- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT07578064
A Randomized, Self-controlled Post-marketing Clinical Study on the Comparison of Shengbai Oral Liquid and Leucogen Tablets in the Treatment of Moderate Neutropenia Caused by Anti-tumor Drugs in Breast Cancer Patients
4 de mayo de 2026 actualizado por: Hongxia Wang
The subjects were randomly assigned to Group A or Group B in a 1:1 ratio, stratified by early/late stage.
Group A: In the first cycle, they took Shengbai Oral Liquid (40 ml, three times a day), and in the second cycle, they took Leucogen Tablets (20 mg, three times a day).
Group B: In the first cycle, they took Leucogen Tablets (20 mg, three times a day), and in the second cycle, they took Shengbai Oral Liquid (40 ml, three times a day).
Descripción general del estudio
Estado
Reclutamiento
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Estimado)
60
Fase
- Fase 4
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: Hongxia wang, PhD
- Número de teléfono: 13524491606 021-64175590
- Correo electrónico: whx365@126.com
Ubicaciones de estudio
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Porcelana, 200032
- Reclutamiento
- Fudan University Shanghai Cancer Center
-
-
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:
- Age range: 18 to 80 years old, gender unrestricted;
- Patients with breast cancer confirmed by histopathology.
- ECOG performance status score ≤ 2; expected survival time ≥ 12 weeks;
- During the period of anti-tumor drug treatment before enrollment (including but not limited to chemotherapy drugs: paclitaxel, capecitabine, vinorelbine; CDK4/6 inhibitors: palbociclib, dalpiciclib, ribociclib, abemaciclib; antibody-drug conjugates: trastuzumab emtansine, trastuzumab deruxtecan, sacituzumab govitecan, larotrectinib), grade II-III neutropenia occurred, and it is planned to continue the original treatment plan and dose for at least 2 cycles.
- The subject meets the criteria for continuing anti-tumor drug treatment; normal bone marrow hematopoietic function, no bleeding tendency (INR < 1.5); blood routine meets the following requirements: Hb ≥ 8g/dl, platelet count ≥ 75×109/L; liver and kidney function meets the following requirements: AST and ALT ≤ 3 ULN, total bilirubin ≤ 2 ULN, serum creatinine ≤ 1.5 ULN; no obvious heart and lung function disorders;
- The subject has high compliance and voluntarily signs the informed consent form.
Exclusion Criteria:
- 1. Having participated in other new drug clinical trials within 4 weeks before enrollment; planning to participate in other new drug clinical trials during the study period; planning to add other anti-tumor treatments during the study period; 2. Having received bone marrow radiotherapy involving 25% of the bone marrow; having undergone hematopoietic stem cell transplantation or bone marrow transplantation; 3. Uncontrolled acute or chronic infection; having severe underlying diseases such as heart, lung, liver or kidney diseases; having primary diseases of the hematopoietic system; having diseases such as hypersplenism, hyperthyroidism, adrenal insufficiency, connective tissue diseases, etc. that can cause a decrease in white blood cells; 4. Uncontrolled digestive system symptoms that affect the administration of the study drug; confirmed or suspected allergy to the study drug or its related components; 5. Uncontrolled psychological or mental disorders; judged by the investigator as unsuitable for participation in this study.
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: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Group A: In the first cycle, they took Shengbai Oral Liquid (40 ml, three times a day), and in the s
In the first cycle, they took Shengbai Oral Liquid (40 ml, three times a day), and in the second cycle, they took Leucogen Tablets (20 mg, three times a day).
|
In the first cycle, they took Shengbai Oral Liquid (40 ml, three times a day), and in the second cycle, they took Leucogen Tablets (20 mg, three times a day).
|
|
Experimental: Group B: In the first cycle, they took Leucogen Tablets (20 mg, three times a day), and in the secon
In the first cycle, they took Leucogen Tablets (20 mg, three times a day), and in the second cycle, they took Shengbai Oral Liquid (40 ml, three times a day).
|
In the first cycle, they took Leucogen Tablets (20 mg, three times a day), and in the second cycle, they took Shengbai Oral Liquid (40 ml, three times a day).
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Lowest neutrophil count (ANC) in the two stages
Periodo de tiempo: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the lowest values of neutrophils (ANC) in each group during the two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Rate of ANC decline (Grade II/III/IV), duration of ANC decline in the two stages
Periodo de tiempo: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the decline rates of grade II /III /IV ANC and the duration of ANC decline in each group during two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
|
Dosage of G-CSF
Periodo de tiempo: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the dosage of G-SCF in each group during the two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
|
The incidence of febrile neutropenia
Periodo de tiempo: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the incidence of febrile neutropenia in each group during two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
|
Infection incidence rate
Periodo de tiempo: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the incidence of infection in each group during the two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
|
Antibiotic utilization rate
Periodo de tiempo: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the utilization rate of antibiotics in each group during the two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
|
The completion rate of anti-tumor drugs
Periodo de tiempo: From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
Compare the completion rates of anti-tumor drugs in each group during the two chemotherapy cycles
|
From the initial treatment to the end of follow-up, approximately 42 or 56 days
|
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)
6 de agosto de 2025
Finalización primaria (Estimado)
30 de septiembre de 2026
Finalización del estudio (Estimado)
31 de diciembre de 2026
Fechas de registro del estudio
Enviado por primera vez
29 de julio de 2025
Primero enviado que cumplió con los criterios de control de calidad
4 de mayo de 2026
Publicado por primera vez (Actual)
11 de mayo de 2026
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
11 de mayo de 2026
Última actualización enviada que cumplió con los criterios de control de calidad
4 de mayo de 2026
Última verificación
1 de mayo de 2025
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- BC-NEU-001
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. .