Last updated: 11/15/2018 21:50:19
An open, randomised study to compare the immunogenicity, safety and reactogenicity of SmithKline Beecham combined hepatitis A/hepatitis B vaccine Twinrix administered following a 2 dose schedule (0-6 mths) to that of Twinrix. Junior administered following a 3 dose schedule (0, 1, 6 months) in healthy volunteers aged 12-15 years
Clinicaltrials.gov ID
Not applicable
EudraCT ID
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: An open, randomised study to compare the immunogenicity, safety and reactogenicity of SmithKline Beecham combined hepatitis A/hepatitis B vaccine Twinrix administered following a 2 dose schedule (0-6 mths) to that of Twinrix. Junior administered following a 3 dose schedule (0, 1, 6 months) in healthy volunteers aged 12-15 years
Trial description: An open, randomised study to compare the immunogenicity, safety and reactogenicity of SmithKline Beecham combined hepatitis A/hepatitis B vaccine Twinrix administered following a 2 dose schedule (0-6 mths) to that of Twinrix. Junior administered following a 3 dose schedule (0, 1, 6 months) in healthy volunteers aged 12-15 years
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:
Levie K et al. (2002) Long term (24 Months) follow-up of a hepatitis A and B vaccine, comparing a two and three dose schedule in adolescents aged 12-15 Years. Vaccine. 20(19-20):2579-2584.
Medical condition
Hepatitis A
Product
Hepatitis A (Inactivated), Hepatitis B (Recombinant) Vaccine
Collaborators
Not applicable
Study date(s)
April 1998 to December 1998
Type
Not applicable
Phase
3
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
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
1998-03-12
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
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