IP Library › Granted Patent US 10,675,330
Granted Patent B2
US 10,675,330 · App. 15/927,553 · Granted Jun 9, 2020

Injectable bone morphogenetic protein

Inventor: Ping Li (Germantown, TN)
Assignee: Warsaw Orthopedic, Inc.
A61K38/1875A61K9/0019A61K9/08A61P19/00A61P19/08
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 10,675,330
App. No.
15/927,553
Granted
Jun 9, 2020
Kind
B2
Abstract

A method of treating a bone defect is provided. The method comprises administering to the bone defect an injectable solution comprising about 20 μg to about 5000 μg of bone morphogenetic protein-2 (BMP-2) in an aqueous carrier. Kits and methods of making are also provided.

Claims (9)

1. A method of treating a bone defect, the method comprising administering to the bone defect an injectable solution comprising 28 μg of bone morphogenetic protein-2 (BMP-2) in an aqueous carrier, wherein the injectable solution has a pH of about 6.0, and wherein the injectable solution is administered as a single dose injection to the bone defect.

2. The method of claim 1 , wherein the BMP-2 is recombinant human BMP-2 (rhBMP-2).

3. The method of claim 1 , wherein the aqueous carrier comprises saline, dextrose, sterile water for injection, phosphate buffered saline, blood, or a combination thereof.

4. The method of claim 1 , wherein the injectable solution further comprises a buffering agent comprising tris(hydroxymethyl)aminomethane (Tris), ethylenediaminetetraacetic acid (EDTA), 2-[4-(2-hydroxyethyl)-1-piperazinyl]ethanesulfonic acid (HEPES), 2-(N-morpholino)ethanesulfonic acid (MES), sodium acetate, sodium citrate, sodium phosphate, potassium phosphate, phosphate buffered saline (PBS), sodium chloride, potassium chloride, calcium chloride, glycerol, sucrose, glycine, L-glutamic acid, polysorbate 80 or a combination thereof.

5. The method of claim 4 , wherein the buffering agent comprises sucrose, glycine, L-glutamic acid, sodium chloride, polysorbate 80 or a combination thereof.

6. The method of claim 4 , wherein the buffering agent in the injectable solution is at a concentration from about 1 mM to 100 mM.

7. The method of claim 1 , wherein the injectable solution further comprises a clotting factor in an amount of about 0.0001% to about 5% of the injectable solution.

8. The method of claim 1 , wherein (i) the injectable solution is administered percutaneously to a long bone fracture; or (ii) the injectable solution is injected directly into a fracture site that has a hematoma.

9. The method of claim 1 , wherein the aqueous carrier is not osteoinductive or osteoconductive.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 21, 2018
From: LI, PING
To: WARSAW ORTHOPEDIC, INC
Reel/Frame 045306/0125 →
Continuity (1)
Related Publication 20190290731A1 · Sep 26, 2019
Cited By (1)
US 12,264,187