Synergistic combination
The invention relates to the combined administration of PDE inhibitors and β2 adrenoceptor agonists for the treatment of respiratory disorders.
1 - 12 . (canceled)
13 . A pharmaceutical composition comprising a PDE inhibitor, which is to be administered orally, from the PDE4 or PDE3/4 inhibitors group combined with a β 2 adrenoceptor agonist in fixed or free combination, wherein said PDE inhibitor is selected from the group consisting of roflumilast; BYK-33043; AWD-12-281; SB-207499; arofylline; ibudilast; a pharmacologically tolerable hydrate, solvate, salt, hydrate of a salt, or solvate of a salt thereof; an N-oxide of roflumilast; and an N-oxide of BYK-33043;
and wherein said β 2 adrenoceptor agonist is selected from the group consisting of 4-hydroxy-3-hydroxymethyl-α-[(tert-butylamino)methyl]benzyl alcohol (salbutamol); (R)-4-hydroxy-3-hydroxymethyl-α-[(tert-butylamino)methyl]benzyl alcohol (levosalbutamol); 1-(3,5-dihydroxyphenyl)-2-(tert-butylamino)-ethanol (terbutaline); 2-hydroxymethyl-3-hydroxy-6-(1-hydroxy-2-tert-butylaminoethyl)pyridine (pirbuterol); (R*,R*)-(±)-N-[2-hydroxy-5-[1-hydroxy-2-[[2-(4-methoxyphenyl)-1-methylethyl]amino]ethyl]phenyl]formamide (formoterol); (+)-4-hydroxy-α 1 -[[[6-(4-phenylbutoxy)hexyl]amino]methyl]-1,3benzenedimethanol (salmeterol); and a pharmacologically tolerable hydrate, solvate, salt, hydrate of a salt or solvate of a salt thereof.
14 . The pharmaceutical composition as claimed in claim 13 , which is a fixed oral combination.
15 . The pharmaceutical composition as claimed in claim 13 , wherein the PDE inhibitor is a compound selected from the group consisting of arofylline; ibudilast; SB-207499; and a pharmacologically tolerable hydrate, solvate, salt, hydrate of a salt or solvate of a salt thereof.
16 . The pharmaceutical composition as claimed in claim 13 , wherein the PDE inhibitor is BYK-33043 or a pharmacologically tolerable hydrate, solvate, salt, hydrate of a salt or solvate of a salt thereof, or an N-oxide of BYK-33043.
17 . The pharmaceutical composition as claimed in claim 13 , wherein the PDE inhibitor is BYK-33043 or a pharmacologically tolerable hydrate, solvate, salt, hydrate of a salt or solvate of a salt thereof, or an N-oxide of BYK-33043, and the β2 adrenoceptor agonist is (±)-4-hydroxy-α 1 -[[[6-(4-phenylbutoxy)hexyl]amino]methyl]-1,3benzenedimethanol (salmeterol) or a pharmacologically tolerable hydrate, solvate, salt, hydrate of a salt or solvate of a salt thereof.
18 . The pharmaceutical composition as claimed in claim 13 , which additionally contains an excipient selected from the group consisting of propellants, surface-active substances, emulsifiers, stabilizers, preservatives, flavorings, fillers, solvents, gel-forming agents, tablet excipients, antioxidants, dispersants, antifoams, flavor corrigents, solubilizers, colorants or permeation promoters, and completing agents.
19 . A method of treating a respiratory tract disorder in a patient, comprising administering a therapeutically effective amount of a PDE inhibitor from the PDE4- or PDE3/4 inhibitors group in combination with a β 2 adrenoceptor agonist to said patient, wherein said PDE inhibitor is administered orally, wherein said PDE inhibitor is selected from the group consisting of roflumilast; BYK-33043; AWD-12-281; SB-207499; arofylline; ibudilast; a pharmacologically tolerable hydrate, solvate, salt, hydrate of a salt, or solvate of a salt thereof; an N-oxide of roflumilast; and an N-oxide of BYK-330439; and wherein said β 2 adrenoceptor agonist is selected from the group consisting of 4-hydroxy-3-hydroxymethyl-α-[(tert-butylamino)methyl]benzyl alcohol (salbutamol); (R)-4-hydroxy-3-hydroxymethyl-α-[(tert-butylamino)methyl]benzyl alcohol (levosalbutamol); 1-(3,5-dihydroxyphenyl)-2-(tert-butylamino)-ethanol (terbutaline); 2-hydroxymethyl-3-hydroxy-6-(1-hydroxy-2-tert-butylaminoethyl)pyridine (pirbuterol); (R*,R*)-(±)-N-[2-hydroxy-5-[1-hydroxy-2-[[2-(4-methoxyphenyl)-1-methylethyl]amino]ethyl]phenyl]formamide (formoterol); (±)-4-hydroxy-α 1 -[[[6-(4-phenylbutoxy)hexyl]amino]methyl]-1,3-benzenedimethanol (salmeterol); and a pharmacologically tolerable hydrate, solvate, salt, hydrate of a salt or solvate of a salt thereof.
20 . The method of claim 19 , wherein the respiratory tract disorder is an allergen-induced or inflammation-induced bronchial disorder.
21 . The method of claim 20 , wherein the allergen-induced or inflammation-induced bronchial disorder is selected from the group consisting of bronchitis, obstructive bronchitis, spastic bronchitis, allergic bronchitis, allergic asthma, bronchial asthma, and COPD.
22 . The method of claim 19 , wherein the PDE inhibitor and the β 2 adrenoceptor agonist are administered simultaneously.
23 . The method of claim 19 , wherein the PDE inhibitor and the β 2 adrenoceptor agonist are administered more or less simultaneously.
24 . The method of claim 19 , wherein the PDE inhibitor and the β 2 adrenoceptor agonist are administered in succession.
25 . A method of treating a respiratory tract disorder in a patient, comprising administering to said patient a therapeutically effective amount of the pharmaceutical composition as claimed in claim 17 .
26 . The method of claim 25 , wherein the respiratory tract disorder is an allergen-induced or inflammation-induced bronchial disorder.
27 . The method of claim 26 , wherein the allergen-induced or inflammation-induced bronchial disorder is selected from the group consisting of bronchitis, obstructive bronchitis, spastic bronchitis, allergic bronchitis, allergic asthma, bronchial asthma, and COPD.
28 . The method of claim 25 , wherein the PDE inhibitor and the β 2 adrenoceptor agonist are administered simultaneously.
29 . The method of claim 25 , wherein the PDE inhibitor and the β 2 adrenoceptor agonist are administered more or less simultaneously.
30 . The method of claim 25 , wherein the PDE inhibitor and the β 2 adrenoceptor agonist are administered in succession.