Last updated: 11/06/2018 23:35:48

Phase III, multi-country, randomised, controlled, partially-blind study to assess the lot-to-lot consistency of the production method of GlaxoSmithKline Biologicals’ DTPw-HBV/ Hib Kft. vaccine and to compare to GlaxoSmithKline Biologicals’ Tritanrix-Hep B™/ Hiberix™ and to Commonwealth Serum Laboratory’s DTPw (Triple Antigen) in a subgroup, when administered as a primary vaccination course to healthy infants at 2, 4 and 6 months of age and co-administered with oral live attenuated poliomyelitis vaccine.

GSK study ID
101223
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Phase III, multi-country, randomised, controlled, partially-blind study to assess the lot-to-lot consistency of the production method of GlaxoSmithKline Biologicals’ DTPw-HBV/ Hib Kft. vaccine and to compare to GlaxoSmithKline Biologicals’ Tritanrix-Hep B™/ Hiberix™ and to Commonwealth Serum Laboratory’s DTPw (Triple Antigen) in a subgroup, when administered as a primary vaccination course to healthy infants at 2, 4 and 6 months of age and co-administered with oral live attenuated poliomyelitis vaccine.
Trial description: Phase III, multi-country, randomised, controlled, partially-blind study to assess the lot-to-lot consistency of the production method of GlaxoSmithKline Biologicals’ DTPw-HBV/ Hib Kft. vaccine and to compare to GlaxoSmithKline Biologicals’ Tritanrix-Hep B™/ Hiberix™ and to Commonwealth Serum Laboratory’s DTPw (Triple Antigen) in a subgroup, when administered as a primary vaccination course to healthy infants at 2, 4 and 6 months of age and co-administered with oral live attenuated poliomyelitis vaccine.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Espinoza F et al. (2010) Primary and booster vaccination in Latin American children with a DTPw-HBV/Hib combination: a randomized controlled trial. BMC Infectious Diseases. 10:297.
Medical condition
Diphtheria-Tetanus-Pertussis-Hepatitis B-Haemophilus influenzae type b Vaccines
Product
GSK323527A
Collaborators
Not applicable
Study date(s)
August 2004 to September 2005
Type
Not applicable
Phase
2/3

Participation criteria

Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable

Trial location(s)

This study does not involve prospective enrollment of participants.

Study documents

Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English

If you wish to request for full study report, please contact - [email protected]

Results overview

Not applicable

Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2005-05-09

Plain language summaries

Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.

Additional information about the trial

Not applicable
Participate in clinical trial
Access to clinical trial data by researchers
Visit website