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临床试验/KCT0009102
KCT0009102尚未招募Unknown

A single-center clinical study to evaluate the safety and efficacy of autologous bone marrow-derived DCs(CellgramDC-WT1) and immune checkpoint inhibitors in patients with metastatic pancreatic cancer who have failed first-line or more standard chemotherapy

Soon Chun Hyang University Hospital Seoul0 个研究点目标入组 10 人开始时间: 待定最近更新:

试验速览

阶段
Unknown
状态
尚未招募
发起方
入组人数
10

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
19(Year) 至 79(Year)(—)
性别
All

入选标准

  • (1) 19 or older and under 80
  • (2) Patients diagnosed histologically with pancreatic cancer, recurrent, metastatic
  • (3) Patients confirmed to have progressed the disease in accordance with RECIST v1.1 after standard chemotherapy of primary or higher
  • (4) Patients who meet full-body performance status ECOG 0-2
  • (5) Patients with at least one measurable lesion according to RECIST v1.1
  • (6) Patients who have not received surgery, radiotherapy, or immunotherapy within the past 4 weeks and have recovered from side effects (However, tissue collection procedures that do not affect the condition of the subject are allowed at the discretion of the researcher)
  • (7) Patients who agreed to use medically recognized contraception during the clinical study participation period
  • (8) Patients who can conduct clinical research in accordance with the clinical research plan
  • (9) Patients who have agreed in writing to participate in this clinical study voluntarily

排除标准

  • (1) Patients with malignant tumors other than non-melanoma skin cancer in the last 3 years
  • (2) Patients who have previously received anti-tumor immunotherapy (such as anti-PD1, anti-PDL-1 or CTLA4 inhibitor) or participated in clinical studies related to immunotherapy or cell therapy
  • (3) Patients with active autoimmune diseases requiring systemic immunosuppression therapy
  • (4) a patient with a history of organ or hematopoietic stem cell transplantation
  • (5) Patients with acute or chronic infections requiring systemic treatment
  • (6) a patient known to be positive for human immunodeficiency virus (HIV) infection/serum
  • (7) Patients with active hepatitis A, B or C
  • (8) an untreated syphilis patient
  • (9) Patients who received a live virus vaccine (e.g. measles, mumps, rubella, chickenpox, yellow fever, rabies, BCG, oral typhoid vaccine, Flu-Mist, etc.) within 30 days
  • (10) Pregnant or breastfeeding patient
  • (11) In addition, if the Tester deems that he/she is not suitable for clinical research

研究者

发起方
Soon Chun Hyang University Hospital Seoul

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