IP Library Granted Patent US 8,772,337
Granted Patent B2
US 8,772,337 · App. 12/666,778 · Granted Jul 8, 2014

Preservative-free prostaglandin-based ophthalmic solution

Inventors: Frederic Pilotaz (Vaulanaveys le Haut, FR); Fabrice Mercier (Clermont Ferrand, FR); Henri Chibret (Joze, FR)
Assignee: Laboratoires Thea
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Quick Facts
Patent No.
US 8,772,337
App. No.
12/666,778
Granted
Jul 8, 2014
Kind
B2
Abstract

The present invention provides an ophthalmic solution without an antimicrobial preservative. The solution includes as an active substance at least one prostaglandin and as a solubilizing agent, a surfactant, where the solubilizing agent is polyoxyl-15-hydroxystearate.

Claims (14)

1. An ophthalmic solution without an antimicrobial preservative comprising as an active substance at least one prostaglandin and as a solubilizing agent, a surfactant wherein the solubilizing agent is polyoxyl-15-hydroxystearate.

2. The solution according to claim 1 , wherein the concentration of the solubilizing agent in the solution is between 1 and 20 g/l.

3. The solution according to claim 1 , wherein the prostaglandin concentration in the solution is between 0.02 and 1.5 g/l.

4. The solution according to claim 1 wherein the prostaglandin is selected from the group consisting of 17-phenyl-13,14 dihydro trinor prostaglandin F 2α isopropyl ester (latanoprost), 20-ethyl prostaglandin F 2α , (+)-fluprostenol isopropyl ester (travoprost), 17-phenyl trinor prostaglandin F 2α amide, 17-phenyl-13,14 dihydro trinor prostaglandin F 2α ethyl amide (bimatoprost), tafluprost prostaglandin F 2α ethanolamide, bimatoprost (free acid)-d 4 , bimatoprost-d 4 , latanoprost ethyl amide, 13,14 dihydro-15-keto-20-ethyl prostaglandin F 2α (unoprostone), and 13,14 dihydro-15-keto-20-ethyl prostaglandin F 2α isopropyl ester (unoprostone isopropyl ester).

5. The solution according to claim 1 , further comprising an antiglaucoma agent selected from the group consisting of beta-blockers, carbonic anhydrase inhibitors and alpha-adrenergic agonists.

6. The solution according to claim 5 , wherein the antiglaucoma agent forms between 0.1 and 0.5% by weight of the solution.

7. The solution according to claim 1 , further comprising an additive selected from the group consisting of isotonicity agents, antioxidants and buffer systems.

8. A single-use or multi-dose vial produced in additive-free LDPE containing the ophthalmic solution of claim 1 .

9. A method of treating glaucoma, reducing intraocular pressure, or providing neuroprotection to retinal tissues in a human or animal in need thereof comprising administering to the human or animal a solution according to claim 1 .

10. A method according to claim 9 , comprising administering to the human or animal, via the topical route, one drop per day of the solution into each eye.

11. The solution according to claim 1 , wherein the concentration of the solubilizing agent in the solution is between 2 and 10 g/l.

12. A method of treating glaucoma in an eye of a human in need thereof comprising topically administering to the eye of the human an effective amount of the solution according to claim 1 .

13. A method of reducing intraocular pressure in an eye of a human in need thereof comprising topically administering to the eye of the human an effective amount of the solution according to claim 1 .

14. A method of providing neuroprotection to retinal tissues in an eye of a human in need thereof comprising topically administering to the eye of the human an effective amount of the solution according to claim 1 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2009
From: PILOTAZ, FREDERIC; MERCIER, FABRICE; CHIBRET, HENRI
To: LABORATOIRES THEA
Reel/Frame 023706/0060 →
Priority Claims (1)
FR 07 05272 · Jul 20, 2007 · national
Continuity (1)
Related Publication 20100210720A1 · Aug 19, 2010