Evaluation of Manufacturing Lot of StaphVAX

Status Completed

Clinical Trial Summary

This study answers a U.S. Food and Drug Administration requirement for evaluation in people of a manufacturing lot of vaccine. Subjects receive one dose of one lot of vaccine. The antibodies in the blood measure the immunogenicity of the vaccine, and typical vaccine safety information is also collected.

Clinical Trial Description

n/a

Study Design

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

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT00211900
Study type	Interventional
Source	Nabi Biopharmaceuticals
Contact
Status	Completed
Phase	Phase 3
Start date	March 2005
Completion date	November 2005

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