Trial | NCT03515252  Report issue

Title

Study of Autologous Immune Killer Cells in Patients With Late Stage Hepatocellular Carcinoma or Lung Cancer
A Phase I Study to Evaluate the Safety and Efficacy of Autologous Immune Killer Cells in Patients With Late Stage Hepatocellular Carcinoma or Lung Cancer

  • Phase

    Phase 1

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Study Participants

    20
This is a phase I clinical study. Blood is drawn from the patient and brought to our laboratory for isolation of immune cells. These immune cells are then proliferated over a two week period and used to produce our patented product IKC (Immune Killer Cells). The IKC will then infused back into the patient to treat the cancer. Each patient will receive a total of six infusions.
This is a phase I clinical study. Blood is drawn from the patient and brought to our laboratory for isolation of immune cells. These immune cells are then proliferated over a two week period and used to produce the patented product IKC (Immune Killer Cells). The IKC will then infused back into the patient to treat the cancer. Each patient will receive a total of six infusions.

For each indication (cancer of the lung or liver) 10 patients are anticipated to be recruited, making a total of 20 subjects. All subjects will receive treatment as this is a single-arm study.
Study Started
Apr 26
2005
Primary Completion
Nov 02
2006
Study Completion
Jun 07
2007
Last Update
May 09
2018

Late stage lung cancer and liver cancer Experimental

Immune Killer Cells (IKC)

Criteria 

Inclusion Criteria:

subjects had voluntarily given written informed consent
subjects had CT scan on lung or liver tumors within the past 4 weeks of the screening visit
subjects who were histologically or pathologically confirmed with locally advanced or metastatic lung cancer or HCC
subjects who did not have valid therapy, ever failed with other therapy, or refused or were not appropriate for other therapies for lung cancer or HCC
subjects' ECOG performance status ≤ 2
subjects with life expectancy ≥ 3 months

Exclusion Criteria:

subjects with medical history of gout
subjects who had participated other clinical trials within 4 weeks before the screening visit
subjects with positive result of HIV or HTLV test within 4 weeks before the screening visit
subjects with clinically significant diseases other than cancer
subjects with myocardial infraction, stroke, or congestive heart failure within 3 months before the screening visit
female subjects who were pregnant or lactating or women of child-bearing potential but unable to take adequate contraception
subjects with history of alcohol, drug or other substance abuse
subjects with disease of bacteremia
No Results Posted