- ICH GCP
- Registro de ensaios clínicos dos EUA
- Ensaio Clínico NCT07668453
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
Visão geral do estudo
Status
Condições
Intervenção / Tratamento
Tipo de estudo
Inscrição (Estimado)
Estágio
- Fase 2
Contactos e Locais
Contato de estudo
- Nome: Yongxiang Xia, Doctor
- Número de telefone: +8613815893869
- E-mail: yx_xia@njmu.edu.cn
Estude backup de contato
- Nome: Yongxiang Xia
- Número de telefone: +8613815893869
- E-mail: yx_xia@njmu.edu.cn
Locais de estudo
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-
Jiangsu
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Nanjing, Jiangsu, China, 210000
- Recrutamento
- Jiangsu Provincial People's Hospital
-
Contato:
- Yongxiang Xia
- E-mail: yx_xia@njmu.edu.cn
-
Contato:
- Yongxiang Xia, Doctor
- Número de telefone: +8613815893869
- E-mail: yx_xia@njmu.edu.cn
-
-
Critérios de participação
Critérios de elegibilidade
Idades elegíveis para estudo
- Adulto
- Adulto mais velho
Aceita Voluntários Saudáveis
Descrição
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
Plano de estudo
Como o estudo é projetado?
Detalhes do projeto
- Finalidade Principal: Tratamento
- Alocação: N / D
- Modelo Intervencional: Atribuição de grupo único
- Mascaramento: Nenhum (rótulo aberto)
Armas e Intervenções
Grupo de Participantes / Braço |
Intervenção / Tratamento |
|---|---|
|
Experimental: 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.
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O que o estudo está medindo?
Medidas de resultados primários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Objective Response Rate (ORR)
Prazo: 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.
|
Medidas de resultados secundários
Medida de resultado |
Descrição da medida |
Prazo |
|---|---|---|
|
Progression-Free Survival (PFS)
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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.
|
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Incidence and severity of Adverse Events (AEs) and Serious Adverse Events (SAEs)
Prazo: 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.
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Colaboradores e Investigadores
Datas de registro do estudo
Datas Principais do Estudo
Início do estudo (Real)
Conclusão Primária (Estimado)
Conclusão do estudo (Estimado)
Datas de inscrição no estudo
Enviado pela primeira vez
Enviado pela primeira vez que atendeu aos critérios de CQ
Primeira postagem (Real)
Atualizações de registro de estudo
Última Atualização Postada (Real)
Última atualização enviada que atendeu aos critérios de controle de qualidade
Última verificação
Mais Informações
Termos relacionados a este estudo
Termos MeSH relevantes adicionais
- Neoplasias por local
- Neoplasias
- Neoplasias do Aparelho Digestivo
- Doenças do aparelho digestivo
- Doenças das vias biliares
- Neoplasias das Vias Biliares
- Aminoácidos, peptídeos e proteínas
- Proteínas
- Produtos químicos orgânicos
- Compostos heterocíclicos, 1 anel
- Compostos heterocíclicos
- Hidrocarbonetos
- Cicloparaffinas
- Hidrocarbonetos, aliciclicos
- Hidrocarbonetos, cíclicos
- Terpenos
- Taxóides
- Ciclodecanos
- Diterpenos
- Desoxicitidina
- Citidina
- Nucleosídeos de pirimidina
- Pirimidinas
- Álbumins
- Paclitaxel
- Paclitaxel ligado à albumina
- Gemcitabina
- Paclitaxel com 130 nm de albumina
Outros números de identificação do estudo
- 26-OBU-JS-BTC-II-010
Plano para dados de participantes individuais (IPD)
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