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OncoMatch/Clinical Trials/NCT06296563

Perioperative Treatment of Resectable Intrahepatic Cholangiocarcinoma With the Combination of Adebrelimab and Apatinib and HAIC

Is NCT06296563 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Adebrelimab and Apatinib for intrahepatic cholangiocarcinoma.

Phase 2RecruitingLei ZHAONCT06296563Data as of May 2026

Treatment: Adebrelimab · ApatinibThe goal of this clinical trial is to explore the efficacy and safety of combined infusion chemotherapy with Adebrelimab and Apatinib in the perioperative treatment of resectable intrahepatic cholangiocarcinoma patients. The main question it aims to answer are: How to improve the survival of patients with intrahepatic cholangiocarcinoma and prolong the recurrence time after surgery. Participants will receive receive neoadjuvant therapy with Adebrelimab combined with apatinib and FOLFOX-HAIC for 2 cycles (1 treatment cycle every 21 days, apatinib only used for the first cycle), and surgery was performed 14-28 days after the end of treatment. After 28 days of surgery, patients will continue to receive adjuvant treatment with Adebrelimab combined with apatinib for a maximum of one year.

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Extracted eligibility criteria

Cancer type

Cholangiocarcinoma

Disease stage

Required: Stage IB, II, IIIA, IIIB

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

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

Cannot have received: PD-1/PD-L1/PD-L2 or co-inhibitory T-cell receptor therapy

Patients who received PD-1, PD-L1, PD-L2, or CTLA-4 inhibitors before enrollment, or patients who directly received another stimulating or co inhibitory T cell receptor (such as CTLA-4, CD137)

Cannot have received: investigational drug

Use any other investigational drugs within 4 weeks prior to enrollment

Lab requirements

Blood counts

anc ≥ 1.5 × 10^9/l; platelet count ≥ 75 × 10^9/l; hemoglobin ≥ 90 g/l

Kidney function

creatinine ≤ 1.5 x uln

Liver function

serum total bilirubin ≤ 1.5 x uln; ast and alt ≤ 2.5 x uln; albumin ≥ 3g/dl

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

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