Merestinib on Bone Metastases in Subjects With Breast Cancer
2021年1月7日 更新者:University of Utah
An Exploratory Phase 1B Study to Assess the Effects of Merestinib on Bone Metastases in Subjects With Breast Cancer
This is an open label, pharmacodynamics, intrapatient dose escalation phase 1B study.
研究概览
研究类型
介入性
注册 (实际的)
2
阶段
- 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。
学习地点
-
-
Utah
-
Salt Lake City、Utah、美国、84112
- Huntsman Cancer Institute
-
-
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
18年 及以上 (成人、年长者)
接受健康志愿者
不
有资格学习的性别
女性
描述
Inclusion Criteria:
- At least 1 bone metastases must be present
- Urinary N-telopeptide level above 20nM BCE/mM creatinine measured at ARUP
- Archived or freshly biopsied primary and/or bone metastatic tumor tissue available in paraffin-embedded blocks or slides that is expected to yield 9 slides
- Life expectancy of ≥ 6 months
- Toxicity related to prior treatments must either have resolved to grade 1 or less, returned to baseline, or be deemed irreversible
- Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 (within 28 days prior to enrollment)
- Planning to remain on current breast cancer therapy for at least 12 weeks.
- At least one prior line of therapy for metastatic breast cancer
- Concurrent treatment with bisphosphonates or denosumab is required.
Exclusion Criteria:
- Unable to swallow or take anything orally
ECG abnormalities:
- Prolonged QTcF (Fredericia's correction) interval on screening ECG (≥ 450 msec)
- QRS ˃ 120 msec
- PR ˃ 210 msec
- Any prior history, or current evidence of second- or third-degree heart block
- Heart rate ˂ 40 beats per minute at screening
- ECG second degree heart block (Mobitz's Type 2 or Wenckebach)
- Complete heart block
- Left bundle branch block or bifascicular block (right bundle branch block and left anterior hemiblock together)
- Episodes of ventricular tachycardia
- Any known prior malignancy (not including non-melanoma skin cancers), unless treated with curative intent
- A serious uncontrolled medical disorder or active infection, which would impair the ability of the subject to receive protocol therapy
- Current or recent (within 3 months) gastrointestinal disease that could impact the absorption (i.e., unmanageable diarrhea or malabsorption at the time of screening)
Inadequate bone marrow function defined as:
- Absolute neutrophil count (ANC) ˂ 1,500 cells/mm3
- Platelet count ˂ 100,000 cells/mm3
- Hemoglobin ˂ 9 g/dL
Inadequate hepatic function defined as:
- Total bilirubin ˃ 1.5 x institutional upper limit of normal (IULN) (Unless due to diagnosis of Gilbert's Syndrome)
- Alanine aminotransaminase (ALT) and aspartate aminotransaminase (AST) ˃ 2.5 x IULN
- Inadequate renal function defined as: Serum creatinine ˃ 1.5 x ULN
- Prothrombin time (PT)/partial thromboplastin time (PTT) ˃ 1.5 times the ULN
- Serum sodium, potassium, and calcium levels not within normal limits.
- Any atrophic macular condition including intermediate or advanced age-related macular degeneration
- Patients receiving medications that are known to be substrates of CYP2C8 (including paclitaxel), CYP2C9, or CYP2C19 or to be oral substrates of CYP3A with narrow therapeutic window (listed on http://medicine.iupui.edu/clinpharm/ddis/main-table). Subjects who have discontinued any of these medications must have a wash-out period of at least 5 days or 5 half-lives of the drug (whichever is longer) prior to the first dose of merestinib
- Exposure to any investigational drug or placebo within 4 weeks of enrollment
- Any other sound medical, psychiatric, and/or social reasons as determined by the investigator
- History of diseases with influence on bone metabolism, such as Paget's disease, osteogenesis imperfecta, active primary or secondary hyperparathyroidism, and primary or secondary hyperthyroidism within 12 months prior to study entry
- Patients with known symptomatic brain metastasis. Subjects with controlled brain metastasis (no radiographic progression at least 4 weeks following radiation and/or surgical treatment and no neurological signs or symptoms) will be allowed
- History of allergy to merestinib or chemically related compounds
- History of osteonecrosis of the jaw
- Change in chemotherapy or hormone therapy within 8 weeks of the start of the study.
- Active gout or inflammatory arthritis requiring treatment
- Use within 28 days of registration of calcitonin, recombinant parathyroid hormone-related peptides, mithramycin, radium, strontium ranelate, or gallium nitrate.
- Adult patients who require monitored anesthesia for PET scanning due to claustrophobia.
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:Merestinib, all patients
|
*The merestinib does escalation timing will depend on the schedule of the other anticancer regimen* Subjects will receive merestinib 40mg PO Qday (dose level 1) for 2 to 4 weeks followed by 80mg PO daily (dose level 2) for 4 to 10 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 |
|---|---|---|
|
Adverse Events that Occur
大体时间:12 weeks, checked at every visit in that time period
|
To assess the tolerability of merestinib in combination with standard breast cancer therapies.
|
12 weeks, checked at every visit in that time period
|
|
Change in urinary N-telopeptide level
大体时间:12 weeks
|
To measure the change in urinary N-telopeptide level after 12 weeks of therapy with merestinib
|
12 weeks
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Absolute and percentage change in serum B-CTX, TRAP-5b, P1NP and BSAP
大体时间:12 weeks
|
To measure the absolute and percentage change in serum β-CTX, TRAP-5b, P1NP, and BSAP at time points from baseline to 12 weeks.
|
12 weeks
|
|
Time to skeletal-related events
大体时间:12 weeks
|
To evaluate determine time to skeletal-related event(s) following initiation of merestinib dosing
|
12 weeks
|
|
Change in pain scores
大体时间:12 weeks
|
To evaluate change in pain as measured by pain scores during and after 12 weeks of merestinib treatment
|
12 weeks
|
|
Change in pain by narcotic use
大体时间:12 weeks
|
To evaluate change in pain as measured by narcotic use) during and after 12 weeks of merestinib treatment
|
12 weeks
|
|
Change in bone lesion uptake
大体时间:12 weeks
|
To evaluate the change in bone lesion uptake on NaF PET scan after 12 weeks of merestinib treatment
|
12 weeks
|
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)
2018年1月11日
初级完成 (实际的)
2019年6月24日
研究完成 (实际的)
2019年6月24日
研究注册日期
首次提交
2017年9月20日
首先提交符合 QC 标准的
2017年9月20日
首次发布 (实际的)
2017年9月25日
研究记录更新
最后更新发布 (实际的)
2021年1月8日
上次提交的符合 QC 标准的更新
2021年1月7日
最后验证
2021年1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.