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Active, not recruiting Phase 2 Interventional

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

ClinicalTrials.gov ID: NCT06040099

Public ClinicalTrials.gov record NCT06040099. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 8:56 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Phase II Single-Arm Study of Durvalumab and Bevacizumab Following Transarterial Radioembolization Using Yttrium-90 Glass Microspheres (TheraSphere™) in Unresectable Hepatocellular Carcinoma Amenable to Locoregional Therapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to measure the efficacy and safety of durvalumab intravenous (IV) solution plus bevacizumab IV solution after transarterial radioembolization (Yttrium 90 glass microspheres TARE) in participants with unresectable hepatocellular carcinoma (HCC) amenable to embolization.

Study identification

NCT ID
NCT06040099
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
AstraZeneca
Industry
Enrollment
58 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 130 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 13, 2024 (Actual)
Primary completion
Jun 30, 2026 (Actual)
Completion
May 27, 2027 (Estimated)
Last update posted
Sep 21, 2026

2024 – 2027

United States locations

U.S. sites
21
U.S. states
17
U.S. cities
19
Facility City State ZIP Site status
Research Site Aurora Colorado 80045 —
Research Site Gainesville Florida 32608 —
Research Site Orlando Florida 32804 —
Research Site Atlanta Georgia 30322 —
Research Site Atlanta Georgia 30342 —
Research Site Chicago Illinois 60611 —
Research Site Boston Massachusetts 02118 —
Research Site Detroit Michigan 48201 —
Research Site St Louis Missouri 63110 —
Research Site Trenton New Jersey 08690 —
Research Site Buffalo New York 14263 —
Research Site New York New York 10029 —
Research Site Chapel Hill North Carolina 27599 —
Research Site Columbus Ohio 43210 —
Research Site Portland Oregon 97239 —
Research Site Philadelphia Pennsylvania 19107 —
Research Site Houston Texas 77030 —
Research Site Charlottesville Virginia 22908 —
Research Site Seattle Washington 98195 —
Research Site Milwaukee Wisconsin 53215 —
Research Site Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06040099, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 21, 2026 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06040099 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →