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OncoMatch/Clinical Trials/NCT06208462

Neoadjuvant Therapy of HAIC(GEMOX) Combined With Adebrelimab and Lenvatinib for Resectable Intrahepatic Cholangiocarcinoma With High-risk Recurrence Factors

Is NCT06208462 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies multiple treatments including Adebrelimab and Lenvatinib for intrahepatic cholangiocarcinoma.

Phase 2RecruitingThe First Affiliated Hospital with Nanjing Medical UniversityNCT06208462Data as of Jun 2026Location: China

Treatment: Adebrelimab · Lenvatinib · Gemcitabine · OxaliplatinClinical Study on the efficacy and safety of HAIC(GEMOX)and Lenvatinib combined with Adebrelimab neoadjuvant therapy for resectable Intrahepatic Cholangiocarcinoma with high-risk recurrence factors.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Adebrelimab

Targeted therapy

Lenvatinib

Chemotherapy

GemcitabineOxaliplatin

Cancer type

Cholangiocarcinoma

Disease stage

Required: Stage IB, II, III, IV

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

Exception: biliary drainage allowed

Prior systemic therapy and tumor-related surgical treatment (biliary drainage allowed)

Cannot have received: PD-1 antibody

have received PD1 antibody

Cannot have received: PD-L1 antibody

have received PDL1 antibody

Cannot have received: CTLA-4 antibody

have received CTLA4 antibody

Cannot have received: VEGFR inhibitor (lenvatinib)

have received Lenvatinib

Cannot have received: chemotherapy

have received ... chemotherapy in the past

Lab requirements

Blood counts

Neutrophils ≥1.5*10^9/L; Platelet ≥80*10^9/L; Hemoglobin ≥9g/dl; Serum albumin ≥3g/dl

Kidney function

Serum creatinine ≤ 1.5 times the upper limit of normal value, creatinine clearance ≥60 ml/min

Liver function

Bilirubin ≤ 1.5 times the upper limit of normal value; ALT and AST ≤ 2 times the upper limit of normal value

The functional indicators of vital organs meet the following requirements ... Neutrophils ≥1.5*10^9/L; Platelet ≥80*10^9/L; Hemoglobin ≥9g/dl; Serum albumin ≥3g/dl; ... Bilirubin ≤ 1.5 times the upper limit of normal value; ALT and AST≤ 2 times the upper limit of normal value; ... Serum creatinine ≤ 1.5 times the upper limit of normal value, creatinine clearance ≥60 ml/min

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

Frequently asked questions

Is NCT06208462 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 IB or II or III or IV 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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