Methods for treating bleeding disorders using sulfated polysaccharides
View Patent ↗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.
1. A method for treating a subject for a bleeding disorder, the method comprising administering a therapeutically effective amount of a composition comprising a procoagulant amount of a non-anticoagulant sulfated polysaccharide (NASP) selected from the group consisting of:
pentosan polysulfate (PPS); and
a modified heparin selected from the group consisting of N-acetyl-heparin (NAH), N-acetyl-de-O-sulfated-heparin (NA-de-o-SH), de-N-sulfated-heparin (De-NSH), and de-N-sulfated-acetylated-heparin (De-NSAH), each having a molecular weight in the range of 10,000 Da to 1,000,000 Da;
and combinations thereof, to said subject;
wherein the NASP is administered at a dosage of about 0.01 mg/kg to about 100 mg/kg, and the bleeding disorder is selected from the group consisting of a chronic or acute bleeding disorder, a congenital coagulation disorder caused by a blood factor deficiency, and an acquired coagulation disorder.
2. The method according to claim 1 , wherein the composition further comprises one or more factors selected from the group consisting of factor XI, factor XII, prekallikrein, high molecular weight kininogen (HMWK), factor V, factor VII, factor VIII, factor IX, factor X, factor XIII, factor II, and von Willebrands factor, tissue factor, factor Vila, factor Va, and factor Xa, factor IXa, factor XIa, factor XIIa, and VIIIa.
3. The method of claim 1 , wherein the bleeding disorder is a blood factor deficiency of one or more factors selected from the group consisting of factor V, factor VII, factor VIII, factor IX, factor X, factor XI, factor XII, factor XIII, and von Willebrand factor; a fibrinogen disorder; a prothrombin disorder; or a platelet dysfunction.
4. The method of claim 1 , wherein the bleeding disorder is caused by prior administration of an anticoagulant or surgery or other invasive procedure.
5. The method of claim 1 , further comprising administering an agent selected from the group consisting of a procoagulant, an activator of the intrinsic coagulation pathway, an activator of the extrinsic coagulation pathway, and a second NASP.
6. The method of claim 5 , wherein the activator of the intrinsic coagulation pathway is selected from the group consisting of factor Xa, factor IXa, factor XIa, factor XIIa, and VIIIa, prekallekrein, and high-molecular weight kininogen.
7. The method of claim 5 , wherein the activator of the extrinsic coagulation pathway is selected from the group consisting of tissue factor, factor VIIa, factor Va, and factor Xa.
8. The method of claim 1 , further comprising administering one or more factors selected from the group consisting of factor XI, factor XII, prekallikrein, high molecular weight kininogen (HMWK), factor V, factor VII, factor VIII, factor IX, factor X, factor XIII, factor II, factor VIIa, and von Willebrands factor.
9. The method of claim 4 , wherein the anticoagulant is selected from the group consisting of heparin, a coumarin derivative, such as warfarin or dicumarol, tissue factor pathway inhibitor (TFPI), antithrombin III, lupus anticoagulant, nematode anticoagulant peptide (NAPc2), active-site blocked factor Vila (factor VIIai), factor IXa inhibitors, factor Xa inhibitors, inhibitors of factors Va and VIIIa, thrombin inhibitors, and an antibody that binds a clotting factor.
10. The method of claim 9 , wherein the anticoagulant is an antibody that binds a clotting factor selected from the group consisting of Factor V, Factor VII, Factor VIII, Factor IX, Factor X, Factor XIII, Factor II, Factor XI, Factor XII, von Willebrands factor, prekallikrein, and high molecular weight kininogen (HMWK).
11. The method according to claim 1 , wherein the NASP is PPS.
12. The method according to claim 1 , wherein the NASP is NAH.
13. The method according to claim 1 , wherein the NASP is NA-de-o-SH.
14. The method according to claim 1 , wherein the NASP is De-NSH.
15. The method according to claim 1 , wherein the NASP is De-NSAH.