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- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07649980
Becotatug Vedotin Plus Pucotenlimab for Advanced Biliary Tract Cancer, Phase II
Becotatug Vedotin Combined With Pucotenlimab in First-Line Treatment-Failed Advanced Biliary Tract Carcinoma: A Phase II Exploratory Clinical Study
Biliary tract carcinoma (BTC), including cholangiocarcinoma and gallbladder cancer, is a highly aggressive digestive system malignancy with limited treatment options after failure of first-line standard chemotherapy.
This open-label, single-arm, Phase II exploratory study aims to evaluate the efficacy and safety of Becotatug Vedotin combined with Pucotenlimab in patients with EGFR-positive advanced BTC who have failed first-line therapy. Participants will receive the combination regimen until the occurrence of disease progression, unacceptable toxicity, withdrawal of informed consent, death, pregnancy, investigator's decision to discontinue treatment, or study termination, whichever occurs first.The primary endpoint is objective response rate (ORR) assessed per RECIST v1.1. Secondary endpoints include progression-free survival (PFS), overall survival (OS), disease control rate (DCR), duration of response (DOR), and safety.
Descripción general del estudio
Estado
Intervención / Tratamiento
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Huikai Li, MD
- Número de teléfono: 86+18622228639
- Correo electrónico: vianvianvip@163.com
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Age ≥ 18 years, male or female.
- Histologically or cytologically confirmed advanced biliary tract cancer (BTC), including intrahepatic cholangiocarcinoma (ICC), extrahepatic cholangiocarcinoma (ECC), and gallbladder cancer (GBC); recurrent biliary tract cancer is also eligible.
- EGFR expression positive by immunohistochemistry (IHC) (+, ++, or +++).
- Failed at least one line of standard systemic therapy.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
- Life expectancy ≥ 3 months.
- At least one measurable lesion per RECIST v1.1 on CT or MRI.
- Child-Pugh class A or B (<7 points).
Adequate organ function as defined below:
- Hematologic: Hemoglobin (Hb) ≥ 90 g/L; white blood cell count (WBC) ≥ lower limit of normal (LLN); absolute neutrophil count (ANC) ≥ 1.5 × 10⁹/L; platelet count ≥ 100 × 10⁹/L.
- Renal: Serum creatinine ≤ 1.5 × upper limit of normal (ULN); creatinine clearance (CrCl) ≥ 55 mL/min.
- Hepatic: Total bilirubin ≤ 1.5 × ULN; ALT and AST ≤ 2.5 × ULN (or ≤ 3 × ULN for total bilirubin and ≤ 5 × ULN for ALT/AST in patients with intrahepatic cholangiocarcinoma or liver metastases).
- Coagulation: International normalized ratio (INR) ≤ 1.5 × ULN; partial thromboplastin time (PTT) within normal range.
- No serious complications such as active gastrointestinal bleeding, perforation, jaundice, gastrointestinal obstruction, or fever (>38°C) not attributable to cancer.
- Females of childbearing potential must have a negative serum or urine pregnancy test within 7 days prior to enrollment, must not be breastfeeding, and must agree to use effective contraception during the study and for 6 months after the last dose. Male participants must agree to use effective contraception during the study and for 6 months after the last dose.
- Expected to have good compliance with protocol-specified follow-up for efficacy and safety assessments.
- Able to understand the study and willing to provide written informed consent.
Exclusion Criteria:
- Diagnosis of another primary malignancy within 5 years prior to enrollment, except for adequately treated carcinoma in situ or basal cell carcinoma of the skin.
- EGFR expression negative by IHC.
- Known central nervous system (CNS) metastases or carcinomatous meningitis, unless clinically stable for ≥ 4 weeks after radiotherapy or surgery and asymptomatic.
- Psychiatric or neurological disorders that compromise the ability to comply with study procedures.
- Prior treatment with MMAE-containing antibody-drug conjugate (ADC) therapy.
- Planned or previous organ or bone marrow transplantation.
- Active or history of autoimmune disease requiring systemic immunosuppressive therapy.
- Receipt of live vaccine within 30 days prior to first dose. Inactivated seasonal influenza vaccines are allowed.
- Uncontrolled cardiac conditions or symptoms.
- Active infection or fever (unless clearly attributable to tumor).
- History or evidence of interstitial lung disease or active non-infectious pneumonitis.
- Any other condition that makes the patient unsuitable for enrollment, including but not limited to: immunodeficiency; active tuberculosis; hepatitis B (eligible if HBV-DNA < 500 IU/mL with normal liver function after antiviral therapy); hepatitis C virus (HCV) infection; uncorrectable electrolyte disturbances; uncontrolled pericardial effusion, pleural effusion, or ascites.
- Known hypersensitivity to any component of the study drugs.
- Use of systemic immunosuppressive agents or corticosteroids (> 10 mg/day prednisone equivalent) within 14 days prior to enrollment.
- Receipt of radiotherapy, chemotherapy, targeted therapy, or immunotherapy within 4 weeks prior to enrollment.
- Participation in another interventional clinical trial within 4 weeks prior to enrollment.
- Pregnancy or breastfeeding.
- Any other condition that, in the investigator's judgment, makes the patient inappropriate for study participation.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Becotatug Vedotin + Pucotenlimab
The combination regimen will be continued until the occurrence of disease progression, unacceptable toxicity, withdrawal of informed consent, death, pregnancy, investigator's decision to discontinue treatment, or study termination, whichever occurs first.
|
2.0mg/kg ,IV,D1,Q3W;The infusion duration is 60 minutes ± 15 minutes, with the first infusion lasting no less than 60 minutes.
Otros nombres:
200mg,IV,D1,Q3W;The infusion duration is 60 minutes ± 15 minutes, with the first infusion lasting no less than 60 minutes.
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Objective Response Rate (ORR)
Periodo de tiempo: From start of treatment until disease progression, assessed up to 36 months.
|
Objective response rate is defined as the proportion of patients achieving complete response (CR) or partial response (PR) assessed per RECIST v1.1.
|
From start of treatment until disease progression, assessed up to 36 months.
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Progression-Free Survival (PFS)
Periodo de tiempo: From start of treatment to disease progression or death, assessed up to 36 months.
|
Time from the first dose of study treatment to the first documented disease progression per RECIST v1.1 or death from any cause, whichever occurs first.
|
From start of treatment to disease progression or death, assessed up to 36 months.
|
|
Overall Survival (OS)
Periodo de tiempo: From start of treatment to death, assessed up to 36 months.
|
Time from the first dose of study treatment to death from any cause.
|
From start of treatment to death, assessed up to 36 months.
|
|
Disease Control Rate (DCR)
Periodo de tiempo: From start of treatment until disease progression, assessed up to 36 months.
|
Proportion of patients achieving complete response (CR), partial response (PR), or stable disease (SD) per RECIST v1.1.
|
From start of treatment until disease progression, assessed up to 36 months.
|
|
Duration of Response (DOR)
Periodo de tiempo: From first response to disease progression or death, assessed up to 24 months from response.
|
Time from the first documented objective response (CR or PR) to the first documented disease progression per RECIST v1.1 or death from any cause, whichever occurs first.
|
From first response to disease progression or death, assessed up to 24 months from response.
|
|
Safety and Tolerability
Periodo de tiempo: From first dose of study drug until 30 days after last dose, up to 36 months
|
Incidence, nature, and severity of adverse events (AEs) and serious adverse events (SAEs) assessed by NCI CTCAE v5.0.
|
From first dose of study drug until 30 days after last dose, up to 36 months
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- EC-2026-0002
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .
Ensayos clínicos sobre Cáncer de vías biliares (BTC)
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University of NottinghamReclutamientoCancer de pancreas | Colangiocarcinoma | Quiste pancreático | Cáncer de vías biliares (BTC) | Carcinoma de colangio | Colangiocarcinoma Cáncer | Cáncer de vías biliares (CCA)Reino Unido
Ensayos clínicos sobre Becotatug Vedotin
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West China HospitalAún no reclutando
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Jiyan LiuWest China Hospital; Lepu Medical Technology (Beijing) Co., Ltd.Aún no reclutando
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Eye & ENT Hospital of Fudan UniversityReclutamientoCarcinoma quístico adenoide | Carcinoma de senos paranasalesPorcelana
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Sun Yat-sen UniversityReclutamientoCancinoma Nasofaríngeo (NPC)Porcelana
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West China HospitalAún no reclutandoCancinoma Nasofaríngeo (NPC)
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Fudan UniversityLepu Biopharma Co., Ltd.Aún no reclutandoCarcinoma cutáneo de células escamosas (CSCC)Porcelana
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Union Hospital, Tongji Medical College, Huazhong...ReclutamientoNeoplasias del Cuello Uterino, Recurrentes; Neoplasias del Cuello Uterino, Metastásicas; Neoplasias de la Vulva; Neoplasias de la VaginaPorcelana
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Tianjin Medical University Cancer Institute and...Aún no reclutandoQuimioterapia | Inhibidor de PD-1 | ESCC | Tislelizumab | Becotatug Vedotin | EGFR ADCPorcelana
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Fudan UniversityFujian Province Tumor Hospital; Ninth People's Hospital, Shanghai Jiao Tong University... y otros colaboradoresAún no reclutando
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Fudan UniversityShanghai Cancer Hospital, ChinaAún no reclutando