drugset / Trial / NCT02339155

Effect of Raxibacumab on Immunogenicity of Anthrax Vaccine Adsorbed

NCT02339155

Phase 4 Completed 573 enrolled Emergent BioSolutions GlaxoSmithKline · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

This study, as a post-marketing commitment to the Food and Drug Administration, is designed to detect the effect of raxibacumab on anthrax vaccine adsorbed (AVA) immunogenicity in a healthy volunteer population. This is a randomized, open-label, parallel group, two arm study to compare the immunogenicity of AVA at 4 weeks after the first AVA dose, when AVA is administered alone or concomitantly with raxibacumab. The study is planned to enroll approximately 30 to 534 subjects in up to 3 cohorts. The total duration of the study will be approximately 26 weeks. The dates reflect cohort 1.

Timeline

Start
2015-02-24
Primary completion
2017-01-03
Completion
2017-06-06

Drugs

EvaluationDrugModalityDoseRoute
Subject BioThrax Vaccine 0.5 ml Subcutaneous
Subject Raxibacumab Monoclonal antibody 40 mg/kg Intravenous
Background Diphenhydramine Unknown 25 mg Oral
Background Diphenhydramine Unknown 50 mg Oral