← Eichor
Study identifier: NCT07239245 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Study to Evaluate the Efficacy and Safety of Neo-Adjuvant TACE and Atezolizumab Plus Bevacizumab Therapy for High-Risk Recurrent Hepatocellular Carcinamo

Condition: Resectable Hepatocellular Carcinoma With High Risk of Recurrence  ·  Sponsor: Cancer Institute and Hospital, Chinese Academy of Medical Sciences

PhasePhase 2
Planned participants30
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

This is an open-label, single-arm, multicenter, prospective, phase II clinical study to evaluate the efficacy and safety of TACE combined with Atezolizumab and Bevacizumab as neoadjuvant treatment in Hepatocellular Carcinoma.

This description comes directly from the study's public registry record.

Talk to the study team

Xinyu Bi  ·  +86 (010)87787100  ·  beexy1971@163.com

Xiaowu Zhang  ·  +86 (010)87788502  ·  zhangxiaowu767@163.com

Always discuss trial participation with your own doctor first.

Locations (4)

Cancer Hospital Chinese Academy of Medical ScienceBeijing, Beijing Municipality, ChinaRecruiting
Henan Cancer HospitalZhengzhou, Henan, ChinaNot Yet Recruiting
The First Hospital of China Medical UniversityShenyang, Liaoning, ChinaNot Yet Recruiting
Shanxi Cancer HospitalTaiyuan, Shanxi, ChinaNot Yet Recruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07239245