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An Open-label, Uncontrolled 4-week Study to Assess the Safety, Efficacy and Pharmacokinetics of Allegra (Dry Syrup Formulation) 15 mg or 30 mg Twice Daily in Pediatric Patients With Perennial Allergic Rhinitis

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Trial Profile

An Open-label, Uncontrolled 4-week Study to Assess the Safety, Efficacy and Pharmacokinetics of Allegra (Dry Syrup Formulation) 15 mg or 30 mg Twice Daily in Pediatric Patients With Perennial Allergic Rhinitis

Status: Completed
Phase of Trial: Phase II/III

Latest Information Update: 14 Jan 2020

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At a glance

  • Drugs Fexofenadine (Primary)
  • Indications Perennial allergic rhinitis
  • Focus Adverse reactions
  • Sponsors Sanofi

Most Recent Events

  • 13 Sep 2011 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
  • 26 May 2011 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.
  • 02 Dec 2010 New trial record

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