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NCT07009470

A Multicenter, Prospective Study of Perioperative Finotonlimab Combined With Bevacizumab in Resectable Hepatocellular Carcinoma Patients With High-Risk Factors for Recurrence

Active, enrolled NA Last updated 6 June 2025
What this trial tests

NA trial testing Finotonlimab (an anti-PD-1 monoclonal antibody) and Anbeizhu (a bevacizumab biosimilar) in HCC in 130 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
10 February 2025
Primary endpoint
28 April 2028
28 October 2028

Quick facts

Lead sponsorTongji Hospital
PhaseNA
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment130
Start date10 February 2025
Primary completion28 April 2028
Estimated completion28 October 2028
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Tongji Hospital

Who can join

Adults 18 to 75, any sex, with HCC. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

For patients with early- to mid-stage hepatocellular carcinoma (HCC), the five-year postoperative recurrence and metastasis rate remains as high as 70%, significantly impacting patient prognosis.Therefore, perioperative therapy may be considered for HCC patients with these high-risk features .

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for HCC

Currently open trials in the same condition.

Other Tongji Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07009470.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing