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
Panoramica dello studio
Stato
Stato
Condizioni
Condizioni
Intervento / Trattamento
Intervento / Trattamento
Tipo di studio
Tipo di studio
Iscrizione (Stimato)
Iscrizione
Fase
Fase
- Fase 3
Contatti e Sedi
Contatto studio
Contatto studio
- Nome: Jingnan Yang
- Numero di telefono: 010-66609990
- Email: CO-Clinicaltrial@innocarepharma.com
Luoghi di studio
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Zhejiang
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Hangzhou, Zhejiang, Cina, 310012
- The First Affiliated Hospital, Zhejiang University school of Medicine
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Contatto:
- Jie Jin
- Numero di telefono: 0571-87236898
- Email: jiej0503@163.com
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Criteri di partecipazione
Criteri di ammissibilità
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
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.
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Nessuno (etichetta aperta)
Numero di armi
Armi e interventi
Gruppo di partecipanti / ArmGruppo di partecipanti / Arm |
Intervento / TrattamentoIntervento / Trattamento |
|---|---|
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Sperimentale: Mesutoclax + Azacitidine
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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 |
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Comparatore attivo: Venetoclax + Azacitidine
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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
Misure di risultato primarie
Misura del risultato |
Lasso di tempo |
|---|---|
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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
Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Response rates
Lasso di tempo: within 3 cycles (each cycle is 28 days) and during study treatment, approximately up to 3 years
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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
|
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Event free survival (EFS)
Lasso di tempo: approximately up to 3 years
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approximately up to 3 years
|
|
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Duration of CR and CRc
Lasso di tempo: during study treatment period, approximately up to 3 years
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Duration of CR and duration of CRc |
during study treatment period, approximately up to 3 years
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EFS with molecular MRD relapse
Lasso di tempo: approximately up to 3 years
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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
|
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Adverse event profile per CTCAE v5.0
Lasso di tempo: from first dose to 28 days post last dose, approximately up to 3 years
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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
|
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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
|
|
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Treatment cycle duration
Lasso di tempo: during study treatment period, approximately up to 3 years
|
during study treatment period, approximately up to 3 years
|
|
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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
|
|
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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
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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
|
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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
Sponsor
Sponsor
Investigatori
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
Studia le date principali
Inizio studio (Stimato)
Inizio studio
Completamento primario (Stimato)
Completamento primario
Completamento dello studio (Stimato)
Completamento dello studio
Date di iscrizione allo studio
Primo inviato
Primo inviato
Primo inviato che soddisfa i criteri di controllo qualità
Primo inviato che soddisfa i criteri di controllo qualità
Primo Inserito (Effettivo)
Primo Inserito
Aggiornamenti dei record di studio
Ultimo aggiornamento pubblicato (Effettivo)
Ultimo aggiornamento pubblicato
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo aggiornamento inviato che soddisfa i criteri QC
Ultimo verificato
Ultimo verificato
Maggiori informazioni
Termini relativi a questo studio
Termini MeSH pertinenti aggiuntivi
- Neoplasie
- Neoplasie per tipo istologico
- Malattie ematologiche
- Leucemia, mieloide
- Leucemia
- Malattie emiche e linfatiche
- Leucemia, mieloide, acuta
- Prodotti chimici organici
- Composti eterociclici, 1-anello
- Composti eterociclici
- Acidi nucleici, nucleotidi e nucleosidi
- Citidina
- Nucleosidi di pirimidina
- Pirimidine
- Composti aza
- Nucleosidi
- Ribonucleosidi
- Azacitidina
- Venetoclax
Altri numeri di identificazione dello studio
Altri numeri di identificazione dello studio
- ICP-CL-01210
Informazioni su farmaci e dispositivi, documenti di studio
Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti
Studia un dispositivo regolamentato dalla FDA degli Stati Uniti
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