Comparative PK Study of 4 Fluticasone/Salmeterol 100/50 mcg Inhalers

  • Research type

    Research Study

  • Full title

    An Open-Label, Randomized, 4-Period, 4-Treatment, Crossover, Single-Dose Study to Compare the Pharmacokinetic and Safety Profiles following 2 Inhalations from 2 Batches of Fluticasone Propionate and Salmeterol Xinafoate Dry Powder Inhaler 100/50 mcg and ADVAIR DISKUS(R) 100/50 mcg in Healthy Volunteers under Fasting Conditions.

  • IRAS ID

    181563

  • Contact name

    Adrian J Stewart

  • Contact email

    adrian.stewart@celerion.com

  • Sponsor organisation

    Lupin Inc

  • Eudract number

    2015-001996-36

  • Duration of Study in the UK

    0 years, 0 months, 26 days

  • Research summary

    Asthma is a chronic inflammatory disease of the bronchial tract characterized by reversible airway obstruction and bronchial hyper-responsiveness. Chronic obstructive pulmonary disease (COPD) is a debilitating respiratory illness characterized by airflow limitation that is not fully reversible and that is usually both progressive and associated with an abnormal inflammatory response of the lungs to noxious particles or gases.

    Fluticasone propionate is a synthetic trifluorinated corticosteroid with potent anti inflammatory activity. Inflammation is an important component of the pathophysiology of asthma and corticosteroids have been shown to inhibit multiple inflammatory cells and mediators involved in the pathophysiology of asthma. Salmeterol xinafoate is a selective LABA. The therapeutic use of a combination of inhaled corticosteroid and an inhaled LABA for the treatment of asthma has been well established, offering advantages in both lung function improvement, as well as important clinical outcomes over the individual components alone.

    The Sponsor is developing a generic formulation of fluticasone propionate and salmeterol xinafoate DPI to be substitutable for the reference (RLD), ADVAIR DISKUS 100/50 mcg.

  • REC name

    HSC REC A

  • REC reference

    15/NI/0116

  • Date of REC Opinion

    22 Jul 2015

  • REC opinion

    Further Information Favourable Opinion