To Evaluate the Safety and Tolerability of SYHX2001 in Patients With Advanced or Metastatic Solid Tumors
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Descripción detallada
Tipo de estudio
Tipo de estudio
Inscripción (Anticipado)
Inscripción
Fase
Fase
- Fase 1
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: Xiaodong Wang
- Número de teléfono: +86 021-60673947
- Correo electrónico: wang_xiaodong@mail.ecspc.com
Ubicaciones de estudio
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Heilongjiang
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Harbin, Heilongjiang, Porcelana
- Reclutamiento
- Harbin Medical University Cancer Hospital
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Contacto:
- Yanqiao Zhang, Professor
- Número de teléfono: 13845120210
- Correo electrónico: yanqiaozhang@126.com
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Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Male or female patients with an age of 18~75years (inclusive).
- Confirmed histologic or cytologic diagnosis of an advanced and/or metastatic solid tumor.
- At least one measurable lesion as defined by RECIST version 1.1.
- Eastern Cooperative Oncology Group Performance Status 0 or 1.
- Life expectancy ≥3 months.
- Major organ function within 14 days prior to treatment meets the following criteria (no blood transfusion, Erythropoietin(EPO), Granulocyte Colony Stimulating Factor(G-CSF) or other medical support): Absolute Neutrophil Count(ANC)≥1.5×10^9/L,Platelet(PLT)≥90×10^9/L,Hemoglobin(Hb)≥100g/L or≥6.2 mmol/L;Creatinine(Cr)≤1.5×upper limit of normal(ULN) and creatinine clearance rate≥50mL/min;Total Bilirubin(TBIL)≤1.5×ULN; Prothrombin time(PT)≤1.5×ULN , Activated Partial Thromboplastin Time(APTT)≤1.5×ULN , Aspartate Aminotransferase(AST)/Alanine Aminotransferase(ALT)≤2.5 × ULN.
- Signed informed consent form.
Exclusion Criteria:
- Chemotherapy, radiotherapy, biotherapy, endocrine therapy, targeted therapy, immunotherapy and other anti-tumor treatment within 4 weeks prior to the first dose of the study drug, or administration of other investigational agents within 4 weeks or 5 half-lives prior to the first dose of the study drug, whichever is longer.
- Major surgery or significant trauma within 4 weeks prior to the first dose of the study drug.
- Adverse reactions from the previous anti-tumor treatment have not yet recovered to ≤ level 1 based on CTCAE 5.0。
- Have a history of severe cardiovascular and cerebrovascular disease.
- Central nervous system metastasis or meningeal metastasis with clinical symptoms, or other evidence shows that the patient's central nervous system metastasis or meningeal metastasis has not been controlled and not suitable for the study according to the judgment of the investigator.
- Known history of hypersensitivity to test drug components.
- Patients with recent active bleeding or a history of bleeding.
- Those with coagulation disorders or taking thrombolytic, anticoagulant or antiplatelet agglutination drugs.
- Gastrointestinal perforation, abdominal fistula, or intra-abdominal abscess within 6 months prior to first dose; or currently under investigator's judgement there are high risk factors for hollow organ perforation/fistula formation).
- Inability to swallow the drug orally, or a condition that seriously affects gastrointestinal absorption in the judgment of the investigator.
- Irritable bowel syndrome with signs/symptoms requiring medication.
- Persistent active diarrhea requiring medical treatment.
- Concomitant use of strong CYP3A4 inhibitors or inducers, strong CYP2D6 inhibitors and strong P-gp inhibitors within 14 days prior to the first dose of the study drug.
- History of autoimmune diseases, immunodeficiency, including HIV positive, or other acquired, congenital immunodeficiency, or organ transplant history.
- Known Hepatitis B Virus (HBV), Hepatitis C Virus (HCV), or other active viral infection.
- Male and female patients of childbearing potential do not agree to use suitable method of contraception during the treatment and 6 months after the last dose of study medication; female patients do not have negative results of serum/urine pregnancy test within 7 days prior to enrollment and would be breastfeeding.
- Not suitable for this study as determined by the investigator due to other reasons.
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)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
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Experimental: SYHX2001
SYHX2001 will be administered orally.
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SYHX2001 tablets, oral
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¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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Dose limiting toxicities (DLT) in stage Ⅰ
Periodo de tiempo: Baseline through Day 28
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Baseline through Day 28
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Maximum tolerated dose (MTD) in stage Ⅰ
Periodo de tiempo: Baseline through Day 28
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Baseline through Day 28
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Recommended phase 2 dose (RP2D)
Periodo de tiempo: Baseline through approximately 2 years
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Baseline through approximately 2 years
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Incidence and severity of adverse events in stage Ⅰ
Periodo de tiempo: Baseline through approximately 2 years
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Baseline through approximately 2 years
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Overall response rate (ORR) in stage Ⅱ
Periodo de tiempo: Up to approximately 2 years
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Up to approximately 2 years
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Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Maximum observed plasma concentration (Cmax) of SYHX2001
Periodo de tiempo: Baseline and up to approximately 2 years
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Baseline and up to approximately 2 years
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Area under the plasma concentration-time curve (AUC) extrapolated from time zero to infinity (AUC[0-inf]) of SYHX2001
Periodo de tiempo: up to approximately 2 years
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up to approximately 2 years
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AUC from time zero to the last quantifiable concentration after dosing (AUC[0-t]) of SYHX2001
Periodo de tiempo: up to approximately 2 years
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up to approximately 2 years
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Terminal phase half-life (t1/2) of SYHX2001
Periodo de tiempo: up to approximately 2 years
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up to approximately 2 years
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Oral clearance (CL/F) of SYHX2001
Periodo de tiempo: up to approximately 2 years
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up to approximately 2 years
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PFS Progression-free survival (PFS)
Periodo de tiempo: up to approximately 2 years
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PFS is defined as the time from first dose until radiographic progression per standard criteria or death due to any cause, whichever is earlier.
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up to approximately 2 years
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Duration of Response (DOR)
Periodo de tiempo: up to approximately 2 years
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DOR is defined as the time from first evidence of response (complete response or partial response per RECIST 1.1) to earlier date of disease progression or death due to any cause.
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up to approximately 2 years
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Number of patients with any adverse events(AEs) and serious adverse events(SAEs) in stage Ⅱ
Periodo de tiempo: up to approximately 2 years
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up to approximately 2 years
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Change from Baseline in symmetrical arginine dimethylation (SDMA) as a pharmacodynamics(PD) measure
Periodo de tiempo: Baseline and up to approximately 2 years
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Baseline and up to approximately 2 years
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Colaboradores e Investigadores
Patrocinador
Patrocinador
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
Inicio del estudio
Finalización primaria (Anticipado)
Finalización primaria
Finalización del estudio (Anticipado)
Finalización del estudio
Fechas de registro del estudio
Enviado por primera vez
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Publicado por primera vez
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización publicada
Última actualización enviada que cumplió con los criterios de control de calidad
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
Otros números de identificación del estudio
- SYHX2001C101
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
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.
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