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临床试验/NCT03329664
NCT03329664Unknown1 期

Safety and Efficacy of ex Vivo Activated and Expanded Autologous Cytokine-induced Killer Cells for Colon Cancer Patients

Sabz Biomedicals1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2020年2月9日最近更新:
适应症

试验速览

阶段
1 期
入组人数
20
试验地点
1
主要终点
Safety of administering CIK cells plus chemotherapy

研究概览

简要总结

This study aims to evaluate the safety and efficacy of activated and expanded autologous cytokine-killer cells in controlling disease recurrence in colon cancer patients with liver metastasis. 20 patients with confirmed stage IV colon carcinoma with metastasis will be assigned into two groups. Patients in both groups will receive the same therapeutic regimen as usual. Patients in one group additionally will be treated with a single infusion of autologous killer cells that had been previously prepared from peripheral blood.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Double (Participant, Care Provider)

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with histologically confirmed colorectal cancer at stage IV
  • ECOG performance status 0-2
  • Adequate cardiac/renal/hepatic function
  • Adequate bone marrow function (blood cell count)

排除标准

  • Patients that have received prior chemotherapy or immune cell therapy
  • Patients that have previously participated in another clinical trial
  • History of positive test result for HIV, HBV, HCV, HTLV-1, syphilis
  • Presence of Active infections
  • Patients with immunodeficiencies, autoimmunities, or severe allergies
  • Receiving immunosuppressive regimens

结局指标

主要结局

Safety of administering CIK cells plus chemotherapy

时间窗: one month post infusion

Patients will be continually assessed for unexpected adverse events or unexpected early mortality 30 days post infusion

Progression-free Survival (PFS)

时间窗: 2 years

The time from treatment initiation day to first documented progressive disease or death due to disease.

Time to progression (TTP)

时间窗: 2 years

the time from randomization until cancer progression, not including death.

次要结局

  • Overall survival (OS)(2 years)
  • Patient quality of life(each 3 months for 2 years)

研究者

申办方类型
Industry
责任方
Principal Investigator
主要研究者

Naser Ahmadbeigi

Doctor

Tehran University of Medical Sciences

研究点 (1)

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