Methods of treating autoimmune, respiratory and inflammatory disorders by inhalation of roflumilast N-oxide
The present disclosure relates to pharmaceutical compositions useful for (and to a method of) treating autoimmune, respiratory and/or inflammatory diseases and conditions. The method involves administering to a subject in need thereof roflumilast N-oxide by inhalation. The present disclosure particularly relates to the treatment of asthma and chronic obstructive pulmonary disease (COPD) by administering roflumilast N-oxide by inhalation.
1. A method of treating chronic obstructive pulmonary disease in a subject in need thereof comprising pulmonary administration of about 600 to about 1200 μg of roflumilast N-oxide or a pharmaceutically acceptable salt thereof in a single dose, wherein the roflumilast N-oxide or pharmaceutically acceptable salt thereof has a d 50 of less than about 6 microns.
2. The method of claim 1 , wherein the d 90 of the roflumilast N-oxide or pharmaceutically acceptable salt thereof is between about 0.5 and about 5 microns.
3. The method of claim 1 , wherein the method comprises pulmonary administration of about 600 to about 1000 μg of roflumilast N-oxide or a pharmaceutically acceptable salt thereof in a single dose.
4. The method of claim 1 , wherein the method comprises pulmonary administration of about 600 to about 800 μg of roflumilast N-oxide or a pharmaceutically acceptable salt thereof in a single dose.
5. The method of claim 1 , wherein the roflumilast N-oxide or pharmaceutically acceptable salt thereof is administered in combination with a long-acting β2 agonist, an M3 antagonist, a corticosteroid, or any combination thereof.
6. The method of claim 5 , wherein the long-acting β2 agonist is selected from carmoterol, GSK-642444, indacaterol, milveterol, arformoterol, formoterol, salbutamol, formoterol, levalbuterol, terbutaline, AZD-3199, BI-1744-CL, LAS-100977, bambuterol, isoproterenol, procaterol, clenbuterol, reproterol, fenoterol, ASF-1020, and any combination thereof.
7. The method of claim 5 , wherein the M3 antagonist is selected from aclidinium, tiotropium, ipratropium and oxitropium, and any combination thereof.
8. The method of claim 5 , wherein the corticosteroid is selected from the group consisting of dexamethasone, fluticasone, fluticasone furoate, prednisolone, betamethasone, budesonide, mometasone, mometasone furoate, triamcinolone acetonide, ciclesonide, TPI-1020, beclomethasone, beclomethasone dipropionate, prednisone, deflazacort, hydrocortisone, QAE-397, flunisolide, and any combination thereof.
9. A method of treating chronic obstructive pulmonary disease in a subject in need thereof comprising pulmonary administration by inhalation of about 600 to about 1200 μg of roflumilast N-oxide or a pharmaceutically acceptable salt thereof in a single dose, wherein the roflumilast N-oxide or pharmaceutically acceptable salt thereof has a d 50 of less than about 6 microns.
10. The method of claim 9 , wherein the d 90 of the roflumilast N-oxide or pharmaceutically acceptable salt thereof is between about 0.5 and about 5 microns.
11. The method of claim 9 , wherein the method comprises pulmonary administration of about 600 to about 1000 μg of roflumilast N-oxide or a pharmaceutically acceptable salt thereof in a single dose.
12. The method of claim 9 , wherein the method comprises pulmonary administration of about 600 to about 800 μg of roflumilast N-oxide or a pharmaceutically acceptable salt thereof in a single dose.
13. The method of claim 9 , wherein the roflumilast N-oxide or pharmaceutically acceptable salt thereof is administered in combination with a long-acting β2 agonist, an M3 antagonist, a corticosteroid, or any combination thereof.
14. The method of claim 13 , wherein the long-acting β2 agonist is selected from carmoterol, GSK-642444, indacaterol, milveterol, arformoterol, formoterol, salbutamol, formoterol, levalbuterol, terbutaline, AZD-3199, BI-1744-CL, LAS-100977, bambuterol, isoproterenol, procaterol, clenbuterol, reproterol, fenoterol, ASF-1020, and any combination thereof.
15. The method of claim 13 , wherein the M3 antagonist is selected from aclidinium, tiotropium, ipratropium and oxitropium, and any combination thereof.
16. The method of claim 13 , wherein the corticosteroid is selected from the group consisting of dexamethasone, fluticasone, fluticasone furoate, prednisolone, betamethasone, budesonide, mometasone, mometasone furoate, triamcinolone acetonide, ciclesonide, TPI-1020, beclomethasone, beclomethasone dipropionate, prednisone, deflazacort, hydrocortisone, QAE-397, flunisolide, and any combination thereof.