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A Study to Assess Adverse Events and Change in Disease Activity of Intravenously (IV) Infused ABBV-324 in Adult Participants With Hepatocellular Cancer (HCC) or Squamous-Cell Non-Small Cell Lung Cancer (LUSC)

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NCT06858813 · readout ≤ 1,503 d

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

Phase
Phase 1
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
232estimated
Sites
22
Countries
China, Israel, Japan +4

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
Start2025-04-14actualWhen 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 posted2025-03-05actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-03-25actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Hepatocellular Cancer
  • Squamous-Cell Non-Small Cell Lung Cancer

Interventions

  • Drug: Lenvatinib
  • Drug: ABBV-324

Primary outcomes

what the primary-completion date above is the date OF
Number of Participants with Adverse Events (AE)s
measured Up to Approximately 4 Years
Number of Participants with Change in Vital Signs
measured Up to Approximately 4 Years
Number of Participants with Change in Electrocardiogram (ECG)
measured Up to Approximately 4 Years
Number of Participants with Change in Clinical Laboratory Tests
measured Up to Approximately 4 Years
Objective Response Rate (ORR)
measured Up to Approximately 4 Years

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