IP Library Granted Patent US 10,149,823
Granted Patent B2
US 10,149,823 · App. 13/949,862 · Granted Dec 11, 2018

Dry powder formulations and methods of use

Inventor: Kambiz Yadidi (Los Angeles, CA)
Assignee: OTITOPIC INC.
A61K9/0075A61K31/616A61M15/0045A61K9/14A61M2202/064A61P7/02Y10S514/958Y10T428/2982
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 10,149,823
App. No.
13/949,862
Granted
Dec 11, 2018
Kind
B2
Abstract

A respirable dry powder can include acetylsalicylic acid or a pharmaceutically acceptable salt thereof. The dry powder can include a mixture of: (i) dry particles have a volume median geometric diameter (VMGD) less than 5 μm; and (ii) dry particles have a volume median geometric diameter (VMGD) of about 15 μm or more.

Claims (12)

1. A method of treating thrombosis or reducing risk of a thromboembolic event in a subject in need thereof, the method comprising administering by pulmonary delivery to the subject dry particles free of excipients from within a dry powder inhaler, wherein the dry particles in the inhaler before the administering are provided in a capsule or blister and consist of acetylsalicylic acid or a pharmaceutically acceptable salt thereof, wherein the dry particles have a mass median aerodynamic diameter (MMAD) of less than 5 μm, and wherein the dry particles deliver at least 50% of administered acetylsalicylic acid to systemic circulation of the subject with about 15 minutes after the administering.

2. The method of claim 1 , wherein the dry powder formulation delivers at least 60% of administered acetylsalicylic acid to systemic circulation of the subject within about 15 minutes of administration.

3. The method of claim 1 , wherein the dry powder formulation delivers at least 70% of administered acetylsalicylic acid to systemic circulation of the subject within about 15 minutes of administration.

4. The method of claim 1 , wherein the dry powder formulation delivers at least 80% of administered acetylsalicylic acid to systemic circulation of the subject within about 15 minutes of administration.

5. The method of claim 1 , wherein the dose of acetylsalicylic acid administered to the subject is about 40 mg or less.

6. The method of claim 5 , wherein the dose of acetylsalicylic acid administered to the subject is about 30 mg or less.

7. A method of treating thrombosis or reducing risk of a thromboembolic event in a subject in need thereof, the method comprising administering by pulmonary delivery to the subject dry particles free of excipients from within a dry powder inhaler, wherein the dry particles in the inhaler before the administering are provided in a capsule or blister and consist of acetylsalicylic acid or a pharmaceutically acceptable salt thereof, wherein the dry particles have a geometric diameter (VMGD) of less than 5 μm, and wherein the dry particles deliver at least 50% of administered acetylsalicylic acid to systemic circulation of the subject with about 15 minutes after the administering.

8. The method of claim 7 , wherein the dry powder formulation delivers at least 60% of administered acetylsalicylic acid to systemic circulation of the subject within about 15 minutes of administration.

9. The method of claim 7 , wherein the dry powder formulation delivers at least 70% of administered acetylsalicylic acid to systemic circulation of the subject within about 15 minutes of administration.

10. The method of claim 7 , wherein the dry powder formulation delivers at least 80% of administered acetylsalicylic acid to systemic circulation of the subject within about 15 minutes of administration.

11. The method of claim 7 , wherein the dose of acetylsalicylic acid administered to the subject is about 40 mg or less.

12. The method of claim 11 , wherein the dose of acetylsalicylic acid administered to the subject is about 30 mg or less.

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 30, 2013
From: YADIDI, KAMBIZ
To: OTITOPIC INC.
Reel/Frame 030905/0301 →
Continuity (2)
Provisional Application 61817435 · Apr 30, 2013
Related Publication 20140322328A1 · Oct 30, 2014