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RECRUITINGPhase 1INTERVENTIONAL

Study of High Efficient Killing Cell Therapy for Advanced NSCLC

Phase I Study of High Efficient Killing Cell Therapy for Advanced Non Small Cell Lung Cancer

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The purpose of this study to preliminarily evaluate the safety and efficacy of High Efficient Killing Cell Therapy for refractory and advanced non-small cell lung cancer

Who May Be Eligible (Plain English)

Who May Qualify: - Male or female patients' age from 18 years to 70 years. - Patients who have a expected to live at least 3 months. - pathologically confirmed non-small cell lung cancer. - failed in previous standard chemotherapy and targeted therapy. - Karnofsky performance status 0-1. - your organs (liver, kidneys, etc.) are working well enough based on blood testss. Who Should NOT Join This Trial: - Pregnant and lactating women. - Patients with T cell lymphoma, syphilis, AIDS or combination - Patients with highly allergic or have a history of severe allergies - Patients with severe hepatic or renal dysfunction - Patients with severe autoimmune conditions (where your immune system attacks your own body) or who is being treated with immunosuppressive agents - Patients with severe infection not controlled or High fever - Patients with organ transplantation or waiting for organ transplantation. - Patients with brain metastasis - Patients with severe coagulopathy (e.g. hemophilia) - Patients without adequate ability to understand, sign willing to sign a consent forms and take part in the clinical research voluntarily. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Male or female patients' age from 18 years to 70 years. * Patients who have a life expectancy of at least 3 months. * pathologically confirmed non-small cell lung cancer. * failed in previous standard chemotherapy and targeted therapy. * Karnofsky performance status 0-1. * adequate organ functions. Exclusion Criteria: * Pregnant and lactating women. * Patients with T cell lymphoma, syphilis, AIDS or combination * Patients with highly allergic or have a history of severe allergies * Patients with severe hepatic or renal dysfunction * Patients with severe autoimmune disease or who is being treated with immunosuppressive agents * Patients with severe infection not controlled or High fever * Patients with organ transplantation or waiting for organ transplantation. * Patients with brain metastasis * Patients with severe coagulopathy (e.g. hemophilia) * Patients without adequate ability to understand, sign informed consents and take part in the clinical research voluntarily.

Treatments Being Tested

BIOLOGICAL

HEKT cell

3 cycles of HEKT cell treatment

Locations (1)

Ruijin Hospital
Shanghai, China