GSK Biologicals' combined diphtheria, tetanus, acellular pertussis vaccine
BiologicalIntramuscular, single dose
NCT Number: NCT01267058
The aim of the study is to assess the safety and immunogenicity of GlaxoSmithKline Biologicals' (formerly known as SmithKline Beecham Biologicals) combined diphtheria-tetanus-acellular pertussis vaccine in healthy adults, from the age of 18 onwards, in Australia.
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Notify Me18 year and older
All sexes
Interventional
Phase 3
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Intramuscular, single dose
Intramuscular, single dose
Intramuscular, single dose
Time frame: Within the 15-day (Day 0 - Day 14) follow-up period after the first injection
Time frame: One month after the first injection
Time frame: One month after the second injection
Time frame: Within the 15-day (Day 0 - Day 14) follow-up period after the second injection
Time frame: Within the 15-day (Day 0 - Day 14) follow-up period after each vaccine administration
Time frame: Within 31 days (Day 0 - Day 30) after each vaccine administration
Time frame: Within 31 days (Day 0 - Day 30) after each vaccine administration
Time frame: Immediately prior to the booster vaccination
Time frame: One year after the vaccination in a subset of subjects from all the groups
Time frame: 2, 3, 4 and 5 years after the vaccination
GlaxoSmithKline
Industry
Single-blind, Clinical Study of the Immunogenicity and Reactogenicity of SB Biologicals' dTpa, pa Vaccines and a Td Vaccine, Given as a Booster Dose to Healthy Adults, From the Age of 18 Years Onwards
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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