Status:

COMPLETED

Study Investigating Administration of Prevenar for Post-Marketing Surveillance

Lead Sponsor:

Wyeth is now a wholly owned subsidiary of Pfizer

Conditions:

Pneumococcal Infections

Eligibility:

All Genders

6-9 years

Brief Summary

The purpose of this study is to identify the following problems and questions with respect to the safety of Pneumococcal 7-Valent Conjugate Vaccine (Diphtheria CRM 197 Protein), Prevenar, during the p...

Eligibility Criteria

Inclusion

  • Infants and children aged 6 weeks to 9 years, provided the conditions pertaining to contraindications, warnings, precautions, and interactions stated in the package insert do not apply.

Exclusion

  • Hypersensitivity to latex or to any component of the vaccine, including diphtheria toxoid
  • Suffering from a current or recent febrile illness.

Key Trial Info

Start Date :

July 1 2004

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

July 1 2008

Estimated Enrollment :

600 Patients enrolled

Trial Details

Trial ID

NCT00195390

Start Date

July 1 2004

End Date

July 1 2008

Last Update

September 25 2008

Active Locations (1)

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Page 1 of 1 (1 locations)

1

Seoul, South Korea, 100-380

Study Investigating Administration of Prevenar for Post-Marketing Surveillance | DecenTrialz