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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

6 de septiembre de 2026 actualizado por: Beijing Sungen Biomedical Technology Co., Ltd

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

A Phase I/IIa clinical study SGT003 in patients with advanced solid tumors.

Descripción general del estudio

Estado

Reclutamiento

Intervención / Tratamiento

Descripción detallada

This is a first-in-human Phase I/IIa clinical study evaluating the safety, tolerability, pharmacokinetic (PK) characteristics, immunogenicity, and preliminary efficacy of SGT003 in patients with advanced solid tumors. The study comprises a Phase I (dose-escalation) stage and a Phase IIa (dose-expansion) stage.

Tipo de estudio

Intervencionista

Inscripción (Estimado)

332

Fase

  • Fase 2
  • Fase 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

Ubicaciones de estudio

    • Beijing Municipality
      • Beijing, Beijing Municipality, Porcelana, 100142
        • Reclutamiento
        • Beijing Cancer Hospital

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:

  1. Patient can fully understand the trial, participates voluntarily, and signs informed consent form (ICF) prior to any study procedures
  2. Patients aged 18 to 75 years at the time of ICF signature.
  3. 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.
  4. ECOG 0 or 1.
  5. Radiographic evidence (CT/MRI, etc.) of disease progression documented during or after the most recent prior treatment.
  6. Patients must have adequate bone marrow reserve and organ function.

Exclusion Criteria:

  1. 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.
  2. Subjects who have received systemic immunosuppressant therapy within 14 days prior to the first administration of the investigational product.
  3. Subjects receiving anticoagulants such as therapeutic-dose heparin or vitamin K antagonists.
  4. Subjects who have received any live or attenuated live vaccine within 28 days prior to the first administration of the investigational product.
  5. Subjects who have undergone major surgery within 4 weeks prior to the first administration of the investigational product.
  6. Subjects with a history of Grade ≥3 immune-related adverse events (irAEs), hypersensitivity reactions, or Grade ≥2 immune-related myocarditis.
  7. 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.
  8. 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

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: 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

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

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 agosto de 2026

Finalización primaria (Estimado)

1 de diciembre de 2028

Finalización del estudio (Estimado)

1 de junio de 2029

Fechas de registro del estudio

Enviado por primera vez

17 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)

9 de septiembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

9 de septiembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

6 de septiembre de 2026

Última verificación

1 de septiembre de 2026

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.

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. .

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