Ciclesonide
Autor: | Neil A Reynolds, Lesley J. Scott |
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Rok vydání: | 2004 |
Předmět: |
Budesonide
Adult Vital capacity Time Factors medicine.drug_class Ciclesonide Drug Administration Schedule chemistry.chemical_compound FEV1/FVC ratio Pregnenediones Administration Inhalation medicine Humans Pharmacology (medical) Metered Dose Inhalers Active metabolite Asthma business.industry Inhaler Esterases medicine.disease chemistry Anesthesia Injections Intravenous Corticosteroid business medicine.drug Half-Life |
Zdroj: | Drugs. 64(5) |
ISSN: | 0012-6667 |
Popis: | Ciclesonide is an inhaled corticosteroid (delivered via a hydrofluoroalkane metered-dose inhaler) that is converted to an active metabolite, desisobutyryl-ciclesonide, in the lung, thereby minimising effects on endogenous cortisol. In two 12-week, randomised studies in patients with asthma, ciclesonide 80 or 320 microg once daily was at least as effective as budesonide 400 microg/day at increasing forced expiratory volume in 1 second (FEV1) and forced vital capacity (FVC) from baseline; ciclesonide 320 microg daily was significantly more effective than budesonide 400 microg once daily in one study. In a randomised, double-blind study in patients with asthma controlled with high-dosages of inhaled corticosteroids, FEV(1) and FVC decreased significantly from baseline at 12 weeks in patients receiving ciclesonide 320 microg daily or budesonide 400 microg daily; peak expiratory flow values decreased significantly only in patients receiving budesonide. Inhaled ciclesonide 80 or 320 microg daily improved asthma symptom scores and decreased the use of rescue medication by a similar, significant amount to budesonide 400 microg/day in two 12-week studies. Inhaled ciclesonide was generally well tolerated in patients with asthma. Ciclesonide did not suppress biochemical markers of adrenal function in 52-week studies. The long-term (52 weeks) systemic effects of ciclesonide remain unknown. |
Databáze: | OpenAIRE |
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