IP Library › Granted Patent US 8,877,196
Granted Patent B2
US 8,877,196 · App. 13/796,530 · Granted Nov 4, 2014

Methods of altering bone growth by administration of sost or wise antagonist or agonist

Inventor: Debra L. Ellies (Kansas City, KS)
Assignee: OssiFi Inc.
A61K38/1709A61K31/59A61K31/713A61L27/12A61K38/1875A61K39/3955A61K45/06A61L27/54A61K39/395A61L2300/256A61L2430/02A61K31/7088A61L2300/432
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Quick Facts
Patent No.
US 8,877,196
App. No.
13/796,530
Granted
Nov 4, 2014
Kind
B2
Abstract

The present invention provides a method of promoting local bone growth by administering a therapeutic amount of a Sost antagonist to a mammalian patient in need thereof. Preferably, the Sost antagonist is an antibody or FAB fragment selectively recognizing any one of SEQ ID NOS: 1-23. The Sost antagonist may be coadministered together or sequentially with a matrix conducive to anchoring new bone growth. Orthopedic and Periodontal devices comprising an implantable portion adapted to be permanently implanted within a mammalian body and bearing an external coating of a Sost antagonist are also disclosed, as it a method of increasing bone density by administering to a mammalian patient a therapeutic amount of a Sost antagonist together with an antiresorptive drug.

Claims (13)

1. A method of increasing bone density in a mammalian patient in need thereof, comprising the steps of:

systemically administering to a said mammalian patient a therapeutic comprising an effective amount of a Sclerostin antagonist sequentially with an antiresorptive drug, said Sclerostin antagonist comprising an antibody or FAB fragment specifically binding a peptide selected from the group consisting of SEQ ID NOS:2-13, 22 and 23, wherein

the antibody interferes with Sclerositn's ability to bind to LRP, thereby systemically increasing bone density.

2. The method according to claim 1 , wherein said patient is a human.

3. The method according to claim 2 , wherein said patient has low bone density.

4. The method according to claim 3 , wherein said antibody or FAB fragment is a monoclonal antibody or FAB fragment.

5. The method according to claim 4 , wherein said monoclonal antibody or FAB fragment is humanized.

6. The method according to claim 3 , wherein said antiresorptive is a bisphosphonate, calcitonin, Vitamin D or SERM.

7. The method according to claim 3 , wherein said antiresorptive is fosamax, actonel, Miacalcic or Evista.

8. The method according to claim 3 , wherein said Sclerostin antagonist is administered to said patient prior to administering said antiresorptive.

9. The method according to claim 3 , wherein said antiresorptive is administered to said patient prior to administering said Sclerostin antagonist.

10. The method according to claim 3 , wherein said patient has previously been treated with an antiresorptive drug.

11. The method according to claim 3 , wherein said patient has not previously been treated with an antiresorptive drug.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNOR'S NAME ON THE COVER SHEET PREVIOUSLY RECORDED AT REEL: 057591 FRAME: 0122. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jan 6, 2022
From: OSTÉOQC, INC.
To: OSSIFI-MAB LLC
Reel/Frame 058700/0155 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 24, 2021
From: OSTÉOQC, INC.; OSSIFI-MAB LLC
To: OSSIFI-MAB LLC
Reel/Frame 057591/0122 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 18, 2014
From: OSSIFI INC.
To: OSTEOQC
Reel/Frame 034283/0182 →
Continuity (4)
Division 13420846 · Mar 15, 2012
Continuation 11962522 · Dec 21, 2007
Provisional Application 60882642 · Dec 29, 2006
Related Publication 20130195856A1 · Aug 1, 2013