A Study of BL-B01D1 Combination Therapy in Patients With Metastatic Castration-resistant Prostate Cancer
2026年7月22日 更新者:Sichuan Baili Pharmaceutical Co., Ltd.
A Phase II/III Clinical Study to Evaluate the Efficacy and Safety of BL-B01D1 Combination Therapy in Patients With Metastatic Castration-resistant Prostate Cancer
This study will first conduct a phase II clinical study, and on the basis of the phase II clinical study, subsequent clinical research will be carried out.
研究概览
研究类型
介入性
注册 (估计的)
180
阶段
- 阶段2
- 第三阶段
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:15013238943
- 邮箱:xiaosa@baili-pharm.com
学习地点
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Beijing Municipality
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Beijing、Beijing Municipality、中国
- The First Medical Center of Chinese PLA General Hospital
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接触:
- Xu Zhang
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Shanghai Municipality
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Shanghai、Shanghai Municipality、中国
- The First Affiliated Hospital of Naval Medical University (Shanghai Changhai Hospital)
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接触:
- Linhui Wang
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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 join this study and sign the informed consent form;
- Age ≥ 18 years;
- Expected survival time ≥ 3 months;
- Unresectable metastatic castration-resistant prostate cancer;
- Meet the definition of mCRPC according to PCWG3 criteria;
- Agree to provide archived tumor tissue specimens from primary or metastatic lesions within 3 years or fresh tissue samples;
- Meet the evaluable lesion requirement defined by any one of the following assessment criteria;
- ECOG performance status score of 0 or 1;
- Toxicities from prior anti-tumor therapy 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 required criteria;
- Urine protein ≤ 1+ or < 1000 mg/24h;
- All enrolled patients must use adequate barrier contraceptive measures throughout the entire treatment period and for 7 months after the end of treatment.
Exclusion Criteria:
- Patients with metastatic castration-resistant prostate cancer who are suitable for radical local therapy;
- Patients with non-prostatic acinar adenocarcinoma confirmed by histopathology or cytology, among others;
- Patients who have previously received antibody-drug conjugates using topoisomerase I inhibitors as the toxin, among others;
- Use of chemotherapy, targeted therapy, biological therapy, etc., within 4 weeks or 5 half-lives prior to study randomization;
- History of severe heart disease or cerebrovascular disease;
- Long-term systemic corticosteroid therapy with prednisone >10 mg/day ongoing before the first dose, among others;
- Active autoimmune diseases and inflammatory diseases;
- Any thrombotic event within 6 months prior to randomization;
- Prolonged QTc interval, complete left bundle branch block, etc.;
- Diagnosis of active malignant tumors within 3 years prior to study randomization;
- Hypertension inadequately controlled by two antihypertensive medications;
- Patients with poorly controlled blood glucose;
- History of ILD requiring steroid therapy, or current ILD, or grade ≥2 radiation pneumonitis;
- Concurrent pulmonary diseases resulting in clinically severe respiratory function impairment;
- Patients with active central nervous system metastases;
- Severe infection occurring within 4 weeks prior to study randomization, etc.;
- Presence of large serous cavity effusion, or serous cavity effusion with symptoms, etc.;
- Imaging findings indicating tumor invasion or encasement of the abdomen, chest, etc.;
- Severe non-healing wounds, ulcers, or fractures within 4 weeks prior to signing informed consent;
- Trial participants with clinically significant bleeding or obvious bleeding tendency within 4 weeks prior to signing informed consent;
- Patients with inflammatory bowel disease, history of extensive bowel resection, history of immune-related enteritis, intestinal obstruction, or chronic diarrhea, etc.;
- Patients with a history of allergy to recombinant humanized antibodies or allergy to the investigational drug;
- History of autologous or allogeneic stem cell transplantation;
- Positive for human immunodeficiency virus antibodies, active hepatitis B virus infection, or hepatitis C virus infection;
- History of severe neurological or psychiatric disorders;
- Receipt of other unapproved clinical investigational drugs or treatments within 4 weeks prior to study randomization;
- Trial participants planning to receive vaccination or having received live vaccines within 28 days prior to study randomization;
- Other conditions deemed by the investigator as unsuitable for participation in this clinical trial due to complications or other circumstances.
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 |
|---|---|
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实验性的:Study treatment
Participants will receive BL-B01D1 + Abiraterone, BL-B01D1 + Olaparib, or BL-B01D1 + Abiraterone + Olaparib in 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.
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静脉滴注给药,周期3周。
其他名称:
Oral administration for a cycle of 3 weeks.
Oral administration for a cycle of 3 weeks.
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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 |
|---|---|---|
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无进展生存(PFS)
大体时间:大约24个月
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通过BICR评估的无进展生存期(PFS)定义为日期受试者之间的时间是随机的,并且对疾病进展的首次观察(基于BICR的基于图像的评估)或死亡。
|
大约24个月
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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客观缓解率 (ORR)
大体时间:最长约 24 个月
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客观缓解率 (ORR) 定义为治疗组和对照组中 CR 和 PR 的数量除以完整分析集 (FAS) 中该组的数量。
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最长约 24 个月
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疾病控制率(DCR)
大体时间:最长约 24 个月
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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。
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最长约 24 个月
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治疗紧急不良事件 (TEAE)
大体时间:最长约 24 个月
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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-B01D1。
将在 BL-B01D1 治疗期间评估 TEAE 的类型、频率和严重程度。
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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
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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。
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大约24个月
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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6月8日
首先提交符合 QC 标准的
2026年6月8日
首次发布 (实际的)
2026年6月11日
研究记录更新
最后更新发布 (实际的)
2026年7月23日
上次提交的符合 QC 标准的更新
2026年7月22日
最后验证
2026年7月1日
更多信息
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.