A Study Comparing BL-B01D1 With Chemotherapy of Physician's Choice in Patients With Unresectable Locally Advanced, Recurrent, or Metastatic HR+/HER2- Breast Cancer After Failure of Prior Endocrine Therapy(PANKU-Breast03)
2026年7月21日 更新者:Sichuan Baili Pharmaceutical Co., Ltd.
A Phase III Randomized Controlled Clinical Study Comparing BL-B01D1 With Chemotherapy of Physician's Choice in Patients With Unresectable Locally Advanced, Recurrent, or Metastatic HR+/HER2- Breast Cancer After Failure of Prior Endocrine Therapy(PANKU-Breast03)
This trial is a registrational Phase III, randomized, open-label, multicenter study to evaluate the efficacy and safety of BL-B01D1 in patients with unresectable locally advanced, recurrent, or metastatic HR+/HER2- breast cancer after failure of prior endocrine therapy.
研究概览
详细说明
In this trial, the experimental group receives BL-B01D1, and the control group receives chemotherapy of physician's choice.
研究类型
介入性
注册 (估计的)
446
阶段
- 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
- 招聘中
- Cancer Hospital Chinese Academy of Medical Sciences
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接触:
- Binghei Xu
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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 sign the informed consent form and comply with the protocol requirements;
- No gender restrictions;
- Age ≥ 18 years;
- Expected survival time ≥ 3 months;
- Patients with unresectable locally advanced, recurrent, or metastatic HR+ HER2- breast cancer;
- Trial participants have not received systemic chemotherapy;
- Trial participants have progressed after at least one line of endocrine therapy, etc.;
- Documented radiographic disease progression prior to enrollment;
- Agree to provide archived tumor tissue specimens or fresh tissue samples from the primary or metastatic lesion within 3 years;
- Must have at least one measurable lesion as defined by RECIST v1.1;
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1;
- 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 (LVEF) ≥ 50%;
- Must meet required organ function levels;
- Urinary protein ≤ 2+ or < 1000 mg/24h;
- For premenopausal women of childbearing potential, a pregnancy test must be performed within 7 days before starting treatment, with a negative serum pregnancy result, and they must not be breastfeeding; all enrolled patients (regardless of gender) must use adequate barrier contraception throughout the treatment period and for 6 months after treatment ends.
Exclusion Criteria:
- Previously treated with ADC drugs that use topoisomerase I inhibitors as the toxin or target EGFR and/or HER3;
- Use of chemotherapy, biotherapy, immunotherapy, etc., within 4 weeks or 5 half-lives before the first dose;
- Previous treatment with anthracycline drugs where the equivalent cumulative dose of doxorubicin exceeds 360 mg/m²;
- History of severe cardiovascular or cerebrovascular diseases;
- Unstable thrombotic events requiring therapeutic intervention within 6 months before screening;
- Prolonged QT interval, complete left bundle branch block, etc.;
- Diagnosis of another malignancy within 3 years before the first dose;
- Hypertension poorly controlled by two antihypertensive medications;
- Poorly controlled blood glucose levels;
- History of ILD requiring steroid therapy, current ILD, or grade ≥2 radiation pneumonitis, etc.;
- Concurrent pulmonary diseases causing clinically severe respiratory function impairment;
- Patients with active central nervous system metastases;
- Presence of large serous cavity effusions or symptomatic serous cavity effusions, etc.;
- Imaging findings indicating tumor invasion or encasement of the abdomen, chest, etc.;
- Severe infection within 4 weeks before study randomization;
- Severe, unhealed wounds, ulcers, or fractures within 4 weeks before signing the informed consent form;
- Trial participants with clinically significant bleeding or a significant bleeding tendency within 4 weeks prior to signing the informed consent form;
- History of inflammatory bowel disease, extensive bowel resection, etc.;
- Patients with a history of allergy to recombinant humanized antibodies or allergy to BL-B01D1 or any of its excipients;
- History of autologous or allogeneic stem cell transplantation;
- Positive for human immunodeficiency virus antibodies, active hepatitis B virus infection, or hepatitis C virus infection;
- Receipt of other unapproved clinical study drugs or treatments within 4 weeks before the first dose;
- Trial participants planning to receive or having received live vaccines within 28 days before the first dose;
- Other conditions deemed by the investigator to be unsuitable for participation in this clinical trial due to complications or other reasons.
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 |
|---|---|
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实验性的:BL-B01D1
参与者在第一个周期(3 周)内接受 BL-B01D1。
具有临床获益的参与者可以接受更多周期的额外治疗。
由于疾病进展或出现无法耐受的毒性或其他原因,将终止给药。
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静脉滴注给药,周期3周。
其他名称:
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有源比较器:Albumin-bound paclitaxel, paclitaxel, or capecitabine
Participants receive Albumin-bound paclitaxel, paclitaxel, or capecitabine in the first cycle.
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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口服,3周为一个周期。
通过静脉输注给药,每个周期为3周。
Administration by intravenous infusion for a cycle of 4 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。
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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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响应持续时间 (DOR)
大体时间:最长约 24 个月
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缓解持续时间(DOR):定义为从首次记录肿瘤缓解之日到首次记录客观肿瘤进展之日或死亡日期的时间段。
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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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抗药物抗体(ADA)
大体时间:最长约 24 个月
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将调查抗 BL-B01D1 抗体 (ADA) 的频率。
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最长约 24 个月
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总生存期(OS)
大体时间:最长大致24个月
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总生存期(OS)定义为从随机分配日期到受试者死亡的时间。
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最长大致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 (实际的)
2026年7月6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10日
首次发布 (实际的)
2026年6月15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21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.