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A US Study to Evaluate Transarterial Radioembolization (TARE) in Combination With Durvalumab and Bevacizumab Therapy in People With Unresectable Hepatocellular Carcinoma Amenable to TARE

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NCT06040099

Sponsored by AstraZeneca (industry) · AZN — their whole pipeline →.

Phase
Phase 2
Status
Active, not recruiting
Study type
Interventional
Design
Na · None · Treatment
Enrollment
58actual
Sites
21
Country
United States

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
Start2024-02-13actualWhen the study began enrolling
Primary completion2026-07-01estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2026-07-01estimatedThe whole study's end, after follow-up
First posted2023-09-15actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-06-30actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Hepatocellular Carcinoma (HCC)

Interventions

  • Drug: Durvalumab — also filed as MEDI4736, IMFINZI
  • Drug: Bevacizumab — also filed as AVASTIN, ZIRABEV
  • Procedure: Transarterial Radioembolization (TARE) — also filed as TheraSphere

Primary outcome

what the primary-completion date above is the date OF
Progression Free Survival (PFS)
measured From Day 1 until date of progressive disease or death [Approximately 3 years]

Publications

Linked on the registry record. A “linked by the registry” entry is NLM's own automated PubMed match, not a claim by the sponsor that the paper reports this study.

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