IP Library › Granted Patent US 8,591,885
Granted Patent B2
US 8,591,885 · App. 11/931,769 · Granted Nov 26, 2013

Carbonic anhydrase inhibitor sustained release intraocular drug delivery systems

Inventors: James N. Chang (Newport Beach, CA); Patrick M. Hughes (Aliso Viejo, CA); Gerald W. Devries (San Clemente, CA)
Assignee: Allergan, Inc.
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Quick Facts
Patent No.
US 8,591,885
App. No.
11/931,769
Granted
Nov 26, 2013
Kind
B2
Abstract

Biocompatible intraocular drug delivery systems include a carbonic anhydrase inhibitor therapeutic agent and a polymeric component in the form of an implant, a microparticle, a plurality of implants or microparticles, and combinations thereof. The therapeutic agent is released in a biologically active form, for example, the therapeutic agent may retain its three dimensional structure when released into an eye of a patient, or the therapeutic agent may have an altered three. The implants may be placed in an eye to treat or reduce the occurrence of one or more ocular conditions, such as retinal damage, including glaucoma and proliferative vitreoretinopathy among others.

Claims (6)

1. A sustained release intraocular drug delivery system comprising: a first therapeutic component selected from the group consisting of acetazolamide, brinzolamide, dorzolamide, and methazolamide, a second therapeutic component selected from ranibizumab and bevacizumab, and a polymeric component comprising hyaluronic acid;

wherein said system is formulated to release at least 10% of its active ingredient in the first two weeks following administration to the posterior chamber of a human eye.

2. The system of claim 1 wherein said system is formulated to release at least 20% of its active ingredient in the first two weeks following administration to the posterior chamber of a human eye.

3. The system of claim 1 wherein said system is formulated to release at least 30% of its active ingredient in the first two weeks following administration to the posterior chamber of a human eye.

4. The system of claim 1 wherein said system is formulated to release at least 40% of its active ingredient in the first two weeks following administration to the posterior chamber of a human eye.

5. The system of claim 1 in which said first therapeutic component is present in a viscous aqueous medium.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 17, 2008
From: CHANG, JAMES N.; HUGHES, PATRICK M.; DE VRIES, GERALD W.
To: ALLERGAN, INC.
Reel/Frame 020658/0760 →
Continuity (6)
Continuation In Part 11370301 · Mar 8, 2006
Continuation In Part 11364687 · Feb 27, 2006
Continuation In Part 11116698 · Apr 27, 2005
Provisional Application 60721600 · Sep 28, 2005
Provisional Application 60567423 · Apr 30, 2004
Related Publication 20110034448A1 · Feb 10, 2011