US2018064807A1PendingUtilityA1

Novel lipids and compositions for the delivery of therapeutics

Assignee: ARBUTUS BIOPHARMA CORPPriority: Nov 10, 2008Filed: Mar 30, 2017Published: Mar 8, 2018
Est. expiryNov 10, 2028(~2.3 yrs left)· nominal 20-yr term from priority
A61P 35/00A61P 37/04A61P 33/00A61K 9/5123C07C 251/38A61K 9/1272A61K 31/713A61K 39/39C07D 491/056A61K 31/7088A61K 48/0033C07C 271/12A61K 47/18A61K 47/20C07D 317/44A61K 47/44C07D 319/06C07D 203/10C12N 2310/14C07C 237/16A61K 2039/55561C07D 491/113A61K 47/22C12N 15/111C07D 317/72C07C 271/20C12N 2320/32C07C 229/08C07C 323/25C07C 229/30A61K 47/28C07D 317/46C07D 317/28C07D 405/12C07C 251/78A61K 47/10A61K 2039/55555A61K 31/7105C12N 15/113C12N 2310/3515Y02A50/30A61K 2039/53A61K 47/24A61K 39/00C07D 211/72C07F 9/1651C07C 307/06C07C 311/11C07C 305/14C07F 9/091C07C 219/10C07C 327/06C07C 259/06C07C 279/04C07C 211/21C07C 323/27C07C 217/46
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Claims

Abstract

The present invention provides lipids that are advantageously used in lipid particles for the in vivo delivery of therapeutic agents to cells. In particular, the invention provides lipids having the following structure:

Claims

exact text as granted — not AI-modified
1 . A cationic lipid having the formula: 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof, wherein
 R 1  and R 2  are each independently for each occurrence optionally substituted C 10 -C 30  alkyl, optionally substituted C 10 -C 30  alkenyl, optionally substituted C 10 -C 30  alkynyl, optionally substituted C 10 -C 30  acyl, or -linker-ligand; 
 R 3  is independently for each occurrence H, optionally substituted C 1 -C 10  alkyl, optionally substituted C 2 -C 10  alkenyl, optionally substituted C 2 -C 10  alkynyl, alkylheterocycle, alkylphosphate, alkylphosphorothioate, alkylphosphorodithioate, alkylphosphonates, alkylamines, hydroxyalkyls, ω-aminoalkyls, ω-(substituted)aminoalkyls, ω-phosphoalkyls, ω-thiophosphoalkyls, optionally substituted polyethylene glycol (PEG, mw 100-40K), optionally substituted mPEG (mw 120-40K), heteroaryl, heterocycle, or linker-ligand; 
 X and Y are each independently O, S, alkyl or N(Q); 
 Q is H, alkyl, ω-amninoalkyl, ω-(substituted)amninoalkyl, ω-phosphoalkyl or ω-thiophosphoalkyl; 
 A 2  is O, S, CH 2 , CHF or CF 2 ; 
 Z′ is O, S, N(Q) or alkyl; and 
 j is 0-10. 
 
     
     
         2 . (canceled) 
     
     
         3 . (canceled) 
     
     
         4 . (canceled) 
     
     
         5 . (canceled) 
     
     
         6 . (canceled) 
     
     
         7 . (canceled) 
     
     
         8 . (canceled) 
     
     
         9 . The cationic lipid of  claim 1 , wherein X and Y are O. 
     
     
         10 . (canceled) 
     
     
         11 . The cationic lipid of  claim 1 , wherein A 2  is —CH 2 —. 
     
     
         12 . (canceled) 
     
     
         13 . (canceled) 
     
     
         14 . The cationic lipid of  claim 1 , wherein Z′ is N(Q). 
     
     
         15 . (canceled) 
     
     
         16 . (canceled) 
     
     
         17 . The cationic lipid of  claim 1 , wherein Z′ is alkyl. 
     
     
         18 . The cationic lipid of  claim 1 , wherein R 3  is alkylamine. 
     
     
         19 . (canceled) 
     
     
         20 . (canceled) 
     
     
         21 . The cationic lipid of  claim 1 , wherein Q is alkyl. 
     
     
         22 . (canceled) 
     
     
         23 . (canceled) 
     
     
         24 . (canceled) 
     
     
         25 . A cationic lipid of the formula 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof, wherein
 R 1  and R 2  are independently optionally substituted C 10 -C 30  alkyl or optionally substituted C 10 -C 30  alkenyl; and 
 X and Y are independently hydrogen or C 1 -C 4  alkyl, or X and Y together with the nitrogen atom to which they are directly bound form a mono- or bi-cyclic heterocycle. 
 
     
     
         26 . (canceled) 
     
     
         27 . (canceled) 
     
     
         28 . (canceled) 
     
     
         29 . (canceled) 
     
     
         30 . (canceled) 
     
     
         31 . (canceled) 
     
     
         32 . (canceled) 
     
     
         33 . (canceled) 
     
     
         34 . (canceled) 
     
     
         35 . (canceled) 
     
     
         36 . (canceled) 
     
     
         37 . (canceled) 
     
     
         38 . (canceled) 
     
     
         39 . (canceled) 
     
     
         40 . The cationic lipid of  claim 25 , wherein the compound is 
       
         
           
           
               
               
           
         
       
       or a pharmaceutically acceptable salt thereof, wherein X and Y are hydrogen or C 1 -C 4  alkyl. 
     
     
         41 . (canceled) 
     
     
         42 . (canceled) 
     
     
         43 . A lipid particle comprising a compound of  claim 1 . 
     
     
         44 . (canceled) 
     
     
         45 . A lipid particle comprising a compound of  claim 25 . 
     
     
         46 . The lipid particle of  claim 43 , wherein the particle further comprises a therapeutic agent. 
     
     
         47 . The lipid particle of  claim 45 , wherein the particle further comprises a therapeutic agent. 
     
     
         48 . (canceled) 
     
     
         49 . The lipid particle of  claim 46 , wherein the therapeutic agent is a nucleic acid. 
     
     
         50 . The lipid particle of  claim 47 , wherein the therapeutic agent is a nucleic acid. 
     
     
         51 . (canceled) 
     
     
         52 . The lipid particle of  claim 49 , wherein the nucleic acid is siRNA or mRNA. 
     
     
         53 . The lipid particle of  claim 50 , wherein the nucleic acid is siRNA or mRNA. 
     
     
         54 . (canceled) 
     
     
         55 . A method of treating a disease or disorder in a subject in need thereof, comprising administering to the subject the lipid particle of  claim 46 . 
     
     
         56 . A method of treating a disease or disorder in a subject in need thereof, comprising administering to the subject the lipid particle of  claim 47 .

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