US2018187158A1PendingUtilityA1
Multifunctional immature dental pulp stem cells and therapeutic applications
Est. expiryMar 15, 2033(~6.6 yrs left)· nominal 20-yr term from priority
A61P 9/00A61P 43/00A61P 35/00A61P 37/02A61P 9/10A61P 37/06A61P 25/14A61P 27/02A61P 29/00A61P 3/02A61P 25/16A61P 25/28A61P 25/02C12N 5/0623C12N 2500/90C12N 2500/25A61K 35/32C12N 2500/84A61P 17/02C12N 2501/392C12N 2506/1361C12N 2500/38C12N 2533/76A61P 17/14C12N 5/0619C12N 2501/39C12N 5/0678A61P 21/00A61P 21/02A61K 35/30A61P 15/08C12N 2501/395C12N 5/0664A61P 25/00C12N 2501/385A61K 45/06C12N 5/0621A61P 13/12A61P 17/00A61K 35/28A61K 2300/00
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Claims
Abstract
The present invention is directed to therapeutic multifunctional immature dental pulp stem cells (IDPSCs), and IDPSCs multi-lineage compositions. The invention is further directed to the use of IDPSCs and compositions to reduce the risk of and/or treat degenerative diseases or for other medicinal and aesthetic purposes.
Claims
exact text as granted — not AI-modified1 - 103 . (canceled)
104 . A pharmaceutical formulation comprising migratory immature dental pulp stem cells (IDPSCs) expressing CD73 (ecto-5′-nucleotidase), p53, and p75.
105 . The pharmaceutical formulation according to claim 104 , wherein the IDPSCs express CD105, CD73, and CD90 and lack expression of CD45, CD34, and HLA-DR.
106 . The pharmaceutical formulation according to claim 104 , wherein the IDPSCs express CD29 (integrin beta 1).
107 . The pharmaceutical formulation according to claim 104 , wherein the migratory IDPSCs are in a unit dosage injectable form.
108 . The pharmaceutical formulation according to claim 107 , wherein the unit dosage injectable form is selected from the group consisting of a solution, a suspension, a dispersion, and an emulsion.
109 . The pharmaceutical formulation according to claim 108 , wherein the unit dosage injectable form is an aqueous dispersion.
110 . The pharmaceutical formulation according to claim 109 , wherein the pH of the aqueous dispersion is between about 6.8 and about 7.5.
111 . The pharmaceutical formulation according to claim 109 , wherein the ionic strength of the aqueous dispersion is between about 0.1 and about 0.2.
112 . The pharmaceutical formulation according to claim 104 , further comprising a fluid lubricant.
113 . The pharmaceutical formulation according to claim 104 , further comprising a carrier.
114 . The pharmaceutical formulation according to claim 113 , wherein the carrier is a solvent or a dispersing medium.
115 . The pharmaceutical formulation according to claim 113 , wherein the carrier comprises water, saline, or phosphate buffered saline.
116 . The pharmaceutical formulation according to claim 104 , further comprising an additive and/or an excipient.
117 . The pharmaceutical formulation according to claim 116 , wherein the additive and/or excipient are present in an amount of 0.001 to 50 weight percent.
118 . A pharmaceutical composition comprising migratory IDPSCs expressing CD73 (ecto-5′-nucleotidase), p53, and p75 and a pharmaceutically acceptable carrier or vehicle for cell therapy.
119 . The pharmaceutical composition according to claim 118 , wherein the IDPSCs express CD105, CD73, and CD90 and lack expression of CD45, CD34, and HLA-DR.
120 . The pharmaceutical composition according to claim 118 , wherein the IDPSCs express CD29 (integrin beta 1).
121 . The pharmaceutical composition according to claim 118 , wherein the carrier is a solvent or a dispersing medium.
122 . The pharmaceutical composition according to claim 118 , wherein the carrier comprises water, saline, or phosphate buffered saline.
123 . The pharmaceutical composition according to claim 118 , further comprising a fluid lubricant.
124 . The pharmaceutical composition according to claim 118 , wherein the vehicle is suitable for systemic administration.Join the waitlist — get patent alerts
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