investigator
measured Through Study Completion, Up to Approximately 56 Months
Stage 2: Overall Survival (OS)
measured Through Study Completion, Up to Approximately 56 Months

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