Treatment of allergic rhinitis using a combination of mometasone and olopatadine
The present invention relates to a method of treating allergic rhinitis in a subject (e.g., a pediatric human subject) in need thereof comprising nasally administering to the subject an effective amount of a fixed-dose pharmaceutical composition comprising mometasone or its salt and olopatadine or its salt.
1. A method of treating allergic rhinitis and/or symptoms associated therewith in a human in need thereof comprising nasally administering to the human an effective amount of a fixed-dose pharmaceutical composition comprising mometasone furoate and olopatadine or its salt, in a weight ratio of from about 1:12 to about 1:53, wherein (i) the composition is nasally administered as 1 or 2 sprays per nostril, at least once daily, (ii) the pharmaceutical composition has a pH between about 3.3 and about 4.1, and (iii) each spray comprises olopatadine hydrochloride equivalent to about 600 mcg of olopatadine and about 25 mcg to about 50 mcg of mometasone furoate.
2. The method of claim 1 , wherein the composition comprises mometasone furoate and olopatadine or its salt in a weight ratio of about 1:13.3 to about 1:26.6.
3. The method of claim 1 , wherein the symptoms are selected from nasal symptoms.
4. The method of claim 3 , wherein the nasal symptoms are selected from nasal congestion, rhinorrhea, itching and sneezing.
5. The method of claim 1 , wherein the allergic rhinitis is seasonal allergic rhinitis.
6. The method of claim 1 , wherein the allergic rhinitis is perennial allergic rhinitis.
7. A method of treating allergic rhinitis in a human in need thereof comprising nasally administering to the human an effective amount of a fixed-dose pharmaceutical composition comprising mometasone furoate and olopatadine or its salt, wherein (i) the composition is nasally administered as 1 or 2 sprays per nostril of the human at least once daily, (ii) each spray comprises about 25 mcg to about 50 mcg of mometasone furoate and about 600 mcg of olopatadine or its salt and (iii) the method provides reduction in at least one treatment-related adverse effect relative to the use of olopatadine alone.
8. The method of claim 7 , wherein the composition comprises mometasone furoate and olopatadine or its salt in a weight ratio of about 1:13.3 to about 1:26.6.
9. The method of claim 7 , wherein the treatment-related adverse effect is epistaxis.
10. The method of claim 7 , wherein the symptoms are selected from 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 7 , wherein the allergic rhinitis is seasonal allergic rhinitis.
13. The method of claim 7 , wherein the allergic rhinitis is perennial allergic rhinitis.
14. A method of treating allergic rhinitis and/or symptoms associated therewith in a human in need thereof comprising nasally administering to the human an effective amount of a fixed-dose pharmaceutical composition comprising mometasone furoate and olopatadine or its salt, in a weight ratio of about 1:12 to about 1:53, wherein (i) the composition is nasally administered as 1 or 2 sprays per nostril, at least once daily, (ii) each spray comprises olopatadine hydrochloride equivalent to about 600 mcg of olopatadine and about 25 mcg to about 50 mcg of mometasone furoate, and (iii) the composition has a total impurity content of no more than 1.0% after storage at about 25° C. and 60% relative humidity for a period of at least 6 months.
15. A method of treating one or more symptoms associated with allergic rhinitis in a human subject in need thereof comprising nasally administering twice daily, two sprays per nostril of a fixed-dose aqueous pharmaceutical composition comprising mometasone furoate and olopatadine hydrochloride, wherein (i) the composition has a pH between about 3.3 and about 4.1, (ii) each spray comprises about 25 mcg of mometasone furoate and about 665 mcg olopatadine hydrochloride, (iii) the composition contains less than 2% of crystallized olopatadine hydrochloride, based on the 100% total weight of olopatadine hydrochloride in the composition, after 3 months of storage at 25° C.±2° C. and 60%±5% relative humidity.
16. The method of claim 15 , wherein the composition contains less than 2% of crystallized olopatadine hydrochloride, based on the 100% total weight of olopatadine hydrochloride in the composition, after 6 months of storage at 25° C.±2° C. and 60%±5% relative humidity.
17. A method of treating one or more symptoms associated with allergic rhinitis in a human subject in need thereof comprising nasally administering twice daily, two sprays per nostril of a fixed-dose aqueous pharmaceutical composition comprising mometasone furoate and olopatadine hydrochloride, wherein (i) the composition has a pH between about 3.3 and about 4.1, (ii) each spray comprises about 25 mcg of mometasone furoate and about 665 mcg olopatadine hydrochloride, (iii) the composition contains less than 2% of crystallized olopatadine hydrochloride, based on the 100% total weight of olopatadine hydrochloride in the composition, after 3 months of storage at 40° C.±2° C. and 75%±5% relative humidity.
18. The method of claim 17 , wherein the composition contains less than 2% of crystallized olopatadine hydrochloride, based on the 100% total weight of olopatadine hydrochloride in the composition, after 6 months of storage at 40° C.±2° C. and 75%±5% relative humidity.