Phase I/IIa Clinical Trial of IMC001 in Patients With Advanced Epithelial Solid Tumors. (IMC001 EpCAM)
Phase I/IIa Clinical Trial Evaluating the Safety and Efficacy of IMC001 in Patients With Advanced Epithelial Solid Tumors.
研究概览
研究类型
注册 (估计的)
阶段
- 阶段2
- 阶段1
联系人和位置
学习地点
-
-
-
Beijing、中国
- Beijing Cancer Hospital
-
-
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:
- to provide a signed and dated informed consent form before conducting any research-related procedures , and willing and able to comply with all research procedures.
- Applicants must be 18 years of age or older and 75 years of age or younger; both male and female applicants are welcome .
- Subjects with histologically or cytologically confirmed locally advanced/metastatic epithelial solid tumors , including but not limited to subjects with advanced gastric cancer/gastroesophageal junction adenocarcinoma, triple-negative breast cancer, biliary tract tumors, ovarian cancer, colorectal cancer, pancreatic cancer, gastrointestinal and pancreatic neuroendocrine tumors, etc.
Disease progression or intolerance to standard systemic therapy , including:
- Gastric cancer and gastroesophageal junction adenocarcinoma that have failed or are intolerant of at least two lines of standard systemic therapy. If first-line three-drug combination therapy has failed or is intolerant, enrollment may be made after thorough investigator evaluation.
- Triple-negative breast cancer: Subjects with unresectable locally advanced or metastatic triple-negative breast cancer who have failed at least two lines of standard systemic therapy. All subjects must have previously received taxane therapy, regardless of the stage of disease at the time of treatment.
- Other subjects with epithelial solid tumors who have failed or are intolerant of standard treatment.
- Tumor tissue samples (primary or metastatic, archived or newly collected) from the expected subjects, tested by the central laboratory, are EpCAM histologically positive (defined as tumor cell positivity ≥10% and staining intensity ≥1+).
- The expected survival period of the subjects is ≥12 weeks .
- According to RECIST 1.1 criteria, there should be at least one stably measurable target lesion (where the largest lesion should be ≤4). In the 3×10⁵ CAR -T cells/kg dose group, subjects with evaluable lesions (unmeasurable lesions) can be admitted.
- ECOG performance status score 0-1 .
The subject has adequate organ and bone marrow function. Laboratory screening must meet the following criteria: all laboratory test results should be within the stable ranges outlined below, and there should be no ongoing supportive treatment. If any laboratory test result is abnormal according to the following criteria, a repeat test may be performed within one week. If the test results still do not meet the following criteria, the subject's screening has failed.
- Blood tests [No intensive blood transfusions (≥2 times within 1 week), platelet transfusions, or cell growth factor injections (excluding recombinant erythropoietin)) within 7 days prior to the test]: Neutrophil count (ANC) ≥1.5×10⁹ / L; Platelet count (PLT) ≥100 × 10⁹ / L; Hemoglobin content (Hb) ≥9.0g / dL; Lymphocyte count ( ALC ) ≥0.5× 10⁹ /L ;
- Liver function: alanine aminotransferase (ALT) ≤ 2.5 × ULN, aspartate aminotransferase (AST) ≤ 2.5 × ULN, serum total bilirubin (TB) ≤ 2 × ULN; for subjects with liver metastases, AST and ALT < 5 × ULN ;
- Kidney function: Serum creatinine ≤1.5×ULN; if serum creatinine >1.5×ULN, creatinine clearance rate >50mL/min is required (according to the Cockcroft-Gault formula); qualitative urine protein ≤1+; if qualitative urine protein ≥2+, a 24-hour urine protein quantification test is required (if the 24-hour urine protein quantification test is <1g, it is acceptable).
- Amylase and lipase ≤1.5×ULN; alkaline phosphatase (ALP) ≤2.5×ULN, and for subjects with bone metastases, ALP <5×ULN ;
- Coagulation function: Activated partial thromboplastin time ≤ 1.5 ULN, prothrombin time ≤ 1.5 × ULN ;
- All toxicities resulting from prior antitumor therapy were reduced to grade 0-1 (according to NCI CTCAE version 5.0) or to a level acceptable to the inclusion criteria. Other toxicities, such as alopecia and vitiligo, which the investigators deemed not to pose a safety risk to the subjects, were excluded .
Reproductive status: Female subjects of reproductive age or male subjects whose sexual partners are women of reproductive age, who are willing to use medically approved and highly effective contraceptive methods, such as intrauterine devices or condoms, from the time they sign the informed consent form until 12 months after cell infusion (women of reproductive age include premenopausal women and women within 24 months after menopause) .
Exclusion Criteria:
- Pregnant and breastfeeding women .
- Positive for human immunodeficiency virus (HIV) antibodies; hepatitis B virus infection ( if the subject is positive for hepatitis B surface antigen, regardless of whether the core antibody is negative or positive, they can also be enrolled if the viral DNA load is negative, and prophylactic antiviral treatment should be considered ); acute or chronic active hepatitis C (positive for HCV antibodies); positive for syphilis antibodies; Epstein-Barr virus (EBV) infection ( positive for IgM or known EBV infection ); cytomegalovirus (CMV) infection (positive for IgM); positive for human T-lymphotropic virus (HTLV). The results of the above pathogen tests are subject to the results of the central laboratory .
- Severe infections that are in an active phase or poorly controlled clinically .
- The patients had uncontrollable pleural effusion, pericardial effusion, and ascites before enrollment .
- Extensive or diffuse lung metastases , extensive or diffuse liver metastases , extensive or diffuse bone metastases .
- Subjects with intestinal obstruction or obstructive jaundice who are deemed unsuitable for participation in this trial by the researchers .
- Blood oxygen saturation ≤95% without oxygen supplementation .
- Patients with other serious lung diseases that may limit their participation in this study, such as pulmonary embolism, chronic obstructive pulmonary disease, symptomatic or poorly controlled interstitial lung disease, or clinically significant abnormalities in pulmonary function tests .
- Subjects with a known history or current hepatic encephalopathy requiring treatment; subjects with a current or history of central nervous system disorders, such as seizures, cerebral ischemia/hemorrhagic disease, dementia, cerebellar disease, or any autoimmune disease involving the central nervous system .
- Central nervous system metastasis or meningeal metastasis .
- Currently, patients have unstable heart disease requiring treatment or heart disease that cannot be controlled by treatment, or hypertension that is poorly controlled according to investigators (defined as systolic blood pressure ≥160 mmHg and/or diastolic blood pressure >100 mmHg after standard antihypertensive drug treatment); or diabetes that is poorly controlled despite standard treatment (fasting blood glucose ≥10.2 mmol/L) .
If any of the following cardiac clinical symptoms or conditions exist within 6 months prior to cell infusion:
- Left ventricular ejection fraction (LVEF) < 50%;
- History of myocardial infarction within the past year; or unstable angina; or percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG); or use of a pacemaker;
- Resting electrocardiogram examination: QTc F > 450ms (male) or QTc F > 470ms (female);
- An electrocardiogram at rest reveals clinically significant abnormalities (such as abnormalities in heart rate, conduction, or morphological characteristics) or complete left bundle branch block or third-degree atrioventricular block or a PR interval >250 ms.
Evidence of a significant coagulation disorder or other obvious risk of bleeding, including:
- Abnormal coagulation function that is clinically significant;
- History of intracranial hemorrhage or spinal cord hemorrhage;
- Patients with tumor lesions invading major blood vessels and posing a significant risk of bleeding;
- Subjects who currently have unstable or active ulcers or active gastrointestinal bleeding;
- An embolic event occurred within 6 months prior to cell reinfusion;
- Within one month prior to cell reinfusion, there has been clinically significant hemoptysis or obvious bleeding from tumor lesions;
- Had a major trauma or major surgery within one month prior to enrollment;
- The presence of any bleeding disorder, such as hemophilia, von Willebrand disease, etc.;
- The patient has received anticoagulation therapy (excluding low molecular weight heparin) for therapeutic purposes within 2 weeks prior to cell reinfusion.
- Subjects are receiving routine anticoagulation therapy (such as warfarin or heparin). Subjects require long-term antiplatelet therapy (aspirin >300 mg/day; clopidogrel >75 mg/day); dipyridamole, ticlopidine, or cilostazol, etc.
- The patient has received systemic steroids equivalent to >15 mg/day of prednisone for more than 3 days within 2 weeks prior to apheresis, excluding inhaled steroids .
- Subjects requiring systemic therapy with corticosteroids or other immunosuppressive drugs during treatment. Subjects with any active autoimmune disease, or a history of autoimmune disease with anticipated relapse (including but not limited to: systemic lupus erythematosus, rheumatoid arthritis, psoriasis, multiple sclerosis, inflammatory bowel disease, and asthma requiring medical intervention with bronchodilators). Exceptions include: type 1 diabetes; skin diseases not requiring systemic treatment (e.g., vitiligo, psoriasis); alopecia; hypothyroidism requiring only hormone replacement therapy; asthma that was completely remitted in childhood and requires no intervention in adulthood; or other conditions not expected to relapse in the absence of external triggers .
Subjects with a prior or concurrent history of other malignant tumors, except in the following circumstances:
- Basal cell or squamous cell carcinoma that has undergone adequate treatment (sufficient wound healing is required before enrollment in the study).
- Cervical cancer or breast cancer in situ, cured and with no signs of recurrence for at least 3 years prior to the study;
- The primary malignant tumor has been completely removed and has been in complete remission for ≥5 years ; d ) The concurrent malignant tumor was an epithelial tumor that expressed EpCAM .
- Subjects who have previously received other gene therapies, including but not limited to CAR-T therapy and TCR-T therapy .
- The following treatments or medications were received before cell reinfusion: chemotherapy, targeted therapy, biotherapy, endocrine therapy, immunotherapy, or other anti-tumor treatments (excluding treatments that meet the protocol requirements before reinfusion, such as lymph node pretreatment and bridging therapy); less than 28 days or less than 5 half-lives since the first infusion treatment in this study (whichever is shorter); or traditional Chinese medicine treatment with anti-tumor indications received within 2 weeks before cell reinfusion .
- of severe allergies, such as anaphylactic shock .
- Subjects with severe mental disorders .
- Subjects who develop new cardiac arrhythmias, including but not limited to arrhythmias that cannot be controlled by medication; hypotension requiring vasopressors; or bacterial, fungal, or viral infections requiring intravenous antibiotics. Subjects receiving antibiotics to prevent infection may continue to participate in the trial at the investigator's discretion .
- The patient had participated in other interventional clinical studies and used investigational drugs within one month prior to the planned infusion of IMC001 .
- Subjects who received a live attenuated vaccine within 4 weeks prior to the planned single-donor administration or who are scheduled to receive a live attenuated vaccine during the study.
- Subjects with any other concurrent serious and /or uncontrolled medical conditions that the investigators deem unsuitable for participation in this trial.
Researchers assessed that participants were unable or unwilling to comply with the requirements of the research protocol .
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 |
|---|---|
|
实验性的:Each subject will be infused once with autologous CAR-T cell injection targeting EpCAM
|
In the Phase I dose-escalation phase of this study, approximately 7-15 subjects with advanced epithelial solid tumors will be recruited to evaluate the safety and tolerability of autologous IMC001 treatment.
DLT (digestive-thickness assessment) will be performed on subjects in each cohort within 28 days after IMC001 infusion; the definition of DLT is detailed below.
The expansion phase will select at least two dose groups, each recruiting 5-10 subjects (in conjunction with the escalation phase, expanding each dose group to approximately 10 subjects), to determine the recommended RP2D dose for progression to Phase IIa.
|
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 |
|---|---|---|
|
Observe dose limiting toxicity (DLTs) of IMC001 within 28 days after administration according to the DLT definition in the protocol
大体时间:Within 28 days after administration of IMC001
|
White blood cells (10 ^ 9/L), red blood cells (10 ^ 12/L), platelet count (10 ^ 9/L), hemoglobin (g/L), treatment-related lymphohistiocytosis (HLH)/hemophagocytic lymphohistiocytosis (HPS), cytokine release syndrome (CRS), immune cell therapy related neurotoxicity syndrome (ICANS)
|
Within 28 days after administration of IMC001
|
|
After treatment with IMC001, the recommended Phase II dose (RP2D) is determined based on dose limiting toxicity (DLT) and clinical response, including potential side effects
大体时间:Complete the incremental and expansion phases for all dose groups, and have the Safety Monitoring Committee (SMC) further evaluate safety and initial efficacy, and determine the recommended dose for entering Phase IIa (RP2D).
|
According to the results of the Safety Monitoring Committee (SMC) meeting, 2-3 dose levels will be selected for expansion, with an additional 5 to 10 subjects (excluding dose escalation subjects) to further evaluate safety and initial efficacy, and determine the recommended dose for entering Phase IIa (RP2D).
|
Complete the incremental and expansion phases for all dose groups, and have the Safety Monitoring Committee (SMC) further evaluate safety and initial efficacy, and determine the recommended dose for entering Phase IIa (RP2D).
|
|
Evaluate the objective response rate (ORR) of tumors based on RECIST 1.1
大体时间:According to the study protocol, periodic imaging assessments will be conducted at scheduled visits until the confirmed PD, 2 years (96 weeks) after infusion, loss to follow-up, withdrawal of informed consent, or death (whichever occurs first)
|
According to RECIST 1.1, the number of people who have achieved complete remission (CR) and partial remission (PR) is evaluated
|
According to the study protocol, periodic imaging assessments will be conducted at scheduled visits until the confirmed PD, 2 years (96 weeks) after infusion, loss to follow-up, withdrawal of informed consent, or death (whichever occurs first)
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Pharmacokinetic evaluation (regarding Cmax)
大体时间:From IMC001 infusion until 96 weeks.
|
Maximum concentration of CAR-T cells in peripheral blood after administration (CAR+cells/μL blood)
|
From IMC001 infusion until 96 weeks.
|
|
Pharmacokinetic evaluation (regarding Tmax)
大体时间:From IMC001 infusion until 96 weeks.
|
Time to reach maximum concentration (Days)
|
From IMC001 infusion until 96 weeks.
|
|
Pharmacokinetic evaluation (approximately AUC0-28d)
大体时间:From IMC001 infusion to 28 days after infusion
|
The area under the CAR-T concentration time curve within 28 days after IMC001 infusion
|
From IMC001 infusion to 28 days after infusion
|
|
Pharmacodynamic evaluation
大体时间:Collect data from IMC001 infusion (day -1, day 0, day 1, day 3, day 7, day 9, day 14, day 21, day 28) until disease progression or peak monitoring occurs, if CAR copy number, death, or other cause is not detected for two consecutive episodes (whichever o
|
The concentration levels of CAR-T related serum cytokines such as CRP, IL-6, and INF - γ at each time point
|
Collect data from IMC001 infusion (day -1, day 0, day 1, day 3, day 7, day 9, day 14, day 21, day 28) until disease progression or peak monitoring occurs, if CAR copy number, death, or other cause is not detected for two consecutive episodes (whichever o
|
其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Replicative lentivirus (RCL)
大体时间:Baseline, 16 weeks, 48 weeks, until subject loss to follow-up, death, withdrawal of informed consent, cell transfusion for 2 years (96 weeks) or termination of the trial (whichever occurs first), with a maximum monitoring period of 15 years.
|
Detecting the presence of replication type lentivirus (RCL) in peripheral blood
|
Baseline, 16 weeks, 48 weeks, until subject loss to follow-up, death, withdrawal of informed consent, cell transfusion for 2 years (96 weeks) or termination of the trial (whichever occurs first), with a maximum monitoring period of 15 years.
|
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
与本研究相关的术语
其他研究编号
- IMC001-RT02
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
在美国制造并从美国出口的产品
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.