KRAS G12D-specific Immune Effector Cells Targeting KRAS G12D-positive Solid Tumors
KRAS G12D-specific Engineered Immune Effectors (EIE) Targeting High-risk Tumors With KRAS G12D Mutation
The purpose of this study is to assess the feasibility, safety and efficacy of KRAS G12D-specific engineered immune effector (EIE) therapy in patients with advanced, KRAS G12D-positive malignancies. Another goal of the study is to characterize the function, expansion and persistence of KRAS G12D-specific effector cells in treated patients.
研究概览
详细说明
Important Regulatory Notice:
This trial record is only for global academic information registration on ClinicalTrials.gov. Neither the sponsor Beijing Meikang Jimian Biotechnology Co., Ltd. nor collaborator Shenzhen Geno-Immune Medical Institute has obtained NMPA clinical trial approval or clinical technology filing permission to carry out interventional cell therapy trials in mainland China.
ClinicalTrials.gov registration alone does not represent legal approval by Chinese health and drug regulatory authorities.
KRAS G12D mutation is one of the most frequent oncogenic drivers in human malignancies including pancreatic ductal adenocarcinoma, colorectal cancer, non-small cell lung cancer and other advanced solid tumors. Patients with metastatic KRAS G12D mutated tumors generally have poor prognosis; after failure of standard chemotherapy, targeted therapy and checkpoint immunotherapy, effective salvage treatment options remain very limited, and overall survival is unsatisfactory. Conventional chemotherapy and existing targeted agents cannot achieve durable tumor control for large proportions of these patients.
The somatic KRAS G12D neoantigen is tumor-specific, absent in normal human tissues, and critical for maintaining malignant phenotypes, which makes it an attractive target for adoptive cell immunotherapy. This trial investigates autologous KRAS G12D-specific EIE therapy. Peripheral blood mononuclear cells (PBMCs) will be collected via leukapheresis and stimulated with autologous dendritic cells primed with KRAS G12D-specific immunogenic peptides. Manufactured EIE products will be phenotypically profiled for CD8+, CD4+ and CD56+ lymphocyte subsets together with antigen specific reactivity. This phase 1/2 study aims to evaluate safety, manufacturing feasibility and preliminary anti-tumor efficacy of autologous KRAS G12D-specific EIEs in subjects with KRAS G12D-positive tumors.
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:Lung-Ji Chang, PhD
- 电话号码:+86 13671121909
- 邮箱:c@mkgimi.com
学习地点
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Guangdong
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Shenzhen、Guangdong、中国、518000
- Shenzhen Geno-immune Medical Institute
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接触:
- Lung-Ji Chang, PhD
- 电话号码:+86 13671121909
- 邮箱:c@mkgimi.com
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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:
- Abilities to understand and the willingness to provide written informed consent;
- ≥ 18 and ≤ 75 years old;
- Histologically confirmed recurrent, refractory or metastatic advanced malignancies with documented KRAS G12D somatic mutation and measurable lesions by RECIST v1.1; patients have progressed after at least one line of standard of care systemic therapy for their malignancy. At time of leukapheresis, patients are either off dexamethasone or receiving dexamethasone ≤ 4 mg/day;
- ECOG performance status 0-2 (or Karnofsky performance score ≥ 60);
- Life expectancy >3 months;
- Satisfactory bone marrow, liver and kidney functions as defined by the following: absolute neutrophile count ≥ 1500/mm^3; hemoglobin > 10 g/dL; platelets > 100000 /mm^3; Bilirubin < 1.5×ULN; alanine aminotransferase (ALT) or aspartate aminotransferase (AST) < 2.5×ULN; creatinine < 1.5×ULN;
- Peripheral blood absolute lymphocyte count must be above 0.8×10^9/L;
- Satisfactory heart functions;
- Must be willing to follow the instructions of doctors;
- Women of reproductive potential (between 15 and 49 years old) must have a negative pregnancy test within 7 days of study start. Male and female patients of reproductive potential must agree to use birth control during the study and 3 months post study.
Exclusion Criteria:
- Receipt of KRAS G12D based therapy within 8 weeks prior to study entry;
- HIV positive;
- Tuberculosis infection not under control;
- History of autoimmune disease, or other diseases requiring long-term administration of steroids or immunosuppressive therapies;
- History of allergic disease, or allergy to immune cells or study product;
- Patients already actively enrolled in other immune cell clinical study;
- Presence of untreated or actively progressing central nervous system metastases not locally controlled;
- Patients, in the opinion of investigators, may not be eligible or not able to comply with the study.
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:KRAS G12D-EIEs
Autologous KRAS G12D-specific engineered immune effectors (EIEs) |
1 to 2 infusions, once a week, for 1x10^5~1x10^7 EIEs/kg via intravenous injection each time |
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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Percentage of adverse effects after KRAS G12D-EIE injection
大体时间:up to one month
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To assess the safety of autologous KRAS G12D-EIEs in vivo. The percentage of patients who have adverse effects will be evaluated by using the NCI CTCAE V4.0 criteria. |
up to one month
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Rate of successful KRAS G12D-EIE generation
大体时间:up to one month
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The percentage of successful KRAS G12D-EIE generation, which are derived from subjects and pass the safety test after standard culture procedures, viable for at least one preparation, will be evaluated. |
up to one month
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Ability of KRAS G12D-EIE cells to induce cancer-specific reactions
大体时间:: after 1 month from KRAS G12D-EIE cell infusion until 24 months after infusion
|
ELISPOT measurement of target-specific T cells in blood sample |
: after 1 month from KRAS G12D-EIE cell infusion until 24 months after infusion
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Ability of KRAS G12D-EIE cells inducing tumor reduction
大体时间:after 1 month from KRAS G12D-EIE cell infusion until 24 months after infusion
|
Objective response (complete response (CR) + partial response (PR)) will be assessed by the Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 criteria. CR is disappearance of all target lesions. Any pathological lesions (whether target or non-target) must have reduction in short axis to <10 mm. Partial response is at least a 30% decrease in the sum of the diameters of target lesions, taking as reference the baseline sum diameters. |
after 1 month from KRAS G12D-EIE cell infusion until 24 months after infusion
|
合作者和调查者
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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