Formulation having mobilizing activity
The present innovation relates to a novel formulation capable of increasing the amount of stem cells and progenitor cells in circulation in the peripheral blood of a mammal; the formulation is characterized in that it contains defibrotide in combination with at least one haematopoietic factor having the capacity to mobilize haematopoietic progenitors, preferably G-CSF. In one embodiment, the formulation includes two separately administrable formulations, one containing a haematopoietic factor having the capacity to mobilize haematopoietic progenitors and the other containing defibrotide. The formulation is effective to achieve an increase in the number of haematopoietic progenitor cells that is greater than an increase in the number of haematopoietic progenitor cells achieved by the haematopoietic factor alone.
1. A method for increasing the amount of stem cells and/or haematopoietic progenitors in the peripheral blood of a mammal, comprising:
administering defibrotide as described in Chemical Abstract Registry No. 83712-60-1 and at least one haematopoietic factor having the capacity to mobilize haematopoietic progenitors to a mammal.
2. The method according to claim 1 , wherein said defibrotide and said haematopoietic factor are administered simultaneously.
3. The method according to claim 1 , wherein said defibrotide and said haematopoietic factor are administered separately.
4. The method according to claim 1 , wherein said defibrotide and said haematopoietic factor are administered sequentially.
5. The method according to claim 1 , wherein the haematopoietic factor is G-CSF, GM-CSF, Flt3 ligand, stem cell factor, thrombopoietin, or interleukin 8.
6. The method according to claim 5 , wherein the haematopoietic factor is G-CSF.
7. The method according to claim 1 , wherein said defibrotide and said haematopoietic factor are independently administered intravenously, orally, intramuscularly, intraperitoneally, or subcutaneously.
8. The method according to claim 1 , wherein said defibrotide is administered by continuous infusion.
9. The method according to claim 8 , wherein said defibrotide is administered at a dosage of 5-15 mg/kg/hour for 2-7 days.
10. The method according to claim 1 , wherein said haematopoietic factor is administered subcutaneously.
11. The method according to claim 10 , wherein said haematopoietic factor is administered at a dosage of 5-24 μg/kg.
12. The method according to claim 1 , wherein the defibrotide is in an aqueous solution.
13. The method according to claim 1 , wherein the haematopoietic factor is in an aqueous solution.
14. The method according to claim 1 , wherein the defibrotide is in a form of an alkali metal salt.
15. The method according to claim 14 , wherein said alkali metal is sodium.
16. The method according to claim 1 , wherein the mammal is a human.