US2018187158A1PendingUtilityA1

Multifunctional immature dental pulp stem cells and therapeutic applications

Assignee: AVITA INT LTDPriority: Mar 15, 2013Filed: Sep 7, 2017Published: Jul 5, 2018
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-modified
1 - 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.

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