- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07561463
Sacituzumab Tirumotecan for Pancreatic Cancer
28 de abril de 2026 actualizado por: LIN YANG, Cancer Institute and Hospital, Chinese Academy of Medical Sciences
A Phase II Trial of Sacituzumab Tirumotecan for Previously Treated Locally Advanced or Metastatic Pancreatic Cancer
This is a multicenter, prospective, open-label Phase II clinical study designed to evaluate the efficacy and safety of sacituzumab govitecan monotherapy in patients with locally advanced or metastatic pancreatic ductal adenocarcinoma who have failed at least one prior line of therapy, and to explore the potential correlation between baseline tumor tissue TROP-2 expression and treatment efficacy.
The study plans to enroll 30 eligible subjects, who will receive sacituzumab govitecan at 5 mg/kg via intravenous infusion every 2 weeks as one treatment cycle, until disease progression or intolerable toxicity occurs.
The primary endpoint is Objective Response Rate (ORR); secondary endpoints include Progression-Free Survival (PFS), Overall Survival (OS), Disease Control Rate (DCR), Duration of Response (DOR), and the incidence and severity of Treatment-Related Adverse Events (TRAEs).
Descripción general del estudio
Estado
Aún no reclutando
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Estimado)
30
Fase
- Fase 2
Contactos y Ubicaciones
Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.
Estudio Contacto
- Nombre: LIN YANG Doctor
- Número de teléfono: 010-13681015148
- Correo electrónico: linyangcicams@126.com
Criterios de participación
Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
No
Descripción
Inclusion Criteria:
- Voluntary participation with written informed consent provided
- Age ≥18 years at the time of signing the informed consent form
- Histologically or cytologically confirmed pancreatic ductal adenocarcinoma (including adenosquamous carcinoma)
- Failure of or disease progression after at least one prior line of systemic therapy for locally advanced or metastatic pancreatic cancer
- At least one measurable target lesion at baseline per RECIST 1.1 criteria (a single measurable lesion must not have received prior radiotherapy, or must have demonstrated clear progression after radiotherapy)
- ECOG performance status score of 0-2
- Adequate organ and bone marrow function (including hematologic, hepatic, renal, and coagulation parameters meeting specified criteria)
- Subjects of childbearing potential must use highly effective contraception, and female subjects must have a negative pregnancy test
- Ability and willingness to comply with study-related procedures.
Exclusion Criteria:
- History of or current presence of central nervous system metastases
- Presence of untreated or unstable spinal cord compression
- High risk of gastrointestinal or intra-abdominal bleeding
- Prior treatment with TROP2-targeted agents or antibody-drug conjugates (ADCs)
- Requirement for strong CYP3A4 inhibitors or inducers within 2 weeks prior to the first dose, or inability to avoid their use during the study
- History of severe dry eye syndrome, meibomian gland disease, or other corneal disorders that may impair corneal healing
- Major surgery within 28 days prior to the first dose (excluding palliative procedures), or receipt of curative radiotherapy within 3 months
- Presence of other malignancies within 3 years prior to the first treatment (except for certain definitively treated cancers)
- Uncontrolled severe systemic diseases such as cardiovascular or cerebrovascular disease, diabetes mellitus, or hypertension
- History of interstitial lung disease or non-infectious pneumonitis, or current related lesions
- Presence of severe underlying pulmonary disease, autoimmune disease, or prior total pneumonectomy
- Active chronic inflammatory bowel disease, gastrointestinal obstruction, or other severe gastrointestinal disorders
- Tumor invasion of critical organs or vessels with associated symptoms, or risk of fistula formation
- Toxicities from prior antitumor therapy not recovered to ≤ Grade 1 (except for low-risk toxicities)
- Active hepatitis B, hepatitis C, HIV infection, or active syphilis
- Known allergy to the investigational drug or its components, or history of severe hypersensitivity to other biologic agents
- Severe infection within 4 weeks prior to dosing, or active infection requiring systemic therapy within 2 weeks
- Receipt of non-specific immunomodulatory therapy or antitumor traditional Chinese medicine within 2 weeks prior to dosing
- Receipt of live vaccines within 30 days prior to dosing or planned during the study period
- Pregnant or breastfeeding women, or individuals of childbearing potential who are not using highly effective contraception as required
- Individuals considered vulnerable populations (e.g., patients with psychiatric disorders or critically ill patients), or any other condition deemed unsuitable for enrollment by the investigator.
Plan de estudios
Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.
¿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: Sacituzumab tirumotecan in Previously Treated Locally Advanced or Metastatic PDAC
|
Sacituzumab tirumotecan 5 mg/kg administered intravenously every 2 weeks
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Objective Response Rate (ORR)
Periodo de tiempo: From the date of first dose to the date of first documented disease progression as assessed by RECIST v1.1, death from any cause, or study discontinuation, whichever occurs first; tumor assessments performed every 6 weeks for up to 100 weeks.
|
Percentage of patients with Complete Response (CR) or Partial Response (PR) per RECIST
|
From the date of first dose to the date of first documented disease progression as assessed by RECIST v1.1, death from any cause, or study discontinuation, whichever occurs first; tumor assessments performed every 6 weeks for up to 100 weeks.
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Investigadores
- Investigador principal: LIN YANG, Doctor, Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Fechas de registro del estudio
Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.
Fechas importantes del estudio
Inicio del estudio (Estimado)
1 de abril de 2026
Finalización primaria (Estimado)
1 de enero de 2027
Finalización del estudio (Estimado)
1 de julio de 2027
Fechas de registro del estudio
Enviado por primera vez
31 de marzo de 2026
Primero enviado que cumplió con los criterios de control de calidad
28 de abril de 2026
Publicado por primera vez (Actual)
1 de mayo de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
1 de mayo de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
28 de abril de 2026
Última verificación
1 de abril de 2026
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- NCC6141
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
No
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
No
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. .