IP Library Granted Patent US 7,749,543
Granted Patent B2
US 7,749,543 · App. 12/351,558 · Granted Jul 6, 2010

Methods useful in the treatment of bone resorption diseases

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 7,749,543
App. No.
12/351,558
Granted
Jul 6, 2010
Kind
B2
Abstract

The invention relates to a combined pharmaceutical preparation comprising parathyroid hormone and a bone resorption inhibitor, said preparation being adapted for (a) the administration of parathyroid hormone during a period of approximately 6 to 24 months; (b) after the administration of parathyroid hormone has been terminated, the administration of a bone resorption inhibitor during a period of approximately 12 to 36 months.

Claims (12)

1. A method for the treatment of osteoporosis in humans comprising:

administering to said human an effective amount of parathyroid hormone during a period of approximately 6 to 24 months; and

after the administration of said parathyroid hormone has been terminated, optionally administering a bone resorption inhibitor during a period of approximately 6 to 36 months.

2. A method according to claim 1 , wherein the parathyroid hormone is selected from (a) full-length parathyroid hormone; (b) biologically active variants of full-length parathyroid hormone; (c) biologically active parathyroid hormone fragments; and (d) biologically active variants of parathyroid hormone fragments.

3. A method according to claim 1 , wherein administering to said human an effective amount of parathyroid hormone, consists of administering a human PTH (1-84) during a period of approximately 6 to 24 months.

4. A method according to claim 1 , wherein administering to said human an effective amount of parathyroid hormone, consists of administering once daily a human PTH (1-84) dose of 50 μg to 100 μg during a period of approximately 6 to 24 months.

5. A method according to claim 1 , wherein the optionally administering a bone resorption inhibitor comprises administering a bone resorption inhibitor selected from the group consisting of bisphosphonate, a selective estrogen receptor modulator, calcitonin, a vitamin D analog, and a calcium salt.

6. A method according to claim 1 , wherein the said human is a post-menopausal female.

7. A method for the enhancement of bone mineral density in a human needing enhancement of bone density, the method comprising:

optionally administering, to a human who has already been subject to treatment with parathyroid hormone during a period of approximately 6 to 24 months, after the administration of parathyroid hormone has been terminated, an effective amount of a bone resorption inhibitor during a period of approximately 6 to 36 months.

8. A method according to claim 7 , wherein the optionally administering a bone resorption inhibitor comprises administering a bone resorption inhibitor selected from the group consisting of bisphosphonate, a selective estrogen receptor modulator, calcitonin, a vitamin D analog, and a calcium salt.

9. A method according to claim 7 , wherein the said human is a post-menopausal female.

Assignments (1)
SECURITY AGREEMENT Recorded Dec 20, 2013
From: NPS PHARMACEUTICALS, INC.
To: DRUG ROYALTY L.P. 3
Reel/Frame 031866/0539 →