drugset / Trial / NCT01244230

Safety, Efficacy and Pharmacokinetic Study of Allegra in Pediatric Patients With Atopic Dermatitis (AD)

NCT01244230

Phase 2/3 Completed 100 enrolled Sanofi
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Primary Objective: To evaluate safety (4 weeks) Secondary Objectives: * To evaluate the long-term safety (12 weeks) * To evaluate the efficacy * To characterize the pharmacokinetic profile

Timeline

Start
2010-11
Primary completion
2011-07
Completion
2011-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Fexofenadine Unknown 15 mg Oral
Subject Fexofenadine Unknown 30 mg Oral

Indications