US2022016110A1PendingUtilityA1
Compositions for the mobilization, homing, expansion and differentiation of stem cells and methods of using the same
Est. expiryMar 15, 2033(~6.7 yrs left)· nominal 20-yr term from priority
A61K 31/405A61K 31/20A61P 19/02A61K 35/32C12N 2501/999A61P 29/00A61P 19/00A61K 31/495A61P 25/00A61K 35/28C12N 5/0663A61P 43/00A61P 19/04
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Claims
Abstract
The invention provides compositions that increase the mobilization, homing, expansion, and/or differentiation of stem cells and methods of using the same for the treatment of mammals.
Claims
exact text as granted — not AI-modified1 - 28 . (canceled)
29 . A method of stimulating chondrogenesis in a subject comprising administering a pharmaceutical composition comprising DA-DKP and a component selected from the group consisting of N-acetyl tryptophan, caprylate, caprylic acid, and combinations thereof to a subject in need thereof.
30 . The method of claim 29 , wherein the pharmaceutical composition comprises a low molecular weight fraction of human serum albumin.
31 . The method of claim 30 , wherein the low molecular weight fraction of human serum albumin is a less than 5000 molecular weight fraction.
32 . The method of claim 30 , wherein the low molecular weight fraction of human serum albumin is produced by filtration.
33 . The method of claim 29 , wherein chondrogenesis is stimulated in a stem cell.
34 . The method of claim 33 , wherein the stem cell is selected from the group consisting of a progenitor cell and mesenchymal stem call (MSC).
35 . The method of claim 29 , wherein the stimulation of chondrogenesis promotes cartilage, bone, and/or ligament repair or induces repair or regeneration of chondral tissue, in the subject.
36 . The method of claim 29 , wherein the chondrogenesis treats or ameliorates a chondrogenic disease in the mammal.
37 . The method of claim 36 , wherein the chondrogenic disease is selected from the group consisting of a congenital cartilage disease, degenerative or fibrotic joint, rheumatoid arthritis and osteoarthritis.
38 . The method of claim 29 , wherein the chondrogenesis treats or repairs a condition selected from the group consisting of a cartilage defect, a skeletal defect, a fracture arising from trauma or surgery.
39 . The method of claim 29 , wherein the DA-DKP administration stimulates the formation of new bone or cartilage tissue.
40 . The method of claim 29 , wherein the administration comprises stimulating stem cells ex vivo and then administering the stimulated stem cells to the mammal.
41 . The method of claim 40 , wherein the stem cells are stimulated ex vivo by culturing a population of stem cells of chondrocyte lineage with DA-DKP, or composition comprising a DA-DKP, for a time sufficient to stimulate chondrogenesis.
42 . The method of claim 40 , wherein the administering comprises implanting the stimulated cells into a desired site in the mammal.
43 . The method of claim 29 , wherein the chondrogenesis results in increased production of collagen.
44 . The method of claim 29 , wherein the chondrogenesis results in increased production of a type 2A1 collagen.
45 . The method of claim 29 , wherein the chondrogenesis results in increased production of a type 1A1 collagen.
46 . The method of claim 29 , wherein the chondrogenesis results in at least a 2-fold increase in the production of collagen or at least a 4-fold increase in the production of collagen.
47 . (canceled)
48 . The method of claim 29 , wherein the chondrogenesis results in at least a 10-fold increase in the production of collagen or at least a 20-fold increase in the production of collagen.
49 . (canceled)
50 . The method of claim 29 , wherein the chondrogenesis results in at least a 25-fold increase in the production of collagen.
51 - 75 . (canceled)Cited by (0)
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