IP Library › Granted Patent US 6,841,147
Granted Patent B2
US 6,841,147 · App. 09/224,683 · Granted Jan 11, 2005

Stem cell factor compositions

Assignee: Amgen, Inc.
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Quick Facts
Patent No.
US 6,841,147
App. No.
09/224,683
Granted
Jan 11, 2005
Kind
B2
Abstract

Novel stem cell factors, oligonucleotides encoding the same, and methods of production, are disclosed. Pharmaceutical compositions and methods of treating disorders involving blood cells are also disclosed.

Claims (24)

1. A composition which comprises a therapeutically effective amount of an isolated stem cell factor (SCF) polypeptide, or a biologically active SCF fragment comprising at least 130 contiguous amino acids of any of sequences set forth in SEQ ID NO:46, SEQ ID NO:61 or SEQ ID NO:63 that enhances hematopoiesis and one or more cytokines in a pharmaceutically acceptable carrier.

2. The composition of claim 1 , wherein SCF polypeptide is a product of a recombinant prokaryote cell or eukaryote cells.

3. The composition of claim 2 , wherein the SCF polypeptide is a human SCF polypeptide.

4. The composition of claim 3 , wherein the SCF polypeptide is selected from the group of polypeptides consisting of the amino acid sequence set out as 1-162, 1-164 and 1-165 in SEQ ID NO:46 said polypeptides optionally consisting of an N-terminal methionine.

5. The composition of claim 3 , wherein the SCF polypeptide is a polypeptide which comprises a polypeptide sequence selected from the group consisting of the amino acid sequence set out as 1-130, 1-133, 1-137, 1-141, 1-145, 1-148, 1-152, 1-156, 1-157, 1-158, 1-159, 1-160, 1-161, 1-163, 1-166, 1-168, 1-173, 1-178, 2-164, 2-165, 5-164, 11-164, 1-180, 1-183, 1-185, 1-188, 1-189, 1-220 and 1-248 in SEQ ID NO:61 said polypeptide optionally consisting of an N-terminal methionine.

6. The composition of claim 3 , wherein the SCF polypeptide is selected from the group consisting of amino acids 1-152, 1-157, 1-160, 1-161 and 1-220 as set out in SEQ ID NO:63 said polypeptide optionally consisting of N-terminal methionine.

7. The method of claim 4 , 5 , or 6 , wherein the stem cell factor is covalently conjugated to a water-soluble polymer.

8. The method of claim 7 , wherein the water soluble polymer is polyethylene glycol.

9. The composition of claim 4 , 5 , or 6 wherein the amount of SCF in the composition is effective to treat hematopoietic disorders.

10. The composition of claim 7 , wherein the amount of SCF in the composition is effective to treat hematopoietic disorders.

11. The composition of claim 9 , wherein the composition contains at least one cytokine selected from the group consisting of Interleukin-1, Interleukin-2, Interleukin-3, Interleukin-4, Interleukin-5, Interleukin-6, Interleukin-7, Interleukin-8, Interleukin-9, Interleukin-10, Interleukin-11, Interleukin-12, erythropoietin, Granulocyte Colony-stimulating Growth Factor, Granulocyte-Macrophage Colony-Stimulating Factor, Colony Stimulating Factor-1, Insulin-like Growth Factor-1, and Leukemic Inhibitory Factor.

12. The composition of claim 10 , wherein the composition contains at least one cytokine selected from the group consisting of Interleukin-1, Interleukin-2, Interleukin-3, Interleukin-4, Interleukin-5, Interleukin-6, Interleukin-7, Interleukin-8, Interleukin-9, Interleukin-10, Interleukin-11, Interleukin-12, erythropoietin, Granulocyte Colony-stimulating Growth Factor, Granulocyte-Macrophage Colony-Stimulating Factor, Colony Stimulating Factor-1, Insulin-like Growth Factor-1, and Leukemic Inhibitory Factor.

13. The composition of claim 4 , 5 , or 6 , wherein the composition contains a pharmaceutically effective carrier for the controlled release of SCF and other cytokines in the composition.

14. The composition of claim 7 , wherein the composition contains a pharmaceutically effective carrier for the controlled release of SCF and other cytokines in the composition.

15. The composition of claim 4 , 5 , or 6 , wherein the composition contains a pharmaceutically effective carrier for parenteral delivery of the composition.

16. The composition of claim 7 , wherein the composition contains a pharmaceutically effective carrier for parenteral delivery of the composition.

17. The composition of claim 4 , 5 , or 6 , wherein the composition contains a pharmaceutically effective carrier for pulmonary delivery of the composition.

18. The composition of claim 7 , wherein the composition contains a pharmaceutically effective carrier for pulmonary delivery of the composition.

19. The composition of claim 4 , 5 , or 6 , wherein the composition contains a pharmaceutically effective carrier for nasal delivery of the composition.

20. The composition of claim 7 , wherein the composition contains a pharmaceutically effective carrier for nasal delivery of the composition.

21. The composition of claim 4 , 5 , or 6 , wherein the composition contains a pharmaceutically effective carrier for the oral delivery of the composition.

22. The composition of claim 7 , wherein the composition contains a pharmaceutically effective carrier for the oral delivery of the composition.

23. The composition of claim 4 , 5 , or 6 , wherein the composition contains a pharmaceutically effective carrier for the topical delivery of the composition.

24. The composition of claim 7 , wherein the composition contains a pharmaceutically effective carrier for the topical delivery of the composition.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2009
From: AMGEN INC
To: BIOVITRUM AB (PUBL)
Reel/Frame 023708/0868 →
Continuity (10)
Division 0900589300 · Jan 12, 1998
Division 0844965300 · May 24, 1995
Division 0817232900 · Dec 21, 1993
Continuation 0798225500 · Nov 25, 1992
Continuation 0768453500 · Apr 10, 1991
Continuation In Part 0758970100 · Oct 1, 1990
Continuation In Part 0757361600 · Aug 24, 1990
Continuation In Part 0753719800 · Jun 11, 1990
Continuation In Part 0742238300 · Oct 16, 1989
Related Publication 20020031491A1 · Mar 14, 2002