IP Library › Granted Patent US 8,741,918
Granted Patent B2
US 8,741,918 · App. 12/144,620 · Granted Jun 3, 2014

Parenteral formulations of dopamine agonists

Inventor: Anthony H. Cincotta (Tiverton, RI)
Assignee: VeroScience LLC
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Quick Facts
Patent No.
US 8,741,918
App. No.
12/144,620
Granted
Jun 3, 2014
Kind
B2
Abstract

This invention relates to stable pharmaceutical compositions for parenteral administration comprising dopamine agonists and peripheral acting agents useful for treatment of metabolic disorders or key elements thereof. The parenteral dosage forms exhibit long stable shelf life and distinct pharmacokinetics.

Claims (10)

1. A stable parenteral dosage form comprising bromocriptine and a pharmaceutically acceptable excipient, and exhibiting a pharmacokinetic profile comprising:

a) a T max at about 1 to about 90 minutes after administration of the parenteral dosage form; and

b) followed by a plasma drug concentration of at least 50% C max for a duration of about 90 to about 360 minutes.

2. The parenteral dosage form of claim 1 exhibiting a pharmacokinetic profile wherein at least about 90% of the bromocriptine is cleared from plasma within about 240 to about 480 minutes of said duration of about 90 to about 360 minutes.

3. The parenteral dosage form of claim 1 wherein said T max is about 5 to about 90 minutes after administration of the parenteral dosage form.

4. The parental dosage form of claim 1 exhibiting a pharmacokinetic profile wherein said T max is about 5 to about 90 minutes after administration of the dosage form and said duration of about 90 to about 360 minutes comprises a post-C max level comprising about one-half C max within about 30 to about 150 minutes of T max.

5. The parental dosage form of claim 1 exhibiting a pharmacokinetic profile wherein said T max is about 5 to about 90 minutes after administration of the dosage form and said duration of about 90 to about 360 minutes comprises a post-C max level comprising about one-half C max within about 90 to about 360 minutes of T max.

6. The parenteral dosage form of claim 1 in the form of a nasal, sublingual, buccal, transdermal, or subcutaneous dosage form.

7. The parenteral dosage form of claim 1 comprising a total of about 0.02 to about 50.0 mg of said bromocriptine.

8. The parenteral dosage form of claim 1 further comprising an anti-hypertensive agent, anti-inflammatory agent, anti-coagulative agent, anti-hypercholesterolemic agent, anti-hypertriglyceridemic agent, anti-hyperglycemic agent or HMGCoA reductase inhibitor.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2011
From: CINCOTTA, ANTHONY H.
To: VEROSCIENCE, LLC
Reel/Frame 025639/0277 →
Continuity (3)
Provisional Application 60945562 · Jun 21, 2007
Provisional Application 61020930 · Jan 4, 2008
Related Publication 20090143390A1 · Jun 4, 2009