- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07649200
Study of SNH-118110 in Advanced Solid Tumors (SNH-118110)
A Phase I Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of SNH-118110 in Patients With Advanced Solid Tumors
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Inscripción (Estimado)
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
- Nombre: Caicun Zhou, MD
- Número de teléfono: 86 021-58822171
- Correo electrónico: CAICUNZHOUDR@TONGJI.EDU.CN
Ubicaciones de estudio
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Porcelana, 200120
- The East Hospital Affiliated to Tongji University, Shanghai
-
-
Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
- Adulto
- Adulto Mayor
Acepta Voluntarios Saludables
Descripción
Inclusion Criteria:
- Ability to understand and voluntarily sign an informed consent form (ICF) prior to any study related procedures.
- Age ≥ 18 years at the time of signing the ICF.
- Histologically or cytologically confirmed diagnosis of advanced solid tumors, with the following additional requirements:
Dose-escalation phase: Patients with advanced solid tumors harboring a RET gene alteration who have failed standard therapy or are intolerant to standard therapy.
Dose-expansion phase:
Cohort 1: Locally advanced or metastatic NSCLC with RET gene fusion who have progressed after at least one prior line of therapy, which must include a RET inhibitor.
Cohort 2: Treatment-naïve patients with locally advanced or metastatic NSCLC harboring a RET gene fusion.
Cohort 3: Other advanced solid tumors harboring RET gene alterations.
- At least one measurable target lesion according to RECIST version 1.1.
- Documentation of a RET fusion or other activating RET gene alteration (based on a local or central laboratory report).
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1, with no deterioration within the 2 weeks prior to the first dose of study drug.
- Life expectancy of at least 3 months.
Exclusion Criteria:
- Presence of other known oncogenic driver mutations.
- Prior anti-tumor therapy within specified washout periods prior to first dose (e.g., small molecules, biologics, radiotherapy, major surgery), or failure to recover from clinically significant toxicities.
- Clinically significant uncontrolled or active conditions, including but not limited to:
Inadequate bone marrow, hepatic, or renal function. Significant cardiovascular disease (e.g., uncontrolled hypertension, prolonged QTc, poor ejection fraction, recent thromboembolic events).
Active or uncontrolled infections, bleeding diathesis, or significant pleural/abdominal/pericardial effusion requiring intervention.
Central nervous system metastases unless stable and asymptomatic off steroids.
- Conditions affecting oral drug absorption or gastrointestinal function.
- History of severe allergic reactions to similar agents.
- Pregnant or lactating women, or patients with serious concurrent medical or psychiatric conditions that would compromise safety or study compliance.
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: SNH-118110
Dose escalation: Multiple doses of SNH-118110 Dose expansion: MTD/MAD/recommended expansion dose
|
Participants will continue treatment until progression of disease or the end of the study.
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Safety evaluation
Periodo de tiempo: Up to approximately 2 years
|
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs).
|
Up to approximately 2 years
|
|
Maximum tolerated dose (MTD) or maximum administered dose (MAD)
Periodo de tiempo: Cycle 1 (up to 21 days)
|
Determination of the MTD or MAD of oral SNH-118110 by the number of participants who experience a dose limiting toxicity (DLT)
|
Cycle 1 (up to 21 days)
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
The maximum concentration (Cmax)
Periodo de tiempo: Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
|
Cmax of SNH-118110
|
Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
|
|
Time of the maximum concentration (Tmax)
Periodo de tiempo: Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
|
Tmax of SNH-118110
|
Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
|
|
Area under the concentration-time curve from time zero (pre-dose) to last time of quantifiable concentration (AUC0-t)
Periodo de tiempo: Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
|
AUC0-t of SNH-118110
|
Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
|
|
Elimination half-life (t1/2)
Periodo de tiempo: Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
|
T1/2 of SNH-118110
|
Cycle 1 day 1 through cycle 2 day 1 (cycle= 21 days)
|
|
Objective response rate (ORR)
Periodo de tiempo: Up to approximately 2 years
|
ORR of SNH-118110 evaluated by investigators per RECIST v1.1
|
Up to approximately 2 years
|
|
Disease control rate (DCR)
Periodo de tiempo: Up to approximately 2 years
|
DCR of SNH-118110 evaluated by investigators per RECIST v1.1
|
Up to approximately 2 years
|
|
Duration of response (DoR)
Periodo de tiempo: Up to approximately 2 years
|
DoR of SNH-118110 evaluated by investigators per RECIST v1.1
|
Up to approximately 2 years
|
|
Progression-free survival (PFS)
Periodo de tiempo: Up to approximately 2 years
|
PFS of SNH-118110 evaluated by investigators per RECIST v1.1
|
Up to approximately 2 years
|
|
Overall survival (OS)
Periodo de tiempo: Up to approximately 2 years
|
Overall survival (OS)
|
Up to approximately 2 years
|
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
- Neoplasias por sitio
- Neoplasias
- Enfermedades de las vías respiratorias
- Neoplasias por tipo histológico
- Enfermedades pulmonares
- Neoplasias Glandulares y Epiteliales
- Adenocarcinoma
- Neoplasias de las vías respiratorias
- Neoplasias torácicas
- Neoplasias Pulmonares
- Carcinoma
- Tumores neuroectodérmicos
- Neoplasias De Células Germinales Y Embrionarias
- Neoplasias De Tejido Nervioso
- Carcinoma Broncogénico
- Neoplasias Bronquiales
- Tumores neuroendocrinos
- Neoplasias ductales, lobulillares y medulares
- Carcinoma Neuroendocrino
- Carcinoma de pulmón de células no pequeñas
- Carcinoma Medular
Otros números de identificación del estudio
- SNH-118110-101
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. .