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Immunogenicity and Safety of PENTAXIM™ in Indian Population - Article


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Clinical Trial: Immunogenicity and Safety of PENTAXIM™ in Indian Population

This study is not yet open for patient recruitment.
Verified by Sanofi-Aventis December 2005

Sponsored by: Sanofi-Aventis
Information provided by: Sanofi-Aventis
ClinicalTrials.gov Identifier: NCT00259337

Purpose

The present clinical study will assess the immunogenicity as primary objective and reactogenicity as secondary objective 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.

Safety:

To describe the safety after each dose of the primary series of the study combined vaccine (PENTAXIM™).

Condition Intervention Phase
Diphtheria
Tetanus
Polio
Pertussis
Haemophilus Influenzae Type B
 Vaccine: Diphteria/Tetanus/Polio/Acellular Pertussis/Hib vaccine
Phase III

MedlinePlus related topics:  Bacterial Infections;   Bronchitis;   Diphtheria;   Lung Diseases;   Polio and Post-Polio Syndrome;   Tetanus

Study Type: Interventional
Study Design: Prevention, Non-Randomized, Open Label, Historical Control, Single Group Assignment, Safety/Efficacy Study

Further study details as provided by Sanofi-Aventis:

Study start: January 2006

Eligibility

Ages Eligible for Study:  42 Days   -   56 Days,  Genders Eligible for Study:  Both

Accepts Healthy Volunteers

Criteria

Inclusion Criteria:

  • Aged 42 to 56 days inclusive on the day of inclusion
  • Born at full term pregnancy (>37 weeks) with a birth weight ≥ 2.5 kg
  • Informed consent form signed by the parent(s) or other legal representative
  • Able to attend all scheduled visits and to comply with all trial procedures

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 corticosteroids 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.
  • Any vaccination preceding trial vaccination (except BCG)
  • History of diphtheria, tetanus, pertussis, poliomyelitis, hepatitis B or Haemophilus influenza type b (confirmed either clinically, serologically or microbiologically).
  • Previous vaccination against the diphtheria, tetanus, pertussis, poliomyelitis, hepatitis B diseases or Haemophilus influenza 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

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00259337

Public Registry Sanofi Pasteur       RegistryContactUs@sanofipasteur.com

India
      New Delhi,  India

Study chairs or principal investigators

Clinical Trials,  Study Director,  sanofi pasteur   

More Information

Study ID Numbers:  E2I41
Last Updated:  December 13, 2005
Record first received:  November 24, 2005
ClinicalTrials.gov Identifier:  NCT00259337
Health Authority: India: Indian Council of Medical Research
ClinicalTrials.gov processed this record on 2006-01-10

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