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Rethinking bioequivalence and equivalence requirements of orally inhaled drug products 被引量:2
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作者 Dina Al-Numani Philippe Colucci Murray P.Ducharme 《Asian Journal of Pharmaceutical Sciences》 SCIE CAS 2015年第6期461-471,共11页
Orally inhaled drug products(OIPs),such as corticosteroids and bronchodilators,are at the forefront of asthma and chronic obstructive pulmonary disease treatments,two diseases that afflict worldwide populations.Introd... Orally inhaled drug products(OIPs),such as corticosteroids and bronchodilators,are at the forefront of asthma and chronic obstructive pulmonary disease treatments,two diseases that afflict worldwide populations.Introducing generics of these products is essential,as the pricing of these medications remain a barrier to adequate patient care.Currently,there is no consensus between regulatory bodies as to the bioequivalence and equivalence requirements of OIPs that are intended for local action in the lungs.This manuscript critically reviews these requirements and presents future directions for clinicians,scientists,and regulators to consider to optimize the development and approval of OIPs. 展开更多
关键词 Inhalation products Pharmacokinetics PHARMACODYNAMICS BIOEQUIVALENCE Therapeutic equivalence clinical endpoint studies
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