Trials / Unknown
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
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Transcatheter 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 |
| BIOLOGICAL | DC-CIK | 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 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.