drugset / Trial / NCT00261079

Fexofenadine in Pruritic Skin Disease

NCT00261079

Phase 4 Completed 435 enrolled Handok Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

Primary objective: * To compare the efficacy and safety profile of Fexofenadine 180mg tablets plus prednicarbate(2.5mg/g) vs prednicarbate(2.5mg/g) alone in the treatment of pruritic skin disease Secondary objective: * To evaluate patient's satisfaction of Allegra treatment

Timeline

Start
2005-04
Primary completion
Completion
2006-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Fexofenadine Unknown 180 mg

Indications

No indication recorded.