IP Library Granted Patent US 7,803,368
Granted Patent B2
US 7,803,368 · App. 11/786,250 · Granted Sep 28, 2010

Pharmacological vitreolysis

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Quick Facts
Patent No.
US 7,803,368
App. No.
11/786,250
Granted
Sep 28, 2010
Kind
B2
Abstract

Methods of treating or preventing a disorder, or a complication of a disorder, of an eye of a subject, comprising contacting a vitreous and/or aqueous humor with a composition comprising a truncated form of plasmin comprising a catalytic domain of plasmin (TPCD) are disclosed. TPCDs include, but are not limited to, miniplasmin, microplasmin and derivatives and variants thereof. The methods of the invention can be used to reduce the viscosity of the vitreous, liquefy the vitreous, induce posterior vitreous detachment, reduce hemorrhagic blood from the eye, clear or reduce materials toxic to the eye, clear or reduce intraocular foreign substances from the eye, increase diffusion of a composition administered to an eye, reduce extraretinal neovascularization and any combinations thereof. The method can be used in the absence of, or as an adjunct to, vitrectomy.

Claims (22)

1. A method of liquefying a vitreous and/or inducing posterior vitreous detachment of an eye of a subject having macular edema, comprising contacting the vitreous and/or an aqueous humor in the eye of the subject having macular edema with an effective amount of a composition comprising microplasmin, wherein the method results in liquefying a vitreous and/or inducing posterior vitreous detachment of the eye of a subject having macular edema.

2. The method of claim 1 , wherein said microplasmin is selected from the group consisting of recombinant microplasmin, stabilized microplasmin, and stabilized, recombinant microplasmin.

3. The method of claim 1 , wherein the composition is a liquid solution, and wherein the step of contacting the vitreous and/or the aqueous humor with the composition comprises injecting the liquid solution into the vitreous and/or the aqueous humor.

4. The method of claim 1 , wherein the subject is a human.

5. The method of claim 1 , wherein the method is performed in the absence of non-pharmacological vitrectomy.

6. The method of claim 1 , wherein the method is performed as an adjunct to vitrectomy.

7. The method of claim 1 , wherein an effective amount of microplasmin is in the range of 0.005 mg to 0.2 mg per eye.

8. A method of treating macular edema, or a complication of macular edema, of an eye of a subject, comprising contacting a vitreous and/or an aqueous humor in the eye of the subject with an effective amount of a composition comprising microplasmin, wherein the method results in vitreous liquefaction and/or posterior vitreous detachment in the eye of the subject, thereby treating the macular edema, or the complication of the macular edema, of the eye of the subject.

9. The method of claim 8 , wherein said microplasmin is selected from the group consisting of recombinant microplasmin, stabilized microplasmin, and stabilized, recombinant microplasmin.

10. The method of claim 8 , wherein the composition is a liquid solution, and wherein the step of contacting the vitreous and/or the aqueous humor with the composition comprises injecting the liquid solution into the vitreous and/or the aqueous humor.

11. The method of claim 8 , wherein the subject is a human.

12. The method of claim 8 , wherein the method is performed in the absence of non-pharmacological vitrectomy.

13. The method of claim 8 , wherein the method is performed as an adjunct to vitrectomy.

14. The method of claim 8 , wherein an effective amount of microplasmin is in the range of 0.005 mg to 0.2 mg per eye.

15. A method of performing a vitrectomy in a subject having macular edema, comprising contacting a vitreous and/or aqueous humor of an eye of the subject having macular edema with an effective amount of a composition comprising microplasmin, prior to or at the same time as the removal of the vitreous.

16. The method of claim 15 , wherein said microplasmin is selected from the group consisting of recombinant microplasmin, stabilized microplasmin, and stabilized, recombinant microplasmin.

17. The method of claim 15 , wherein the composition is a liquid solution, and wherein the step of contacting the vitreous and/or the aqueous humor with the composition comprises injecting the liquid solution into the vitreous and/or the aqueous humor.

18. The method of claim 15 , wherein the subject is a human.

19. The method of claim 15 , wherein an effective amount of microplasmin is in the range of 0.005 mg to 0.2 mg per eye.

20. The method of claim 4 , wherein the human subject is administered human microplasmin.

21. The method of claim 11 , wherein the human subject is administered human microplasmin.

22. The method of claim 18 , wherein the human subject is administered human microplasmin.

Assignments (3)
CHANGE OF NAME Recorded Feb 13, 2019
From: THROMBOGENICS N.V.
To: OXURION NV
Reel/Frame 049255/0733 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 23, 2009
From: PAKOLA, STEVE; DE SMET, MARC
To: THROMB-X NV
Reel/Frame 022589/0970 →
CHANGE OF NAME Recorded Apr 23, 2009
From: THROMB-X NV
To: THROMBOGENICS NV
Reel/Frame 022590/0012 →