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

3 november 2026 uppdaterad av: 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

Studieöversikt

Studietyp

Interventionell

Inskrivning (Beräknad)

318

Fas

  • Fas 3

Kontakter och platser

Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.

Studiekontakt

Studieorter

    • Zhejiang
      • Hangzhou, Zhejiang, Kina, 310012
        • The First Affiliated Hospital, Zhejiang University school of Medicine
        • Kontakt:

Deltagandekriterier

Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.

Urvalskriterier

Åldrar som är berättigade till studier

18 år och äldre (Vuxen, Äldre vuxen)

Tar emot friska volontärer

Nej

Kön som är behöriga för studier

Allt

Beskrivning

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.

Studieplan

Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.

Hur är studien utformad?

Designdetaljer

  • Primärt syfte: Behandling
  • Tilldelning: Randomiserad
  • Interventionsmodell: Parallellt uppdrag
  • Maskning: Ingen (Open Label)

Vapen och interventioner

Deltagargrupp / Arm
Intervention / Behandling
Experimentell: 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

Aktiv komparator: 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.

Vad mäter studien?

Primära resultatmått

Resultatmått
Tidsram
overall survival (OS)
Tidsram: through the study completion, approximately up to 4 years
through the study completion, approximately up to 4 years

Sekundära resultatmått

Resultatmått
Åtgärdsbeskrivning
Tidsram
Response rates
Tidsram: 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)
Tidsram: approximately up to 3 years
approximately up to 3 years
Duration of CR and CRc
Tidsram: 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
Tidsram: 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
Tidsram: approximately up to 3 years

Transfusion independence rate

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

Samarbetspartners och utredare

Det är här du hittar personer och organisationer som är involverade i denna studie.

Utredare

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

Studieavstämningsdatum

Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.

Studera stora datum

Studiestart (Beräknad)

1 november 2026

Primärt slutförande (Beräknad)

1 december 2029

Avslutad studie (Beräknad)

1 juni 2030

Studieregistreringsdatum

Först inskickad

28 oktober 2026

Först inskickad som uppfyllde QC-kriterierna

3 november 2026

Första postat (Faktisk)

9 november 2026

Uppdateringar av studier

Senaste uppdatering publicerad (Faktisk)

9 november 2026

Senaste inskickade uppdateringen som uppfyllde QC-kriterierna

3 november 2026

Senast verifierad

1 november 2026

Mer information

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Nej

Studerar en amerikansk FDA-reglerad produktprodukt

Nej

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