IP Library Granted Patent US 8,859,526
Granted Patent B2
US 8,859,526 · App. 12/893,798 · Granted Oct 14, 2014

Methods for treating bleeding disorders using sulfated polysaccharides

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Quick Facts
Patent No.
US 8,859,526
App. No.
12/893,798
Granted
Oct 14, 2014
Kind
B2
Abstract

Methods for treating bleeding disorders using non-anticoagulant sulfated polysaccharides (NASPs) as procoagulants are disclosed. NASPs can be administered as single agents, or in combination with one another, or with other medications (such as factors VII, VIII and IX) to promote hemostasis. In particular, the use of NASPs in treatment of bleeding disorders, including congenital coagulation disorders, acquired coagulation disorders, and trauma induced hemorrhagic conditions is described.

Claims (12)

1. A composition comprising:

a non-anticoagulant sulfated polysaccharide (NASP) selected from the group consisting of glycosaminoglycans, carrageenans, substituted heparins, periodate-oxidized heparins, fucoidans, fucopyranon sulfates, dermatan sulfates, pentosan polysulfates, chemically sulfated laminarin, chemically sulfated alginic acid, chemically sulfated pectin and dextran sulfates;

one or more factors selected from the group consisting of factor XI, factor XII, prekallikrein, high molecular weight kininogen, factor V, factor VII, factor VIII, factor IX, factor X, factor XIII, factor II, von Willebrands factor, tissue factor, factor VIIa, factor Va, and factor Xa, factor IXa, factor Xla, factor XIIa, and Villa; and

one or more pharmaceutically acceptable excipients;

wherein the concentration of the NASP in the composition is from 10 nM to 500 nM.

2. The composition according to claim 1 , wherein the NASP is a compound selected from the group consisting of fucoidan, pentosan polysulfate, N-acetyl heparin, N-acetyl-de-O-sulfated-heparin, de-N-sulfated heparin and de-N-sulfated-acetylated heparin.

3. The composition according to claim 1 , wherein the NASP has a molecular weight which ranges from 500 to 25000 daltons.

4. The composition according to claim 1 , wherein the factor is Factor VIIIA.

5. The composition according to claim 4 , wherein the factor is Factor VIIA.

6. The composition according to claim 5 , wherein the factor is Factor IXA.

7. The composition according to claim 1 , wherein the composition is a liquid.

8. The composition according to claim 1 , wherein the composition is present in a syringe.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 31, 2021
From: BAXALTA GMBH; BAXALTA INCORPORATED
To: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Reel/Frame 055188/0953 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2015
From: BAXTER INTERNATIONAL INC.
To: BAXALTA GMBH; BAXALTA INCORPORATED
Reel/Frame 036370/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2015
From: BAXTER HEALTHCARE SA
To: BAXALTA GMBH; BAXALTA INCORPORATED
Reel/Frame 036375/0001 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2010
From: JOHNSON, KIRK W.
To: AVIGEN, INC.
Reel/Frame 025530/0470 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2010
From: AVIGEN, INC.
To: BAXTER HEALTHCARE S.A.; BAXTER INTERNATIONAL INC.
Reel/Frame 025530/0770 →