IP Library Granted Patent US 9,707,192
Granted Patent B2
US 9,707,192 · App. 14/328,652 · Granted Jul 18, 2017

Lipolytic methods

Inventor: John Daniel Dobak (La Jolla, CA)
Assignee: NEOTHETICS, INC.
A61K31/138A61K9/0014A61K9/0019A61K9/0021A61K31/167A61K31/195A61K31/4535A61K31/567A61K31/573A61K31/58A61K47/10A61K47/14A61K47/34A61K47/36A61K9/5031
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Quick Facts
Patent No.
US 9,707,192
App. No.
14/328,652
Granted
Jul 18, 2017
Kind
B2
Abstract

Compositions, formulations, methods, and systems for treating regional fat deposits comprise contacting a targeted fat deposit with a composition comprising long acting beta-2 adrenergic receptor agonist and a compound that reduces desensitization of the target tissue to the long acting beta-2 adrenergic receptor agonist, for example, glucocorticosteroids and/or ketotifen. Embodiments of the composition are administered, for example, by injection, and/or transdermally.

Claims (18)

1. A method of administration to subcutaneous tissue for reducing regional fat in a subject, the method comprising contacting the subcutaneous tissue of the subject with a pharmaceutically effective amount of a lipophilic long-acting selective beta-2 adrenergic receptor agonist, or a salt, solvate, or combinations thereof in an amount that is up to about 250 micrograms per week, provided that the contacting is less frequently than once per day, and wherein the lipophilic long-acting selective beta-2 adrenergic receptor agonist comprises at least one of salmeterol, formoterol, bambuterol, or any salt, solvate, or any combination thereof.

2. The method of claim 1 , provided that the lipophilic long-acting selective beta-2 adrenergic receptor agonist comprises salmeterol xinafoate.

3. The method of claim 1 , provided that the lipophilic long-acting selective beta-2 adrenergic receptor agonist comprises formoterol fumarate.

4. The method of claim 1 , provided that the contacting comprises administration by subcutaneous injection.

5. The method of claim 2 , provided that the contacting comprises administration by subcutaneous injection.

6. The method of claim 1 , provided that the contacting comprises transdermal administration.

7. The method of claim 2 , provided that the contacting comprises transdermal administration.

8. The method of claim 1 , provided that the lipophilic long-acting selective beta-2 agonist comprises salmeterol, or any salt, solvate, or any combination thereof, and the pharmaceutically effective amount is up to about 100 micrograms per day contacted.

9. The method of claim 1 , provided that the lipophilic long-acting selective beta-2 agonist comprises formoterol, or any salt, solvate, or combination thereof, and the pharmaceutically effective amount is up to about 50 micrograms per day contacted.

10. The method of claim 1 , provided that at least one of the lipophilic long-acting selective beta-2 adrenergic receptor agonist is administered by single needle injection or by needleless injection.

11. The method of claim 1 , provided that the subcutaneous tissue comprises periorbital fat, submental fat, abdominal fat, waist fat, hip fat, or thigh fat.

12. The method of claim 2 , provided that the administration is subcutaneously or transdermally.

13. A method of reducing regional fat accumulation in a subject comprising administering to the regional fat accumulation a composition, by subcutaneous injection or transdermal administration, that comprises a lipophilic long-acting selective beta-2 agonist, or a salt, solvate, or combinations thereof that is up to 250 micrograms per week, provided that the administration is less frequently than once per day, and wherein the lipophilic long-acting selective beta-2 adrenergic receptor agonist comprises at least one of salmeterol, formoterol, bambuterol, or any salt, solvate, or any combination thereof.

14. The method of claim 13 , provided that the lipophilic long-acting selective beta-2 agonist comprises salmeterol, or any salt, solvate, or any combination thereof.

15. The method of claim 13 , provided that the lipophilic long-acting selective beta-2 agonist comprises salmeterol xinafoate.

16. The method of claim 13 , provided that the lipophilic long-acting selective beta-2 adrenergic receptor agonist comprises formoterol fumarate.

17. The method of claim 13 , provided that the lipophilic long-acting selective beta-2 agonist comprises salmeterol, or any salt, solvate, or any combination thereof, in an amount that is up to about 100 micrograms per day administered.

18. The method of claim 13 , provided that the lipophilic long-acting selective beta-2 agonist comprises formoterol, or any salt, solvate, or any combination thereof, in an amount that is up to about 50 micrograms per day administered.

Assignments (2)
CHANGE OF NAME Recorded Sep 5, 2014
From: LITHERA, INC.
To: NEOTHETICS, INC.
Reel/Frame 033694/0006 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2014
From: DOBAK, JOHN DANIEL
To: LITHERA, INC.
Reel/Frame 033366/0582 →
Continuity (7)
Continuation 13204423 · Aug 5, 2011
Continuation 12763030 · Apr 19, 2010
Division 11457436 · Jul 13, 2006
Provisional Application 60732981 · Nov 3, 2005
Provisional Application 60729531 · Oct 24, 2005
Provisional Application 60699155 · Jul 14, 2005
Related Publication 20140322305A1 · Oct 30, 2014