A Phase III Study Comparing Mesutoclax + Azacitidine Versus Venetoclax + Azacitidine in Untreated Acute Myeloid Leukemia (AML) Patients
A Randomized, Open-label, Multicenter Phase III Study of Mesutoclax Combined With Azacitidine Versus Venetoclax Combined With Azacitidine in the Treatment of Treatment Naive Acute Myeloid Leukemia (AML) Who Are Elderly or Ineligible for Intensive Chemotherapy
A Phase III study comparing Mesutoclax + azacitidine versus venetoclax + azacitidine in newly diagnosed acute myeloid leukemia (AML) patients
Descripción general del estudio
Estado
Estado
Condiciones
Condiciones
Intervención / Tratamiento
Intervención / Tratamiento
Tipo de estudio
Tipo de estudio
Inscripción (Estimado)
Inscripción
Fase
Fase
- Fase 3
Contactos y Ubicaciones
Estudio Contacto
Estudio Contacto
- Nombre: Jingnan Yang
- Número de teléfono: 010-66609990
- Correo electrónico: CO-Clinicaltrial@innocarepharma.com
Ubicaciones de estudio
-
-
Zhejiang
-
Hangzhou, Zhejiang, Porcelana, 310012
- The First Affiliated Hospital, Zhejiang University school of Medicine
-
Contacto:
- Jie Jin
- Número de teléfono: 0571-87236898
- Correo electrónico: jiej0503@163.com
-
-
Criterios de participación
Criterio de elegibilidad
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Study participants with newly diagnosed AML (excluding acute promyelocytic leukemia [APL]) confirmed per the 2022 World Health Organization (WHO) classification criteria.
- Age ≥65 years; or age ≥18 years and <65 years and ineligible for intensive chemotherapy.
- The participant is expected to have a survival time of at least 12 weeks.
- For participants aged ≥65 years: ECOG Performance Status (PS) 0-2; for participants aged ≥18 years and <65 years: ECOG PS 0-3.
- Participants must have adequate hepatic and renal function.
- Male participants must agree to refrain from unprotected sexual intercourse and sperm donation from the first dose of investigational product through 90 days after the last dose.
- Female participants must meet one of the following: postmenopausal; permanently sterilized; or, for females of reproductive potential, have a negative serum pregnancy test within 7 days prior to the first study dose. Females of reproductive potential must agree to use one highly effective contraceptive method plus a supplementary barrier contraceptive method with their partner from the date of ICF signature until 180 days after the last dose.
- The participant is able to communicate adequately with the investigator and comply with study procedures as specified in the protocol.
- The participant or their legally authorized representative voluntarily provides written informed consent.
Exclusion Criteria:
- Prior antitumor treatment for myeloid hematologic malignancies.
- Prior history of chronic myeloid leukemia (CML), myelodysplastic syndrome/myeloproliferative neoplasm (MDS/MPN).
- Known central nervous system (CNS) involvement of leukemia.
- Peripheral blood white blood cell count >25×10^9/L prior to randomization.
- Active hepatitis B virus or hepatitis C virus infection.
- History of immunodeficiency, including positive human immunodeficiency virus (HIV) antibody.
- Use of strong or moderate CYP3A/P-gp inhibitors or inducers (medications, dietary supplements, etc.) within 5 half-lives before the first dose of investigational product.
- Diagnosis of another active malignant neoplasm within the past 2 years.
- Severe active infection requiring intravenous antimicrobial therapy.
- History of severe cardiovascular disease.
- Prior history of central nervous system disorders.
- History of severe bleeding diathesis.
- Known alcohol or substance dependence.
- Participants whom the investigator judges cannot adhere to the protocol due to uncontrolled medical, psychological, familial, social or geographic conditions; or participants who are unwilling or unable to follow protocol-required procedures.
- Pregnant or breastfeeding female participants.
- Malabsorption syndrome or other conditions that preclude oral administration or may interfere with drug absorption.
- Known hypersensitivity to the active ingredients/excipients of mesutoclax tablets, venetoclax, azacitidine, or mannitol.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Número de brazos
Armas e Intervenciones
Grupo de participantes/brazoGrupo de participantes/brazo |
Intervención / TratamientoIntervención / Tratamiento |
|---|---|
|
Experimental: Mesutoclax + Azacitidine
|
125 mg QD, orally, until disease progression or other reasons for treatment discontinuation, whichever comes first. 75 mg/m2, Day 1-7 or Day 1-5 and Day 8-9 of each Cycle, by injection |
|
Comparador activo: Venetoclax + Azacitidine
|
75 mg/m2, Day 1-7 or Day 1-5 and Day 8-9 of each Cycle, by injection 400 mg QD, orally, until disease progression or other reasons for treatment discontinuation, whichever comes first. |
¿Qué mide el estudio?
Medidas de resultado primarias
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
overall survival (OS)
Periodo de tiempo: through the study completion, approximately up to 4 years
|
through the study completion, approximately up to 4 years
|
Medidas de resultado secundarias
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Response rates
Periodo de tiempo: within 3 cycles (each cycle is 28 days) and during study treatment, approximately up to 3 years
|
Rate of complete remission with negative measurable residual disease (CRMRD-), complete remission (CR) rate, and composite complete remission (CRc) rate (CRc includes CR, CR with incomplete hematologic recovery [CRi] , and/or CR with partial hematological recovery(CRh)) |
within 3 cycles (each cycle is 28 days) and during study treatment, approximately up to 3 years
|
|
Event free survival (EFS)
Periodo de tiempo: approximately up to 3 years
|
approximately up to 3 years
|
|
|
Duration of CR and CRc
Periodo de tiempo: during study treatment period, approximately up to 3 years
|
Duration of CR and duration of CRc |
during study treatment period, approximately up to 3 years
|
|
EFS with molecular MRD relapse
Periodo de tiempo: approximately up to 3 years
|
Mesured from the date of randomization to date of treatment failure, hematological relapse, MRD relapse, or death from any cause, whichever comes first |
approximately up to 3 years
|
|
Transfusion independence rate
Periodo de tiempo: approximately up to 3 years
|
Transfusion independence rate |
approximately up to 3 years
|
|
Adverse event profile per CTCAE v5.0
Periodo de tiempo: from first dose to 28 days post last dose, approximately up to 3 years
|
Incidence, category, severity, and other characteristics of adverse events (AEs), assessed per NCI Common Terminology Criteria for Adverse Events (CTCAE) Version 5.0 |
from first dose to 28 days post last dose, approximately up to 3 years
|
|
Numbers of Treatment cycle
Periodo de tiempo: during study treatment period, approximately up to 3 years
|
during study treatment period, approximately up to 3 years
|
|
|
Treatment cycle duration
Periodo de tiempo: during study treatment period, approximately up to 3 years
|
during study treatment period, approximately up to 3 years
|
|
|
Days of treatment per cycle
Periodo de tiempo: during study treatment period, approximately up to 3 years
|
during study treatment period, approximately up to 3 years
|
|
|
Patient Reported Outcomes (PRO) by European Organization for Research and Treatment of Cancer -Quality of Life Questionnaire (EORTC-QLQ-C30)
Periodo de tiempo: from first dose to 28 days post last dose, approximately up to 3 years
|
PROs assessed by EORTC-QLQ-C30 , changes in rating compared to baseline. |
from first dose to 28 days post last dose, approximately up to 3 years
|
|
PRO by EuroQol 5-Dimension 5-Level (EQ-5D-5L)
Periodo de tiempo: from first dose to 28 days post last dose, approximately up to 3 years
|
PROs assessed by EQ-5D-5L, changes in rating compared to baseline. |
from first dose to 28 days post last dose, approximately up to 3 years
|
Colaboradores e Investigadores
Patrocinador
Patrocinador
Investigadores
Investigadores
- Investigador principal: Qian Jiang, Peking University People's Hospital
- Investigador principal: Jie Jin, First Affiliated Hospital of Zhejiang University
- Investigador principal: Jianxiang Wang, Chinese Academy of Medical Sciences
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Inicio del estudio
Finalización primaria (Estimado)
Finalización primaria
Finalización del estudio (Estimado)
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
- Neoplasias
- Neoplasias por tipo histológico
- Enfermedades hematológicas
- Leucemia Mieloide
- Leucemia
- Enfermedades hemic y linfáticas
- Leucemia Mieloide Aguda
- Químicos orgánicos
- Compuestos heterocíclicos, 1 anillo
- Compuestos heterocíclicos
- Ácidos nucleicos, nucleótidos y nucleósidos
- Citidina
- Nucleósidos de pirimidina
- Pirimidinas
- Compuestos AZA
- Nucleósidos
- Ribonucleósidos
- Azacitidina
- venetoclax
Otros números de identificación del estudio
Otros números de identificación del estudio
- ICP-CL-01210
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. .