A Study of BL-M08D1 in Combination With Immunochemotherapy in Patients With Diffuse Large B-Cell Lymphoma
2026年9月8日 更新者:Sichuan Baili Pharmaceutical Co., Ltd.
A Phase Ib/II Clinical Study to Evaluate the Efficacy and Safety of BL-M08D1 for Injection in Combination With Immunochemotherapy in Patients With Diffuse Large B-Cell Lymphoma
This Phase Ib/II study is a clinical trial to explore the efficacy and safety of BL-M08D1 for injection in combination with immunochemotherapy in patients with diffuse large B-cell lymphoma.
研究概览
地位
尚未招聘
条件
研究类型
介入性
注册 (估计的)
204
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:Sa Xiao, PHD
- 电话号码:+86 15013238943
- 邮箱:xiaosa@baili-pharm.com
学习地点
-
-
Guangdong
-
Guangzhou、Guangdong、中国
- Sun Yat-sen University Cancer Center
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接触:
- Qingqing Cai
-
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Jiangsu
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Suzhou、Jiangsu、中国
- The First Affiliated Hospital of Soochow University
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接触:
- Depei Wu
-
-
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:
- Voluntarily sign the informed consent form and comply with the protocol requirements;
- No gender restriction;
- Age ≥18 years and ≤75 years;
- Expected survival time ≥3 months;
- Patients with diffuse large B-cell lymphoma;
- Agree to provide archived tumor tissue specimens within 3 years or fresh tissue samples;
- Must have at least one measurable lesion;
- Eastern Cooperative Oncology Group (ECOG) performance status score ≤2;
- Toxicity from prior anti-tumor therapy must have recovered to ≤ Grade 1 as defined by NCI-CTCAE v6.0;
- No severe cardiac dysfunction, with left ventricular ejection fraction ≥50%;
- Organ function levels must meet the requirements;
- Urine protein ≤1+ or <1000 mg/24h;
- For premenopausal women with childbearing potential, a serum pregnancy test must be performed within 7 days before starting treatment, and the serum pregnancy test must exclude pregnancy; patients must not be breastfeeding; all enrolled trial participants must take adequate barrier contraceptive measures throughout the entire treatment period and for 6 months after treatment completion;
- Trial participants must be able and willing to comply with the visit schedule, treatment plan, laboratory tests, and other study-related procedures specified in the protocol.
Exclusion Criteria:
- Use of chemotherapy, biological therapy, immunotherapy, etc., within 4 weeks or 5 half-lives prior to the first dose;
- History of severe heart disease or cerebrovascular disease within 6 months before screening;
- Prolonged QT interval, complete left bundle branch block, third-degree atrioventricular block, or frequent and uncontrolled arrhythmias;
- Active autoimmune diseases and inflammatory diseases;
- Diagnosis of active malignancy within 5 years prior to the first dose;
- Unstable thrombotic events requiring therapeutic intervention within 6 months prior to the first dose;
- Hypertension inadequately controlled by antihypertensive medications;
- Trial participants with poorly controlled blood glucose;
- History of interstitial lung disease requiring corticosteroid therapy, or current ILD, or radiation pneumonitis of grade ≥2;
- Use of glucocorticoids at a dose >30 mg/day prednisone or equivalent, for purposes other than control of lymphoma symptoms;
- Concurrent pulmonary diseases resulting in clinically severe impairment of respiratory function;
- Patients with central nervous system involvement;
- Previous or current central nervous system disorders;
- Contraindications to any component of the study intervention, including but not limited to previous allergic reactions;
- Receipt of autologous hematopoietic stem cell transplantation or CAR-T cell therapy, etc., within 12 weeks prior to the first dose;
- Positive for human immunodeficiency virus antibody, active tuberculosis, active hepatitis B virus infection, or active hepatitis C virus infection;
- Active infection requiring systemic therapy within 4 weeks prior to the first study drug administration;
- Pleural, abdominal, or pelvic effusion or pericardial effusion requiring drainage and/or accompanied by symptoms within 4 weeks prior to the first study drug administration;
- Imaging findings indicating that the tumor has invaded or encased major blood vessels in the abdomen, chest, neck, pharynx, etc., or the pericardium or heart;
- Use of another investigational drug within 4 weeks or 5 half-lives prior to the first dose;
- Pregnant or breastfeeding women;
- Other conditions that, in the investigator's opinion, make the participant unsuitable for enrollment in this clinical trial.
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:随机化
- 介入模型:并行分配
- 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:BL-M08D1+R-GemOx or BL-M08D1+R-CHOP
Participants receive BL-M08D1+R-GemOx or BL-M08D1+R-CHOP for the first cycle (3 weeks).
Participants with clinical benefit could receive additional treatment for more cycles.
The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.
|
静脉滴注给药,周期3周。
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Oral administration for a cycle of 3 weeks.
|
|
有源比较器:R-GemOx or R-CHOP
Participants receive R-GemOx or R-CHOP for the first cycle (3 weeks).
Participants with clinical benefit could receive additional treatment for more cycles.
The administration will be terminated because of disease progression or intolerable toxicity occurring or other reasons.
|
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Administration by intravenous infusion for a cycle of 3 weeks.
Oral administration for a cycle of 3 weeks.
|
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 |
|---|---|---|
|
客观缓解率 (ORR)
大体时间:最长约 24 个月
|
ORR 定义为达到 CR(所有目标病灶消失)或 PR(目标病灶直径总和至少减少 30%)的参与者百分比。
根据 RECIST 1.1,经历确认的 CR 或 PR 的参与者百分比。
|
最长约 24 个月
|
|
Recommended Phase II Dose (RP2D)
大体时间:Up to approximately 24 months
|
The RP2D is defined as the dose level chosen by the sponsor (in consultation with the investigators) for phase II study, based on safety, tolerability, efficacy, PK, and PD data collected during the dose escalation study of BL-M08D1.
|
Up to approximately 24 months
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
疾病控制率(DCR)
大体时间:最长约 24 个月
|
疾病控制率 (DCR):根据 RECIST 1.1 标准将最佳总体缓解 (BOR) 评为完全缓解 (CR)、部分缓解 (PR) 和疾病稳定 (SD) 的所有随机受试者的百分比。
|
最长约 24 个月
|
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治疗中出现的不良事件(TEAE)
大体时间:最长约 24 个月
|
TEAE 被定义为在治疗期间身体暂时出现的结构、功能或化学的任何不利和非故意的变化,或先前存在的病症的任何恶化(即频率和/或强度的任何临床上显着的不利变化) BL-M08D1。
将在 BL-M08D1 治疗期间评估 TEAE 的类型、频率和严重程度。
|
最长约 24 个月
|
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响应持续时间(DOR)
大体时间:大约24个月
|
响应的持续时间(DOR)定义为首先记录肿瘤反应到首次记录客观肿瘤进展或死亡日期的日期。
|
大约24个月
|
|
Progression-free Survival (PFS)
大体时间:Up to approximately 24 months
|
Progression-free survival (PFS) as assessed by BICR is defined as the time between the date subjects were randomized and the first observation of disease progression (based on BICR's image-based assessment) or death.
|
Up to approximately 24 months
|
|
Complete Remission Rate (CRR)
大体时间:Up to approximately 24 months
|
Complete Remission Rate (CRR) refers to the proportion of patients in a clinical trial who achieve a complete remission (CR) after receiving a specific treatment.
|
Up to approximately 24 months
|
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9月1日
初级完成 (估计的)
2028年12月1日
研究完成 (估计的)
2028年12月1日
研究注册日期
首次提交
2026年9月8日
首先提交符合 QC 标准的
2026年9月8日
首次发布 (实际的)
2026年9月14日
研究记录更新
最后更新发布 (实际的)
2026年9月14日
上次提交的符合 QC 标准的更新
2026年9月8日
最后验证
2026年9月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
- 肿瘤
- 免疫系统疾病
- 组织学类型的肿瘤
- 淋巴系统疾病
- 淋巴增生性疾病
- 免疫增生性疾病
- 淋巴瘤,非霍奇金
- 淋巴瘤,B细胞
- 淋巴瘤
- 半身和淋巴疾病
- 淋巴瘤,大 B 细胞,弥漫性
- 氨基酸,肽和蛋白质
- 蛋白质
- 有机化学品
- 杂环化合物,1形
- 杂环化合物
- 杂环化合物,2环
- 杂环化合物,融合环
- 碳氢化合物
- 生物碱
- 多环化合物
- 吲哚
- 抗体,单克隆
- 抗体
- 免疫球蛋白
- 免疫蛋白
- 血蛋白
- 血清球蛋白
- 球蛋白
- 协调配合物
- 脱氧胞苷
- 胞苷
- 嘧啶核苷
- 嘧啶
- 怀孕
- 怀孕
- 类固醇
- 融合环化合物
- 磷酰胺芥末
- 氮芥末化合物
- 芥末化合物
- 碳氢化合物,卤素
- 磷酰胺
- 有机磷化合物
- 妊娠二培养子
- VINCA生物碱
- Secologanin色素生物碱
- 吲哚生物碱
- 吲哚衍生物
- 吲哚王
- 抗体,单克隆,鼠的衍生
- 奥沙利铂
- 利妥昔单抗
- 吉西他滨
- 强的松
- 环磷酰胺
- 长春新碱
其他研究编号
- BL-M08D1-201
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
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.