US2017128526A1PendingUtilityA1
Stem cell derived factors for treating pathologic conditions
Assignee: BRIGHAM & WOMENS HOSPITAL INCPriority: Aug 19, 2005Filed: May 27, 2016Published: May 11, 2017
Est. expiryAug 19, 2025(expired)· nominal 20-yr term from priority
C12N 15/09A61K 38/1709A61K 9/0085A61K 9/0053C12N 15/63C07K 14/435A61K 38/17A61K 9/0019A61K 38/18A61P 9/00A61K 45/06A61P 9/10C07K 14/475C12N 5/10
63
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Claims
Abstract
A purified paracrine factor of a mesenchymal stem cell, such as a Secreted frizzled related protein (Sfrp) is useful to reduce cell death an/or tissue injury associated with ischemic conditions.
Claims
exact text as granted — not AI-modified1 - 15 . (canceled)
16 . A pharmaceutical composition comprising a purified paracrine factor of a mesenchymal stem cell (MSC), wherein said factor comprises SEQ ID NO:17 or a fragment thereof and one or more pharmaceutically acceptable excipients.
17 . The pharmaceutical composition of claim 16 , wherein the pharmaceutically acceptable excipient is one or more of isotonic saline, glucose, cyclodextrin, or polyvinylpyrrolidone (PVP).
18 . The pharmaceutical composition of claim 16 , wherein the composition is formulated for oral, nasal, topical, parenteral, subcutaneous, intraperitoneal, intramuscular, or intravenous administration.
19 . The pharmaceutical composition of claim 16 , wherein the composition is formulated for direct intracoronary injection (a) through the chest wall; (b) into a coronary artery; or (c) using percutaneous catheter-based methods.
20 . The pharmaceutical composition of claim 19 , wherein the composition is formulated for injection into myocardium, pericardium, or endocardium.
21 . The pharmaceutical composition of claim 16 , wherein the composition is formulated into a capsule or a tablet for oral administration, ointment, suppository, paste, spray, dermal patch, cream, gel, resorbable sponge, or foam.
22 . The pharmaceutical composition of claim 16 , wherein the composition further comprises one or more of (a) an anti-apoptotic agent; or (b) a therapeutic agent for treating, preventing, or alleviating a symptom of a cardiac disorder.
23 . The pharmaceutical composition of claim 16 , wherein the composition further comprises one or more of VEGF, thyrosin beta 4, Sfrp-1, Sfrp-2, Sfrp-3, adipsin, adrenomedullin, chemokine (C—C motif) ligand 2, cysteine rich protein 61, lysyl oxidase-like 2, or a serine proteinase inhibitor.
24 . The pharmaceutical composition of claim 16 , wherein the composition comprises at least 60%, 75%, 90%, or 99% by weight of SEQ ID NO:17 or a fragment thereof.
25 . The pharmaceutical composition of claim 16 , wherein said factor comprises amino acids 45-430 of SEQ ID NO:17.
26 . The pharmaceutical composition of claim 21 , wherein said composition is a slow-release composition.
27 . The pharmaceutical composition of claim 16 , wherein said composition is formulated for administration to brain or spinal cord.
28 . The pharmaceutical composition of claim 16 , wherein said pharmaceutically acceptable excipients comprise one or more of an isotonic saline solution, a glucose solution, polyvinylpyrrolidone (PVP), cyclodextrins, or another standard pharmaceutically acceptable excipient.
29 . The pharmaceutical composition of claim 21 , wherein the composition is formulated into a capsule or a tablet for oral administration and further comprises one or more of a cytoprotective compound, gelatin, cellulose, starch, sugar bentonite, a lubricant, lactose, mannitol, a filler, or a tableting agent.
30 . The pharmaceutical composition of claim 16 , comprising about 0.1 mg/kg to about 150 mg/kg of the polypeptide encoded by SEQ ID NO:17 or a fragment thereof.
31 . The pharmaceutical composition of claim 20 , comprising 1-1000 μg of the polypeptide encoded by SEQ ID NO:17 or a fragment thereof.
32 . A stent or catheter comprising the pharmaceutical formulation of claim 16 .Cited by (0)
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