- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07811037
A Phase I/IIa Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics, Immunogenicity, and Preliminary Efficacy of SGT003 in Patients With Advanced Solid Tumors
A Multicenter, Dose-Escalation and Expansion Phase I/IIa Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetic Characteristics, Immunogenicity, and Preliminary Efficacy of SGT003 in Patients With Advanced Solid Tumors
Descripción general del estudio
Descripción detallada
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 2
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Shuchang Jiang
- Número de teléfono: +86 13552250017
- Correo electrónico: shuchang.jiang@hotgen.com.cn
Ubicaciones de estudio
-
-
Beijing Municipality
-
Beijing, Beijing Municipality, Porcelana, 100142
- Reclutamiento
- Beijing Cancer Hospital
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Patient can fully understand the trial, participates voluntarily, and signs informed consent form (ICF) prior to any study procedures
- Patients aged 18 to 75 years at the time of ICF signature.
Study population:
- Phase I (dose-escalation study): Patients with advanced solid tumors confirmed histologically or cytologically, who have failed at least one standard therapy for advanced disease, are intolerant to standard therapy, or have no available standard treatment options.
- Phase IIa (dose-expansion study): Patients with advanced solid tumors who have received at least first-line but not up to third-line standard systemic therapy and experienced disease progression or intolerance to such therapy.
- ECOG 0 or 1.
- Radiographic evidence (CT/MRI, etc.) of disease progression documented during or after the most recent prior treatment.
- Patients must have adequate bone marrow reserve and organ function.
Exclusion Criteria:
- Subjects who have received chemotherapy, radiotherapy, biotherapy, endocrine therapy, immunosuppressive therapy or other anti-tumor therapy within 4 weeks prior to the first administration of the investigational product.
- Subjects who have received systemic immunosuppressant therapy within 14 days prior to the first administration of the investigational product.
- Subjects receiving anticoagulants such as therapeutic-dose heparin or vitamin K antagonists.
- Subjects who have received any live or attenuated live vaccine within 28 days prior to the first administration of the investigational product.
- Subjects who have undergone major surgery within 4 weeks prior to the first administration of the investigational product.
- Subjects with a history of Grade ≥3 immune-related adverse events (irAEs), hypersensitivity reactions, or Grade ≥2 immune-related myocarditis.
- Subjects with active autoimmune disease or prior autoimmune disease with a risk of recurrence. Exceptions: well-controlled type 1 diabetes, hypothyroidism controlled solely by hormone replacement therapy, and skin diseases that do not require systemic treatment.
- Subjects with current or prior active interstitial lung disease (ILD). Subjects with radiation-induced pulmonary fibrosis that does not require steroid therapy are eligible.
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: SGT003
Use SGT003 for Injection
|
Dosage Form: Injection Strength: 50 mg (5 mL) per vial Dosage and Administration: Subjects will receive SGT003 (investigational product) via intravenous (IV) infusion on Day 1 (D1) of each cycle. Dose: During the Phase I dose-escalation, subjects will be dosed according to the assigned dose cohort; during the Phase IIa dose-expansion stage, subjects will be dosed according to the selected expansion dose. Duration of Administration: For each subject, the first infusion will be completed within 90 minutes. If no infusion-related reaction (IRR) and/or hypersensitivity reaction occurs, the subsequent infusion duration may be shortened to no less than 60 minutes. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Adverse Events (AEs), immune-related Adverse Events (irAEs)
Periodo de tiempo: First dose up to 28 days (+3 days) after EOT, or prior to initiation of other anti-tumor therapy, whichever occurs first.
|
This includes clinically significant changes in vital signs, physical examination, electrocardiogram, echocardiogram and clinical laboratory tests, as graded by National Cancer Institute (NCI) Common Terminology for Adverse Events (CTCAE) version 6.0.
|
First dose up to 28 days (+3 days) after EOT, or prior to initiation of other anti-tumor therapy, whichever occurs first.
|
|
Phase I: Dose Limit Toxicity (DLTs)
Periodo de tiempo: Within the first dose cycle (Day1-Day21) of SGT003
|
Evaluated at each dose level of SGT003 graded by NCI CTCAE v6.0.
|
Within the first dose cycle (Day1-Day21) of SGT003
|
|
Phase I: Maximum Toxicity Dose(MTD)
Periodo de tiempo: Within the first dose cycle (Day1-Day21) of SGT003
|
The MTD is based on the incidence of DLTs
|
Within the first dose cycle (Day1-Day21) of SGT003
|
|
Phase I: Recommended Phase II dose (RP2D)
Periodo de tiempo: Within the first dose cycle (Day1-Day21) of SGT003
|
The RP2D is based on the results of safety、PK/PD and preliminary efficacy of SGT003 in the stage of dose escalation
|
Within the first dose cycle (Day1-Day21) of SGT003
|
|
Phase IIa: Objective Response Rate (ORR)
Periodo de tiempo: from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first. average Up to 24 months
|
The ratio of CR and PR Evaluated by RECIST1.1 and iRECIST,
|
from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first. average Up to 24 months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Area under the plasma concentration-time curve (AUC)
Periodo de tiempo: From first study treatment to EOT, average of 24 months
|
area under the plasma concentration-time curve
|
From first study treatment to EOT, average of 24 months
|
|
Peak concentration (Cmax)
Periodo de tiempo: From first study treatment to EOT, average of 24 months
|
peak concentration
|
From first study treatment to EOT, average of 24 months
|
|
Time to peak concentration(Tmax)
Periodo de tiempo: From first study treatment to EOT, average of 24 months
|
time to peak concentration
|
From first study treatment to EOT, average of 24 months
|
|
Immunogenicity
Periodo de tiempo: Starting from the first administration of investigational product until 28 days (+3 days) after EOT.
|
ADA detection rate, ADA incidence rate, Nab detection rate (if applicable), Nab incidence rate (if applicable)
|
Starting from the first administration of investigational product until 28 days (+3 days) after EOT.
|
Otras medidas de resultado
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Phase I. Objective Response Rate (ORR)
Periodo de tiempo: average Up to 24 months
|
Evaluated by RECIST1.1 and iRECIST, from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
|
average Up to 24 months
|
|
Phase I and phase IIa. Duration of Response (DOR)
Periodo de tiempo: average Up to 24 months
|
Evaluated by RECIST1.1 and iRECIST, from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
|
average Up to 24 months
|
|
Phase I and phase IIa. Disease Control Rate (DCR)
Periodo de tiempo: average Up to 24 months
|
The ratio of CR、PR and SD Evaluated by RECIST1.1 and iRECIST, whichever occurs first.
|
average Up to 24 months
|
|
Phase I and phase IIa. Time to Response (TTR)
Periodo de tiempo: average up to 24 months
|
The period from the date of randomization to the occurrence of CR/PR,evaluated by RECIST1.1 and iRECIST, , until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
|
average up to 24 months
|
|
Phase I and phase IIa. Progression-Free Survival (PFS)
Periodo de tiempo: average Up to 24 months
|
from date of randomization, until disease progression, initiation of new anti-tumor therapy, withdrawal of informed consent, death, loss to follow-up, or study termination, whichever occurs first.
Evaluated by RECIST1.1 and iRECIST,
|
average Up to 24 months
|
|
Phase IIa. Overall Survival (OS)
Periodo de tiempo: average up to 24 months
|
the period from date of randomization to death
|
average up to 24 months
|
Colaboradores e Investigadores
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
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
Otros números de identificación del estudio
- SG-SGT003-101
- CTR20262751 (Identificador de registro: China Center for Drug Evaluation (CDE), NMPA)
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. .