IP Library Granted Patent US 11,872,308
Granted Patent B2
US 11,872,308 · App. 18/128,705 · Granted Jan 16, 2024

Dry powder formulations of epinephrine and associated methods

Inventors: Scott Lyman (Raleigh, NC); Barry Bleske (Albuquerque, NM); Ted William Lanpher (Half Moon Bay, CA)
Assignee: BELHAVEN BIOPHARMA INC.
A61K9/0075A61K9/0043A61K31/137A61K31/277A61K31/417A61K47/02A61K47/26A61K47/38
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Quick Facts
Patent No.
US 11,872,308
App. No.
18/128,705
Granted
Jan 16, 2024
Kind
B2
Abstract

Provided herein are dry powder formulations comprising epinephrine alone or in combination with at least one enabling agent suitable for nasal application. Also provided are unit dose forms and devices comprising such formulations and methods of using such formulations for the treatment of various conditions including anaphylaxis, anaphylactoid reaction, respiratory conditions, hemodynamic collapse, and for administration during cardiopulmonary arrest and other life-threatening conditions.

Claims (42)

1. An intranasal device for administration of a pharmaceutical composition comprising:

a reservoir and a means for discharging one or more doses of the pharmaceutical composition, wherein the reservoir contains a quantity of the pharmaceutical composition;

wherein the pharmaceutical composition is a dry powder comprising:

epinephrine or a pharmaceutically acceptable salt thereof, wherein the pharmaceutical composition provides a dose of about 0.01 mg to about 10 mg of the epinephrine or the pharmaceutically acceptable salt thereof;

a polysorbate, wherein the pharmaceutical composition comprises about 0.01% w/v to about 5% w/v of the polysorbate; and

a carrier;

wherein the pharmaceutical composition does not include an alpha-adrenergic blocker; and

wherein the intranasal device further includes a nasal probe and an actuator.

2. The intranasal device of claim 1 , wherein a median particle diameter of the epinephrine or the pharmaceutically acceptable salt thereof is about 20 μm to about 75 μm.

3. The intranasal device of claim 1 , wherein the pharmaceutical composition further comprises an anticaking agent.

4. The intranasal device of claim 1 , wherein the pharmaceutical composition further comprises at least one antihistamine.

5. The intranasal device of claim 1 , wherein the pharmaceutical composition further comprises at least one steroid.

6. The intranasal device of claim 1 , wherein the pharmaceutical composition further comprises a catechol-o-methyl transferase (COMT) inhibitor.

7. The intranasal device of claim 1 , wherein the pharmaceutical composition further comprises one or more agents selected from a group consisting of a mucosal permeation or penetration enhancer, a mucoadhesive, a mucosal transit slowing agent, a mucosal transport enhancer, or any combination thereof.

8. The intranasal device of claim 1 , wherein the intranasal device has 360° functionality and is constructed and configured to dispense a dose from any position.

9. The intranasal device of claim 1 , wherein the intranasal device further includes an intranasal device global positioning system (GPS) device or is coupled to a GPS device, wherein the intranasal device GPS or the GPS device is constructed and configured to provide location data.

10. The intranasal device of claim 1 , wherein the intranasal device further includes a communications interface, wherein the communications interface is constructed and configured to transmit data wirelessly to at least one remote device.

11. The intranasal device of claim 1 , wherein the carrier includes mannitol, a cyclodextrin, citric acid, lactose, and/or sodium carboxymethylcellulose.

12. The intranasal device of claim 1 , wherein the pharmaceutical composition does not include a preservative.

13. The intranasal device of claim 1 , wherein the quantity of the pharmaceutical composition is between about 5 mg and about 75 mg.

14. The intranasal device of claim 1 , wherein the intranasal device further includes a sensor that is adapted to detect a displacement or a deformation of a portion of the intranasal device when the dry powder is dispensed from the reservoir.

15. The intranasal device of claim 14 , wherein the intranasal device further includes a display and a power supply, a timer, a clock, and/or a printed circuit board, wherein the display is constructed and configured to display a time of dose dispensation.

16. A kit for intranasal administration of a pharmaceutical composition comprising:

at least one intranasal device, wherein each of the at least one intranasal device includes a reservoir and a means for discharging one or more doses of the pharmaceutical composition, wherein the reservoir contains a quantity of the pharmaceutical composition; and

a pouch and/or a hard case, wherein the at least one intranasal device is enclosed in the pouch and/or the hard case;

wherein the pharmaceutical composition is a dry powder comprising:

epinephrine or a pharmaceutically acceptable salt thereof, wherein the pharmaceutical composition provides a dose of about 0.01 mg to about 10 mg of the epinephrine or the pharmaceutically acceptable salt thereof;

a polysorbate, wherein the pharmaceutical composition comprises about 0.01% w/v to about 5% w/v of the polysorbate; and

a carrier;

wherein the pharmaceutical composition does not include an alpha-adrenergic blocker; and

wherein the at least one intranasal device further includes a nasal probe and an actuator.

17. The kit of claim 16 , wherein the hard case includes a desiccant plastic.

18. The kit of claim 16 , wherein the pouch and/or the hard case is water resistant or waterproof.

19. The kit of claim 16 , wherein the pouch and/or the hard case is Modular Lightweight Load-carrying Equipment (MOLLE)-compatible.

20. An intranasal device for administration of a pharmaceutical composition comprising:

a reservoir and a means for discharging one or more doses of the pharmaceutical composition, wherein the reservoir contains a quantity of the pharmaceutical composition;

wherein the pharmaceutical composition is a spray-dried powder comprising:

epinephrine or a pharmaceutically acceptable salt thereof, wherein the pharmaceutical composition provides a dose of about 0.01 mg to about 10 mg of the epinephrine or the pharmaceutically acceptable salt thereof;

polysorbate 80, wherein the pharmaceutical composition comprises about 0.01% w/v to about 2% w/v of the polysorbate 80; and

a carrier;

wherein the pharmaceutical composition does not include an alpha-adrenergic blocker; and

wherein the intranasal device further includes a nasal probe and an actuator.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 10, 2023
From: LYMAN, SCOTT; BLESKE, BARRY EUGENE; LANPHER, TED WILLIAM
To: BELHAVEN BIOPHARMA INC.
Reel/Frame 063273/0231 →
Continuity (3)
Continuation 17836588 · Jun 9, 2022
Provisional Application 63209221 · Jun 10, 2021
Related Publication 20230233460A1 · Jul 27, 2023
Cited By (3)
US 12,605,517 US 12,653,972 US 12,661,315