SHR2554 Plus Liposomal Mitoxantrone as First-line Treatment for Peripheral T-cell Lymphoma (PTCL)
2026年7月21日 更新者:Institute of Hematology & Blood Diseases Hospital, China
An Open-label, Multicenter, Phase Ib/II Exploratory Clinical Study of EZH2 Inhibitor SHR2554 in Combination With Liposomal Mitoxantrone for the First-line Treatment of Peripheral T-cell Lymphoma
This is a single-arm, multicenter, Phase Ib/IIa study designed to explore the efficacy and safety of SHR2554 in combination with liposomal mitoxantrone for the treatment of patients with treatment-naive peripheral T-cell lymphoma (PTCL).
The study is divided into a Phase Ib safety lead-in phase and a Phase IIa dose expansion phase.
研究概览
研究类型
介入性
注册 (估计的)
44
阶段
- 阶段2
- 阶段1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:Liang Huang
- 电话号码:+86 022-23608126
- 邮箱:huangliang@ihcams.ac.cn
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Age ≥18 years old,regardless of gender;
- Centrally confirmed histopathological/cytologic diagnosis of PTCL with the following subtypes:Peripheral T-cell lymphoma, not otherwise specified (PTCL, NOS);Follicular helper T (TFH) cell lymphoma of lymph nodes, including angioimmunoblastic, follicular, NOS; Enteropathy-associated T-cell lymphoma(EATL); Monomorphic epitheliotropic intestinal T-cell lymphoma (MEITL)and any other PTCL subtypes deemed by the investigator to be eligible for inclusion.
- No prior anti-tumor therapy.
- There must be at least one measurable or evaluable lesion that meets the Lugano 2014 criteria for lymphoma: Measurable lesion: Nodal lesions with major diameter greater than 1.5cm and minor diameter greater than 1.0cm as assessed by PET/CT or Computed Tomography (CT) and/or Magnetic Resonance Imaging (MRI); Or the length of extranodal lesions >1.0cm; 2)Evaluable lesions: PET-CT showed increased uptake in lymph nodes or extranodal regions (higher than liver) and imaging features consistent with lymphoma;
- ECOG performance status score: 0-2;
- Expected survival time ≥3 months;
- Have adequate organ and bone marrow functiont;
- No concurrent hemophagocytic lymphohistiocytosis (HLH). If a patient has clinically diagnosed HLH, enrollment eligibility will be determined by the investigator based on an evaluation of the patient's general physical condition following targeted anti-HLH therapy.
- Women of childbearing potential must have a negative serum pregnancy test within 7 days before the first dose of medication; Effective contraception should be used from the time of informed consent until 6 months after the last dose of study drug.
- Capable of understanding the study procedures and voluntarily signing a written informed consent form (ICF).;
Exclusion Criteria:
- Prior treatment with epigenetic agents before enrollment;
- Patients with a history of severe cardiac disease, history of radiation therapy to the mediastinal/pericardial region, cumulative anthracycline dose > 550 mg (doxorubicin equivalent), prior use of mitoxantrone, baseline left ventricular ejection fraction (LVEF) < 50%, or history of exposure to other cardiotoxic drugs;
- History of other primary aggressive malignancies that are not in remission, or have been in remission for less than 3 years;
- Primary central nervous system (CNS) lymphoma or secondary CNS involvement.
- Known allergy or hypersensitivity to the study drugs or their related metabolites;
- Currently participating in another clinical study, or less than 4 weeks elapsed from the end of treatment in a previous clinical study to the planned start of study treatment;
- Pregnant or lactating women;
- Active infections;
- Medical History and Concurrent Conditions;
- History of Human Immunodeficiency Virus (HIV) infection and/or Acquired Immunodeficiency Syndrome (AIDS);
- Patients with mental disorders or those unable to provide informed consent
- Any other condition deemed by the investigator to be unsuitable for study enrollment;
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:SHR2554 combined with Liposomal Mitoxantrone
|
Patients will receive 6 cycles of SHR2554 combined with liposomal mitoxantrone as induction therapy.
All patients who achieve a complete response (CR) after induction therapy are eligible for transplantation.
Patients achieving CR or partial response (PR), as well as those post-transplantation, may receive SHR2554 maintenance therapy in 28-day cycles.
Maintenance therapy will continue until disease progression or other reasons for discontinuation.
The maximum duration of SHR2554 administration in the maintenance phase will not exceed 24 months.
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Incidence of Dose-Limiting Toxicities (DLT)
大体时间:Cycle 1 (28 days)
|
Adverse events (AE) defined as DLT events per protocol
|
Cycle 1 (28 days)
|
|
Complete response (CR) rate
大体时间:up to 6 months after enrollment
|
The proportion of subjects evaluated as complete response (CR) according to Lugano 2014 efficacy evaluation criteria
|
up to 6 months after enrollment
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Adverse events(AE)
大体时间:From the first day of medication to 28 days after the last dose
|
The safety of the drug was evaluated by NCI-CTC AE 6.0 standard.
Hematologic and non-hematologic toxicity.
|
From the first day of medication to 28 days after the last dose
|
|
Objective response rate (ORR)
大体时间:up to 6 months after enrollment
|
The proportion of subjects evaluated as complete response (CR) and partial response (PR) according to Lugano 2014 efficacy evaluation criteria
|
up to 6 months after enrollment
|
|
Duration of Response (DOR)
大体时间:up to 2.5 years post first treatment
|
The time from the first assessment of CR/PR to the first assessment of PD or death from any cause in the subject
|
up to 2.5 years post first treatment
|
|
Duration of complete response (CR)
大体时间:up to 2.5 years post first treatment
|
The time from the first assessment of CR to the first assessment of PD or death from any cause in the subject
|
up to 2.5 years post first treatment
|
|
Progression-free Survival (PFS)
大体时间:Up to 2.5 years
|
From the time subjects were enrolled to the time of disease progression (in any way) or death from any cause.
|
Up to 2.5 years
|
|
Overall survival (OS)
大体时间:Up to 2.5 years
|
From the date of inclusion to date of death, irrespective of cause.
|
Up to 2.5 years
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年8月1日
初级完成 (估计的)
2028年8月1日
研究完成 (估计的)
2030年3月1日
研究注册日期
首次提交
2026年7月21日
首先提交符合 QC 标准的
2026年7月21日
首次发布 (实际的)
2026年7月24日
研究记录更新
最后更新发布 (实际的)
2026年7月24日
上次提交的符合 QC 标准的更新
2026年7月21日
最后验证
2026年7月1日
更多信息
与本研究相关的术语
其他研究编号
- IIT2026083
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
不
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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