For Healthcare Professionals

Evaluate Durvalumab and Tremelimumab +/- Lenvatinib in Combination With TACE in Patients With Locoregional HCC

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About the study

A global study to evaluate transarterial chemoembolization (TACE) in combination with durvalumab, tremelimumab and lenvatinib therapy in patients with locoregional hepatocellular carcinoma
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Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. No evidence of extrahepatic disease
  2. Disease not amenable to curative surgery or transplantation or curative ablation but disease amenable to TACE
  3. Child Pugh score class A
  4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 at enrollment
  5. Measurable disease by Modified Response Criteria in Solid Tumors (mRECIST) criteria
  6. Adequate organ and marrow function

EXCLUSION CRITERIA

Exclusion Criteria:


  1. History of symptomatic congestive heart failure, unstable angina pectoris, uncontrolled cardia arrhythmia
  2. History of hepatic encephalopathy
  3. Major portal vein thrombosis visible on baseline imaging
  4. Uncontrolled arterial hypertension
  5. Co-infection with HBV and HDV

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Study Locations

Enter your ZIP code/Postal code/PIN code to locate study sites near you:

How to Apply


Contact the study center to learn if this study is a good match for you.
Phone iconCall 1-877-240-9479Email iconEmail Study Center

Study Details


Contition

Hepatocellular Carcinoma

Age

18 - 120

Phase

PHASE3

Participants Needed

725

Est. Completion Date

Feb 26, 2027

Treatment Type

INTERVENTIONAL


Sponsor

AstraZeneca

ClinicalTrials.gov NCT Identifier

NCT05301842

Study Number

D910VC00001_CN

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