Lowering Viral Load With Nucleos(T)Ide Analogues Prior to Peginterferon Alfa-2b Treatment to Increase Sustained Response in HBeAg-positive Chronic Hepatitis B (PEGON)
This study is currently recruiting participants.
Verified January 2013 by Foundation for Liver Research
Sponsor:
Foundation for Liver Research
Information provided by (Responsible Party):
Foundation for Liver Research
ClinicalTrials.gov Identifier:
NCT01532843
First received: February 10, 2012
Last updated: January 3, 2013
Last verified: January 2013
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Purpose
Treatment with a nucleoside analogue and subsequent viral decline has shown to partially restore immune hyporesponsiveness in chronic hepatitis B patients. Recent pilot studies investigating whether the effect of lowering viral load with nucleoside analogue therapy prior to the initiation of peginterferon results in higher sustained off-treatment responses showed contradictory findings.
The aim of this study is to investigate sustained off-treatment response to peginterferon alfa-2b in chronic HBeAg-positive hepatitis B patients who are pretreated with nucleos(t)ide analogues, thereby lowering viral load
| Condition | Intervention | Phase |
|---|---|---|
|
Chronic Hepatitis B |
Drug: peginterferon alpha-2b |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Lowering Viral Load With Nucleos(T)Ide Analogues Prior to Peginterferon Alfa-2b Treatment to Increase Sustained Response in HBeAg-positive Chronic Hepatitis B (PEGON-study) |
Resource links provided by NLM:
Drug Information available for:
Peginterferon Alfa-2b
Recombinant Hepatitis B vaccine
Hepatitis A Vaccines
U.S. FDA Resources
Further study details as provided by Foundation for Liver Research:
Primary Outcome Measures:
- Sustained response [ Time Frame: at week 72 ] [ Designated as safety issue: No ]Sustained response to therapy, defined as the combined presence of HBeAg seroconversion and HBV DNA < 200 IU/mL
| Estimated Enrollment: | 80 |
| Study Start Date: | June 2012 |
| Estimated Study Completion Date: | December 2014 |
| Estimated Primary Completion Date: | September 2014 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Active Comparator: peginterferon alpha-2b & nucleos(t)ide analogue
peginterferon alfa-2b 1.5 μg/kg per week s.c. for 48 weeks
|
Drug: peginterferon alpha-2b
peginterferon alpha-2b 1.5 μg/kg per week s.c.for 48 weeks
Other Name: Pegintron
|
|
No Intervention: Nucleos(t)ide analogue
Continuation of Nucleos(t)ide analogue mono-therapy
|
Eligibility| Ages Eligible for Study: | 18 Years to 70 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Chronic hepatitis B (HBsAg positive > 6 months)
- HBeAg positive, anti-HBe negative within 4 weeks prior to initiation of peginterferon alfa-2b
- HBV DNA < 2000 IU/ml within one month prior to initiation of peginterferon alfa-2b after a minimum of 12 months treatment with either Entecavir (one of all 3 brands) or Tenofovir
- ALT < 5x ULN
- Compensated liver disease
- Age ≥ 18 years and ≤ 70 years
- Written informed consent
Exclusion Criteria:
- Treatment with any investigational drug within 30 days of entry to this protocol
- Treatment with Telbivudine
- Severe hepatitis activity as documented by ALT > 5 x ULN
- History of decompensated cirrhosis (defined as jaundice in the presence of cirrhosis, ascites, bleeding gastric or esophageal varices or encephalopathy)
- Pre-existent neutropenia (neutrophils < 1,500/mm3) or thrombocytopenia (platelets < 90,000/mm3)
- Co-infection with hepatitis C virus or human immunodeficiency virus (HIV)
- Other acquired or inherited causes of liver disease: alcoholic liver disease, obesity induced liver disease, drug related liver disease, auto-immune hepatitis, hemochromatosis, Wilson's disease or alpha-1 antitrypsin deficiency
- Alpha fetoprotein > 50 ng/ml
- Hyper- or hypothyroidism (subjects requiring medication to maintain TSH levels in the normal range are eligible if all other inclusion/exclusion criteria are met)
- Immune suppressive treatment within the previous 6 months
- Contra-indications for alfa-interferon therapy like suspected hypersensitivity to interferon or Peginterferon or any known pre-existing medical condition that could interfere with the patient's participation in and completion of the study.
- Pregnancy, breast-feeding
- Other significant medical illness that might interfere with this study: significant pulmonary dysfunction in the previous 6 months, malignancy other than skin basocellular carcinoma in previous 5 years, immunodeficiency syndromes (e.g. HIV positivity, auto-immune diseases, organ transplants other than cornea and hair transplant)
- Any medical condition requiring, or likely to require chronic systemic administration of steroids, during the course of the study
- Substance abuse, such as alcohol (> 80 g/day), I.V. drugs and inhaled drugs in the past 2 years.
- Any other condition which in the opinion of the investigator would make the patient unsuitable for enrollment, or could interfere with the patient participating in and completing the study
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01532843
Contacts
| Contact: Harry LA Janssen, MD PhD | +31-10-7035942 | M.HOOGENDOORN@ERASMUSMC.NL |
| Contact: Pauline Arends, MD | +31-10-7031618 | p.arends@erasmusmc.nl |
Locations
| China | |
| Ruijin Hospital "Jiaolong University" | Recruiting |
| Shanghai, China, 200025 | |
| Contact: Qing Xie, MD PhD | |
| Principal Investigator: Qing Xie, MD PhD | |
| Zhong Shan Hospital "Fu Dan University" | Recruiting |
| Shanghai, China, 200083 | |
| Contact: Jiyao Wang, MD PhD | |
| Contact: Ning Ping Zhang, MD zhang.ningping@zs-hospital.sh.cn | |
| Principal Investigator: Jiyao Wang, MD PhD | |
| Public Health Center "Fu Dan University" | Recruiting |
| Shanghai, China, 200083 | |
| Contact: Qin Zhang, MD PhD | |
| Principal Investigator: Qin Zhang, MD PhD | |
| Netherlands | |
| Erasmus MC, University Medical Center | Recruiting |
| Rotterdam, Netherlands | |
| Contact: Harry LA Janssen, MD PhD | |
Sponsors and Collaborators
Foundation for Liver Research
Investigators
| Principal Investigator: | Harry LA Janssen, MD PHD | Erasmus MC, University Medical Center Rotterdam |
More Information
No publications provided
| Responsible Party: | Foundation for Liver Research |
| ClinicalTrials.gov Identifier: | NCT01532843 History of Changes |
| Other Study ID Numbers: | HBV 11-02 |
| Study First Received: | February 10, 2012 |
| Last Updated: | January 3, 2013 |
| Health Authority: | Netherlands: The Central Committee on Research Involving Human Subjects (CCMO) |
Keywords provided by Foundation for Liver Research:
|
Hepatitis B sustained response peginterferon nucleos(t)ide analogues |
Additional relevant MeSH terms:
|
Hepatitis Hepatitis A Hepatitis B Hepatitis, Chronic Hepatitis B, Chronic Hepatitis, Viral, Human Peginterferon alfa-2b Liver Diseases Digestive System Diseases Virus Diseases Enterovirus Infections |
Picornaviridae Infections RNA Virus Infections Hepadnaviridae Infections DNA Virus Infections Interferon-alpha Antiviral Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions Immunologic Factors Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on May 16, 2013