IP Library Granted Patent US 10,376,465
Granted Patent B2
US 10,376,465 · App. 15/277,062 · Granted Aug 13, 2019

Monovalent metal cation dry powders for inhalation

Inventors: Michael M. Lipp (Framingham, MA); Jean C. Sung (Cambridge, MA)
Assignee: Pulmatrix Operating Company, Inc.
A61K9/0073A61K9/0075A61K31/137A61K31/407A61K31/439A61K31/4745A61K31/496A61K31/5383A61K31/56A61K31/58A61K31/7036A61K38/00A61K38/28A61K39/00A61K39/395A61K47/02A61K47/183C07K16/00
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 10,376,465
App. No.
15/277,062
Granted
Aug 13, 2019
Kind
B2
Abstract

The present invention is directed toward respirable dry powders and particles for systemic delivery of pharmaceutically active agents or delivery to the respiratory tract. The dry powders contain one or more monovalent metal cations (such as Na + ), are small and dispersible.

Claims (7)

1. A respirable dry powder comprising respirable dry particles that comprise sodium sulfate, leucine, an active agent, wherein said active agent is an anti-fungal, and an optional excipient; wherein the respirable dry powder comprising respirable dry particles is characterized by a volume median geometric diameter (VMGD) at 1 bar as measured using a HELOS/RODOS system between 0.5 microns and 5 microns, a tap density of greater than 0.4 g/cc to about 1.2 g/cc, and a dispersibility ratio of 1 bar/4 bar of about 1.5 or less.

2. The respirable dry powder of claim 1 , wherein the sodium sulfate is present in an amount between about 20% and about 60%, wherein the weight percentages are on a dry basis of the respirable dry particles.

3. The respirable dry powder of claim 1 , wherein the leucine is present in an amount of about 50% or less, wherein the weight percentage is on a dry basis of the respirable dry particles.

4. The respirable dry powder of claim 1 , wherein the anti-fungal agent is present in an amount between about 10% and about 50%, wherein the weight percentages are on a dry basis of the respirable dry particles.

5. The respirable dry powder of claim 1 , wherein the active agent is present in an amount between about 50% and about 99.9%, wherein the weight percentages are on a dry basis of the respirable dry particles.

6. A method of treating a pulmonary disease comprising administering to the respiratory tract of a patient in need thereof an effective amount of the respirable dry powder of claim 1 .

7. The method of claim 6 , wherein the pulmonary disease is asthma, airway hyperresponsiveness, seasonal allergic allergy, bronchiectasis, chronic bronchitis, emphysema, chronic obstructive pulmonary disease, cystic fibrosis, or idiopathic pulmonary fibrosis.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 3, 2016
From: LIPP, MICHAEL M.; SUNG, JEAN C.
To: PULMATRIX, INC.
Reel/Frame 039922/0133 →
CHANGE OF NAME Recorded Oct 3, 2016
From: PULMATRIX, INC.
To: PULMATRIX OPERATING COMPANY, INC
Reel/Frame 040205/0815 →
Continuity (4)
Continuation 13876312
Provisional Application 61387883 · Sep 29, 2010
Provisional Application 61481879 · May 3, 2011
Related Publication 20170143624A1 · May 25, 2017
Cited By (1)
US 12,337,064