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

3 novembre 2026 aggiornato da: 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

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Stimato)

318

Fase

  • Fase 3

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Luoghi di studio

    • Zhejiang
      • Hangzhou, Zhejiang, Cina, 310012
        • The First Affiliated Hospital, Zhejiang University school of Medicine
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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

Comparatore attivo: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Lasso di tempo
overall survival (OS)
Lasso di tempo: through the study completion, approximately up to 4 years
through the study completion, approximately up to 4 years

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Response rates
Lasso di tempo: 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)
Lasso di tempo: approximately up to 3 years
approximately up to 3 years
Duration of CR and CRc
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: approximately up to 3 years

Transfusion independence rate

approximately up to 3 years
Adverse event profile per CTCAE v5.0
Lasso di tempo: 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
Lasso di tempo: during study treatment period, approximately up to 3 years
during study treatment period, approximately up to 3 years
Treatment cycle duration
Lasso di tempo: during study treatment period, approximately up to 3 years
during study treatment period, approximately up to 3 years
Days of treatment per cycle
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Investigatore principale: Qian Jiang, Peking University People's Hospital
  • Investigatore principale: Jie Jin, First Affiliated Hospital of Zhejiang University
  • Investigatore principale: Jianxiang Wang, Chinese Academy of Medical Sciences

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Stimato)

1 novembre 2026

Completamento primario (Stimato)

1 dicembre 2029

Completamento dello studio (Stimato)

1 giugno 2030

Date di iscrizione allo studio

Primo inviato

28 ottobre 2026

Primo inviato che soddisfa i criteri di controllo qualità

3 novembre 2026

Primo Inserito (Effettivo)

9 novembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

9 novembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

3 novembre 2026

Ultimo verificato

1 novembre 2026

Maggiori informazioni

Termini relativi a questo studio

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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