- ICH GCP
- US Clinical Trials Registry
- Klinisk forsøg NCT07925190
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
Studieoversigt
Status
Betingelser
Intervention / Behandling
Undersøgelsestype
Tilmelding (Anslået)
Fase
- Fase 3
Kontakter og lokationer
Studiekontakt
- Navn: Jingnan Yang
- Telefonnummer: 010-66609990
- E-mail: CO-Clinicaltrial@innocarepharma.com
Studiesteder
-
-
Zhejiang
-
Hangzhou, Zhejiang, Kina, 310012
- The First Affiliated Hospital, Zhejiang University school of Medicine
-
Kontakt:
- Jie Jin
- Telefonnummer: 0571-87236898
- E-mail: jiej0503@163.com
-
-
Deltagelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Ingen (Åben etiket)
Våben og indgreb
Deltagergruppe / Arm |
Intervention / Behandling |
|---|---|
|
Eksperimentel: 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. |
Hvad måler undersøgelsen?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
overall survival (OS)
Tidsramme: through the study completion, approximately up to 4 years
|
through the study completion, approximately up to 4 years
|
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Response rates
Tidsramme: 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)
Tidsramme: approximately up to 3 years
|
approximately up to 3 years
|
|
|
Duration of CR and CRc
Tidsramme: 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
Tidsramme: 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
Tidsramme: approximately up to 3 years
|
Transfusion independence rate |
approximately up to 3 years
|
|
Adverse event profile per CTCAE v5.0
Tidsramme: 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
Tidsramme: during study treatment period, approximately up to 3 years
|
during study treatment period, approximately up to 3 years
|
|
|
Treatment cycle duration
Tidsramme: during study treatment period, approximately up to 3 years
|
during study treatment period, approximately up to 3 years
|
|
|
Days of treatment per cycle
Tidsramme: 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)
Tidsramme: 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)
Tidsramme: 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
|
Samarbejdspartnere og efterforskere
Efterforskere
- Ledende efterforsker: Qian Jiang, Peking University People's Hospital
- Ledende efterforsker: Jie Jin, First Affiliated Hospital of Zhejiang University
- Ledende efterforsker: Jianxiang Wang, Chinese Academy of Medical Sciences
Datoer for undersøgelser
Studer store datoer
Studiestart (Anslået)
Primær færdiggørelse (Anslået)
Studieafslutning (Anslået)
Datoer for studieregistrering
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først opslået (Faktiske)
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Faktiske)
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Yderligere relevante MeSH-vilkår
- Neoplasmer
- Neoplasmer efter histologisk type
- Hæmatologiske sygdomme
- Leukæmi, myeloid
- Leukæmi
- Hemiske og lymfatiske sygdomme
- Leukæmi, Myeloid, Akut
- Organiske kemikalier
- Heterocykliske forbindelser, 1-ring
- Heterocykliske forbindelser
- Nukleinsyrer, nukleotider og nukleosider
- Cytidin
- Pyrimidin -nukleosider
- Pyrimidiner
- AZA -forbindelser
- Nukleosider
- Ribonucleosider
- Azacitidin
- Venetoclax
Andre undersøgelses-id-numre
- ICP-CL-01210
Lægemiddel- og udstyrsoplysninger, undersøgelsesdokumenter
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