A Phase 2 Study of Luvometinib Combined With Anlotinib in KRAS-mutated NSCLC
A Multicenter, Open-label, Single-arm Phase 2 Study to Evaluate the Efficacy and Safety of Luvometinib Combined With Anlotinib in Patients With KRAS-mutated Metastatic Non-small Cell Lung Cancer
研究概览
地位
研究类型
注册 (估计的)
阶段
- 阶段2
联系人和位置
学习联系方式
- 姓名:BAOHUI HAN
- 电话号码:+86 13817833343
- 邮箱:18930858216@163.com
研究联系人备份
- 姓名:Wei Zhang
- 电话号码:+86 18017321318
- 邮箱:zhwei2002@sjtu.edu.cn
学习地点
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Shanghai Municipality
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Shanghai、Shanghai Municipality、中国、200000
- 招聘中
- Shanghai Chest Hospital
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接触:
- BAOHUI HAN
- 电话号码:+86 13817833343
- 邮箱:18930858216@163.com
-
接触:
- Wei Zhang
- 电话号码:+86 18017321318
- 邮箱:zhwei2002@sjtu.edu.cn
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-
参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria
- aged between ≥ 18 years and ≤75 years; regardless of male or female.
- Histologically and/or cytologically confirmed diagnosis of non-small cell lung caner,and the clinical stage is IV(AJCC 4th); Received at least one line of systemic treatment(including platinum-based chemotherapy ± PD-(L)1) during the stage IV, and disease progression occured during or after the treatment.
- KRAS mutation positive.
- ECOG score 0-1. 5. Expected survival time ≥ 3 months.
6.At least one intracranial measurable lesion according to RECIST v1.1 criteria.
7.Adequate organ function within 7 days before enrollment. 8. Recovery to ≤grade 1 or return to baseline from previous treatment-related adverse events (according to CTCAE 5.0), except for adverse events such as hair loss that are judged by the investigators to be safe and do not violate other inclusion criteria.
9. Avoid excessive exposure to sunlight, and be willing to use sufficient sunscreen when there is expected to be sunlight exposure.
10. Take contraceptive measures as required.
Exclusion Criteria
1.Patients who have previously received any of the following treatments:
- Prior treatment with MEK inhibitors、anlotinib or other VEGFR-TKI(such as cabozantinib, sorafenib, apatinib,etc);
- Major surgery within 28 days or minor surgery within 14 days prior to the first dose, or need to undergo major surgery during the study treatment;
- Systemic anti-cancer treatment (including chemotherapy, targeted therapy, immunotherapy, and other clinical trial drug treatments) within 28 days prior to the first dose or within 5 drug half-lives (whichever is shorter).
- Treatment with traditional Chinese medicine, Chinese patent medicine or modern Chinese medicine preparations with anti-tumor indications within 7 days prior to the first dose;
- Radical radiotherapy within 28 days prior to the first dose; palliative radiotherapy allowed if ≥14 days before first dose;
- Live or live-attenuated vaccine within 28 days prior to the first dose; other vaccines (e.g., inactivated COVID-19 vaccine) within 14 days prior to the first dose;
History of allogeneic organ transplantation or allogeneic stem cell transplantation, or autologous stem cell transplantation within 3 months prior to the first dose.
2.Active CNS metastases; brainstem, leptomeningeal, spinal cord metastases or spinal cord compression.
3.Small cell lung cancer (including mixed SCLC/NSCLC) or cavitary central squamous cell carcinoma.
4.Receipt of ≥4 prior lines of systemic anticancer therapy. 5.Active autoimmune disease requiring systemic therapy in the past 2 years,except: stable disease on replacement therapy without systemic treatment; non-systemic dermatologic conditions (vitiligo, psoriasis) or alopecia.
6.Active infection requiring systemic therapy within 2 weeks before first dose. 7.Uncontrolled hypertension. 8.Dysphagia, active gastrointestinal disease, malabsorption, or any condition impairing study drug absorption.
9.Retinal vein occlusion (RVO), retinal pigment epithelial detachment (RPED), uncontrolled glaucoma, or other ocular disease interfering with ocular toxicity assessment.
10.Current or previous idiopathic pulmonary fibrosis/pneumonitis; active ILD, pneumonitis (including clinically significant radiation pneumonitis), pulmonary fibrosis; history of tracheal fistula; continuous oxygen requirement due to severe dyspnea or respiratory insufficiency.
11.Active HBV or HCV; known AIDS or positive HIV; active tuberculosis or syphilis.
12.Tumor invasion into major vessels, heart, pericardium, trachea, esophagus, or high risk of esophagotracheal/esophagopleural fistula.
13.Significant hemoptysis within 1 month before first dose; clinically significant bleeding, bleeding tendency, coagulopathy, or history of ≥Grade 3 thrombosis.
14.Symptomatic or recurrent pleural effusion, ascites, or pericardial effusion requiring frequent drainage.
15.Other malignancy diagnosed within 5 years before first dose.
学习计划
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:非随机化
- 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:Arm1: safety run-in part
Oral treatment with luvometinib + anlotinib combination, including different doses.
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Dose A:luvometinib 8mg and anlotinib 8mg; Dose B1:luvometinib 12mg and anlotinib 8mg; Dose B2: luvometinib 8mg and anlotinib 10mg; Dose C: luvometinib 12mg and anlotinib 10mg.
其他名称:
in this part, patients will receive the combined treatment of luvometinib and anlotinib at the recommended doses.
其他名称:
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实验性的:Arm2: expansion part
Select the optimal doses of luvometinib + anlotinib combination from the safety run-in period and continue enrolling about 30 patients to evaluate the efficacy and further safety.
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Dose A:luvometinib 8mg and anlotinib 8mg; Dose B1:luvometinib 12mg and anlotinib 8mg; Dose B2: luvometinib 8mg and anlotinib 10mg; Dose C: luvometinib 12mg and anlotinib 10mg.
其他名称:
in this part, patients will receive the combined treatment of luvometinib and anlotinib at the recommended doses.
其他名称:
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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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the objective response rate (ORR) per RECIST v1.1
大体时间:up to 24 months
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ORR assessed per RECIST v1.1 criteria,and defined as the proportion of patients with confirmed complete response (CR) and partial response (PR)
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up to 24 months
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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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Duration of overall response (DOR)
大体时间:up to 24 months
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DOR is defined as the time from the date of the first CR or PR to the first recorded tumor progression or death (death due to any cause), whichever occurs earlier
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up to 24 months
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Time to response (TTR)
大体时间:up to 24 months
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TTR is defined as the time from the first dose of the investigational drug to the first confirmed CR or PR
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up to 24 months
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Disease Control Rate (DCR)
大体时间:up to 24 months
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DCR is defined as the proportion of patients with complete response (CR), partial response (PR) or stable disease(SD)
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up to 24 months
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Progress Free Survival (PFS)
大体时间:up to 24 months
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PFS is defined as the time from the first dose to the first recorded progressive disease or death from any cause, whichever is first
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up to 24 months
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safety of the combination therapy of luvometinib and anlotinib
大体时间:up to 24 months
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including the types and frequencies of adverse event (AE) that occurred during the treatment period, Serious adverse events (SAE), adverse events that led to reduction of dose, and adverse events that resulted in discontinuation of dose.
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up to 24 months
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PK of the combination therapy of luvometinib and anlotinib
大体时间:up to 24 months
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including the types and frequencies of adverse event (AE) that occurred during the treatment period, Serious adverse events (SAE), adverse events that led to reduction of dose, and adverse events that resulted in discontinuation of dose.
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up to 24 months
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合作者和调查者
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
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