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CompletedNCT01101074

Observational Safety and Effectiveness Study of Adjuvanted Swine Origin A (H1N1) Pandemic Subunit Egg Derived Vaccine

A Prospective Observational Study of Safety and Effectiveness Following Administration of Adjuvanted Swine Origin A (H1N1) Pandemic Subunit Egg Derived Vaccine

Status
Completed
Phase
Study type
Observational
Enrollment
135,469 (actual)
Sponsor
Novartis Vaccines · Industry
Sex
All
Age
6 Months
Healthy volunteers
Accepted

Summary

This observational study will evaluate the safety and effectiveness following administration of adjuvanted Swine Origin A (H1N1) Pandemic Subunit Egg Derived Vaccine through both an ad hoc active monitoring system and a passive surveillance of hospitalization in a large cohort.

Conditions

Interventions

TypeNameDescription
OTHERThis is non-intervention observational studyThis is non-intervention observational study

Timeline

Start date
2009-10-01
Primary completion
2010-01-01
Completion
2010-09-01
First posted
2010-04-09
Last updated
2011-10-12

Locations

1 site across 1 country: Italy

Source: ClinicalTrials.gov record NCT01101074. Inclusion in this directory is not an endorsement.

Observational Safety and Effectiveness Study of Adjuvanted Swine Origin A (H1N1) Pandemic Subunit Egg Derived Vaccine (NCT01101074) · Clinical Trials Directory