Completed

Immunogenicity and Safety of Sanofi Pasteur Pentaxim Combined Vaccine in Infants in Thailand

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What is being tested

Diphtheria, Tetanus, Polio, Acellular Pertussis and Hib Vac

Biological
Who is being recruted

Neuroinflammatory Diseases+25

+ Actinomycetales Infections

+ Bacterial Infections and Mycoses

From 2 to 2 Months
See all eligibility criteria
How is the trial designed

Prevention Study

Phase 4
Interventional
Study Start: December 2005
See protocol details

Summary

Principal SponsorSanofi
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: December 1, 2005

Actual date on which the first participant was enrolled.

The present clinical study will assess the immunogenicity and reactogenicity of Sanofi Pasteur's DTacP-IPV// PRP\~T combined vaccine (Pentavac™ or Pentaxim™) as a three-dose primary vaccination at 2, 4, and 6 months of age followed by a booster dose during the second year of life and concomitant hepatitis B vaccine at 2 and 6 months of age in infants in Thailand.

Official TitleImmunogenicity and Safety of Sanofi Pasteur Pentaxim Combined Vaccine in Infants in Thailand
Principal SponsorSanofi
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

186 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 2 to 2 Months

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Neuroinflammatory DiseasesActinomycetales InfectionsBacterial Infections and MycosesBacterial InfectionsBordetella InfectionsCentral Nervous System DiseasesCentral Nervous System InfectionsClostridium InfectionsCorynebacterium InfectionsDiphtheriaEnterovirus InfectionsHaemophilus InfectionsInfectionsMyelitisNervous System DiseasesNeuromuscular DiseasesPicornaviridae InfectionsPoliomyelitisRespiratory Tract DiseasesRespiratory Tract InfectionsRNA Virus InfectionsSpinal Cord DiseasesTetanusVirus DiseasesWhooping CoughPasteurellaceae InfectionsGram-Negative Bacterial InfectionsGram-Positive Bacterial Infections

Criteria

Inclusion Criteria: * Aged 53 to 70 days inclusive on the day of inclusion Exclusion Criteria: * Participation in another clinical trial in the 4 weeks preceding the (first) trial vaccination * Planned participation in another clinical trial during the present trial period * 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. * Blood or blood-derived products received in the past. * Mother known as seropositive to HIV or hepatitis B * Any vaccination in the 5 weeks preceding the first trial vaccination (except Bacille Calmette-Guerin \[BCG\]) * History of diphtheria, tetanus, pertussis, poliomyelitis, Haemophilus influenzae type b infection or hepatitis B (confirmed either clinically, serologically or microbiologically). * Previous vaccination against the diphtheria, tetanus, pertussis, poliomyelitis diseases or Haemophilus influenzae type b infection with the trial vaccine or another vaccine. * Thrombocytopenia or a bleeding disorder contraindicating intramuscular vaccination * History of/current seizures * Febrile illness (rectal temperature ≥ 38.0°C or axillary temperature ≥ 37.4°C) or acute illness on the day of inclusion.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental

Study Objectives

Primary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.
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CompletedNo study centers