Last updated:  11/07/2018 00:14:31
Assessment of the clinical acceptability, immunogenicity and long-term preventive efficacy of GlaxoSmithKline (previously SmithKline Beecham and SmithKline-Rit) Biologicals’ recombinant DNA anti-hepatitis B vaccine in hemophiliacs.
Clinicaltrials.gov ID 
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EudraCT ID 
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EU CT Number 
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Trial status 
                  Study complete
                
Study complete
Trial overview
Official title: Assessment of the clinical acceptability, immunogenicity and long-term preventive efficacy of GlaxoSmithKline (previously SmithKline Beecham and SmithKline-Rit) Biologicals’ recombinant DNA anti-hepatitis B vaccine in hemophiliacs.
Trial description: Assessment of the clinical acceptability, immunogenicity and long-term preventive efficacy of GlaxoSmithKline (previously SmithKline Beecham and SmithKline-Rit) Biologicals’ recombinant DNA anti-hepatitis B vaccine in hemophiliacs.
Primary purpose:
Not applicable
Trial design:
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Masking:
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Allocation:
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Primary outcomes:
Not applicable
Secondary outcomes: 
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Interventions:
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Enrollment:
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Primary completion date:
Not applicable
Observational study model:
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Time perspective:
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Clinical publications:
Mannucci PM et. al. Immunogenicity of a Recombinant Hepatitis B vaccine in Hemophiliacs. American Journal of Hematology; 1988; 29: 211-214.
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
Not applicable
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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