Evaluating the Safeness of Trivalent Subunit Inactivated Influenza

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Prevention

See also
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NCT number	NCT01123954
Study type	Interventional
Source	Novartis
Contact
Status	Completed
Phase	Phase 2
Start date	January 2010
Completion date	April 2010

Evaluating the Safeness of Trivalent Subunit Inactivated Influenza Vaccines in Preventing Flu on Vietnamese Volunteers

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms