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
調査の概要
研究の種類
入学 (推定)
段階
- フェーズ 3
連絡先と場所
研究連絡先
- 名前:Jingnan Yang
- 電話番号:010-66609990
- メール:CO-Clinicaltrial@innocarepharma.com
研究場所
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-
Zhejiang
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Hangzhou、Zhejiang、中国、310012
- The First Affiliated Hospital, Zhejiang University school of Medicine
-
コンタクト:
- Jie Jin
- 電話番号:0571-87236898
- メール:jiej0503@163.com
-
-
参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
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.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:ランダム化
- 介入モデル:並列代入
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的: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 |
|
アクティブコンパレータ: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. |
この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
|
overall survival (OS)
時間枠:through the study completion, approximately up to 4 years
|
through the study completion, approximately up to 4 years
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Response rates
時間枠: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)
時間枠:approximately up to 3 years
|
approximately up to 3 years
|
|
|
Duration of CR and CRc
時間枠: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
|
|
EFS with molecular MRD relapse
時間枠: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
時間枠:approximately up to 3 years
|
Transfusion independence rate |
approximately up to 3 years
|
|
Adverse event profile per CTCAE v5.0
時間枠: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
時間枠: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
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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
|
協力者と研究者
捜査官
- 主任研究者:Qian Jiang、Peking University People's Hospital
- 主任研究者:Jie Jin、First Affiliated Hospital of Zhejiang University
- 主任研究者:Jianxiang Wang、Chinese Academy of Medical Sciences
研究記録日
主要日程の研究
研究開始 (推定)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
追加の関連 MeSH 用語
その他の研究ID番号
- ICP-CL-01210
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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