OncoMatch

OncoMatch/Clinical Trials/NCT05608200

Lenvatinib+Sintilimab+TACE vs. Lenvatinib+TACE for Advanced HCC

Is NCT05608200 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies multiple treatments including Lenvatinib, sintilimab plus TACE and Lenvatinib plus TACE for hepatocellular carcinoma non-resectable.

Phase 3RecruitingSecond Affiliated Hospital of Guangzhou Medical UniversityNCT05608200Data as of Jun 2026Location: China

Treatment: Lenvatinib, sintilimab plus TACE · Lenvatinib plus TACEThis study is conducted to evaluate the efficacy and safety of lenvatinib, sintilimab plus TACE (Len-Sin-TACE) compared with lenvatinib plus TACE (Len-TACE) for patients with advanced hepatocellular carcinoma (HCC).

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Extracted eligibility criteria

Treatments studied

Other

Lenvatinib, sintilimab plus TACELenvatinib plus TACE

Cancer type

Hepatocellular Carcinoma

Disease stage

Required: Stage BCLC STAGE C, CNLC IIIA, CNLC IIIB

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: systemic therapy

Patients who received prior systemic therapy ... for HCC

Cannot have received: immunotherapy

Patients who received prior ... immunotherapy ... for HCC

Cannot have received: TACE

Patients who received prior ... TACE ... for HCC

Cannot have received: transcatheter arterial radioembolization

Patients who received prior ... transcatheter arterial radioembolization (TARE) ... for HCC

Cannot have received: transcatheter arterial embolization

Patients who received prior ... transcatheter arterial embolization (TAE) ... for HCC

Cannot have received: hepatic arterial infusion chemotherapy

Patients who received prior ... hepatic arterial infusion chemotherapy (HAIC) ... for HCC

Cannot have received: radiation therapy

Patients who received prior ... radiation therapy for HCC

Lab requirements

Blood counts

white blood cell count <3.0×10^9/L, platelets <50×10^9/L, prothrombin time prolongation ≥ 4s

Liver function

Child-Pugh class A/B

Child-Pugh class A/B; hematologic examination: white blood cell count <3.0×10^9/L, platelets <50×10^9/L; Prothrombin time prolongation ≥ 4s

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT05608200 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

What disease stage is eligible?

Stage BCLC STAGE C or CNLC IIIA or CNLC IIIB is required.

Is there an age limit?

Yes. Patients must be 75 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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