A Study of JNJ-101684362 (HLD-0117) in Patients With Metastatic Breast Cancer (HLD-0117)
A Phase 1 Study of JNJ-101684362 (HLD-0117) in Patients With Estrogen Receptor Positive (ER+) Metastatic Breast Cancer (MBC)
The purpose of this study is to find out the maximum tolerated dose (MTD) and/or recommended dose(s) for expansion (RDEs) of JNJ-101684362 (HLD-0117), to evaluate the safety of JNJ-101684362 (HLD-0117) , and how well the participants can tolerate it in Part 1 (dose escalation) of the study.
研究概览
研究类型
注册 (估计的)
阶段
- 阶段1
联系人和位置
学习联系方式
- 姓名:Study Contact
- 电话号码:844-434-4210
- 邮箱:Participate-In-This-Study1@its.jnj.com
学习地点
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Adelaide、澳大利亚、5000
- 招聘中
- Cancer Research SA
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Connecticut
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New Haven、Connecticut、美国、06510
- 招聘中
- Yale University School Of Medicine
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Florida
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Sarasota、Florida、美国、34236
- 招聘中
- Florida Cancer Specialists
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Massachusetts
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Boston、Massachusetts、美国、02114
- 招聘中
- Massachusetts General Hospital
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Tennessee
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Nashville、Tennessee、美国、37203
- 招聘中
- SCRI Oncology Partners
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Texas
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San Antonio、Texas、美国、78229
- 招聘中
- South Texas Accelerated Research Therapeutics, LLC (START)
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Virginia
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Fairfax、Virginia、美国、22031
- 招聘中
- Next Virginia
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参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
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Female (assigned at birth), greater than or equal to (>=) 18 years old, and able to provide informed consent
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Histologically confirmed metastatic or locally advanced breast cancer
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Postmenopausal status defined by surgical or natural menopause, or ovarian suppression with a GnRH agonist
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Prior therapy including
- Must have received at least one endocrine therapy in the metastatic setting.
- Must have received at least one cyclin-dependent kinase (CDK) 4/6i, either in the adjuvant and/or metastatic setting.
- For Part 1 and Part 2 Cohorts 2A, 2B, 2C, and 2D: Participants may have received up to two prior distinct cytotoxic regimens (for example, taxanes, antibody-drug conjugates (ADCs), etc.) in the metastatic setting, unless discussed and approved by the medical monitor.
- For Part 2 Cohort 2E: Participants must have received more than two prior distinct cytotoxic regimens (for example, taxanes, ADCs, etc.) in the metastatic setting.
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Radiologic disease progression on the most recent therapy
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Patients must have disease evaluable per response evaluation criteria in solid tumors (RECIST) v1.1
- For Part 1 and Part 2B, 2C, and 2E: Participants may have either evaluable or measurable disease per RECIST v1.1.
- For Part 2 Cohort 2A: Participants should have measurable soft tissue disease per RECIST v1.1.
- For Part 2 Cohort 2D: Participants should have evaluable but not measurable disease.
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Willingness to provide baseline and on-treatment tumor biopsies, unless not feasible or medically appropriate
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For Part 1 and Part 2 (all cohorts):
- Participants must have documented >=10% ER staining and human epidermal growth factor receptor 2 (HER2) negative (per american society of clinical oncology [ASCO] college of american pathologists [CAP] guidelines) on the most recent tumor biopsy sample obtained.
- For Part 2 Cohort 2B: Participants must have recent estrogen receptor 1 gene (ESR1) wild type from tumor or circulating tumor deoxy ribonucleic acid (ctDNA) testing performed after the most recent endocrine therapy prior to enrollment.
- For Part 2 Cohort 2C: Participants must have ESR1 mutation detected from tumor or ctDNA testing performed prior to enrollment.
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Eastern cooperative oncology group (ECOG) performance status 0-1 and life expectancy of at least 3 months
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Adequate organ function Recovery from prior therapy-related toxicities to Grade <=1 (except alopecia; neuropathy and endocrinopathies <=Grade 2)
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Ability to swallow oral medication and comply with study procedures
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Stable dose (>=30 days) of bisphosphonates or denosumab, if applicable
Exclusion Criteria:
- Participants with Inflammatory breast cancer or leptomeningeal disease or brain metastases, with the exception of patients with definitively treated brain metastases that are clinically stable and asymptomatic for >2 weeks and who are off or receiving low-dose corticosteroid treatment (<=10 mg prednisone or equivalent) for at least 2 weeks prior to start of study treatment.
- Recent major bleeding or uncontrolled bleeding disorder
- Ongoing corticosteroid use >10 mg/day (prednisone equivalent)
- Recent anticancer or investigational therapy within 14 days (28 days for fulvestrant)
- Untreated or unstable spinal cord compression
- Significant cardiovascular disease within 6 months or ongoing uncontrolled cardiac conditions
- Active or uncontrolled infection (controlled HIV or treated hepatitis C allowed)
- Uncontrolled renal, pancreatic, or liver disease (excluding stable conditions such as Gilbert's syndrome or liver metastases)
- Another malignancy requiring treatment within 2 years (except low-risk, curatively treated cancers)
- Major surgery within 28 days
- Any condition that may interfere with safety or study compliance
- Pregnancy or breastfeeding
学习计划
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:顺序分配
- 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:Arm 1
JNJ-101684362 (HLD-0117): Participants with estrogen receptor positive (ER+) metastatic breast cancer (MBC) will receive JNJ-101684362 (HLD-0117) orally once daily as monotherapy in Part 1 until recommended dose(s) for expansion has been developed. Participants in Part 2 will receive JNJ-101684362 (HLD-0117) at the RP2Ds developed in Part 1. |
A treatment cycle consists of 28 days. Treatment may continue until disease progression or study discontinuation (withdrawal of consent, intercurrent illness, unacceptable adverse event or any other changes unacceptable for further treatment, etc.) |
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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Dose Limiting Toxicities (DLTs)
大体时间:28 days
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Frequency of dose-limiting toxicities (DLTs) |
28 days
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AEs, ECGs, Labs and Clinical Changes
大体时间:28 days
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Frequency and severity of adverse events (AEs) and abnormal electrocardiogram (ECG), laboratory and clinical changes from baseline |
28 days
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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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Objective response rate (ORR)
大体时间:56 Days
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Objective response rate (ORR) per RECIST in evaluable patients |
56 Days
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Duration of response (DOR)
大体时间:28 days
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DOR is defined as the time from the first occurrence of a documented objective response to disease progression or death from any cause, whichever occurs first. |
28 days
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Progression-free survival (rPFS)
大体时间:56 days
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Radiographic progression-free survival (rPFS) |
56 days
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Disease Control Rate (DCR)
大体时间:24 weeks
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Disease Control Rate (DCR) |
24 weeks
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Clinical Benefit Rate (CBR)
大体时间:24 weeks
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CBR is defined as the proportion of patients who achieve partial response (PR) or complete response (CR), or stable disease (SD) lasting at least 24 weeks, as assessed according to RECIST v1.1. |
24 weeks
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合作者和调查者
调查人员
- 研究主任:Janssen Research & Development, LLC Clinical Trial、Janssen Research & Development, LLC
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
与本研究相关的术语
其他研究编号
- HLD-0117-ONC-101
- HLD-0117-ONC-101 (其他标识符:Janssen Research & Development, LLC)
- 2026-527749-23-00 (注册表标识符:EUCT number)
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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