Stabilized oxymetazoline formulations and their uses
The present invention provides stabilized cream formulations of oxymetazoline and uses thereof. The present invention also provides a method of treating facial erythema associated with rosacea in a patient in need of such treatment, comprising topically administering once or twice daily to the site of erythema on the face of the patient a pharmaceutical composition comprising 0.5%, 1.0% or 1.5% oxymetazoline or a pharmaceutically acceptable salt thereof as the sole active ingredient.
1. A method of treating persistent facial erythema associated with rosacea in a female adult human patient in need of such treatment, the method comprising topically administering once daily to one or more sites of erythema on the face of the adult human patient, a pharmaceutical composition comprising 1.0% w/w oxymetazoline hydrochloride as the sole active ingredient, wherein the pharmaceutical composition is a cream.
2. The method of claim 1 , wherein the female patient is aged 45 to 64.
3. The method of claim 1 , wherein the pharmaceutical composition further comprises methylparaben, propylparaben, phenoxyethanol, sodium citrate, citric acid, disodium edetate, butylated hydroxytoluene, lanolin, medium chain triglycerides, diisopropyl adipate, oleyl alcohol, PEG-300, PEG-6 stearate, PEG-32 stearate, glycol stearate, cetostearyl alcohol, ceteareth-6, stearyl alcohol, ceteareth-25, and purified water.
4. The method of claim 1 , wherein the pharmaceutical composition comprises about 1.0% w/w oxymetazoline HCl, about 0.2% w/w methylparaben, about 0.05% w/w propylparaben, about 0.8% w/w phenoxyethanol, about 0.3% w/w sodium citrate dihydrate, about 0.2% w/w anhydrous citric acid, about 0.01% w/w disodium edetate, about 0.05% w/w butylated hydroxytoluene, about 2% w/w anhydrous lanolin, about 7% w/w medium chain triglycerides, about 7% w/w diisopropyl adipate, about 7% w/w oleyl alcohol, about 4% w/w polyethylene glycol PEG-300, about 8% w/w polyethylene glycol PEG-6/polyethylene glycol PEG-32/glycol stearate, about 8% w/w cetostearyl alcohol, about 2% w/w ceteareth-6/stearyl alcohol, about 2% w/w ceteareth-25, and purified water.
5. The method of claim 1 , wherein the administering results in an at least 2-grade improvement from baseline on Clinician's Erythema Assessment (CEA) scale, Subject Self-Assessment of Erythema (SSA), or both.
6. The method of claim 1 , wherein the administering results in an at least 1-grade improvement from baseline on Clinician's Erythema Assessment (CEA) scale, Subject Self-Assessment of Erythema (SSA), or both.
7. The method of claim 1 , wherein the administering once daily for 28 days results in a mean C max ±standard deviation (SD) of 66.4±67.1 pg/mL in said adult human patient.
8. The method of claim 1 , wherein the administering once daily for 28 days results in mean±SD AUC 0-24 of 1050±992 pg·hr/mL in said adult human patient.
9. The method of claim 1 , wherein the administering comprises topically applying a pea sized amount of the pharmaceutical composition to the one or more sites of erythema on the face of the adult human patient.
10. A method of treating persistent facial erythema associated with rosacea in a female adult human patient in need of such treatment, the method comprising topically administering once daily to the face of the adult human patient, a pharmaceutical composition comprising 1.0% w/w oxymetazoline hydrochloride as the sole active ingredient, wherein the pharmaceutical composition is a cream.
11. The method of claim 10 , wherein the female patient is aged 45 to 64.
12. The method of claim 10 , wherein the topically administering comprises applying a thin layer of said pharmaceutical composition over the entire face avoiding the eyes and lips.
13. The method of claim 10 , wherein the pharmaceutical composition further comprises methylparaben, propylparaben, phenoxyethanol, sodium citrate, citric acid, disodium edetate, butylated hydroxytoluene, lanolin, medium chain triglycerides, diisopropyl adipate, oleyl alcohol, PEG-300, PEG-6 stearate, PEG-32 stearate, glycol stearate, cetostearyl alcohol, ceteareth-6, stearyl alcohol, ceteareth-25, and purified water.
14. The method of claim 10 , wherein the pharmaceutical composition further comprises about 1.0% w/w oxymetazoline HCl, about 0.2% w/w methylparaben, about 0.05% w/w propylparaben, about 0 8% w/w phenoxyethanol, about 0.3% w/w sodium citrate dihydrate, about 0.2% w/w anhydrous citric acid, about 0.01% w/w disodium edetate, about 0.05% w/w butylated hydroxytoluene, about 2% w/w anhydrous lanolin, about 7% w/w medium chain triglycerides, about 7% w/w diisopropyl adipate, about 7% w/w oleyl alcohol, about 4% w/w polyethylene glycol PEG-300, about 8% w/w polyethylene glycol PEG-6/polyethylene glycol PEG-32/glycol stearate, about 8% w/w cetostearyl alcohol, about 2% w/w ceteareth-6/stearyl alcohol, about 2% w/w ceteareth-25, and purified water.
15. The method of claim 10 , wherein the administering results in an at least 2-grade improvement from baseline on Clinician's Erythema Assessment (CEA) scale, Subject Self-Assessment of Erythema (SSA), or both.
16. The method of claim 10 , wherein the administering once daily for 28 days results in a mean C max ±SD of 66.4±67.1 pg/mL in the adult patient.
17. The method of claim 10 , wherein the administering once daily for 28 days results in a mean AUC 0-24 ±SD of 1050±992 pg·hr/mL in the adult patient.