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- Essai clinique 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
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- Phase 3
Contacts et emplacements
Coordonnées de l'étude
- Nom: Jingnan Yang
- Numéro de téléphone: 010-66609990
- E-mail: CO-Clinicaltrial@innocarepharma.com
Lieux d'étude
-
-
Zhejiang
-
Hangzhou, Zhejiang, Chine, 310012
- The First Affiliated Hospital, Zhejiang University school of Medicine
-
Contact:
- Jie Jin
- Numéro de téléphone: 0571-87236898
- E-mail: jiej0503@163.com
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
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.
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: 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 |
|
Comparateur actif: 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. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
overall survival (OS)
Délai: through the study completion, approximately up to 4 years
|
through the study completion, approximately up to 4 years
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Response rates
Délai: 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)
Délai: approximately up to 3 years
|
approximately up to 3 years
|
|
|
Duration of CR and CRc
Délai: 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
Délai: 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
Délai: approximately up to 3 years
|
Transfusion independence rate |
approximately up to 3 years
|
|
Adverse event profile per CTCAE v5.0
Délai: 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
Délai: during study treatment period, approximately up to 3 years
|
during study treatment period, approximately up to 3 years
|
|
|
Treatment cycle duration
Délai: during study treatment period, approximately up to 3 years
|
during study treatment period, approximately up to 3 years
|
|
|
Days of treatment per cycle
Délai: 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)
Délai: 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)
Délai: 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
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Qian Jiang, Peking University People's Hospital
- Chercheur principal: Jie Jin, First Affiliated Hospital of Zhejiang University
- Chercheur principal: Jianxiang Wang, Chinese Academy of Medical Sciences
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
- Tumeurs
- Tumeurs par type histologique
- Maladies hématologiques
- Leucémie myéloïde
- Leucémie
- Maladies hémiques et lymphatiques
- Leucémie, myéloïde, aiguë
- Produits chimiques organiques
- Composés hétérocycliques, 1 anneau
- Composés hétérocycliques
- Acides nucléiques, nucléotides et nucléosides
- Cytidine
- Nucléosides pyrimidine
- Pyrimidines
- Composés Aza
- Nucléosides
- Ribonucléosides
- Azacitidine
- vénitoclax
Autres numéros d'identification d'étude
- ICP-CL-01210
Informations sur les médicaments et les dispositifs, documents d'étude
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