Long-term Persistence Study in Healthy Adults Previously Vaccinated With Twinrix Adult

Hepatitis B Clinical Trial

Official title:

An Open Single Centre Study to Evaluate the Long-term Antibody Persistence and Immune Memory Between 16 and 20 Years After the Primary Study HAB-032 (208127/022) in Which Healthy Adults Were Vaccinated With Twinrix Adult Following a Three-dose Schedule.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01037114
• Other study ID #: 112266
• Status: Completed
• Phase: Phase 4
• Start date: January 27, 2010
• Est. completion date: February 28, 2014

Study information

• Verified date: January 2018
• Source: GlaxoSmithKline
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will evaluate the persistence of the immune response to HAV (hepatitis A virus) antigens and HBs (hepatitis B surface) antigens in healthy adults previously vaccinated with Twinrix Adult in the primary study, HAB-032 (208127/022). The subjects will be invited for blood sampling 16, 17, 18, 19 and 20 years after the primary vaccination to evaluate the antibody persistence. For subjects in whom low circulating antibodies are detected, the presence of immune memory against hepatitis A & B antigens will be investigated by the administration of a challenge dose of the appropriate vaccine (Havrix and/or Engerix-B) at the next planned visit.

No new subjects will be recruited during this study.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: February 28, 2014
• Est. primary completion date: February 28, 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

All subjects must satisfy the following criteria at entry into each of the long-term follow-up visits:

• Subjects who the investigator believes that they can and will comply with the requirements of the protocol should be enrolled in the study.

• A male or female who received the complete primary vaccination course in the primary study 208127/022.

• Written informed consent obtained from the subject.

All subjects must satisfy the following criteria at entry into the challenge dose phase:

• Subjects who the investigator believes that they can and will comply with the requirements of the protocol.

• A male or female who received the complete primary vaccination course in the primary study 208127/022.

• Written informed consent obtained from the subject.

• Subjects who participated in the LTFU phase of the 208127/022 study and for whom the antibody concentrations were below the cut-off at the last available follow-up time-point.

• Female subjects of non-childbearing potential may be enrolled in the study.

• Female subjects of childbearing potential may be enrolled in the study, if the subject:

• has practiced adequate contraception for 30 days prior to vaccination, and

• has a negative pregnancy test on the day of vaccination, and

• has agreed to continue adequate contraception for two months after the administration of the challenge dose.

Exclusion Criteria:

The following criteria should be checked before entry into each of the long-term follow-up visits. If any exclusion criterion applies, the subject must not be included in the study:

• Use of any investigational or non-registered product within 30 days prior to blood sampling.

• Administration of a hepatitis A, hepatitis B or combined hepatitis A and B vaccine outside the study procedures, since the primary study 208127/022.

• History of hepatitis A or hepatitis B infection since the primary study 208127/022.

• Administration of hepatitis A or hepatitis B immunoglobulins and/or any blood products within three months prior to blood sampling.

The following criteria should be checked before the challenge dose is administered. If any apply, the subject must not be included in the challenge dose phase:

• Use of any investigational or non-registered product within 30 days prior to study start or planned use during the study.

• Administration of a hepatitis A, hepatitis B or combined hepatitis A and B vaccine between the last LTFU visit and the challenge dose visit.

• History of hepatitis A or hepatitis B infection between the last LTFU visit and the challenge dose visit.

• History of anaphylactic reactions following the administration of vaccines.

• History of any reaction or hypersensitivity likely to be exacerbated by any component of the vaccines.

• Acute disease and/or fever at the time of enrolment.

• Pregnant or lactating female.

• Female planning to become pregnant or planning to discontinue contraceptive precautions.

Related Conditions & MeSH terms

• Hepatitis
• Hepatitis A
• Hepatitis B

Intervention

Procedure:
• Blood sampling
Blood sampling at Year 16, 17, 18, 19 and 20 and at the time of challenge dose administration and 14 days and one month after challenge dose administration (if challenge dose needed).

Biological:
• Engerix-B
Engerix-B will be administered to subjects who are not seroprotected against hepatitis B.
• Havrix
Havrix will be administered to subjects who are seronegative for anti-HAV antibodies.

Locations

Country	Name	City	State
Belgium	GSK Investigational Site	Gent

Sponsors (1)

Lead Sponsor	Collaborator
GlaxoSmithKline

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Subjects Seropositive for Anti-hepatitis A Virus Antibodies (Anti-HAV) and Anti-hepatitis B Surface Antigen (Anti-HBs) Antibodies and With Anti-HBs Antibody Concentrations >= 10 Milliinternational Units Per Milliliter (mIU/mL)	Seropositivity for anti-HAV antibodies is defined as antibody concentrations >= 15 milliinternational units per milliliter (mIU/mL). Seropositivity for anti-HBs antibodies is defined as antibody concentrations >= 6.2 mIU/mL.	At Years 16, 17, 18, 19 and 20.
Primary	Anti-HAV and Anti-HBs Geometric Mean Concentrations (GMCs)	Concentrations were expressed as GMCs in mIU/mL.	At Years 16, 17, 18, 19 and 20.
Secondary	Anti-HBs Concentrations After the Challenge Dose of Engerix-B	Concentration was given in mIU/mL.; Only 1 subject was eligible for the challenge dose of Engerix-B at the Year 16 time point. Therefore the values for this subject are given without a measure of dispersion.	Before, 14 days and one month (30 days) after the challenge dose of Engerix-B.
Secondary	Anti-HAV Concentrations After the Challenge Dose of Havrix	Concentration was given in mIU/mL. Only 2 subjects were eligible for the challenge dose of Havrix, one at Year 18 and another at Year 20 time point. Therefore the values for these subject are given without a measure of dispersion.	Before, 14 days and one month (30 days) after the challenge dose of Havrix.
Secondary	Number of Subjects With Anamnestic Response to the Challenge Dose of Engerix-B	At Year 16 only 1 subject was eligible for the challenge dose of Engerix-B.; Anti-HBs anamnestic response to the challenge dose was defined as: Anti-HBs antibody concentrations >= 10 mIU/mL at one month post-challenge dose in subjects seronegative at the pre-challenge time point.; At least a 4-fold increase in anti-HBs antibody concentrations, at one month post-challenge dose in subjects seropositive at the pre-challenge time point.	30 days after the challenge dose of Engerix-B.
Secondary	Number of Subjects With Anamnestic Response to the Challenge Dose of Havrix	Anti-HAV anamnestic response to the challenge dose was defined as: Anti-HAV antibody concentrations = 15 mIU/mL at one month post-challenge dose, in subjects seronegative at the pre-challenge time point.; At least a 2-fold increase in anti-HAV antibody concentrations one month after the challenge dose, in subjects having anti-HAV antibody concentrations = 100 mIU/mL at the pre-challenge time point.; Or at least a 4-fold increase in anti-HAV antibody concentrations one month after the challenge dose, in seropositive subjects having anti-HAV antibody concentrations < 100 mIU/mL at the pre-challenge time-point.	30 days after the challenge dose of Havrix.
Secondary	Number of Subjects Reporting Unsolicited Adverse Events (AEs)	At Year 16, 1 subject was administered a challenge dose of Engerix-B and at Y18 and Y20, 2 subjects were administered a challenge dose of Havrix.; An AE is any untoward medical occurrence in a clinical investigation subject, temporally associated with the use of a medicinal product, whether or not considered related to the medicinal product.	31 days (Days 0-30) after the challenge dose of Engerix-B and Havrix.
Secondary	Number of Subjects With Serious Adverse Events (SAEs)	Only 1 subject received a challenge dose at Year 16 of Engerix-B.; An SAE is any untoward medical occurrence that: results in death, is life threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, is a congenital anomaly/birth defect in the offspring of a study subject, or may evolve into one of the outcomes listed above.	During the 31-day (Days 0-30) follow-up period after the Engerix-B challenge dose.
Secondary	Number of Subjects With Serious Adverse Events (SAEs)	One subject received a challenge dose of Havrix at Year 18 and another at Year 20.; Serious adverse events (SAEs) assessed include medical occurrences that result in death, are life threatening, require hospitalization or prolongation of hospitalization or result in disability/incapacity.	During the 31-day (Days 0-30) follow-up period after the Havrix challenge dose.
Secondary	Number of Subjects Reporting SAEs Related to Study Participation or a Concurrent GSK Medication	An SAE is any untoward medical occurrence that: results in death, is life threatening, requires hospitalization or prolongation of existing hospitalization, results in disability/incapacity, is a congenital anomaly/birth defect in the offspring of a study subject, or may evolve into one of the outcomes listed above.	Up to Year 20.

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