Use of Ciclesonide for the Treatment of Respiratory Disease in a Smoking Patient
The invention relates to a new method of treatment of respiratory diseases, in particular the treatment of asthmatic smoking patients. The method comprises the administration of a pharmaceutical composition comprising ciclesonide.
1 . A method for treating a respiratory disease in a patient, wherein said patient is a smoking patient, comprising administering to the patient a therapeutically effective and pharmacologically tolerable dose of a composition containing ciclesonide, or a pharmaceutically acceptable salt, solvate or physiologically functional derivative thereof.
2 . The method according to claim 1 , wherein the dose comprises 20, 40, 60, 80, 100, 120, 140, 160, 180, 200 or 320 μg ciclesonide.
3 . The method according to claim 1 , wherein the dose is a daily dose in a continuous treatment regimen.
4 . The method according to claim 3 , wherein the treatment period is more than one day.
5 . The method according to claim 4 , wherein the treatment period is more than one week.
6 . The method according to claim 5 , wherein the composition comprises a pharmaceutically acceptable carrier and/or one or more excipients.
7 . The method according to claim 1 , wherein ciclesonide is selected from the group consisting of [11β,16α(R)]-16,17-[(Cyclohexylmethylene)bis(oxy)]-11-hydroxy-21-(2-methyl-1-oxopropoxy)pregna-1,4-diene-3,20-dione, [11β,16α(S)]-16,17-[(Cyclohexylmethylene)bis(oxy)]-11-hydroxy-21-(2-methyl-1-oxoprop-oxy)pregna-1,4-diene3,20-dione, [11β,16α(R,S)]-16,17-[(Cyclohexylmethylene)bis(oxy)]-11-hydroxy-21-(2-methyl-1-oxoprop-oxy)pregna-1,4-diene3,20-dione, 16α,17-(22R)-Cyclohexylmethylendioxy-11β,21-dihydroxy-pregna-1,4-dien-3,20-dion, 16α,17-(22S)-Cyclohexylmethylendioxy-11β,21-dihydroxy-pregna-1,4-dien-3,20-dion and 16α,17-(22R,S)-Cyclohexylmethylendioxy-11β,21-dihydroxy-pregna-1,4-dien-3,20-dion.
8 . The method according to claim 1 , comprising a once daily dosage regimen.
9 . The method according to claim 1 , wherein the composition is suitable for administration by inhalation.
10 . The method according to claim 9 , wherein the composition comprises ciclesonide dissolved in a pharmaceutically acceptable carrier.
11 . The method according to claim 10 , wherein the composition is a pharmaceutical aerosol formulation comprising a therapeutically effective amount of ciclesonide and a hydrofluorocarbon propellant, and cosolvent in an amount effective to solubilize ciclesonide and optionally a surfactant.
12 . The method according to claim 11 , wherein the cosolvent is ethanol.
13 . The method according to claim 12 , wherein the composition is a pharmaceutical aerosol formulation comprising particles of ciclesonide in a therapeutically effective amount and a hydrofluorocarbon propellant, and 0.01 to 5% w/w based upon propellant of polar cosolvent and optionally a surfactant.
14 . The method according to claim 9 , wherein the composition is a dry powder and the carrier is a saccharide.
15 . The method according to claim 14 , wherein the carrier is lactose monohydrate.
16 . The method according to claim 15 , wherein the respiratory disease is selected from the group consisting of asthma, nocturnal asthma, exercise-induced asthma, chronic obstructive pulmonary diseases (COPD), chronic bronchitis, wheezy bronchitis, emphysema, respiratory tract infection, upper respiratory tract disease, rhinitis, allergic rhinitis and seasonal rhinitis.
17 . The method according to claim 1 , wherein the respiratory disease is mild or moderate asthma.
18 . The method according to claim 1 , wherein the ciclesonide consists essentially of R epimer.
19 . The method according to claim 1 , wherein the patient has a smoking history of less than 10 pack per year of cigarettes or less than two pipe packs per year.
20 . The method according to claim 19 , wherein the patient has a smoking history of less than 10 pack per year of cigarettes or less than two pipe packs per year and has at least three months of smoking abstinence.
21 . The method of claim 11 , wherein the hydrofluorocarbon propellant is selected from the group consisting of 1,1,1,2-tetrafluoroethane, 1,1,1,2,3,3,3-heptafluoropropane and a mixture thereof.
22 . The method of claim 13 , wherein the hydrofluorocarbon propellant is selected from the group consisting of 1,1,1,2-tetrafluoroethane, 1,1,1,2,3,3,3-heptafluoropropane and a mixture thereof.