Claims for Patent: 7,795,427

Summary for Patent: 7,795,427

Title:	Methods for inhibiting osteoclast differentiation, formation, or function and for increasing bone mass
Abstract:	The invention provides methods and compositions for modulating osteoclastogenesis and for treating bone diseases characterized by bone loss or a decrease in bone mass or density, by administering a compound or agent that modulates the adenosine A1 receptor, in particular, an inhibitor or antagonist of the A1 receptor.
Inventor(s):	Cronstein; Bruce N. (New York, NY), Kara; Firas Mohamed (Woodside, NY)
Assignee:	New York University (New York, NY)
Application Number:	11/705,689
Patent Claims:	1. A method for inhibiting osteoclast differentiation, formation, or function in a patient in need thereof, comprising administering to said patient an agent that blocks or antagonizes the adenosine A1 receptor, in an amount sufficient to inhibit osteoclast differentiation, formation or function, wherein the agent is a small organic molecule. 2. The method of claim 1, wherein the adenosine A1 receptor antagonist is CVT-124. 3. The method of claim 1, wherein the adenosine A1 receptor antagonist is administered orally or parenterally. 4. The method of claim 1, wherein the adenosine A1 receptor antagonist is administered intravenously, subcutaneously, intramuscularly, or intravasally. 5. The method of claim 1, wherein the adenosine A1 receptor antagonist is administered via an implanted device. 6. The method of claim 5, wherein the implanted device is an osmotic pump. 7. The method of claim 1, wherein the adenosine A1 receptor antagonist is administered in combination with a therapeutically effective amount of one or more other compounds or agents effective for treating a bone disease or condition characterized by loss of bone or a decrease in bone mass. 8. The method of claim 7, wherein the one or more other compounds or agents effective for treating a bone disease or condition is selected from the group consisting of an antiresorptive drug, a bone-forming agent, an estrogen receptor antagonist and a drug that has a stimulatory effect on osteoblasts. 9. The method of claim 8, wherein the antiresorptive drug is selected from the group consisting of a bisphosphonate, an estrogen or estrogen analogue, a selective estrogen receptor modulator (SERM) and a calcium source, Tibolone, calcitonin, and a calcitriol. 10. The method of claim 8, wherein the bone-forming agent is parathyroid hormone (PTH) or a peptide fragment thereof, PTH-related protein (PTHrp), a bone morphogenetic protein, osteogenin, NaF, a PGE.sub.2 agonist, a statin, and a RANK ligand (RANKL). 11. The method of claim 10, wherein the PTH peptide fragment is teriparatide. 12. The method of claim 8, wherein the drug that has a stimulatory effect on osteoblasts is vitamin D, or a vitamin D derivative. 13. The method of claim 8, wherein the estrogen receptor antagonist is selected from the group consisting of raloxifene, bazedoxifene and lasofoxifene. 14. The method of claim 9, wherein the bisphosphonate is selected from the group consisting of alendronate, risedronate, ibandronate and zoledronate. 15. A method of increasing bone mass or ameliorating loss of bone mass in a subject suffering from a condition characterized by low bone mass, the method comprising administering to said subject a therapeutically effective amount of an adenosine A1 receptor antagonist, wherein the A1 receptor antagonist is a small organic molecule. 16. The method of claim 15, wherein the condition is selected from the group consisting of osteoporosis, juvenile osteoporosis, bone loss due to/ or associated with the onset of menopause, osteoporotic fractures, giant cell tumors of bone, renal osteodystrophy, osteogenesis imperfecta, hypercalcemia, hyperparathyroidism, osteomalacia, osteohalisteresis, osteolytic bone disease, osteonecrosis, Paget's disease of bone, bone loss due to rheumatoid arthritis, inflammatory arthritis, osteomyelitis, corticosteroid treatment, malignancy-induced osteoporosis and bone lysis, periodontal bone loss, age-related loss of bone mass, osteotomy and bone loss associated with prosthetic ingrowth, and other forms of osteopenia. 17. The method of claim 15, wherein the adenosine A1 receptor antagonist is CVT-124. 18. The method of claim 15, wherein the adenosine A1 receptor antagonist is administered orally or parenterally. 19. The method of claim 15, wherein the adenosine A1 receptor antagonist is administered intravenously, subcutaneously, intramuscularly, or intravasally. 20. The method of claim 15, wherein the adenosine A1 receptor antagonist is administered via an implanted device. 21. The method of claim 20, wherein the implanted device is an osmotic pump. 22. The method of claim 15, wherein the adenosine A1 receptor antagonist is administered in combination with a therapeutically effective amount of one or more other compounds or agents effective for treating a bone disease or condition characterized by loss of bone or a decrease in bone mass. 23. The method of claim 22, wherein the one or more other compounds or agents effective for treating a bone disease or condition is selected from the group consisting of an antiresorptive drug, a bone-forming agent, an estrogen receptor antagonist and a drug that has a stimulatory effect on osteoblasts. 24. The method of claim 23, wherein the antiresorptive drug is selected from the group consisting of a bisphosphonate, an estrogen or estrogen analogue, a selective estrogen receptor modulator (SERM) and a calcium source, Tibolone, calcitonin, a calcitriol and hormone replacement therapy. 25. The method of claim 23, wherein the bone-forming agent is parathyroid hormone (PTH) or a peptide fragment thereof, PTH-related protein (PTHrp), a bone morphogenetic protein, osteogenin, NaF, a PGE.sub.2 agonist, a statin, and a RANK ligand (RANKL). 26. The method of claim 25, wherein the PTH peptide fragment is teriparatide. 27. The method of claim 23, wherein the drug that has a stimulatory effect on osteoblasts is vitamin D, or a vitamin D derivative. 28. The method of claim 23, wherein the estrogen receptor antagonist is selected from the group consisting of raloxifene, bazedoxifene and lasofoxifene. 29. The method of claim 24, wherein the bisphosphonate is alendronate, risedronate, ibandronate and zoledronate.

Details for Patent 7,795,427

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Nps Pharmaceuticals, Inc.	NATPARA	parathyroid hormone	For Injection	125511	01/23/2015		2026-02-14