IP Library Granted Patent US 11,819,569
Granted Patent B2
US 11,819,569 · App. 16/396,272 · Granted Nov 21, 2023

Treating inflammation with inhaled aspirin

Inventor: Kambiz Yadidi (Los Angeles, CA)
Assignee: VECTURA INC.
A61K9/0075A61K31/616A61M15/0045A61K9/14A61M2202/064A61P7/02A61P29/00Y10T428/2982
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 11,819,569
App. No.
16/396,272
Granted
Nov 21, 2023
Kind
B2
Abstract

The subject technology relates generally to pulmonary delivery of NSAIDs, such as aspirin.

Claims (12)

1. A method of treating or reducing the risk of a thromboembolic event in a subject in need thereof, the method comprising administering by pulmonary delivery to the subject a dry powder composition from within a dry powder inhaler, wherein the dry powder composition in the inhaler before the administering is provided in a capsule or blister and comprises acetylsalicylic acid or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable excipient and the dry powder composition comprises 95% or more by weight of acetylsalicylic acid or a pharmaceutically acceptable salt thereof, wherein the dry powder composition has a mass median aerodynamic diameter (MMAD) of less than 5 μm, and wherein the dry powder composition delivers at least 50% of administered acetylsalicylic acid or a pharmaceutically acceptable salt thereof to systemic circulation of the subject within about 15 minutes after the administering.

2. The method of claim 1 , wherein the dry powder composition delivers at least 60% of administered acetylsalicylic acid or a pharmaceutically acceptable salt thereof to systemic circulation of the subject within about 15 minutes of administration.

3. The method of claim 1 , wherein the dry powder composition delivers at least 70% of administered acetylsalicylic acid or a pharmaceutically acceptable salt thereof to systemic circulation of the subject within about 15 minutes of administration.

4. The method of claim 1 , wherein the dry powder composition delivers at least 80% of administered acetylsalicylic acid or a pharmaceutically acceptable salt thereof to systemic circulation of the subject within about 15 minutes of administration.

5. The method of claim 1 , wherein the thromboembolic event is selected from myocardial infarction, deep venous thrombosis, pulmonary embolism and thrombotic stroke.

6. The method according to claim 1 , wherein the dry powder composition does not contain lactose.

7. A method for treating or reducing the risk of a thrombotic event in a subject in need thereof, the method comprising administering by pulmonary delivery to the subject a dry powder composition from within a dry powder inhaler, wherein the dry powder composition in the inhaler before the administering is provided in a capsule or blister and comprise 95% or more by weight of acetylsalicylic acid or a pharmaceutically acceptable salt thereof, the dry powder composition has a volume median geometric diameter (VMGD) of less than 5 μm, and wherein the dry powder composition delivers at least 50% of administered acetylsalicylic acid or a pharmaceutically acceptable salt thereof to systemic circulation of the subject within about 15 minutes after the administering.

8. The method of claim 7 , wherein the dry powder composition delivers at least 60% of administered acetylsalicylic acid or a pharmaceutically acceptable salt thereof to systemic circulation of the subject within about 15 minutes of administration.

9. The method of claim 7 , wherein the dry powder composition delivers at least 70% of administered acetylsalicylic acid or a pharmaceutically acceptable salt thereof to systemic circulation of the subject within about 15 minutes of administration.

10. The method of claim 7 , wherein the dry powder composition delivers at least 80% of administered acetylsalicylic acid or a pharmaceutically acceptable salt thereof to systemic circulation of the subject within about 15 minutes of administration.

11. The method of claim 7 , wherein thromboembolic event is selected from myocardial infarction, deep venous thrombosis, pulmonary embolism and thrombotic stroke.

12. The method according to claim 7 , wherein the dry powder composition does not contain lactose.

Assignments (3)
CHANGE OF NAME Recorded May 12, 2025
From: VECTURA INC.
To: ASPEYA US INC.
Reel/Frame 071251/0047 →
CONFIRMATION OF ASSIGNMENT Recorded Apr 24, 2023
From: OTITOPIC INC.
To: VECTURA INC.
Reel/Frame 063448/0621 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2019
From: YADIDI, KAMBIZ
To: OTITOPIC INC.
Reel/Frame 049801/0833 →
Continuity (4)
Continuation 16216924 · Dec 11, 2018
Continuation 13949862 · Jul 24, 2013
Provisional Application 61817435 · Apr 30, 2013
Related Publication 20190247304A1 · Aug 15, 2019
Cited By (1)
US 12,508,227