drugset / Trial / NCT00861211

Safety and Efficacy Study of Oral Senicapoc on Allergen Challenge in Atopic Asthmatic Subjects

NCT00861211

Phase 2 Completed 34 enrolled Icagen
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of the study is to determine whether senicapoc can decrease changes in FEV1 following allergen challenge in atopic allergic subjects.

Timeline

Start
2008-10
Primary completion
2009-03
Completion
2009-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Senicapoc Small molecule 40 mg Oral

Indications