IP Library Granted Patent US 8,986,685
Granted Patent B2
US 8,986,685 · App. 13/644,728 · Granted Mar 24, 2015

Compositions and methods for increasing bone mineralization

Inventors: Mary E. Brunkow (Seattle, WA); David J. Galas (Mercer Island, WA); Brian Kovacevich (Renton, WA); John T. Mulligan (Seattle, WA); Bryan W. Paeper (Seattle, WA); Jeffrey Van Ness (Seattle, WA); David G. Winkler (Arlington, MA)
Assignee: UCB Pharma S.A.
A61K45/06C07K14/51C07K16/18C07K16/22C12Q1/6883G01N33/6872A61K39/3955A01K2217/05A01K2217/075A61K48/00C07K2317/11C07K2317/23C07K2319/00C12N2799/021C12Q2600/156C12Q2600/158C12Q2600/172
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Quick Facts
Patent No.
US 8,986,685
App. No.
13/644,728
Granted
Mar 24, 2015
Kind
B2
Abstract

Described herein are pharmaceutical compositions comprising an anti-sclerostin antibody and an inhibitor of bone resorption.

Claims (11)

1. A pharmaceutical composition comprising (a) an antibody, or an antibody fragment thereof, wherein the antibody or antibody fragment binds to a polypeptide encoded by SEQ ID NO: 1 with an affinity K a of greater than or equal to 10 7 M −1 , and (b) an inhibitor of bone resorption.

2. The pharmaceutical composition of claim 1 , wherein the inhibitor of bone resorption is selected from the group consisting of calcitonin, estrogen, a bisphosphonate, a growth factor having anti-resorptive activity and tamoxifen.

3. The pharmaceutical composition according to claim 1 , wherein the inhibitor of bone resorption is a bisphosphonate.

4. The pharmaceutical composition according to claim 1 , wherein the inhibitor of bone resorption is estrogen.

5. The pharmaceutical composition according to claim 1 , wherein the antibody fragment is selected from the group consisting of F(ab′) 2 , F(ab) 2 , Fab′, Fab, and Fv.

6. The pharmaceutical composition according to claim 1 , wherein the antibody is selected from the group consisting of a murine monoclonal antibody, a human monoclonal antibody, a humanized monoclonal antibody, and an antibody fragment of any of the foregoing.

7. The pharmaceutical composition according to any one of claims 1 - 6 , further comprising a pharmaceutically acceptable carrier, excipient or diluent.

8. A method of increasing bone mineral content in a human comprising administering to the human (a) an antibody, or an antibody fragment thereof, wherein the antibody binds to a polypeptide encoded by SEQ ID NO: 1 with an affinity K a of greater than or equal to 10 7 M −1 , and (b) an inhibitor of bone resorption, in amounts effective to increase bone mineral content.

9. The method of claim 8 , wherein the inhibitor of bone resorption is selected from the group consisting of calcitonin, estrogen, a bisphosphonate, a growth factor having anti-resorptive activity and tamoxifen.

10. The method of claim 8 , wherein the inhibitor of bone resorption is a bisphosphonate.

11. The method of claim 8 , wherein the inhibitor of bone resorption is estrogen.

Assignments (2)
NUNC PRO TUNC ASSIGNMENT Recorded Oct 25, 2013
From: DARWIN DISCOVERY LIMITED
To: UCB S.A.
Reel/Frame 031479/0219 →
NUNC PRO TUNC ASSIGNMENT Recorded Oct 25, 2013
From: UCB S.A.
To: UCB PHARMA S.A.
Reel/Frame 031479/0358 →
Continuity (5)
Continuation 11931853 · Oct 31, 2007
Continuation 10095248 · Mar 7, 2002
Continuation 09449218 · Nov 24, 1999
Provisional Application 60110283 · Nov 27, 1998
Related Publication 20130121995A1 · May 16, 2013