- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07808177
Clinical Evaluation of 177Lu-FAP-VG11 Injection in Patients With Fibroblast Activation Protein -Positive Advanced Solid Tumours
9 de septiembre de 2026 actualizado por: Xiaorong Sun, Shandong Cancer Hospital and Institute
An Exploratory Clinical Study to Evaluate the Safety, Tolerability and Biodistribution Characteristics of 177 Lu FAP VG11 Injection in Patients With Advanced Solid Tumours
This is an exploratory clinical study evaluating the safety, tolerability and biodistribution characteristics of 177Lu-FAP-VG11 injection in patients with FAP-positive advanced solid tumours.
Descripción general del estudio
Estado
Reclutamiento
Intervención / Tratamiento
Descripción detallada
This is an exploratory, single-arm, dose-escalation, open-label early Phase I clinical study to evaluate the safety, tolerability, dosimetry and preliminary efficacy of 177Lu-FAP-VG11 injection in FAP-positive patients with advanced solid tumors.
Tipo de estudio
Intervencionista
Inscripción (Estimado)
7
Fase
- Fase temprana 1
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: Xiaorong Sun
- Número de teléfono: 0531-67626287
- Correo electrónico: xrsun@sdfmu.edu.cn
Ubicaciones de estudio
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-
Shandong
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Jinan, Shandong, Porcelana, 250000
- Reclutamiento
- Cancer Hospital of Shandong First Medical University
-
Contacto:
- Xiaorong Sun
- Número de teléfono: 0531-67626287
- Correo electrónico: xrsun@sdfmu.edu.cn
-
-
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:
- Patients with advanced solid tumors who have failed standard therapy or for whom no standard therapy is available.
- Patients whose tumors are assessed as FAP-positive (high FAP expression with SUVmax uptake above liver background) by FAP-targeted diagnostic PET/CT imaging.
- In the investigator's judgment, no other treatment option with curative or life-prolonging potential is available.
- Male or non-pregnant, non-lactating females, aged ≥18 years.
- Eastern Cooperative Oncology Group (ECOG) performance status score ≤2.
- Life expectancy >6 months.
- Female patients: Women of childbearing potential must agree to use highly effective contraceptive methods from screening until 6 months after the last dose of study drug.
- Male patients: Subjects must use a condom during sexual intercourse during the study and for 14 weeks after the last study treatment to prevent partner pregnancy and to avoid transmission of the study drug via semen; in addition, subjects should refrain from sperm donation during treatment and for 6 months after the last study drug administration.
- Subjects must provide written informed consent voluntarily before participation in the trial.
- Willing and able to comply with scheduled visits, treatment plans, laboratory tests, and other study procedures.
Exclusion Criteria:
- Clinically symptomatic central nervous system metastases or meningeal metastases, or other evidence that the patient's central nervous system or meningeal metastases are not controlled, and deemed unsuitable for enrollment by the investigator.
- Major organ surgery (excluding needle biopsy) or significant trauma within 4 weeks prior to the first use of study drug, or need for elective surgery during the study period.
- History of immunodeficiency, including positive HIV test, or other acquired or congenital immunodeficiency diseases, or history of organ transplantation, or severe autoimmune disease history deemed unsuitable for enrollment by the investigator; or allogeneic organ transplantation requiring immunosuppressive therapy.
- Receipt of systemic or local radioisotope therapy within 3 months prior to the first dose.
- Receipt of other investigational drugs not yet marketed within 4 weeks prior to the first use of study drug, or within five half-lives of the other investigational drug.
- Definitive history of neurological or psychiatric disorders, including epilepsy or dementia.
- Pregnancy or lactation, or unwillingness to use adequate contraceptive methods.
- Any severe concomitant disease that, in the investigator's opinion, would make the patient's participation in the study inadvisable or could affect compliance with the protoco.
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: 177Lu-FAP-VG11 injection treatment
Patients will be treated with 177Lu-FAP-VG11 Injection
|
Patients will receive 177Lu-FAP-VG11 administration at an interval of 6 weeks between each dose.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Dose-Limiting Toxicities (DLT)
Periodo de tiempo: Through study completion, assessed up to 2 years.
|
Evaluating the safety and tolerability of the 177Lu-FAP-VG11 injection in patients.
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Through study completion, assessed up to 2 years.
|
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Maximum Tolerate dose (MTD)
Periodo de tiempo: Through study completion, assessed up to 2 years.
|
Evaluating the safety and tolerability of the 177Lu-FAP-VG11 injection in patients.
|
Through study completion, assessed up to 2 years.
|
|
Adverse Events
Periodo de tiempo: Through study completion, assessed up to 2 years.
|
Patients adverse events Incidence and severity of treatment emergent adverse events will be assessed as per CTCAE v6.0.All Adverse Events (AEs) occurring during the clinical study period will be monitored.
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Through study completion, assessed up to 2 years.
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Biodistribution
Periodo de tiempo: Through study completion, assessed up to 2 years.
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Evaluation of drug biodistribution in major human organs.
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Through study completion, assessed up to 2 years.
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Radiation dosimetry
Periodo de tiempo: Through study completion, assessed up to 2 years.
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Standard uptake value (SUV).
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Through study completion, assessed up to 2 years.
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Radiation dosimetry
Periodo de tiempo: Through study completion, assessed up to 2 years.
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Organ accumulation (%ID).
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Through study completion, assessed up to 2 years.
|
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Radiation dosimetry
Periodo de tiempo: Through study completion, assessed up to 2 years.
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Absorbed dose (AD).
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Through study completion, assessed up to 2 years.
|
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Radiation dosimetry
Periodo de tiempo: Through study completion, assessed up to 2 years.
|
Effective dose (ED) in tumors and target organs.
|
Through study completion, assessed up to 2 years.
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Objective Response Rate (ORR)
Periodo de tiempo: Through study completion, assessed up to 2 years.
|
ORR is defined as the the proportion of subjects who achieve a best overall response of Complete Response (CR) or Partial Response (PR).
|
Through study completion, assessed up to 2 years.
|
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Duration of Response (DOR)
Periodo de tiempo: Through study completion, assessed up to 2 years.
|
DOR is defined as the time from the earliest date of documented CR or PR until documented disease progression or death, whichever occurs first.
|
Through study completion, assessed up to 2 years.
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
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 (Actual)
17 de junio de 2026
Finalización primaria (Estimado)
6 de mayo de 2027
Finalización del estudio (Estimado)
6 de mayo de 2029
Fechas de registro del estudio
Enviado por primera vez
18 de agosto de 2026
Primero enviado que cumplió con los criterios de control de calidad
6 de septiembre de 2026
Publicado por primera vez (Actual)
8 de septiembre de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
14 de septiembre de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
9 de septiembre de 2026
Última verificación
1 de agosto de 2026
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- SDZLEC2026-049-001
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. .