IP Library Granted Patent US 11,052,096
Granted Patent B2
US 11,052,096 · App. 17/072,779 · Granted Jul 6, 2021

Steroidal compositions

Inventors: Chandrashekar Giliyar (Plymouth, MN); Nachiappan Chidambaram (Sandy, UT); Mahesh V. Patel (Salt Lake City, UT); Srinivasan Venkateshwaran (Salt Lake City, UT)
Assignee: Lipocine Inc.
A61K31/569A61K9/0053A61K9/4858A61K9/4866A61K9/4875A61K31/568A61K47/10A61K47/14A61K47/44
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Quick Facts
Patent No.
US 11,052,096
App. No.
17/072,779
Granted
Jul 6, 2021
Kind
B2
Abstract

Provided herein are steroid containing compositions suitable for providing therapeutically effective amounts of at least one steroid to individuals. Also provided herein are compositions comprising testosterone and/or testosterone derivatives suitable for providing therapeutically effective and safe amounts of testosterone over periods of time. Further provided are methods of treating andro- and/or testosterone deficiency in individuals by administering to the individuals compositions described herein.

Claims (11)

1. A method of treating a hypogonadal male comprising orally administering to the male twice-daily a composition comprising a capsule and a semi-solid formulation encased within the capsule, the formulation comprising:

a) 20-25 percent by weight of testosterone undecanoate (TU),

b) 10-21 percent by weight of hydrophilic surfactant, and

c) 48-70 percent by weight of lipophilic carrier selected from lipophilic surfactant, triglycerides, or Vitamin E compounds,

wherein the formulation in the capsule administered twice daily comprises about 120 mg to about 400 mg of TU, and wherein the composition, when orally administered to a plurality of hypogonadal males provides, a mean plasma concentration of testosterone at steady state of between 300 ng/dL and 1000 ng/dL in at least 75% of the males, a plasma C max concentration of testosterone less than 1800 ng/dL in at least 95% of males, less than 1500 ng/dL in at least 85% of males, and less than 2500 ng/dL in all males.

2. The method of claim 1 , wherein administration of the composition provides a serum T max at 3 to 9 hours.

3. The method of claim 1 , wherein the formulation further comprises a 5-alpha reductase inhibitor.

4. The method of claim 1 , wherein the formulation further comprises a digestible oil.

5. The method of claim 4 , wherein the hydrophilic surfactant is polyoxyethylene ( 40 ) hydrogenated castor oil and the lipophilic surfactant is oleic acid.

6. The method of claim 1 , wherein the composition releases about 40 wt. % TU within the first 30 minutes and about 60 wt. % TU after 4 hours in an aqueous medium.

7. The method of claim 1 , wherein the formulation in the capsule administered twice daily comprises about 120 mg to about 240 mg of TU.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 16, 2020
From: GILIYAR, CHANDRASHEKAR; CHIDAMBARAM, NACHIAPPAN; PATEL, MAHESH V.; VENKATESHWARAN, SRINIVASAN
To: LIPOCINE, INC.
Reel/Frame 054081/0061 →
Continuity (2)
Continuation 12350930 · Jan 8, 2009
Related Publication 20210038615A1 · Feb 11, 2021
Cited By (1)
US 12,310,978