drugset / Trial / NCT00119067

Summary

Anthrax Clinical Trial Objectives: To assess whether: * Anthrax vaccine (AVA or BioThrax, BioPort Corp. Lansing MI) administered by the intramuscular (IM) route elicits antibody responses that are not inferior (i.e., "non-inferior") to that achieved by the currently licensed schedule. * BioThrax administered by the IM route and containing fewer numbers of doses elicits antibody responses that are not inferior (i.e., "non-inferior") to that achieved by the currently licensed schedule. * Differences in reactogenicity exist between the IM and subcutaneous (SQ) administration of BioThrax. Additionally for the final report we will assess whether: * Occurrence of adverse events following AVA administration is influenced by selected risk factors.

Timeline

Start
2002-05
Primary completion
2010-02
Completion
2010-02

Outcome

Met primary endpoint

paper The 8-IM group's m2 response was non-inferior to the 8-SQ group for the three primary endpoints PMID 24373307 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject BioThrax Vaccine — Intramuscular

Indications

No indication recorded.