AzTrials
AzTrials

Hepatitis BPhase 4NCT00356564

Persistence of the Immune Response to Hepatitis B in 7-9 Years Old Children Previously Vaccinated With DTPa-HBV-IPV/Hib

A Phase 4 study testing hepatitis B vaccine in people with Hepatitis B, run by GlaxoSmithKline at 42 sites in Germany.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

Persistence of seroprotective antibody concentrations \& immunological memory shown by the ability to mount a response to a challenge dose of HBV vaccine Read more about this study

Who is it for?
Ages 7 to 9 yearsHealthy volunteers can take part
Conditions the study is for
Hepatitis B
What is being tested?
hepatitis B vaccine
Type of treatment
Vaccines
How many people
350 participants
Where
42 sitesGermany
Study dates
Jul 2006to Dec 2006
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 7 to 9 years
  • All sexes
  • Healthy volunteers accepted
  • Child

Who may be able to join

  • A male or female aged 7 to 9 years at the time of study entry .
  • Subjects who have received a total of 4 doses of DTPa-HBV-IPV/Hib vaccine or a total of 4 doses of HBV vaccine in previous vaccination studies.
  • Evidence of previous hepatitis B booster vaccination or disease since administration of the fourth dose of DTPa-HBV-IPV/Hib or HBV vaccine.

Who cannot join

None listed.

Trial locations and contacts

42 sites in 1 country.

42 sites in 1 country

Germany42 sites
  • GSK Investigational Site

    Aichach, Bavaria, 86551

  • GSK Investigational Site

    Altenholz, Schleswig-Holstein, 24161

  • GSK Investigational Site

    Bad Lobenstein, Thuringia, 07356

  • GSK Investigational Site

    Bad Sobernheim, Rhineland-Palatinate, 55566

  • GSK Investigational Site

    Berlin, State of Berlin, 10249

  • GSK Investigational Site

    Berlin, State of Berlin, 10999

  • GSK Investigational Site

    Berlin, State of Berlin, 13355

  • GSK Investigational Site

    Berlin, State of Berlin, 13507

  • GSK Investigational Site

    Bischofswerda, Saxony, 01877

  • GSK Investigational Site

    Bobingen, Bavaria, 86399

  • GSK Investigational Site

    Bredstedt, Schleswig-Holstein, 25821

  • GSK Investigational Site

    Dresden, Saxony, 01307

  • GSK Investigational Site

    Erding, Bavaria, 85435

  • GSK Investigational Site

    Erkrath, North Rhine-Westphalia, 40699

  • GSK Investigational Site

    Ettenheim, Baden-Wurttemberg, 77955

  • GSK Investigational Site

    Flensburg, Schleswig-Holstein, 24937

  • GSK Investigational Site

    Flensburg, Schleswig-Holstein, 24944

  • GSK Investigational Site

    Hamburg, Free and Hanseatic City of Hamburg, 22415

  • GSK Investigational Site

    Husum, Schleswig-Holstein, 25813

  • GSK Investigational Site

    Kaufering, Bavaria, 86916

  • GSK Investigational Site

    Kehl, Baden-Wurttemberg, 77694

  • GSK Investigational Site

    Kempten (Allgäu), Bavaria, 87435

  • GSK Investigational Site

    Kiel, Schleswig-Holstein, 24161

  • GSK Investigational Site

    Krefeld, North Rhine-Westphalia, 47798

  • GSK Investigational Site

    Landsberg am Lech, Bavaria, 86899

  • GSK Investigational Site

    Lohr, Bavaria, 97816

  • GSK Investigational Site

    Mainz, Rhineland-Palatinate, 55131

  • GSK Investigational Site

    Marburg/Lahn, Hesse, 35039

  • GSK Investigational Site

    Munich, Bavaria, 81241

  • GSK Investigational Site

    Munich, Bavaria, 81243

  • GSK Investigational Site

    Niebüll, Schleswig-Holstein, 25899

  • GSK Investigational Site

    Nördlingen, Bavaria, 86720

  • GSK Investigational Site

    Oberkirch, Baden-Wurttemberg, 77704

  • GSK Investigational Site

    Offenburg, Baden-Wurttemberg, 77654

  • GSK Investigational Site

    Pegnitz, Bavaria, 91257

  • GSK Investigational Site

    Rudolstadt, Thuringia, 07407

  • GSK Investigational Site

    Salzgitter, Lower Saxony, 38226

  • GSK Investigational Site

    Schoeneberg - Kuebelberg, Rhineland-Palatinate, 66901

  • GSK Investigational Site

    Trier, Rhineland-Palatinate, 54290

  • GSK Investigational Site

    Tutzing, Bavaria, 82327

  • GSK Investigational Site

    Weilheim, Bavaria, 82362

  • GSK Investigational Site

    Willich, North Rhine-Westphalia, 47877

Other trials in Germany

About this study

Official title: Multicentre Study to Assess Persistence of Antibodies Against Hepatitis B and Immune Response to a Hepatitis B Challenge Dose in Healthy Children 7 to 9 Years Old Previously Vaccinated With 4 Doses of GSK Biologicals' DTPa-HBV-IPV/Hib Vaccine

Persistence of seroprotective antibody concentrations \& immunological memory shown by the ability to mount a response to a challenge dose of HBV vaccine

Conditions
Hepatitis B
Being tested
hepatitis B vaccine
Keywords
Prophylaxis for hepatitis B disease
Medical subject headings
Hepatitis B

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • hepatitis B vaccineBiological

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Anti-HBs antibody concentration

Secondary outcomes (2)
  1. Persistence of antibodies to the other DTPa-HBV-IPV/Hib vaccine antigens.

  2. Sol & unsol symptoms after HBV vaccination, SAEs

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Jul 2006 (estimated)
  2. Study startJul 2006
  3. Study completionDec 2006

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Prevention
Allocation
Non-randomised
Intervention model
Parallel groups
Masking
None (open label)
Enrolment
350 participants
IDs, dates and publications
ClinicalTrials.gov ID
NCT00356564
Sponsor's protocol ID
106744
Status last verified
Oct 2016
First submitted
25 Jul 2006
Last updated
12 Oct 2016
Results posted
No
Individual data sharing
Yes: Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.

Publications

  • Zinke M, Disselhoff J; DTP a-HBV-IPV-110 and -111 study groups; Gartner B, Jacquet JM. Immunological persistence in 4-6 and 7-9 year olds previously vaccinated in infancy with hexavalent DTPa-HBV-IPV/Hib. Hum Vaccin. 2010 Feb;6(2):189-93. doi: 10.4161/hv.6.2.10117.

    PubMed 20009522

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing hepatitis B vaccine in people with Hepatitis B, run by GlaxoSmithKline at 42 sites in Germany.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 0 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 12 Oct 2016. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 42 sites in Germany. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Anti-HBs antibody concentration. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00356564, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Oct 2016.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in