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OpenTrials
Completed

NCT Number: NCT01267058

Booster Study of Combined Diphtheria-tetanus-acellular Pertussis Vaccine in Healthy Adults

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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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • At least 18 years of age at the time of the vaccination
  • Written informed consent has been obtained

Exclusion criteria

  • Evidence of confirmed pertussis disease within the previous 5 years
  • History of diphtheria or tetanus vaccination within the past 5 years Females must not be pregnant or lactating They must either surgically sterilized or one year post-menopausal or if they are of childbearing potential, they must be abstinent or have used adequate contraceptive precautions (or one month prior to the booster vaccination, and must agree to continue such precautions for 2 months after completion of the vaccination.
  • History of diphtheria or tetanus disease
  • History of allergic disease likely to be stimulated by the vaccination
  • Major congenital defects or serious chronic illness
  • History of progressive neurological disease
  • Immunosuppressive therapy
  • Any suspected or confirmed immune disorder
  • Immunoglobulin therapy or administration of any blood products within the previous three months or during the study period
  • Acute febrile illness (>37.5°C, axillary or oral temperature) at the time of planned vaccination
  • Administration of an investigational or non registered drug or vaccine within 30 days prior to the start of the present trial
  • Simultaneous administration of a vaccine not foreseen by the study protocol, within 30 days prior to the start of the present trial
  • Any severe or serious adverse experience having occurred after previous administration of DTP vaccine i.e:
  • an immediate anaphylactic or unacceptable reaction to the investigator's opinion, to a previous dose of diphtheria tetanus pertussis whole-cell vaccine, i.e. :
  • encephalopathy
  • fever > 40.5°C (105°F), rectal temperature, occurring after vaccination with diphtheria tetanus pertussis whole-cell vaccine and not due to another identifiable cause.
  • collapse or shock-like state
  • persistent, inconsolable crying lasting > 3 hours
  • seizures with or without fever
  • systemic allergic or neurologic reactions following a previous dose of tetanus and diphtheria toxoids vaccine
  • Exclusion from long term follow-up of antibody persistence : Evidence of confirmed pertussis, diphtheria or tetanus disease or vaccination against these diseases since previous study visit

Treatment and study plan

GSK Biologicals' combined diphtheria, tetanus, acellular pertussis vaccine

Biological

Intramuscular, single dose

GSK Biologicals' acellular pertussis vaccine

Biological

Intramuscular, single dose

Commonwealth Serum Laboratories' combined diphtheria and tetanus vaccine

Biological

Intramuscular, single dose

Primary outcomes

  1. Occurrence of solicited local and general symptoms

    Time frame: Within the 15-day (Day 0 - Day 14) follow-up period after the first injection

Secondary outcomes

  1. Immunogenicity with respect to components of the study vaccines

    Time frame: One month after the first injection

  2. Immunogenicity with respect to components of the study vaccines

    Time frame: One month after the second injection

  3. Occurrence of solicited local symptoms and fever

    Time frame: Within the 15-day (Day 0 - Day 14) follow-up period after the second injection

  4. Occurrence of general solicited symptoms to vaccination, other than fever

    Time frame: Within the 15-day (Day 0 - Day 14) follow-up period after each vaccine administration

  5. Occurrence of unsolicited symptoms

    Time frame: Within 31 days (Day 0 - Day 30) after each vaccine administration

  6. Occurrence of serious adverse experiences to vaccination

    Time frame: Within 31 days (Day 0 - Day 30) after each vaccine administration

  7. Immunogenicity with respect to components of the study vaccines

    Time frame: Immediately prior to the booster vaccination

  8. Immunogenicity with respect to components of the study vaccines

    Time frame: One year after the vaccination in a subset of subjects from all the groups

  9. Immunogenicity with respect to components of the study vaccines

    Time frame: 2, 3, 4 and 5 years after the vaccination

Sponsors and collaborators

Lead sponsor

GlaxoSmithKline

Industry

Registry information

Official study title

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

Important dates

Study start
1997
Primary completion
1998
Study completion
1998
First posted
Dec 24, 2010
Registry last updated
Dec 24, 2010

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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