Sustained release formulations for the treatment of intraocular pressure or glaucoma
View Patent ↗The present embodiments provide for methods of treating elevated intraocular pressure or glaucoma using a sustained release medicament consisting of prostaglandin in benzyl benzoate that is injected intraocularly no more frequently than once every two months.
1. A liquid medicament for use in the treatment of elevated intraocular pressure or glaucoma in a subject, the medicament consisting of prostaglandin in benzyl benzoate, the prostaglandin present at about 0.1% (w/w) to about 5% (w/w), inclusive, the medicament for a dosing regimen in which about 5 μL to about 60 μL, inclusive, is injected into the anterior chamber or vitreous of the eye once per interval of no less than about two months.
2. The medicament of claim 1 , wherein the liquid medicament is injected once per interval of no less than about three months.
3. The medicament of claim 2 , wherein the liquid medicament is injected once per interval of no less than about six months.
4. The medicament of claim 1 , wherein the prostaglandin is latanoprost.
5. The medicament of claim 4 , wherein the liquid medicament is from about 20 μL to about 25 μL, inclusive, and the medicament contains latanoprost at a concentration of about 0.1% (w/w) to about 1% (w/w), inclusive.
6. The medicament of claim 5 , wherein the liquid medicament is injected once per interval of no less than about two months.
7. The medicament of claim 5 , wherein the liquid medicament is injected once per interval of no less than about three months.
8. The medicament of claim 5 , wherein the liquid medicament is injected once per interval of no less than about six months.
9. A sustained release unit dose for treating elevated intraocular pressure or glaucoma in a subject, wherein the unit dose is a liquid consisting of latanoprost at a concentration of about 0.25% (w/w) to about 5% (w/w), inclusive, in benzyl benzoate, wherein the unit dose is about 5 μL to about 60 μL, inclusive, is administered by intravitreal injection, and optionally thereafter is re-administered no more frequently than once about every two months.
10. The sustained release unit dose as in claim 9 , wherein the unit dose contains latanoprost at about 0.1% (w/w) to about 1% (w/w), inclusive, and optionally is re-administered no more frequently than once about every three months.
11. The sustained release unit dose as in claim 9 , wherein said unit dose is about 20 μL of about 1% (w/w) latanoprost in benzyl benzoate and is equivalent to about 224 μg of latanoprost dose.
12. The sustained release unit dose as in claim 9 , wherein said unit dose is about 50 μL of about 1% (w/w) latanoprost in benzyl benzoate and is equivalent to about 559 μg of latanoprost dose.
13. The sustained release unit dose as in claim 9 , wherein said unit dose is about 20 μL of about 2% (w/w) latanoprost in benzyl benzoate and is equivalent to about 447 μg of latanoprost dose.
14. The sustained release unit dose as in claim 9 , wherein said unit dose is about 50 μL of about 2% (w/w) latanoprost in benzyl benzoate and is equivalent to about 1118 μg of latanoprost dose.
15. The sustained release unit dose as in claim 9 , wherein said unit dose is about 20 μL of about 4% (w/w) latanoprost in benzyl benzoate and is equivalent to about 894 μg of latanoprost dose.
16. The sustained release unit dose as in claim 9 , wherein said unit dose is about 50 μL of about 4% (w/w) latanoprost in benzyl benzoate and is equivalent to about 2236 μg of latanoprost dose.
17. The sustained release unit dose as in claim 9 , wherein said unit dose is expressed as about 224 μg, 447 μg, 559 μg, 894 μg, 1118 μg, or about 2236 μg equivalent latanoprost dose.