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OncoMatch/Clinical Trials/NCT06298968

Combined Therapy Using Gemcitabine and Cisplatin Chemotherapy, Lenvatinib and Adebrelimab for Patients With Advanced and Unresectable Intrahepatic Cholangiocarcinoma

Is NCT06298968 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies combined therapy using gemcitabine and cisplatin chemotherapy, Lenvatinib and Adebrelimab for intrahepatic cholangiocarcinoma.

Phase 2RecruitingNanfang Hospital, Southern Medical UniversityNCT06298968Data as of Jun 2026Location: China

Treatment: combined therapy using gemcitabine and cisplatin chemotherapy, Lenvatinib and AdebrelimabIn this phase 2 study, the investigators aim to evaluate the efficacy and safety of combined therapy using gemcitabine and cisplatin chemotherapy, Lenvatinib and Adebrelimab for patients with advanced and unresectable intrahepatic cholangiocarcinoma

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Extracted eligibility criteria

Treatments studied

Chemotherapy

combined therapy using gemcitabine and cisplatin chemotherapy, Lenvatinib and Adebrelimab

Cancer type

Cholangiocarcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

Cannot have received: anti-PD-1 therapy

previous treatment with PD1 antibody

Cannot have received: anti-PD-L1 therapy

previous treatment with programmed death ligand -1 (PD-L1) antibody

Cannot have received: anti-CTLA-4 therapy

previous treatment with cytotoxic T lymphocyte-associated antigen-4 (CTLA4) antibody

Lab requirements

Blood counts

Neutrophils ≥1.5*10^9/L; platelets≥100*10^9/L; hemoglobin≥9g/dl; serum albumin≥3g/dl

Kidney function

serum creatinine ≤ 1.5 ULN, creatinine clearance rate ≥ 60ml / min

Liver function

bilirubin ≤ 2 times ULN; ALT and AST ≤ 2 times ULN

Functional indicators of vital organs meet the following requirements a Neutrophils ≥1.5*109/L; platelets≥100*109/L; hemoglobin≥9g/dl; serum albumin≥3g/dl; b Thyroid stimulating hormone (TSH) ≤ 1 times the upper limit of normal value(ULN), T3, T4 are in the normal range; c bilirubin ≤ 2 times ULN; Alanine aminotransferase (ALT) and Aspartate aminotransferase (AST) ≤ 2 times ULN; serum creatinine ≤ 1.5 ULN, creatinine clearance rate ≥ 60ml / min;

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

Frequently asked questions

Is NCT06298968 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior anti-PD-1 therapy, anti-PD-L1 therapy, anti-CTLA-4 therapy disqualifies patients from enrollment.

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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