IP Library › Granted Patent US 12,668,590
Granted Patent B2
US 12,668,590 · App. 18/199,827 · Granted Jun 30, 2026

Composition and method for treating metabolic disorders

Inventor: Anthony H. Cincotta (Tiverton, RI)
Assignee: VeroScience LLC
C07D457/06A61K31/48A61K31/4985C07C59/265C07D498/14
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Quick Facts
Patent No.
US 12,668,590
App. No.
18/199,827
Filed
May 19, 2023
Granted
Jun 30, 2026
Kind
B2
Art Unit
1627
USPC
514/250
Abstract

Bromocriptine citrate administered to a vertebrate, animal or human, can be used for any purpose including, e.g., the long-term modification and regulation of metabolic disorders, including prediabetes, obesity, insulin resistance, hyperinsulinemia, hyperglycemia and type 2 diabetes mellitus (T2DM) and/or, e.g., the treatment of other medical disorder(s) including immune or endocrine disorders or diseases. Bromocriptine citrate is administered over a limited or extended period at a time of day dependent on re-establishing the normal circadian rhythm of central dopaminergic activity of healthy members of a similar species and sex. Insulin resistance, hyperinsulinemia and hyperglycemia, T2DM, prediabetes, MS or all, can be controlled in humans on a long term basis by such treatment inasmuch as the daily administration of bromocriptine citrate resets neuronal activity timing in the neural centers of the brain to produce long term effects.

Claims (14)

1 . The method of treating obesity which comprises administering to a subject in need of such treatment a pharmaceutical composition comprising an effective amount for treating the obesity of bromocriptine citrate.

2 . The method of claim 1 wherein the effective amount is between 0.05 μg and 0.5 mg/kg of body weight per day.

3 . The method of claim 1 which comprises administering the pharmaceutical composition at a time of day that will increase central dopaminergic activity of the subject at the time of day of the circadian peak of central dopaminergic activity in a healthy individual of the same species and sex.

4 . The method of claim 3 which comprises administering the pharmaceutical composition between 0400 and 1200 hours of the day.

5 . The method of claim 1 wherein the pharmaceutical composition comprises a tablet.

6 . The method of claim 5 wherein the tablet comprises a sublingual tablet.

7 . The method of claim 1 which comprises administering the pharmaceutical composition via the sublingual route.

8 . The method of claim 3 which comprises administering the pharmaceutical composition within two hours after awakening.

9 . The method of claim 3 which comprises administering the pharmaceutical composition between 4 hours before and four hours after the onset of daily locomotor activity.

10 . The method of claim 3 which comprises administering the pharmaceutical composition between two hours before and two hours after the onset of daily locomotor activity.

11 . The method of claim 1 which comprises administering the pharmaceutical composition in an oral dosage form.

12 . The method of claim 1 which comprises parenterally administering the bromocriptine citrate.

13 . The method of claim 1 which comprises co-administering at least one of an alpha-I adrenergic antagonist, an alpha 2 adrenergic agonist, a serotonergic inhibitor or a serotonin 5HT1b agonist with the bromocriptine citrate.

14 . The method of claim 1 which comprises administering the pharmaceutical composition via the sublingual route.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 19, 2023
From: CINCOTTA, ANTHONY H., PHD
To: VEROSCIENCE LLC
Reel/Frame 063709/0657 →
Continuity (6)
Continuation 18079564 · Dec 12, 2022
Continuation 17117999 · Dec 10, 2020
Continuation 15796362 · Oct 27, 2017
Division 15492891 · Apr 20, 2017
Provisional Application 62325342 · Apr 20, 2016
Related Publication 20230286974A1 · Sep 14, 2023
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