- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT05407909
To Evaluate the Safety and Tolerability of SYHX2001 in Patients With Advanced or Metastatic Solid Tumors
8 de agosto de 2022 actualizado por: CSPC ZhongQi Pharmaceutical Technology Co., Ltd.
This is a Phase 1, open-label, multicenter, dose escalation and expansion study to evaluate the safety, tolerability, pharmacokinetics, and pharmacodynamics of the experimental drug(SYHX2001) in previously treated patients with advanced or metastatic cancer.
Descripción general del estudio
Estado
Reclutamiento
Condiciones
Intervención / Tratamiento
Descripción detallada
This is a multicenter, open-label, dose-escalation, dose-expansion Phase 1 study of SYHX2001(name of the experimental drug) in patients with advanced or metastatic cancers who have exhausted standard treatment.
The study will consist of 2 parts, a dose escalation part and a cohort expansion part.
Once the recommended phase 2 dose (RP2D) has been determined in the dose escalation part, a cohort expansion part involving up to three separate cohorts will be conducted.
For patients, the study will include a screening phase, a treatment phase, and a post treatment follow-up phase.
An end-of-study visit will be conducted within 30 days after the last dose of SYHX2001.
Tipo de estudio
Intervencionista
Inscripción (Anticipado)
176
Fase
- 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
- 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
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
18 años a 75 años (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Todos
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
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 |
|---|---|
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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
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
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
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)
27 de julio de 2022
Finalización primaria (Anticipado)
6 de enero de 2026
Finalización del estudio (Anticipado)
6 de enero de 2026
Fechas de registro del estudio
Enviado por primera vez
30 de mayo de 2022
Primero enviado que cumplió con los criterios de control de calidad
3 de junio de 2022
Publicado por primera vez (Actual)
7 de junio de 2022
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
9 de agosto de 2022
Última actualización enviada que cumplió con los criterios de control de calidad
8 de agosto de 2022
Última verificación
1 de agosto de 2022
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- SYHX2001C101
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Indeciso
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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