Persistence of Hepatitis B Antibody Levels & Immune Response to a Hepatitis B Vaccine Challenge
This study has been completed.
Sponsor:
GlaxoSmithKline
Information provided by (Responsible Party):
GlaxoSmithKline
ClinicalTrials.gov Identifier:
NCT00411697
First received: December 13, 2006
Last updated: April 12, 2012
Last verified: April 2012
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Purpose
The purpose of this study is to determine at 5 years of age the persistence of immunity to hepatitis B that was conferred by infant vaccination with Infanrix hexa™.
The Protocol Posting has been updated in order to comply with the FDA Amendment Act, Sep 2007.
| Condition | Intervention | Phase |
|---|---|---|
|
Hepatitis B |
Biological: Engerix™-B Kinder |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Non-Randomized Endpoint Classification: Efficacy Study Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Prevention |
| Official Title: | Assess Long-term Persistence of Hepatitis B Antibodies & Immune Response to a Hepatitis B Vaccine (Engerix-B Kinder) Challenge in Children Aged 4-5 Yrs (Previously Primed & Boosted in the 1st 2 Yrs of Life With DTPa-HBV-IPV/Hib Vaccine) |
Resource links provided by NLM:
Further study details as provided by GlaxoSmithKline:
Primary Outcome Measures:
- Anti-hepatitis B surface antigen (HBs) antibody concentrations [ Time Frame: One month after the challenge dose of HBV vaccine ] [ Designated as safety issue: No ]
Secondary Outcome Measures:
- Anti-HBs antibody concentrations [ Time Frame: Before and after challenge dose of HBV vaccine ] [ Designated as safety issue: No ]
- Occurrence of serious adverse events [ Time Frame: During the entire study period. ] [ Designated as safety issue: Yes ]
| Enrollment: | 301 |
| Study Start Date: | December 2006 |
| Estimated Study Completion Date: | May 2007 |
| Primary Completion Date: | May 2007 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Experimental: Group A |
Biological: Engerix™-B Kinder
Intramuscular injection, 1 dose
Other Name: Engerix™-B Kinder
|
Eligibility| Ages Eligible for Study: | 4 Years to 5 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Criteria
Inclusion Criteria:
- Subjects who the investigator believes that their parents/guardians can and will comply with the requirements of the protocol
- A male or female of 4 to 5 years of age at the time of enrolment.
- With documented evidence of previous vaccination with four consecutive doses of Infanrix hexa™ in Germany.
- Written informed consent obtained from the parents or guardians of the subject at the time of enrolment.
- Healthy subjects as established by medical history and clinical examination before entering into the study.
Exclusion Criteria:
- Concurrently participating in another clinical study, at any time during the study period, in which the subject has been or will be exposed to an investigational or a non-investigational product .
- Evidence of previous hepatitis B booster vaccination since administration of the fourth dose of Infanrix hexa™ booster in the second year of life.
- History of or intercurrent hepatitis B disease.
- Hepatitis B vaccination at birth.
- Planned administration/administration of a vaccine not foreseen by the study protocol during the period starting from 30 days before booster vaccination and ending 30 days after.
- Administration of immunoglobulins and/or any blood products within the three months preceding booster vaccination or planned administration during the study period.
- Chronic administration (defined as more than 14 days) of immunosuppressants or other immune-modifying drugs within six months prior to the HBV vaccine challenge.
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00411697
Locations
| Germany | |
| GSK Investigational Site | |
| Bad Saulgau, Baden-Wuerttemberg, Germany, 88348 | |
| GSK Investigational Site | |
| Bietigheim/Bissingen, Baden-Wuerttemberg, Germany, 74321 | |
| GSK Investigational Site | |
| Boennigheim, Baden-Wuerttemberg, Germany, 74357 | |
| GSK Investigational Site | |
| Ehingen, Baden-Wuerttemberg, Germany, 89584 | |
| GSK Investigational Site | |
| Ettenheim, Baden-Wuerttemberg, Germany, 77955 | |
| GSK Investigational Site | |
| Kehl, Baden-Wuerttemberg, Germany, 77694 | |
| GSK Investigational Site | |
| Kirchzarten, Baden-Wuerttemberg, Germany, 79199 | |
| GSK Investigational Site | |
| Oberstenfeld, Baden-Wuerttemberg, Germany, 71720 | |
| GSK Investigational Site | |
| Offenburg, Baden-Wuerttemberg, Germany, 77654 | |
| GSK Investigational Site | |
| Pforzheim, Baden-Wuerttemberg, Germany, 75172 | |
| GSK Investigational Site | |
| Stuttgart, Baden-Wuerttemberg, Germany, 70469 | |
| GSK Investigational Site | |
| Tettnang, Baden-Wuerttemberg, Germany, 88069 | |
| GSK Investigational Site | |
| Tuttlingen, Baden-Wuerttemberg, Germany, 78532 | |
| GSK Investigational Site | |
| Cham, Bayern, Germany, 93413 | |
| GSK Investigational Site | |
| Muenchen, Bayern, Germany, 81735 | |
| GSK Investigational Site | |
| Muenchen, Bayern, Germany, 81241 | |
| GSK Investigational Site | |
| Olching, Bayern, Germany, 82140 | |
| GSK Investigational Site | |
| Tegernsee, Bayern, Germany, 83684 | |
| GSK Investigational Site | |
| Frankenthal, Rheinland-Pfalz, Germany, 67227 | |
| GSK Investigational Site | |
| Trier, Rheinland-Pfalz, Germany, 54290 | |
| GSK Investigational Site | |
| Trier, Rheinland-Pfalz, Germany, 54294 | |
| GSK Investigational Site | |
| Leipzig, Sachsen, Germany, 04317 | |
| GSK Investigational Site | |
| Berlin, Germany, 12679 | |
| GSK Investigational Site | |
| Berlin, Germany, 13507 | |
| GSK Investigational Site | |
| Berlin, Germany, 10315 | |
| GSK Investigational Site | |
| Berlin, Germany, 13055 | |
| GSK Investigational Site | |
| Berlin, Germany, 13355 | |
Sponsors and Collaborators
GlaxoSmithKline
Investigators
| Study Director: | GSK Clinical Trials | GlaxoSmithKline |
More Information
Publications:
| Responsible Party: | GlaxoSmithKline |
| ClinicalTrials.gov Identifier: | NCT00411697 History of Changes |
| Other Study ID Numbers: | 106789 |
| Study First Received: | December 13, 2006 |
| Last Updated: | April 12, 2012 |
| Health Authority: | Germany: Paul-Ehrlich-Institut |
Additional relevant MeSH terms:
|
Hepatitis Hepatitis A Hepatitis B Liver Diseases Digestive System Diseases Hepatitis, Viral, Human Virus Diseases Enterovirus Infections |
Picornaviridae Infections RNA Virus Infections Hepadnaviridae Infections DNA Virus Infections Hepatitis B Antibodies Immunologic Factors Physiological Effects of Drugs Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 21, 2013