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OncoMatch/Clinical Trials/NCT06904196

Lenvatinib Plus SIRT vs Lenvatinib in TACE-Refractory HCC

Is NCT06904196 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Lenvatinib plus SIRT and Lenvatinib for hepatocellular carcinoma non-resectable.

Phase 2RecruitingSecond Affiliated Hospital of Guangzhou Medical UniversityNCT06904196Data as of Jun 2026Location: China

Treatment: Lenvatinib plus SIRT · LenvatinibThis study is conducted to evaluate the efficacy and safety of lenvatinib plus SIRT (LEN+SIRT) compared with lenvatinib (LEN) alone for patients with hepatocellular carcinoma (HCC) refractory to transarterial chemoembolization (TACE).

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Extracted eligibility criteria

Treatments studied

Targeted therapy

Lenvatinib

Other

Lenvatinib plus SIRT

Cancer type

Hepatocellular Carcinoma

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: hepatic arterial infusion chemotherapy

Patients who received prior hepatic arterial infusion chemotherapy (HAIC)

Cannot have received: radiotherapy

Patients who received prior radiotherapy

Cannot have received: systemic therapy

Patients who received prior systemic therapy, for HCC

Lab requirements

Blood counts

platelet count ≥50×10^9/L, leukocyte >3.0×10^9/L, Neutrophil count ≥1.5×10^9/L, haemoglobin ≥85 g/L

Kidney function

creatinine≤1.5×ULN

Liver function

ALT and AST≤5×ULN, albumin ≥28 g/L, total bilirubin ≤3× ULN, prolongation of prothrombin time ≤4 seconds

Adequate organ and hematologic function with platelet count ≥50×10^9/L, leukocyte >3.0×10^9/L, Neutrophil count ≥1.5×10^9/L, haemoglobin ≥85 g/L, ALT and AST≤5×ULN, albumin ≥28 g/L, total bilirubin ≤3× ULN, creatinine≤1.5×ULN, and prolongation of prothrombin time ≤4 seconds

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

Frequently asked questions

Is NCT06904196 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.

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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