drugset / Trial / NCT00425620

Amphotericin B Suspension in Refractory Chronic Sinusitis

NCT00425620

Phase 3 Completed 300 enrolled Accentia Biopharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of the study is to evaluate the safety and efficacy of Amphotericin B suspension versus placebo in the complete resolution of key chronic sinusitis symptoms during 16 weeks of treatment in patients with refractory, postsurgical CS.

Timeline

Start
2006-12
Primary completion
Completion
2007-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Amphotericin B Unknown Intranasal