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A Clinical Trial on Hepatitis B Vaccine Activated-Dendritic Cells Combined With Anti-HBV Drugs in CHB (CTHBVACADCHB)

Sun Yat-sen University logo

Sun Yat-sen University

Status and phase

Unknown
Phase 2
Phase 1

Conditions

Chronic Hepatitis B

Treatments

Drug: Entecavir
Drug: HPDC-T cells & Telbivudine
Drug: IFN-a-2a
Drug: Telbivudine
Biological: HPDC-T cells & Entecavir
Drug: HPDC-T cells & IFN-a-2a

Study type

Interventional

Funder types

Other

Identifiers

NCT02615639
SunYatSenIDD

Details and patient eligibility

About

The anti-virus effects is not satisfying in some of Chronic Hepatitis B(CHB) patients who have been on anti-Hepatitis B Virus (HBV) drugs therapy. Dendritic cell (DC) is critical in Hepatitis B Virus (HBV) specific immunity in the process of producing HBV promoter specific cytotoxic T cells (CTLs) and specific T helper cells (HTLs), however they are defective in CHB patients. Therefore, if it were going to remove HBV completely, it mainly depends if the body itself can produce enough HBV specific cytotoxic T cells (CTLs) and specific T helper cells (HTLs). Our research is to plus Hepatitis B Vaccine Activated-DCs therapy to CHB patients who have been on anti-HBV drugs but with poor effects, supposing to significantly improve anti-HBV efficacy, even to clean HBV from the patients.

Full description

Patients who have been on anti-HBV therapy Complying with the inclusion criteria will be enrolled into our research, Nucleoside analogues (NAs,entecavir) treatment for more than 1 year or interferon(IFN)-a-2a (IFN-a-2a,Pegasys) treatment for more than 24 weeks. The patients will be randomly assigned to experimental group and control group with the ratio of 2:1, one group (control group) will go on receive the anti-HBV drugs treatment solely; another group (experimental group) after enrollment will immediately receive the Hepatitis B Vaccine activated-DCs (HPDC-T cells) for 24 weeks (every 2 weeks once for 24 weeks, 12 times in total), at the same time co-use anti-HBV drugs treatment, as for Pegasys, it will go on to be used for 12 weeks after HPDC-T cells treatment completed.

The technical route of HBV-T cells prepared: First, investigators collect fresh blood of CHB, mononuclear cells were isolated, and induced to HBsAg pulsed DCs in Hepatitis B vaccine (Shenzhen kangtai, Shenzhen, China) and interleukin-4(IL-4)/granulocyte-macrophage colony-stimulating factor(GM-CSF) (Perprotech, New Jersey, USA) (7 days), then co-culture of DCs and Peripheral Blood Mononuclear Cell(PBMCs )7days, obtain HBV specific T cells, return to the patient finally.

Enrollment

450 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • chronic hepatitis B patients, aged 18~65,Chinese
  • have been on entecavir(ETV) or telbivudine(LDT) treatment for more than 1 year,and HBV DNA<100 IU/ml(Roche Cobas);or have been on
  • have been on PEG-IFN treatment for more than 24 weeks,and 20 < HBV DNA < 20000 IU/ml(Roche Cobas).
  • HBsAg 100~5000 IU/ml
  • HBeAg 10~500 COI

Exclusion criteria

  • Superinfection or co-infection with hepatitis A, C, D, E, cytomegalovirus and HIV, or Epstein-Barr virus;
  • other liver diseases such as alcoholic liver disease, drug-induced hepatitis, Wilson disease and autoimmune hepatitis;
  • ascites or gastrointestinal bleeding or peptic ulcer or esophageal varix by electronic gastroscope examination;
  • liver cirrhosis (including compensated and decompensated cirrhosis) and liver failure;
  • severe bacterial or fungal infections;
  • a history of diabetes or cardiac disease or hypertension or nephrosis;
  • pregnant women.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

450 participants in 6 patient groups

HPDC-T cells & entecavir
Experimental group
Description:
HPDC-T cells 1-5×10\^5 intravenous injection, every 2 weeks for 24 weeks , and entecavir(ETV) 0.5mg tablet by mouth, every night.
Treatment:
Biological: HPDC-T cells & Entecavir
entecavir
Active Comparator group
Description:
entecavir 0.5mg tablet by mouth, every night.
Treatment:
Drug: Entecavir
HPDC-T cells & IFN-a-2a
Experimental group
Description:
HPDC-T cells 1-5×10\^5 intravenous injection, every 2 weeks for 24 weeks ,and IFN-a-2a 180ug subcutaneous injection, every week for 9 months.
Treatment:
Drug: HPDC-T cells & IFN-a-2a
IFN-a-2a
Active Comparator group
Description:
IFN-a-2a 180ug subcutaneous injection, every week for 9 months.
Treatment:
Drug: IFN-a-2a
HPDC-T cells & Telbivudine
Experimental group
Description:
HPDC-T cells 1-5×10\^5 intravenous injection, every 2 weeks for 24 weeks ,and Telbivudine 600mg tablet by mouth, every night.
Treatment:
Drug: HPDC-T cells & Telbivudine
Telbivudine
Active Comparator group
Description:
Telbivudine 600mg tablet by mouth, every night.
Treatment:
Drug: Telbivudine

Trial contacts and locations

0

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Central trial contact

Yurong Gu, MD.; Yuehua Huang, MD.&PHD.

Data sourced from clinicaltrials.gov

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