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NCT07128251

A Single-Arm, Multicenter, Exploratory Clinical Study of Transarterial Chemoembolization (TACE) Combined With Iparomlimab and Tuvonralimab Injection and Bevacizumab Injection for the Treatment of Unresectable, Non-Metastatic Hepatocellular Carcinoma (HCC)

Not yet recruiting Phase 2 Last updated 17 August 2025
What this trial tests

Phase 2 trial testing TACE treatment in Hepatocellular Carcinoma (HCC) in 47 participants. Not yet recruiting.

Timeline
20 August 2025
Primary endpoint
30 January 2028
30 December 2029

Quick facts

Lead sponsorAnhui Provincial Hospital
PhasePhase 2
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment47
Start date20 August 2025
Primary completion30 January 2028
Estimated completion30 December 2029

Drugs / interventions tested

Conditions studied

Sponsor

Anhui Provincial Hospital

Who can join

Adults 18 to 75, any sex, with Hepatocellular Carcinoma (HCC) or Immunotherapy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a single-arm, multicenter, exploratory clinical study designed to evaluate the efficacy and safety of TACE combined with Iparomlimab and Tuvonralimab Injection and Bevacizumab Injection in patients with unresectable, non-metastatic HCC. The primary endpoint is PFS as assessed by the investigator based on RECIST v1.1 criteria.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other trials of TACE treatment

Trials testing the same drug.

Other recruiting trials for Hepatocellular Carcinoma (HCC)

Currently open trials in the same condition.

Other Anhui Provincial 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/NCT07128251.

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