A Phase I/II Study of FG-M108 Plus FG-B901 in Advanced CLDN18.2-Positive Solid Tumors
2026年7月10日 更新者:FutureGen Biopharmaceutical (Beijing) Co., Ltd
An Open-Label, Multicenter Phase I/II Clinical Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Efficacy of FG-M108 Injection in Combination With FG-B901 Injection in Patients With Unresectable Locally Advanced or Metastatic Solid Tumors
This open-label, multicenter Phase I/II trial evaluates the combination of FG-M108 and FG-B901 in patients with unresectable locally advanced or metastatic solid tumors that are positive for Claudin 18.2 and have progressed on, are intolerant to, or lack standard therapy.
The Phase I dose-escalation part (using a BF-BOIN design) assesses safety, tolerability, and pharmacokinetics, and determines the recommended Phase II dose (RP2D) of FG-B901 when given with fixed-dose FG-M108.
The Phase IIa expansion cohorts, grouped by tumor type, further evaluate safety and preliminary efficacy, with antitumor activity measured by RECIST 1.1 and iRECIST, while also exploring biomarker correlates.
Key eligibility requires CLDN18.2
positivity (≥10% tumor cells with ≥1+ membrane staining by IHC), ECOG performance status 0-1, and measurable disease.
Up to approximately 30 participants will be enrolled per cohort in Phase IIa.
The study aims to provide initial evidence on the combination's safety, tolerability, PK, immunogenicity, and clinical activity in this hard-to-treat population.
研究概览
研究类型
介入性
注册 (估计的)
120
阶段
- 阶段2
- 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。
学习联系方式
- 姓名:Zhaoyu Jin Yu
- 电话号码:+8610-60709130
- 邮箱:pr@futuregenbiopharm.com
学习地点
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Ha’erbin、中国
- Harbin Medical University Cancer Hospital
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接触:
- Yanqiao Zhang
- 电话号码:+8610-86298278
- 邮箱:yanqiaozhanggcp@163.com
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Shenyang、中国
- The First Hospital of China Medical University
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接触:
- Funan Liu
- 电话号码:+8610-83282066
- 邮箱:lfn540@126.com
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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, understand the study, are willing to comply with and have the ability to complete all trial procedures;
- Age 18-75 years (inclusive), any gender;
- Have histologically or cytologically confirmed locally advanced or metastatic solid tumors, and have failed standard therapy, or are intolerant to standard therapy, or for whom standard therapy is not available;
- CLDN18.2 positive (defined as ≥10% of tumor cells showing membrane staining ≥1+ by central laboratory IHC)
- ECOG 0-1
- Expected survival ≥3 months;
- Have at least one measurable tumor lesion according to RECIST 1.1 criteria;
- Adequate cardiac, bone marrow, liver, renal function;
Exclusion Criteria:
- Have received a live vaccine within 3 months prior to the first dose;
- Received radiotherapy within 4 weeks before the first dose
- Received Chinese herbal medicine with antitumor indications within 2 weeks before the first dose
- Previously received any therapy targeting CLDN18.2
- History of other malignancies within 3 years before the first dose
- Experienced Grade ≥3 immune-related adverse events (irAEs) from prior immunotherapy or discontinued immunotherapy due to irAEs, or have irAEs from prior immunotherapy that the investigator judges to still have clinical impact
- Toxicity from prior antitumor therapy has not recovered to NCI CTCAE v5.0 Grade 0-1
- History of severe allergic reactions, or hypersensitivity, or intolerance to any known component of the investigational products or other monoclonal antibodies
- Have brain or leptomeningeal metastases with symptoms
- Presence of clinically symptomatic body cavity effusions (pleural effusion, ascites, pericardial effusion, etc.) requiring local therapy or repeated drainage, or effusions that are poorly controlled per investigator judgment
- Uncontrolled or clinically significant cardiovascular and cerebrovascular diseases
- Clinically uncontrolled diseases such as diabetes, thyroid disorders (hormone replacement therapy does not affect enrollment), or other severe systemic diseases requiring systemic treatment
- Active or progressive infection requiring systemic treatment within 2 weeks before the first dose
- Known or suspected active autoimmune disease requiring systemic treatment
- Pregnant or breastfeeding female participants
- Known history of Hepatitis C or chronic active Hepatitis B
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: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:剂量扩展队列
一旦确定有效剂量,将开放1~2个扩展队列来评估所选剂量的有效性和安全性。
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Accelerated titration method, IV infusion Q3W; Adaptive BOIN design, IV infusion Q3W.
(21-day cycles)
1~2 dose levels of FG-B901 will be tested according to an accelerated titration method followed by a adaptive BOIN design
300 mg/m2, IV infusion Q3W (21-day cycles)
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实验性的:Dose Escalation Cohort
Experimental : Monotherapy Dose Escalation Cohort Eight dose levels of FG-B901 combined with fixed-dosed FG-M108 will be tested according to an accelerated titration method followed by a adaptive BOIN design.
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Accelerated titration method, IV infusion Q3W; Adaptive BOIN design, IV infusion Q3W.
(21-day cycles)
1~2 dose levels of FG-B901 will be tested according to an accelerated titration method followed by a adaptive BOIN design
300 mg/m2, IV infusion Q3W (21-day cycles)
|
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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客观缓解率 (ORR)
大体时间:最长24个月
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ORR定义为根据RECIST 1.1标准由研究者评估,获得完全缓解(CR)或部分缓解(PR)最佳总体疗效的参与者比例。
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最长24个月
|
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疾病控制率 (DCR)
大体时间:长达24个月
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DCR定义为根据研究者按照RECIST 1.1标准评估,获得最佳总体缓解为完全缓解(CR)、部分缓解(PR)或疾病稳定(SD)的参与者比例。
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长达24个月
|
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通过不良事件(AEs)评估安全性
大体时间:最长24个月
|
不良事件(AE)指临床研究期间发生的任何不良医学事件,无论是否与药品相关,包括体征、症状、异常实验室检测结果和疾病。
临床研究期间不良事件的发生率和严重程度会被记录和分析。
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最长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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总生存期(OS)
大体时间:最长24个月
|
OS定义为从随机分组到因任何原因死亡的时间。
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最长24个月
|
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无进展生存期(PFS)
大体时间:最长24个月
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无进展生存期(PFS)定义为从随机分组开始,至研究者评估根据RECIST 1.1标准首次影像学确认疾病进展或任何原因导致死亡的时间(以先发生者为准)。
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最长24个月
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缓解持续时间 (DOR)
大体时间:最长24个月
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缓解持续时间定义为从首次缓解(完全缓解/部分缓解)之日起至研究者根据RECIST 1.1标准评估的疾病进展日期或因任何原因导致死亡的日期(以先发生者为准)之间的时间。
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最长24个月
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Time to progression (TTP)
大体时间:Up to 24 months
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TTP
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Up to 24 months
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Maximum measured plasma concentration of FG-B901 and FG-M108
大体时间:Up to 24 months
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Cmax
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Up to 24 months
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Time to maximum plasma concentration of FG-B901 and FG-M108
大体时间:Up to 24 months
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Tmax
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Up to 24 months
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Half-life of FG-B901 and FG-M108
大体时间:Up to 24 months
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T1/2
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Up to 24 months
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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 (估计的)
2026年7月30日
初级完成 (估计的)
2028年8月31日
研究完成 (估计的)
2029年2月28日
研究注册日期
首次提交
2026年7月10日
首先提交符合 QC 标准的
2026年7月10日
首次发布 (实际的)
2026年7月15日
研究记录更新
最后更新发布 (实际的)
2026年7月15日
上次提交的符合 QC 标准的更新
2026年7月10日
最后验证
2026年7月1日
更多信息
与本研究相关的术语
其他研究编号
- FG-B901-02
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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.