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Clinical Trial 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


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00261079
Study type Interventional
Source Handok Pharmaceuticals Co., Ltd.
Contact
Status Completed
Phase Phase 4
Start date April 2005
Completion date October 2006

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