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A Phase III Study Comparing Mesutoclax + Azacitidine Versus Venetoclax + Azacitidine in Untreated Acute Myeloid Leukemia (AML) Patients

3 de noviembre de 2026 actualizado por: Beijing InnoCare Pharma Tech Co., Ltd.

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

Aún no reclutando

Condiciones

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Estimado)

318

Fase

  • Fase 3

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

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

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 y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  1. Study participants with newly diagnosed AML (excluding acute promyelocytic leukemia [APL]) confirmed per the 2022 World Health Organization (WHO) classification criteria.
  2. Age ≥65 years; or age ≥18 years and <65 years and ineligible for intensive chemotherapy.
  3. The participant is expected to have a survival time of at least 12 weeks.
  4. For participants aged ≥65 years: ECOG Performance Status (PS) 0-2; for participants aged ≥18 years and <65 years: ECOG PS 0-3.
  5. Participants must have adequate hepatic and renal function.
  6. 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.
  7. 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.
  8. The participant is able to communicate adequately with the investigator and comply with study procedures as specified in the protocol.
  9. The participant or their legally authorized representative voluntarily provides written informed consent.

Exclusion Criteria:

  1. Prior antitumor treatment for myeloid hematologic malignancies.
  2. Prior history of chronic myeloid leukemia (CML), myelodysplastic syndrome/myeloproliferative neoplasm (MDS/MPN).
  3. Known central nervous system (CNS) involvement of leukemia.
  4. Peripheral blood white blood cell count >25×10^9/L prior to randomization.
  5. Active hepatitis B virus or hepatitis C virus infection.
  6. History of immunodeficiency, including positive human immunodeficiency virus (HIV) antibody.
  7. 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.
  8. Diagnosis of another active malignant neoplasm within the past 2 years.
  9. Severe active infection requiring intravenous antimicrobial therapy.
  10. History of severe cardiovascular disease.
  11. Prior history of central nervous system disorders.
  12. History of severe bleeding diathesis.
  13. Known alcohol or substance dependence.
  14. 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.
  15. Pregnant or breastfeeding female participants.
  16. Malabsorption syndrome or other conditions that preclude oral administration or may interfere with drug absorption.
  17. Known hypersensitivity to the active ingredients/excipients of mesutoclax tablets, venetoclax, azacitidine, or mannitol.

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: 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

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

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

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

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

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 (Estimado)

1 de noviembre de 2026

Finalización primaria (Estimado)

1 de diciembre de 2029

Finalización del estudio (Estimado)

1 de junio de 2030

Fechas de registro del estudio

Enviado por primera vez

28 de octubre de 2026

Primero enviado que cumplió con los criterios de control de calidad

3 de noviembre de 2026

Publicado por primera vez (Actual)

9 de noviembre de 2026

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

9 de noviembre de 2026

Última actualización enviada que cumplió con los criterios de control de calidad

3 de noviembre de 2026

Última verificación

1 de noviembre de 2026

Más información

Términos relacionados con este 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.

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. .