IP Library Granted Patent US 8,080,682
Granted Patent B2
US 8,080,682 · App. 11/892,595 · Granted Dec 20, 2011

Substituted acylanilides and methods of use thereof

Assignee: University of Tennessee Research Foundation
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Quick Facts
Patent No.
US 8,080,682
App. No.
11/892,595
Granted
Dec 20, 2011
Kind
B2
Abstract

This invention provides SARM compounds and uses thereof in treating a variety of diseases or conditions in a subject, including, inter alia, a muscle wasting disease and/or disorder or a bone-related disease and/or disorder.

Claims (19)

1. A compound represented by the structure of formula (I):

2. A composition comprising the compound of claim 1 , and a pharmaceutically acceptable carrier, diluent or salt, or a combination thereof.

3. A method of binding a compound to an androgen receptor, comprising the step of contacting the androgen receptor with the selective androgen receptor modulator compound of claim 1 or its isomer, pharmaceutically acceptable salt, or any combination thereof, in an amount effective to bind the compound to the androgen receptor.

4. A method of treating a subject suffering from prostate cancer, comprising the step of administering to said subject compound of claim 1 or its isomer, pharmaceutically acceptable salt, or any combination thereof, in an amount effective to treat prostate cancer in said subject.

5. A method of delaying the progression of prostate cancer in a subject suffering from prostate cancer, comprising the step of administering to said subject the compound of claim 1 , or its isomer, pharmaceutically acceptable salt or any combination thereof in an amount effective to delay the progression of prostate cancer in said subject.

6. A method of treating a bone-related disorder in a subject, increasing a bone mass in a subject or promoting bone formation in a subject, comprising the step of administering to said subject the compound of claim 1 or its isomer, pharmaceutically acceptable salt or any combination thereof, in an amount effective to treat said bone-related disorder, increase said bone mass, or promote said bone formation in said subject.

7. The method of claim 6 , wherein said subject suffers from osteoporosis, osteopenia, increased bone resorption, bone fracture, bone frailty, loss of bone mineral density (BMD), or any combination thereof.

8. The method of claim 6 , wherein said method increases the strength of a bone of said subject.

9. The method of claim 6 , wherein said compound stimulates or enhances osteoblastogenesis.

10. The method of claim 6 , wherein said compound inhibits osteoclast proliferation.

11. A method of treating, reducing the incidence of, delaying the progression of, reducing the severity of, or alleviating the symptoms associated with a muscle wasting disorder in a subject, comprising the step of administering to said subject the compound of claim 1 or its isomer, pharmaceutically acceptable salt or any combination thereof, in an amount effective to treat said muscle wasting disorder in said subject.

12. The method of claim 11 , wherein said muscle wasting disorder is due to a pathology, illness, disease or condition.

13. The method of claim 12 , wherein said pathology, illness, disease or condition is neurological, infectious, chronic or genetic.

14. The method of claim 12 , wherein said pathology, illness, disease or condition is a muscular dystrophy, a muscular atrophy, x-linked spinal-bulbar muscular atrophy (SBMA), a cachexia, malnutrition, leprosy, diabetes, renal disease, chronic obstructive pulmonary disease (COPD), cancer, end stage renal failure, sarcopenia, emphysema, osteomalacia, HIV infection, AIDS, or cardiomyopathy.

15. The method of claim 11 , wherein said muscle wasting disorder is an age-associated muscle wasting disorder; a disuse deconditioning-associated muscle wasting disorder; or the muscle wasting disorder is due to chronic lower back pain; burns; central nervous system (CNS) injury or damage; peripheral nerve injury or damage; spinal cord injury or damage; chemical injury or damage; or alcoholism.

16. A method of treating reducing the severity of, reducing the incidence of, delaying the onset of, or reducing pathogenesis of cachexia in a subject, comprising the step of administering an effective amount of the compound of claim 1 or its isomer, pharmaceutically acceptable salt or any combination thereof to said subject.

17. A method of reducing a fat mass in a subject comprising the step of administering an effective amount of a compound of claim 1 or its isomer, pharmaceutically acceptable salt or any combination thereof to said subject.

18. A method of increasing a lean mass in a subject comprising the step of administering an effective amount of a compound of claim 1 or its isomer, pharmaceutically acceptable salt or any combination thereof to said subject.

19. The compound of claim 1 , wherein said compound is an isomer or a pharmaceutically acceptable salt or any combination thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 3, 2008
From: DALTON, JAMES T.; MILLER, DUANE D.
To: UNIVERSITY OF TENNESSEE RESEARCH FOUNDATION
Reel/Frame 020746/0434 →
Continuity (3)
Provisional Application 60839665 · Aug 24, 2006
Provisional Application 60907749 · Apr 16, 2007
Related Publication 20080076829A1 · Mar 27, 2008