Clinical trial · Interventional
Anti-angiogenic Targeted Drugs Plus Rg3 to Improve the Efficacy of TACE for Unresectable Hepatocellular Carcinoma
A Multicentre Randomized Controlled Study of Anti-angiogenic Targeted Drugs Combined With Ginsenoside Rg3 to Improve the Efficacy of Transcatheter Arterial Chemoembolization (TACE) in the Treatment of Unresectable Hepatocellular Carcinoma
- Source
- ClinicalTrials.gov
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Run
- ING-CLINICALTRIALS-20260908-000001
Summary
Brief summary (as posted)
The aim of this study is to compare the efficacy and safety of transcatheter arterial chemoembolization (TACE) combined with the anti-angiogenic targeted drugs and ginsenoside Rg3 versus TACE alone in patients with unresectable Barcelona Clinic Liver Cancer (BCLC) stage B/C hepatocellular carcinoma (HCC), who has normal liver function and no extrahepatic metastasis.
Conditions
Conditions (1)
Free-text conditions as registered, with the CancerIndex entity they were reconciled to and the match type.
| Condition (as posted) | Mapped entity | Match | Confidence |
|---|---|---|---|
| Hepatocellular Carcinoma | Hepatocellular Carcinoma | ONTOLOGY_EXACT | 0.98 |
Interventions
Interventions (3)
| Intervention | Type | Mapped drug | Match |
|---|---|---|---|
| Anti-angiogenic Targeted Drugs | Drug | — | UNRESOLVED |
| Ginsenoside Rg3 | Drug | — | UNRESOLVED |
| TACE | Procedure | — | UNRESOLVED |
Design
Arms and outcomes
Arms (2)
- type
- EXPERIMENTAL
- label
- Combined group
- description
- Anti-angiogenic targeted drug + Rg3 + TACE
- interventionNames
- Drug: Anti-angiogenic Targeted Drugs
- Drug: Ginsenoside Rg3
- Procedure: TACE
- type
- ACTIVE_COMPARATOR
- label
- Single group
- description
- TACE alone
- interventionNames
- Procedure: TACE
Primary outcomes (1)
- measure
- Progression-free survival (PFS)
- timeFrame
- Up to 2 years
Eligibility
Eligibility (as posted)
- Sex
- All
- Minimum age
- 18 Years
- Maximum age
- 75 Years
Show eligibility criteria text
Inclusion Criteria: 1. Aged 18-75 2. Unresectable HCC patients clinically diagnosed or confirmed by histopathology and/or cytology according to Guidelines for Diagnosis and Treatment of Primary Liver Cancer in China (2019 edition); 3. At least one measurable lesion (according to mRECIST); 4. BCLC stage B or C (China Liver Cancer Staging \[CNLC\] IIa, IIb and IIIa); 5. The maximum diameter of a single lesion ≤10cm; No more than 10 lesions; or combined with portal vein thrombus (PVTT) type I and II (Cheng's classification); 6. Child-pugh score \<7; 7. Eastern Cooperative Oncology Group (ECOG) PS 0-1; Exclusion Criteria: 1. Mixed hepatocellular carcinoma and intrahepatic cholangiocarcinoma (HCC-ICC) confirmed by pathology; 2. Extrahepatic metastasis; 3. Previously received hepatectomy, liver transplantation, interventional therapy, ablative therapy and other local therapies for HCC; 4. PVTT type III/IV (Cheng's classification), major hepatic vein invasion or primary to secondary bile duct invasion; 5. A history of gastrointestinal bleeding or a definite tendency of gastrointestinal bleeding in the past 4 weeks; 6. Cardiovascular diseases with significant clinical significance; 7. Active infection; 8. Other significant clinical and laboratory abnormalities that investigators believe affect safety evaluation.
References
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