Treatment of allergic rhinitis using a combination of mometasone and olopatadine
The present patent application relates to a method of treating allergic rhinitis in a subject (preferably a human) by administering a combination of mometasone or its salt and olopatadine or its salt.
1. A method of treating one or more symptoms associated with allergic rhinitis in a human subject in need thereof comprising nasally administering to the human subject a fixed-dose pharmaceutical composition comprising mometasone furoate and olopatadine hydrochloride, wherein (i) the composition is nasally administered as 2 sprays per nostril of the human subject twice daily, (ii) each spray of the composition comprises about 25 mcg mometasone furoate and olopatadine hydrochloride equivalent to about 600 mcg olopatadine, and (iii) the twice daily administration of the pharmaceutical composition provides a faster onset of action than twice daily administration of olopatadine hydrochloride equivalent to about 1200 mcg olopatadine per nostril alone.
2. The method according to claim 1 , wherein the pharmaceutical composition is a suspension comprising mometasone furoate in particulate form and olopatadine hydrochloride in solution.
3. The method according to claim 1 , wherein the composition is administered for a period of at least 1 week as 2 sprays per nostril twice daily.
4. The method according to claim 1 , wherein the allergic rhinitis is perennial allergic rhinitis.
5. The method according to claim 1 , wherein the allergic rhinitis is seasonal allergic rhinitis.
6. The method according to claim 1 , wherein the human subject exhibits a positive skin prick test to an allergen.
7. A method of treating one or more symptoms associated with seasonal allergic rhinitis in a human subject in need thereof comprising nasally administering to the human subject a fixed-dose pharmaceutical composition in the form of a suspension comprising mometasone furoate in particulate form and olopatadine hydrochloride in solution, wherein (i) the composition is administered as 2 sprays per nostril of the human subject, twice daily, (ii) each spray of the composition comprises about 25 mcg mometasone furoate and about 665 mcg olopatadine hydrochloride, and (iii) the twice daily administration of the pharmaceutical composition provides a faster onset of action than twice daily administration of olopatadine hydrochloride equivalent to about 1200 mcg olopatadine alone.
8. The method according to claim 7 , wherein the composition is administered twice daily for a period of 2 weeks.
9. The method according to claim 7 , wherein the human subject exhibits a positive skin prick test to an allergen.
10. The method of claim 1 , wherein the one or more symptoms are nasal symptoms.
11. The method of claim 10 , wherein the nasal symptoms are selected from nasal congestion, rhinorrhea, itching and sneezing.
12. The method of claim 10 , wherein the nasal symptoms comprise sneezing.
13. The method of claim 7 , wherein the one or more symptoms are nasal symptoms.
14. The method of claim 13 , wherein the nasal symptoms are selected from nasal congestion, rhinorrhea, itching and sneezing.
15. The method of claim 13 , wherein the nasal symptoms comprise sneezing.