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An Open-label, Single-arm, Multicenter Exploratory Study of Adebrelimab Combined With Gemcitabine and Albumin-bound Paclitaxel as First-line Treatment for Biliary Tract Malignancies

The purpose of this clinical trial is to evaluate the safety and effectiveness of a new combination therapy for patients with biliary tract cancer that cannot be removed by surgery. Participants will receive an immunotherapy drug called adebrelimab combined with two chemotherapy drugs (gemcitabine and albumin-bound paclitaxel) as their first-line treatment. This is an open-label, single-arm study, meaning all enrolled patients will receive this same combination treatment. The main goal of the study is to determine the Objective Response Rate (ORR), which measures the proportion of patients whose tumors shrink in response to the treatment. Researchers will also evaluate how long patients live without the disease getting worse (Progression-Free Survival), overall survival, quality of life, and any side effects experienced. The study plans to enroll 30 participants.

연구 개요

연구 유형

중재적

등록 (추정된)

30

단계

  • 2 단계

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

  • 이름: Yongxiang Xia, Doctor
  • 전화번호: +8613815893869
  • 이메일: yx_xia@njmu.edu.cn

연구 연락처 백업

연구 장소

    • Jiangsu
      • Nanjing, Jiangsu, 중국, 210000
        • 모병
        • Jiangsu Provincial People's Hospital
        • 연락하다:
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

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아니

설명

Inclusion Criteria:

  • Age 18 to 75 years, male or female. Eastern Cooperative Oncology Group (ECOG) performance status score of 0 or 1. No prior local or systemic treatment for biliary tract malignancy. Histologically or cytologically confirmed initially unresectable or inoperable biliary tract cancer; recurrent biliary tract tumor after surgery; or patients who received post-operative adjuvant therapy must have been off treatment for more than 6 months. Adequate organ and hematological function. Life expectancy of ≥ 3 months. Laboratory results within 7 days prior to the first dose meeting the following criteria:Absolute neutrophil count (ANC) ≥ 1.5 × 10^9/L, Platelets ≥ 75 × 10^9/L, Hemoglobin ≥ 90 g/L (without blood transfusion or G-CSF within 2 weeks prior to screening); Serum albumin ≥ 30 g/L, Total bilirubin ≤ 1.5 × ULN, ALT and AST ≤ 3 × ULN, Serum creatinine ≤ 1.5 × ULN or Creatinine clearance > 50 mL/min; INR ≤ 1.2 or PT exceeding the normal control range by ≤ 2 seconds; Urine protein < 2+ (if ≥ 2+, 24-hour urine protein quantification must be < 1.0 g). Women of childbearing potential must agree to abstain from sexual intercourse or use a reliable and effective method of contraception from the time of signing the informed consent form until at least 120 days after the last dose of the study drug. Women of childbearing potential must have a negative serum pregnancy test within 72 hours prior to the first dose and must not be lactating. Male subjects with female partners of childbearing potential must agree to abstain from sexual intercourse or use a reliable and effective method of contraception from the time of signing the informed consent form until at least 120 days after the last dose of the study drug, and must not donate sperm during this period.

Exclusion Criteria:

  • Pathological diagnosis of mixed hepatocellular carcinoma or containing other non-cholangiocarcinoma malignant components. Prior systemic therapy. History of or concurrent other malignancies, except for adequately treated non-melanoma skin cancer, carcinoma in situ of the cervix, and papillary thyroid cancer. Active pulmonary tuberculosis infection within 1 year prior to enrollment; or history of active tuberculosis infection over 1 year ago without formal anti-tuberculosis treatment or with tuberculosis still in the active phase. History of autoimmune diseases or immunodeficiency, including but not limited to myasthenia gravis, myositis, autoimmune hepatitis, systemic lupus erythematosus, rheumatoid arthritis, inflammatory bowel disease, antiphospholipid syndrome, Wegener's granulomatosis, Sjögren's syndrome, Guillain-Barré syndrome, or multiple sclerosis. Requiring long-term systemic corticosteroid therapy (dose equivalent to > 10 mg/day prednisone) or any other form of immunosuppressive therapy. Subjects using inhaled or topical corticosteroids are allowed. Severe cardiopulmonary or renal dysfunction. Uncontrolled arterial hypertension (systolic blood pressure ≥ 140 mmHg or diastolic blood pressure ≥ 90 mmHg); history of hypertensive crisis or hypertensive encephalopathy. HBV DNA > 2000 IU/ml, or active HCV infection (HCV antibody positive and HCV-RNA level above the lower limit of detection). Active infection requiring systemic therapy. Human immunodeficiency virus (HIV 1/2 antibody) positive. History of psychotropic drug abuse, alcoholism, or drug addiction. History of allergy to study drugs. Other factors that, in the judgment of the investigator, may affect the safety of the subject or compliance with the trial

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 치료
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: Experimental Arm

Participants in this single arm will receive Adebrelimab (1200 mg, IV, Day 1), Gemcitabine (800 mg/m^2, IV, Days 1 and 8), and albumin-bound paclitaxel (100 mg/m^2, IV, Days 1 and 8) every 3 weeks (21 days) for 6 to 8 cycles. Adebrelimab is administered first, followed by chemotherapy after an interval of at least 30 minutes.

Maintenance phase: After 6-8 cycles of initial treatment, Adebrelimab will be continued for up to 2 years, while Gemcitabine and albumin-bound paclitaxel will be administered alternately every cycle.

Treatment continues until disease progression/recurrence, unacceptable toxicity, withdrawal of consent, or other specified discontinuation criteria are met.

1200 mg, intravenous (IV) infusion, administered on Day 1 of each 21-day cycle.
800 mg/m^2, intravenous (IV) infusion, administered on Days 1 and 8 of each 21-day cycle.
100 mg/m^2, intravenous (IV) infusion, administered on Days 1 and 8 of each 21-day cycle.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Objective Response Rate (ORR)
기간: From the first dose of study treatment until disease progression or death, assessed up to approximately 24 months.
The proportion of patients whose tumor volume shrinks to a predefined value and maintains the minimum time requirement, defined as the sum of Complete Response (CR) and Partial Response (PR). Assessed by investigators according to RECIST 1.1 criteria.
From the first dose of study treatment until disease progression or death, assessed up to approximately 24 months.

2차 결과 측정

결과 측정
측정값 설명
기간
Progression-Free Survival (PFS)
기간: From the first dose of study treatment until disease progression or death, assessed up to approximately 24 months.
The time from the start of treatment to the first observation of disease progression or death from any cause. Assessed according to RECIST 1.1 criteria.
From the first dose of study treatment until disease progression or death, assessed up to approximately 24 months.
Overall Survival (OS)
기간: From the first dose of study treatment until death from any cause, assessed up to approximately 36 months.
The time from the start of treatment to death from any cause.
From the first dose of study treatment until death from any cause, assessed up to approximately 36 months.
Disease Control Rate (DCR)
기간: From the first dose of study treatment until disease progression or death, assessed up to approximately 24 months.
The proportion of patients who achieve Complete Response (CR), Partial Response (PR), or Stable Disease (SD) after treatment. Assessed according to RECIST 1.1 criteria.
From the first dose of study treatment until disease progression or death, assessed up to approximately 24 months.
Duration of Response (DoR)
기간: From the first confirmed response until disease progression or death, assessed up to approximately 24 months.
The time from the first confirmed disease response to the first confirmed disease progression or termination of the response status due to any cause (such as disease recurrence or patient death).
From the first confirmed response until disease progression or death, assessed up to approximately 24 months.
Incidence and severity of Adverse Events (AEs) and Serious Adverse Events (SAEs)
기간: From the signing of informed consent up to 90 days after the last dose of study medication.
Evaluated based on the incidence and severity of AEs and SAEs according to the NCI-CTCAE v5.0 standard.
From the signing of informed consent up to 90 days after the last dose of study medication.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2025년 10월 20일

기본 완료 (추정된)

2027년 6월 30일

연구 완료 (추정된)

2027년 12월 31일

연구 등록 날짜

최초 제출

2026년 6월 22일

QC 기준을 충족하는 최초 제출

2026년 6월 22일

처음 게시됨 (실제)

2026년 6월 25일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 6월 25일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 6월 22일

마지막으로 확인됨

2026년 6월 1일

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