Sonrotoclax in Combination With Azacitidine for Previously Untreated Higher-risk Myelodysplastic Syndromes
A Prospective, Single-Center, Phase Ⅱ Clinical Study on the Efficacy and Safety of Sonrotoclax Combined With Azacitidine in Previously Untreated Patients With Higher-risk Myelodysplastic Neoplasms
To evaluate the efficacy and safety profile of sotoclax combined with azacitidine in newly diagnosed higher-risk MDS patients, including ORR, CR rate, PFS, OS and treatment-related adverse events
調査の概要
状態
研究の種類
入学 (推定)
段階
- フェーズ2
- フェーズ 3
連絡先と場所
研究連絡先
- 名前:Zhurhohan Yu
- 電話番号:+8617280290731
- メール:1148629702@qq.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:
-
Aged ≥ 18 years.
-
Diagnosed with myelodysplastic syndromes (MDS) based on bone marrow morphology, immunophenotyping, cytogenetics, and molecular testing, consistent with the WHO 2016 or 2022 classification criteria.
-
High-risk MDS defined by any of the following risk stratification systems:
- nbsp; a) IPSS-R score > 3.5; or
- nbsp; b) IPSS score > 1; or
- nbsp; c) IPSS-M score > 0.
-
No prior anti-tumor treatment for MDS, including hypomethylating agents or chemotherapy.
-
Eastern Cooperative Oncology Group (ECOG) performance status of 0-2.
-
Expected survival time ≥ 12 weeks.
-
Adequate major organ function as defined below:
- nbsp; a) Creatinine clearance ≥ 50 mL/min;
- nbsp; b) Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × upper limit of normal (ULN); Total bilirubin ≤ 1.5 × ULN;Left ventricular ejection fraction (LVEF) ≥ 45%.
-
Written informed consent must be obtained from the patient, legal representative, or guardian prior to any study-related procedures. The study protocol has been approved by the institutional ethics committee.
Exclusion Criteria:
- Diagnosis of acute promyelocytic leukemia (APL).
- Prior treatment with any BCL-2 inhibitor.
- History of other malignant tumors within the past 3 years (excluding cured malignancies).
- Presence of active and uncontrolled infectious diseases.
- Central nervous system (CNS) involvement.
- Severe and uncontrolled cardiac disease.
- Dry tap on bone marrow aspiration or grade 2-3 myelofibrosis.
- Pregnancy or breastfeeding status.
- Any other condition deemed inappropriate for study enrollment by the investigator.
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:防止
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- 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 |
|---|---|
|
他の:Sonrotoclax plus Azacitidine in Newly-Diagnosed Higher-Risk Myelodysplastic Syndromes (MDS)
Patients with newly-diagnosed higher-risk MDS receive 28-day cycles of sonrotoclax (BGB-11417) plus azacitidine. Azacitidine 75 mg/m² is given subcutaneously or intravenously on Days 1-7. Sonrotoclax (RP2D 160 mg daily, Days 1-14 per cycle) undergoes 4-day dose ramp-up (20-40-80-160 mg) in Cycle 1, followed by full target dose in later cycles. |
Patients with newly-diagnosed higher-risk MDS receive 28-day cycles of sonrotoclax (BGB-11417) plus azacitidine. Azacitidine 75 mg/m² is given subcutaneously or intravenously on Days 1-7. Sonrotoclax (RP2D 160 mg daily, Days 1-14 per cycle) undergoes 4-day dose ramp-up (20-40-80-160 mg) in Cycle 1, followed by full target dose in later cycles. |
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 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Overall Response Rate (ORR)
時間枠:Up to 24 months
|
Description: The proportion of participants achieving objective response (CR or PR) per response criteria. Unit of Measure: Proportion |
Up to 24 months
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Complete Remission (CR) rate
時間枠:Up to 24 months
|
Description: The proportion of participants achieving complete remission per response criteria. Unit of Measure: Proportion |
Up to 24 months
|
|
Duration of Response (DOR)
時間枠:Up to 36 months
|
Description: Time from the first documented objective response to disease progression or death from any cause. Unit of Measure: Time (months) |
Up to 36 months
|
|
Progression-Free Survival (PFS)
時間枠:Up to 36 months
|
Outcome Measure: Progression-Free Survival (PFS) Description: Time from randomization to disease progression or death from any cause. Unit of Measure: Time (months) |
Up to 36 months
|
|
Overall Survival (OS)
時間枠:Up to 36 months
|
Outcome Measure: Overall Survival (OS) Description: Time from randomization to death from any cause. Unit of Measure: Time (months) |
Up to 36 months
|
|
Hematological/non-hematological adverse events
時間枠:From first study treatment dose to 30 days after last dose
|
Description: Incidence of hematological and non-hematological adverse events, graded per CTCAE. Unit of Measure: Incidence (proportion) |
From first study treatment dose to 30 days after last dose
|
協力者と研究者
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
- 2026-MDS-1
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
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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