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UnknownNCT02487017

DC-CIK Combined With TACE in the Treatment of Hepatocellular Carcinoma

Phase 2 Study of DC-CIK Cells Combined With TACE in the Treatment of Hepatocellular Carcinoma

Status
Unknown
Phase
Phase 2
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Shenzhen Hornetcorn Bio-technology Company, LTD · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

Evaluation of DC-CIK cells combined TACE treatment for HCC

Detailed description

60 patients with Hepatocellular Carcinoma, who had received Transcatheter Arterial Chemoembolization (TACE) , will be randomly divided into group A (receive DC-CIK+ TACE treatment) or group B (just receive TACE), and the randomize ratio will be 1:1.

Conditions

Interventions

TypeNameDescription
PROCEDURETranscatheter Arterial Chemoembolization (TACE)Transcatheter Arterial Chemoembolization (TACE): 5-FU 400mg/m2 Hepatic arterial infusion ,lipiodol amount is usually 20 ml,the perfusion time should not be less than 20 min
BIOLOGICALDC-CIKTranscatheter Arterial Chemoembolization (TACE): 5-FU 400mg/m2 Hepatic arterial infusion ,lipiodol amount is usually 20 ml, the perfusion time should not be less than 20 min DC-CIK: 8×10\^9 DC-CIK cells for each infusion, IV (in the vein) for each infusion at least 3 cycles, each cycle received four infusions on day 14, 16, 30 and 32

Timeline

Start date
2015-05-01
Primary completion
2018-12-01
Completion
2018-12-01
First posted
2015-07-01
Last updated
2016-05-24

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT02487017. Inclusion in this directory is not an endorsement.