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A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, 12-Week, Clinical Study Designed to Assess the Efficacy and Safety of BDP Nasal Aerosol (80 mcg, Once Daily) in Pediatric Subjects (4 to 11 Years of Age) With PAR

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A Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, 12-Week, Clinical Study Designed to Assess the Efficacy and Safety of BDP Nasal Aerosol (80 mcg, Once Daily) in Pediatric Subjects (4 to 11 Years of Age) With PAR

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 02 Nov 2021

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At a glance

  • Drugs Beclometasone (Primary)
  • Indications Perennial allergic rhinitis
  • Focus Registrational; Therapeutic Use
  • Sponsors Teva Pharmaceutical Industries

    • Most Recent Events

    • 23 Feb 2015 Results presented at the 2015 Annual Meeting of the American Academy of Allergy, Asthma and Immunology, according to Teva Pharmaceutical Industries media release.
    • 30 Oct 2014 According to the Teva Pharmaceutical Industries pipeline, company plans to submit a supplemental NDA to the FDA based on results from this study by the end of 2014.
    • 01 Nov 2013 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.

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