A Dose–Response Study to Examine the Methodology for Demonstrating the Local Therapeutic Equivalence of the Fluticasone Propionate Component of an Orally Inhaled Combination Therapy of Fluticasone Propionate/Salmeterol Dry Powder-Reference-Cited by-同舟云学术

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A Dose–Response Study to Examine the Methodology for Demonstrating the Local Therapeutic Equivalence of the Fluticasone Propionate Component of an Orally Inhaled Combination Therapy of Fluticasone Propionate/Salmeterol Dry Powder

Published:2019-12-01 Issue:6 Volume:32 Page:364-373
ISSN:1941-2711
Container-title:Journal of Aerosol Medicine and Pulmonary Drug Delivery
language:en
Short-container-title:Journal of Aerosol Medicine and Pulmonary Drug Delivery

Author:

Allan Richard¹,Haughie Scott¹,Kerwin Edward²,Ward Jon¹

Affiliation:

1. Mylan Pharma UK Limited, Sandwich, United Kingdom.

2. Clinical Research Institute of Southern Oregon, Medford, Oregon.

Publisher

Mary Ann Liebert Inc

Subject

Pharmacology (medical),Pharmaceutical Science,Pulmonary and Respiratory Medicine

Link

https://www.liebertpub.com/doi/pdf/10.1089/jamp.2018.1520

Reference20 articles.

1. Global strategy for asthma management and prevention: GINA executive summary

2. Dose-Ranging Study to Evaluate the Efficacy and Safety of Four Doses of Fluticasone Propionate/Salmeterol Multidose Dry Powder Inhaler (FS MDPI) Compared with Fluticasone Propionate (Fp) Mdpi and FS DPI in Subjects with Persistent Asthma

3. ATS Core Curriculum 2017: Part III. Adult Critical Care Medicine

4. A comprehensive study on regulatory requirements for development and filing of generic drugs globally

5. Pharmacodynamic Studies to Demonstrate Bioequivalence of Oral Inhalation Products

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