JS212 in Combination With JS111 as First-Line Treatment in EGFR-Mutant Advanced NSCLC
A Phase II, Open-Label, Single-Arm Study of JS212 in Combination With JS111 as First-Line Treatment in Patients With Epidermal Growth Factor Receptor (EGFR)-Mutant Advanced Non-Small Cell Lung Cancer (NSCLC)
This is a single-arm clinical study evaluating the safety, tolerability, and preliminary efficacy of JS212 in combination with JS111 as first-line treatment in participants with epidermal growth factor receptor (EGFR)-mutant locally advanced or metastatic non-small cell lung cancer (NSCLC) who have not received prior systemic therapy for advanced disease.
The study consists of a safety lead-in stage followed by a clinical expansion stage. Approximately 20 participants are planned to be enrolled across the two stages. Participants will receive JS212 by intravenous infusion on Day 1 of each 21-day cycle and JS111 at 160 mg orally once daily until treatment discontinuation criteria are met.
During the safety lead-in stage, up to 10 participants will be enrolled and monitored for significant toxicities during the first 21 days after initial administration. The Safety Monitoring Committee (SMC) will review available safety, tolerability, and efficacy data and determine the JS212 dose to be further evaluated, whether an additional higher or lower dose should be explored, and whether the study may proceed to the clinical expansion stage.
研究概览
详细说明
This is a single-arm clinical study designed to evaluate the safety, tolerability, and preliminary antitumor activity of JS212 in combination with JS111 as first-line treatment in participants with EGFR-mutant locally advanced or metastatic NSCLC who have not previously received systemic therapy for EGFR-mutant advanced disease.
Participants will receive JS212 by intravenous infusion on Day 1 once every 3 weeks (Q3W), in combination with JS111 at 160 mg administered orally once daily (QD). Each treatment cycle is 21 days. Study treatment will continue until disease progression, unacceptable toxicity, withdrawal of consent, or another protocol-defined treatment discontinuation criterion is met.
The study includes two sequential stages: a safety lead-in stage and a clinical expansion stage. Approximately 20 participants are planned to be enrolled in total, although the final sample size may be adjusted by the Safety Monitoring Committee based on accumulating safety, tolerability, and efficacy data.
Safety Lead-in Stage
Up to 10 participants will be enrolled in the safety lead-in stage. The first 21 days following the initial administration of JS212 and JS111 will constitute the significant toxicity observation period.
The SMC will review the accumulated data and determine the JS212 dose to be used in combination with JS111 during the clinical expansion stage.
Before study initiation or during study conduct, the SMC may also consider emerging safety, tolerability, pharmacologic, and efficacy data from other ongoing studies of JS212 administered as monotherapy or in combination with other agents. Based on these data, the SMC may recommend modification of the JS212 dose, evaluation of another dose level, or omission of the safety lead-in stage and direct initiation of the clinical expansion stage, as specified in the SMC Charter.
Clinical Expansion Stage
After review of the safety lead-in data, participants enrolled in the clinical expansion stage will receive the SMC-selected dose of JS212 in combination with JS111 at 160 mg QD. The clinical expansion stage will further characterize the safety, tolerability, and preliminary antitumor activity of the combination.
Treatment will be administered in 21-day cycles and will continue until disease progression, unacceptable toxicity, withdrawal of consent, or another protocol-defined treatment discontinuation criterion is met. The study is expected to enroll approximately 20 participants in total across the safety lead-in and clinical expansion stages. The SMC may adjust the number of participants based on emerging study data.
Study Objectives
The primary objective is to evaluate the safety and tolerability of JS212 in combination with JS111 and to determine the JS212 dose to be further evaluated in combination with JS111.
The secondary or exploratory objective is to evaluate the preliminary antitumor activity of JS212 in combination with JS111 as first-line treatment in participants with EGFR-mutant locally advanced or metastatic NSCLC.
研究类型
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:kui Zhang
- 电话号码:+8618168028925
- 邮箱:kui_zhang@junshipharma.com
学习地点
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Anhui
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Hefei、Anhui、中国、230088
- The First Affiliated Hospital of Anhui Medical University
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接触:
- Hospital
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接触:
- Huan Zhou, Ph.D
- 电话号码:086 13665527160
- 邮箱:zhouhuanbest@vip.163.com
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首席研究员:
- Huan Zhou, Ph.D
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Shanghai Municipality
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Shanghai、Shanghai Municipality、中国、200030
- Shanghai Chest Hospital
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接触:
- Zhiren Yang, Ph.D.
- 电话号码:086 13965082087
- 邮箱:503091240@qq.com
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接触:
- University
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首席研究员:
- Zhiren Yang, Ph.D
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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:
Participants must meet all of the following criteria to be eligible for enrollment in this study:
- Male or female participants aged 18 to 75 years, inclusive, at the time of signing the informed consent form.
- Histologically or cytologically confirmed recurrent or metastatic solid tumor that is unresectable and not amenable to curative radiotherapy or chemoradiotherapy.
- Confirmed EGFR-sensitizing mutation, defined as an exon 19 deletion or L858R mutation, either occurring alone or together with other EGFR mutations, including concomitant T790M mutation. Local laboratory test reports are acceptable, provided that testing is performed using a well-validated assay, an assay that has passed external quality assessment, a laboratory qualified for molecular pathology diagnosis or genetic testing, or an assay approved by the National Medical Products Administration (NMPA). Participants must not have received prior systemic antitumor therapy for locally advanced or metastatic nonsquamous NSCLC. Participants with recurrent NSCLC who previously received adjuvant or neoadjuvant therapy, including chemotherapy, radiotherapy, or other treatment, or definitive radiotherapy or chemoradiotherapy, may be enrolled if the interval between the last treatment and disease recurrence is more than 6 months.
- At least 1 measurable lesion according to Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST v1.1).
- Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1.
- Life expectancy of at least 12 weeks.
- Adequate major organ function.
- Women of childbearing potential (WOCBP) who are sexually active with a nonsterilized male partner must have a negative serum pregnancy test within 7 days before the first dose and must agree to have no plans for pregnancy and to use highly effective contraception from the time of signing the informed consent form until 7 months after the last dose of JS212 or 2 months after the last dose of JS111, whichever contraception period is longer.
- Nonsterilized male participants who are sexually active with a female partner of childbearing potential must agree to use effective contraception, as described in Appendix 2, from the time of signing the informed consent form until 4 months after the last dose of JS212 or JS111. Sperm donation is prohibited during this period.
- The participant voluntarily agrees to participate in the study and signs the informed consent form.
Exclusion Criteria:
Participants meeting any of the following criteria will be excluded from the study:
1. Any of the following disease-related conditions:
- Histologically or cytologically confirmed tumor containing a small-cell lung cancer component, large-cell neuroendocrine carcinoma, sarcomatoid features, or a squamous cell carcinoma component greater than 10%;
- Known leptomeningeal metastases;
- Symptomatic brain parenchymal metastases. Participants with asymptomatic brain metastases may be enrolled if considered stable by the investigator.
- Uncontrolled pleural effusion or pericardial effusion, or ascites requiring repeated drainage once per month or more frequently;
- Spinal cord compression not treated with surgery and/or radiotherapy, or previously diagnosed spinal cord compression without clinical evidence of disease stability for at least 4 weeks before enrollment following treatment.
2. Receipt of any of the following treatments:
- Chemotherapy or other systemic antitumor therapy within 3 weeks or 5 half-lives before the first dose, whichever is shorter; small-molecule targeted therapy within 2 weeks before the first dose; or limited-field local radiotherapy, such as palliative radiotherapy for bone metastases, within 2 weeks before the first dose;
- Use of a strong CYP3A inhibitor or inducer within 14 days before the first dose of study treatment, or anticipated need for continued treatment with such medications during the study;
- Current treatment with medications known to prolong the QT interval or potentially cause torsades de pointes, or anticipated need for continued treatment with such medications during the study;
- Receipt of any investigational drug within 4 weeks or 5 half-lives before the first dose of study treatment, whichever is shorter;
- Concurrent enrollment in another clinical study, unless it is an observational, noninterventional study or the participant is in the follow-up phase of an interventional clinical study;
- Major surgery, such as craniotomy, thoracotomy, or laparotomy, within 4 weeks before the first dose of study treatment;
- Prior treatment with any EGFR tyrosine kinase inhibitor, any antibody-drug conjugate with a topoisomerase I inhibitor payload, or any antibody and/or antibody-drug conjugate targeting EGFR and/or HER3;
3. Toxicities from prior antitumor therapy that have not recovered to Grade 1 or lower according to CTCAE.
4. Known allergy or hypersensitivity to any study treatment or any of its excipients.
5. Any of the following cardiac findings:
1. Fridericia-corrected QT interval (QTcF) at rest of ≥450 milliseconds in male participants or ≥470 milliseconds in female participants, based on the mean of 3 QTcF measurements obtained during screening; 2. Clinically significant arrhythmia, including but not limited to complete left bundle branch block, third-degree atrioventricular block, second-degree atrioventricular block, or PR interval >250 milliseconds; 3. Risk factors for torsades de pointes, such as clinically significant hypokalemia as judged by the investigator, a family history of long QT syndrome, or a family history of arrhythmia, such as pre-excitation syndrome; 4. Left ventricular ejection fraction (LVEF) <50%. 6. Any condition that may affect the absorption, distribution, metabolism, or elimination of oral medication, including inability to swallow medication, frequent vomiting, persistent uncontrolled diarrhea, extensive gastrointestinal resection, Crohn's disease, or ulcerative colitis.
7. Confirmed or suspected interstitial lung disease, drug-induced pneumonitis, a history of idiopathic pneumonitis or idiopathic pulmonary fibrosis, or another moderate or severe pulmonary disease that substantially impairs lung function, except for Grade 1 or lower radiation pneumonitis.
8. Any severe or uncontrolled ocular disorder, particularly severe dry eye syndrome, keratoconjunctivitis sicca, severe exposure keratitis, or another condition that may increase the risk of epithelial injury, as judged by the physician; or an ocular abnormality requiring surgery or expected to require surgery during the study, except for cataracts not requiring urgent surgery.
9. Severe infection of CTCAE Grade 3 or higher within 4 weeks before the first dose of study treatmen.
10. A history of immunodeficiency, including a positive human immunodeficiency virus test, another acquired or congenital immunodeficiency disorder, a history of organ transplantation or allogeneic bone marrow transplantation, or autologous hematopoietic stem cell transplantation.
11. Active tuberculosis infection identified by medical history or computed tomography, a history of active tuberculosis infection within 1 year before enrollment, or a history of active tuberculosis infection more than 1 year before enrollment without adequate standard treatment.
12. Active hepatitis B, defined as hepatitis B surface antigen (HBsAg) positivity with hepatitis B e antibody (HBeAb) or hepatitis B core antibody (HBcAb) positivity and HBV DNA ≥1000 copies/mL or ≥200 IU/mL; or active hepatitis C, defined as hepatitis C virus antibody positivity with HCV RNA above the lower limit of detection of the assay.
13. Any other malignancy diagnosed within 5 years before the first dose that required treatment, except for malignancies with a low risk of metastasis and a 5-year survival rate greater than 90%, such as adequately treated basal cell or squamous cell carcinoma of the skin, carcinoma in situ of the cervix or breast, adequately treated localized prostate cancer, or adequately treated papillary thyroid carcinoma.
14. Female participants who are pregnant, breastfeeding, or planning to become pregnant during the study.
15. Uncontrolled concomitant disease, including but not limited to symptomatic congestive heart failure within 6 months before the first dose of study treatment, uncontrolled hypertension, unstable angina pectoris, uncontrolled arrhythmia.
16. Any other factor that, in the investigator's judgment, may cause the participant to discontinue the study prematurely, including a current or prior medical condition, including psychiatric illness, requiring concomitant treatment; a clinically significant laboratory abnormality; or family or social circumstances that may affect participant safety or the collection of study data.
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: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:注射用JS212 + JS111胶囊(AP-L1898)
JS212:JS212将在每个21天周期的第1天通过静脉输注给药。 JS111:每日一次(QD)160毫克 |
在每个21天周期的第1天通过静脉输注给药。
160 mg once daily (QD)
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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 |
|---|---|---|
|
安全性(不良事件)
大体时间:长达6年
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不良事件(AEs)的发生率和严重程度,以及异常的实验室或临床检查结果。
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长达6年
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ORR
大体时间:up to 3 years
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Objective response rate (ORR), assessed per RECIST v1.1
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up to 3 years
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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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无进展生存期
大体时间:最长6年
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由研究者评估的无进展生存期(PFS)(RECIST v1.1)
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最长6年
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缓解持续时间
大体时间:最长6年
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由BICR和研究者评估的缓解持续时间(DoR)
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最长6年
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DCR
大体时间:最长6年
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由BICR和研究者评估的疾病控制率(DCR)
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最长6年
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OS
大体时间:最多6年
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总生存期(OS)
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最多6年
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合作者和调查者
赞助
研究记录日期
研究主要日期
学习开始 (估计的)
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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