Device and method for treating ophthalmic diseases

• US 6,436,427 B1
• Filed: 10/09/2001
• Issued: 08/20/2002
• Est. Priority Date: 03/22/1996
• Status: Expired due to Term

• Current Assignee: Neurotech USA, Inc. (Woodbrook Group Holdings, Inc.)
• Original Assignee: Neurotech S.A. (LivaNova Plc)
• Inventors: Baetge, E. Edward, Hammang, Joseph P., Spear, Peter D., Tsiarias, William G.
• Primary Examiner(s): AZPURU, CARLOS A
• Application Number:
  US09/973,325
• Publication Number:
  US 20020061327A1
• Time in Patent Office: 315 Days
• Field of Search: 424/427, 623/4
• US Class Current: 424/427
• CPC Class Codes: A61F 9/0017 implantable in, or in contact with, the eye, e.g. ocular inserts
• CPC Class Codes: A61K 9/0051 Ocular inserts, ocular implants

Abstract

The invention provides a method for delivering biologically active molecules to the eye by implanting biocompatible capsules containing a cellular source of the biologically active molecule. Also provided is a method of treating ophthalmic diseases using biocompatible capsules.

Claims

1. A method for delivering a biologically active molecule to the eye comprising:

implanting a capsule into the anterior chamber, posterior chamber, or vitreous of the eye, the capsule comprising a core containing living cells providing a cellular source of the biologically active molecule and a surrounding biocompatible jacket, the jacket permitting diffusion of the biologically active molecule into the eye, the capsule configured in a shape adapted to implantation in the anterior chamber, posterior chamber, or vitreous of the eye and optionally having a tether that is adapted to secure the capsule in place wherein the dosage of the biologically active molecule that diffuses into the eye is between 50 pg and 1000 ng per eye per patient per day.

2. The method of claim 1 herein the tether is selected from the group consisting of a loop, a disk, and a suture eyelet.

3. The method of claim 1 wherein the biologically active molecule is an anti-angiogenic factor.

4. The method of claim 3 wherein the anti-angiogenic factor is selected from the group consisting of vasculostatin;

angiostatin, endostatin, anti-integrins, vascular endothelial growth factor inhibitors (VEGF-inhibitors), platelet factor 4, heparinase, bFGF-binding molecules, the VEGF receptor Flt, and the VEGF receptor Flk.

5. A method for treating ophthalmic disorders in a patient suffering therefrom, comprising implanting into one or both eyes of the patient, a biocompatible capsule, the capsule comprising:

(a) a core comprising a cellular source of a biologically active molecule, and

(b) a jacket surrounding said core, the jacket comprising a biocompatible material that permits diffusion of the biologically active molecule to the eye in a therapeutically effective amount,

wherein the dosage of the biologically active molecule that diffuses into the eye is between 50 pg and 1000 ng per eye per patient per day and wherein the ophthalmic disorder is selected from the group consisting of uveitis, retinitis pigmentosa, glaucoma, age-related macular degeneration, and diabetic retinopathy.

6. The method of claim 5 wherein the biologically active molecule is an anti-angiogenic factor.

7. The method of claim 6 wherein the anti-angiogenic factor is selected from the group consisting of vasculostatin;

angiostatin, endostatin, anti-integrins, vascular endothelial growth factor inhibitors (VEGF-inhibitors), platelet factor 4, heparinase, bFGF-binding molecules, the VEGF receptor Flt, and the VEGF receptor Flk.