# US 10,869,833 B2 · Drug delivery devices for delivery of ocular therapeutic agents

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- Number: US 10,869,833 B2
- Document ID: US10869833B2
- Status: Granted
- Kind: B2
- Application number: 15/787,600
- Filed: 2017-10-18
- Published: 2018-08-16
- Granted: 2020-12-22
- Earliest claimed: 2010-05-17
- Applicants: Novaer Holdings, Inc.
- Inventors: Casey Kopczynski; Cheng-Wen Lin; Chris Sutay
- Web page: https://patentgrep.com/patent/US10869833B2

## CPC

- A61K 9/0051: {Ocular inserts or implants}
- A61F 9/0017: {implantable in, or in contact with, the eye, e.g. ocular inserts}
- A61K 31/00: Medicinal preparations containing organic active ingredients
- A61K 31/215: of carboxylic acids
- A61K 47/32: Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers {, poly(meth)acrylates, or polyvinyl pyrrolidone}
- A61K 47/36: Polysaccharides; Derivatives thereof, e.g. gums, starch, alginate, dextrin, hyaluronic acid, chitosan, inulin, agar or pectin
- A61P 27/02: Ophthalmic agents
- A61P 27/06: Antiglaucoma agents or miotics
- A61P 43/00: Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
- A61K: PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES (devices or methods specially adapted for bringing pharmaceutical products into particular physical or administering forms A61J3/00; chemical aspects of, or use of materials for deodorisation of air, for disinfection or sterilisation, or for bandages, dressings, absorbent pads or surgical articles A61L; soap compositions C11D)
- A61F: FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS (dental prosthetics A61C)
- A61P: SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS

## Abstract

Drug delivery devices comprising a non-bioabsorbable polymer structure configured to support a composition comprising an active agent. The devices include a plurality of portions fused together and a recess configured to support the composition. At least one of the portions includes an impermeable polymer and at least one other portion includes a rate-limiting water-permeable polymer. The rate-limiting water-permeable polymer allows for transportation of the active agent to an exterior of the device.

## Claims

### Claim 1

A device for insert in the eye, the device comprising:
a first portion comprising a rate-limiting water-permeable polymer;
a second portion fused to the first portion, the second portion including a composition comprising latanoprost free acid salt as an active agent; and
a third portion fused to the second portion, the third portion comprising a rate-limiting water-permeable polymer,
wherein the rate-limiting water-permeable polymer allows for transportation of the active agent to an exterior of the device and wherein the rate-limiting water-permeable polymer is configured to release the latanoprost free acid salt at a rate of 0.00025 to 0.0075 μg/h when the drug delivery device is to be placed episclerally or at a rate of 0.0005 to 0.015 μg/h when the drug delivery device is to be placed supraconjunctivally, and
wherein the device is configured to release 70% to 90% of the latanoprost free acid salt over a period of at least 30 days.

### Claim 2 (depends on 1)

The device set forth in claim 1, wherein at least one of the first portion and third portion comprises a polymer selected from the group consisting of: ethylene vinyl acetate with a vinyl acetate content of about 10% to about 50% by weight (EVA-10-50) and ethylene vinyl alcohol with a vinyl alcohol content of about 40% to about 80% by weight (EVOH-40-80).

### Claim 3 (depends on 1)

A method of treating an ocular condition comprising implanting the device of claim 1 into a conjunctiva of an eye.

### Claim 4 (depends on 3)

The method of claim 3, wherein the device is implanted episclerally in the eye and the active agent is released at a rate of about 0.00025 to about 0.0075 micrograms/hr.

### Claim 5 (depends on 4)

The method of claim 4, wherein the active agent comprises latanoprost arginine salt.

### Claim 6 (depends on 3)

The method of claim 3, wherein the device is implanted supraconjunctivally in the eye and the active agent is released at a rate of 0.00025 to 0.0075 micrograms/hr.

### Claim 7 (depends on 6)

The method of claim 6, wherein the active agent comprises latanoprost arginine salt.

### Claim 8 (depends on 1)

The device of claim 1, wherein the device is substantially cylindrical-shaped.

### Claim 9 (depends on 1)

The device of claim 1, wherein the portion and the third portion are manufactured from the same polymer.

### Claim 10 (depends on 1)

The device of claim 1, wherein the first polymer portion and the third portion are manufactured from a non-water soluble polymer.

### Claim 11 (depends on 10)

The device of claim 10, wherein the non-water soluble polymer is ethylene vinyl acetate having a vinyl acetate content of from 9% to 50% by weight.

### Claim 12 (depends on 11)

The device of claim 11, wherein the ethylene vinyl acetate content in the first portion and the third portion are the same.

### Claim 13 (depends on 11)

The device of claim 11, wherein the ethylene vinyl acetate content in the first portion and the third portion are different.

### Claim 14 (depends on 3)

The method of claim 3, wherein the device is inserted into the upper fornix of the eye or the lower fornix of the eye.
