IP Library Granted Patent US 11,654,213
Granted Patent B2
US 11,654,213 · App. 16/839,832 · Granted May 23, 2023

Implantable scaffolds for treatment of sinusitis and method of reducing inflammation

Inventors: Changcheng You (Northbridge, MA); Quynh Pham (Methuen, MA); Danny Concagh (Medfield, MA)
Assignee: LYRA THERAPEUTICS, INC.
A61L27/34A61F2/186A61F2/90A61K31/58A61L27/18A61L27/54A61L27/56A61L27/58A61M25/10A61M31/002A61F2210/0004A61F2250/0031A61F2250/0067A61L2300/222A61L2300/41A61L2300/604A61L2300/608A61M2025/105A61M2210/0681
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Quick Facts
Patent No.
US 11,654,213
App. No.
16/839,832
Granted
May 23, 2023
Kind
B2
Abstract

This disclosure describes, inter alia, materials, devices, kits and methods that may be used to treat chronic sinusitis. More specifically, a drug-eluting scaffold is implanted in the middle meatus to treat chronic sinusitis for weeks to months.

Claims (8)

1. A method for reducing inflammation of the nasal tissue caused by a sinus condition in an individual in need of treatment, said method comprising delivering an expandable implant to the sinus cavity where the implant self-expands and is in apposition with the walls of the sinus cavity, wherein the implant comprises a plurality of strands, said strands comprising a conformal coating comprising an anti-inflammatory agent in an amount effective to reduce inflammation, and a conformal topcoat layer, which is disposed over the conformal coating wherein release of the anti-inflammatory agent from the implant is continuous for a period of at least 12 weeks after delivery to the sinus cavity such that inflammation is reduced, wherein the thickness of the topcoat layer causes the anti-inflammatory agent to be released in a more linear fashion.

2. The method of claim 1 wherein the sinus condition is chronic sinusitis.

3. The method of claim 1 wherein less than 15% of the anti-inflammatory agent is released during the first week after delivery of the implant.

4. The method of claim 3 wherein 20 to 80% of the agent is released during the first 12 weeks after delivery of the implant.

5. The method of claim 3 wherein 30 to 70% of the agent is released during the first 12 weeks after delivery of the implant.

6. The method of claim 3 wherein 40 to 60% of the agent is released during the first 12 weeks after delivery of the implant.

7. The method of claim 1 wherein the anti-inflammatory agent is mometasone furoate.

8. The method of claim 7 wherein the quantity of mometasone furoate initially present in the implant per unit area ranges from 0.1 μg/mm 2 to 20 μg/mm 2 .

Assignments (2)
CHANGE OF NAME Recorded Jul 28, 2020
From: 480 BIOMEDICAL INC.
To: LYRA THERAPEUTICS, INC.
Reel/Frame 053332/0150 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 8, 2020
From: YOU, CHANGCHENG; PHAM, QUYNH; CONCAGH, DANNY
To: 480 BIOMEDICAL INC.
Reel/Frame 053150/0480 →
Continuity (7)
Continuation 16180413 · Nov 5, 2018
Continuation 15492103 · Apr 20, 2017
Continuation In Part 15197686 · Jun 29, 2016
Provisional Application 62186030 · Jun 29, 2015
Provisional Application 62289982 · Feb 2, 2016
Provisional Application 62332134 · May 5, 2016
Related Publication 20200316253A1 · Oct 8, 2020