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CompletedNCT00320463Updated Oct 12, 2016

Compare Immunogenicity & Safety of 2 Formulations of GSK Biologicals' DTPa-HBV-IPV/Hib Vaccine Given in Healthy Infants

A Phase 3 interventional study of DTPa-HBV-IPV/Hib vaccine in Diphtheria, Hepatitis B and Poliomyelitis, sponsored by GlaxoSmithKline. Completed at 4 sites in Russian Federation. Open to participants aged 11 Weeks to 17 Weeks, including healthy volunteers. Per ClinicalTrials.gov, last updated 2016-10-12.

Sponsored by GlaxoSmithKline · Phase 3, Interventional, and Prevention

Phase
Phase 3
Study type
Interventional
Enrollment
415
Allocation
Randomized
Ages
11 Weeks to 17 Weeks
Sex
All
01

Study summary

In this study, infants will be randomly allocated into three groups:

  • one group of subjects will receive DTPa-HBV-IPV/Hib vaccine (new formulation)
  • the second group of subjects will receive DTPa-HBV-IPV/Hib vaccine (current formulation)
  • the third group of subjects will receive DTPa-HBV-IPV vaccine The study will be double-blind for the two groups receiving the DTPa-HBV-IPV/Hib vaccine (new or current formulation). The study will be single-blind for the group receiving DTPa-HBV-IPV vaccine.
Read the detailed description

A study to compare the immunogenicity \& safety of 2 formulations of GlaxoSmithKline (GSK) Biologicals' DTPa-HBV-IPV/Hib vaccine given in healthy infants at 3,4 \& 5 months age. The immunogenicity \& safety of DTPa-HBV-IPV vaccine will also be evaluated in a 3rd group of subjects Subjects in the group that will receive DTPa-HBV-IPV/Hib vaccine (current formulation) will be the control group for the group that will receive DTPa-HBV-IPV/Hib vaccine (new formulation)

02

Conditions studied

  • Diphtheria
  • Hepatitis B
  • Poliomyelitis
  • Tetanus
  • Acellular Pertussis
03

In context

Hepatitis B

1,656 studies on the registry are indexed under Hepatitis B; 196 are open to participants now.

This study's enrollment of 415 is above the median of 120 across 1,187 interventional studies indexed under Hepatitis B.

Browse Hepatitis B studies →

Lead sponsor

GlaxoSmithKline is the lead sponsor of 3,562 studies on the registry; 117 are open to participants now.

Of its 258 completed or terminated interventional studies of FDA-regulated products, 232 (90%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
11 Weeks to 17 Weeks
Sexes eligible
All
Accepts healthy volunteers
Yes

Eligibility criteria

"Inclusion criteria:

  • A healthy male or female infant between, and including, 11 and 17 weeks of age at the time of the first vaccination.
  • Infant born to known hepatitis B surface antigen (HBsAg) seronegative mother (documented laboratory result of HBsAg assay from the maternal blood sample is available).
  • Born after a normal gestation period (between 36 and 42 weeks).
  • Written informed consent obtained from the parent or guardian of the subject.

Exclusion criteria:

  • Use of any investigational or non-registered product (drug or vaccine) other than the study vaccine(s) within 30 days preceding the first dose of study vaccine, or planned use during the study period.
  • Chronic administration of immunosuppressants or other immune-modifying drugs within six months prior to the first vaccine dose.
  • Any chronic drug therapy to be continued during the study period.
  • Planned administration/ administration of a vaccine not foreseen by the study protocol during the period starting from 30 days before each dose of study vaccine and ending 30 days after the last vaccine dose.
  • Previous vaccination against diphtheria, tetanus, pertussis, poliomyelitis, hepatitis B and/or Haemophilus influenzae diseases.
  • Known history of or exposure to diphtheria, tetanus, pertussis, poliomyelitis, hepatitis B and/or Haemophilus influenzae diseases since birth.
  • History of allergic disease or reactions likely to be exacerbated by any component of the vaccines.

"

05

Study design

Phase
Phase 3
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double
Enrollment
415 participants

Interventions

  • BiologicalDTPa-HBV-IPV/Hib vaccine
06

What researchers measure

Primary outcomes

  1. One month after vaccination, measurement of antibodies against all vaccine antigens.

Secondary outcomes

  1. Immunogenicity: One month after vaccination, vaccine response for the pertussis antigens.

  2. Reactogenicity & safety: After each dose, solicited (day 0-3, local & general) & unsolicited (day 0-30) symptoms. Over the full course of the study: serious adverse events (SAEs)."

07

Study locations

4 sites
  • GSK Investigational Site
    Murmansk, 183046, Russian Federation
  • GSK Investigational Site
    Perm, 614022, Russian Federation
  • GSK Investigational Site
    Syktyvkar, 167002, Russian Federation
  • GSK Investigational Site
    Syktyvkar, 167011, Russian Federation
08

References and documents

Individual participant data

Plan to share: Yes — Patient-level data for this study will be made available through www.clinicalstudydatarequest.com following the timelines and process described on this site.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 12, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT00320463
Lead sponsor
GlaxoSmithKline
Responsible party
Sponsor
First posted
May 3, 2006
Start date
Apr 2006
Completion
Jan 2007
Last update
Oct 12, 2016

Study contacts

GSK Clinical Trials
study director · GlaxoSmithKline
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Oct 2016. You cannot join it, but the record below documents what was studied.

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