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CompletedNCT00254969Updated Apr 17, 2012

Immunogenicity and Safety of Pentaxim in South African Infants

A Phase 3 interventional study of Diphtheria, Tetanus, Polio, Acellular Pertussis and Hib in Diphtheria, Tetanus and Haemophilus Infections, sponsored by Sanofi. Completed at 1 site in South Africa. Open to participants aged 24 Hours and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2012-04-17.

Sponsored by Sanofi · Phase 3, Interventional, and Prevention

Phase
Phase 3
Study type
Interventional
Enrollment
212
Allocation
Non-randomized
Ages
24 Hours and older
Sex
All
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Study summary

The present clinical study will assess the immunogenicity and reactogenicity of Aventis Pasteur's DTacP-IPV// PRP\~T combined vaccine (Pentavac™ or Pentaxim™) as a three-dose primary vaccination at 6, 10 and 14 weeks of age followed by a booster dose during the second year of life in order to meet the requirements for application for the use of the product in the Expanded Program on Immunization (EPI) in South Africa.

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Conditions studied

  • Diphtheria
  • Tetanus
  • Haemophilus Infections
  • Pertussis
  • Poliomyelitis

Keywords

  • Diphteria
  • tetanus
  • haemophilus influenzae type b
  • poliomyelitis
  • pertussis
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In context

Whooping Cough

238 studies on the registry are indexed under Whooping Cough; 15 are open to participants now.

This study's enrollment of 212 is below the median of 375 across 180 interventional studies indexed under Whooping Cough.

Browse Whooping Cough studies →

Lead sponsor

Sanofi is the lead sponsor of 1,508 studies on the registry; 90 are open to participants now.

Of its 198 completed or terminated interventional studies of FDA-regulated products, 118 (60%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
24 Hours and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Aged \< 24 hours on the day of inclusion

Exclusion criteria

Exclusion Criteria:

  • At visit 01 (screening)
  • Illness at a stage that could interfere with trial conduct or completion.
  • Any vaccination preceding the trial participation (except Bacille Calmette-Guerin [BCG])
  • Acute illness on the day of screening. At visit 01 and visit 02 (screening and first study vaccination).
  • Planned participation in another clinical trial during the present trial period
  • Blood or blood-derived products received since birth.
  • Mother known as seropositive to HIV or hepatitis B.
  • Known thrombocytopenia or a bleeding disorder contraindicating intramuscular vaccination
  • History of/current seizures at visit 02 (first study vaccination)
  • Participation in another clinical trial preceding the first trial vaccination
  • Congenital or acquired immunodeficiency; immunosuppressive therapy such as long-term systemic corticosteroid therapy.
  • Systemic hypersensitivity to any of the vaccine components or history of a life-threatening reaction to the trial vaccine or a vaccine containing the same substances
  • Chronic illness at a stage that could interfere with trial conduct or completion.
  • Any vaccination preceding the first trial vaccination (except BCG)
  • History of diphtheria, tetanus, pertussis, poliomyelitis, Haemophilus influenzae type b and hepatitis B infection (confirmed either clinically, serologically or microbiologically).
  • Previous vaccination against diphtheria, tetanus, pertussis, poliomyelitis, Haemophilus influenzae type b and hepatitis B infection with the trial vaccine or another vaccine.
  • Febrile illness (rectal temperature ≥ 38.0°C or axillary temperature ≥ 37.4°C) or acute illness on the day of first vaccination
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Study design

Phase
Phase 3
Primary purpose
Prevention
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
212 participants (actual)

Study arms

  • Experimental
    1

    Biological: Diphtheria, Tetanus, Polio, Acellular Pertussis and Hib

Interventions

  • BiologicalDiphtheria, Tetanus, Polio, Acellular Pertussis and Hib

    0.5 mL, Im

    Also known as: PENTAXIM™

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What researchers measure

Primary outcomes

  1. To provide information concerning the immunogenicity of DTacP-IPV//PRP~T combined vaccine.

    Time frame: 1 month post-vaccination

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Study locations

1 site
  • Soweto, South Africa
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References and documents

Publications

  • Madhi SA, Cutland C, Jones S, Groome M, Ortiz E. One-year post-primary antibody persistence and booster immune response to a DTaP-IPV//PRP~T vaccine (Pentaxim) given at 18 - 19 months of age in South African children primed at 6, 10 and 14 weeks of age with the same vaccine. S Afr Med J. 2011 Nov 28;101(12):879-83. PubMed 22273029 ↗

Related links

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 17, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00254969
Lead sponsor
Sanofi
Responsible party
Sponsor
First posted
Nov 17, 2005
Start date
Oct 2005
Primary completion
May 2008
Completion
Jan 2010
Last update
Apr 17, 2012

Study contacts

Medical Director
study director · Sanofi Pasteur Inc.

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2012. You cannot join it, but the record below documents what was studied.

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