US2017143631A1PendingUtilityA1

Lipid formulation

Assignee: ARBUTUS BIOPHARMA CORPPriority: Jun 10, 2009Filed: Jun 20, 2016Published: May 25, 2017
Est. expiryJun 10, 2029(~2.9 yrs left)· nominal 20-yr term from priority
A61K 48/0033C12N 2310/321A61K 31/7088C12N 2310/14C12N 2320/32C07C 29/58A61K 31/713C12N 2310/346A61K 31/22C07C 227/18A61K 47/549A61K 38/4846C07D 475/04A61K 47/14C12N 2310/3515A61P 25/28A61K 31/712A61K 9/1272C12N 15/113A61K 9/1278C12N 2310/341C12N 2310/351C12N 2310/322C07C 229/12C12N 2310/315A61P 9/00C12N 15/1137C07C 227/40A61K 38/1709A61K 47/6911A61K 47/551A61K 31/7105C12N 2310/3533C12N 2310/3521A61K 2300/00Y02A50/30
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Claims

Abstract

The invention features a cationic lipid of formula I, an improved lipid formulation comprising a cationic lipid of formula I and corresponding methods of use. Also disclosed are targeting lipids, and specific lipid formulations comprising such targeting lipids.

Claims

exact text as granted — not AI-modified
1 . (canceled) 
     
     
         2 . A lipid formulation comprising a cationic lipid of formula I: 
       
         
           
           
               
               
           
         
         or a pharmaceutically acceptable salt thereof, and a therapeutic agent, wherein the therapeutic agent is a nucleic acid, wherein the nucleic acid is mRNA. 
       
     
     
         3 . The lipid formulation of  claim 2 , comprising 40-65% of the cationic lipid of formula I, 5-10% of a neutral lipid, 25-40% of a sterol, and 0.5-10% of a PEG or PEG-modified lipid. 
     
     
         4 . The lipid formulation of  claim 3 , wherein the neutral lipid is selected from DSPC, DPPC, DMPC, POPC, DOPE and SM. 
     
     
         5 . The lipid formulation of  claim 3 , wherein the sterol is cholesterol. 
     
     
         6 . The lipid formulation of  claim 3 , wherein the PEG lipid is PEG-C 14  to PEG-C 22 , PEG-Cer 14  to PEG-C 20 , or PEG-DSPE. 
     
     
         7 . The lipid formulation of  claim 3 , wherein the formulation is prepared by an in-line mixing method. 
     
     
         8 . The lipid formulation of  claim 3 , comprising about 57.5% of the cationic lipid of formula I, about 7.5% of the neutral lipid, about 31.5% of the sterol, and about 3.5% of the PEG or PEG-modified lipid. 
     
     
         9 . The lipid formulation of  claim 8 , wherein the formulation is prepared by an extrusion method. 
     
     
         10 - 12 . (canceled) 
     
     
         13 . The lipid formulation of  claim 3 , wherein the ratio of lipid:nucleic acid is about 3 to about 15. 
     
     
         14 . The lipid formulation of  claim 13 , wherein the ratio of lipid:nucleic acid is about 5 to about 13. 
     
     
         15 . The lipid formulation of  claim 2 , further comprising at least one apolipoprotein. 
     
     
         16 . The lipid formulation of  claim 15 , wherein the apolipotprotein is ApoE, active polymorphic forms, isoforms, variants and mutants, and fragments or truncated forms thereof. 
     
     
         17 . The lipid formulation of  claim 2 , further comprising a targeting lipid. 
     
     
         18 . The formulation of  claim 17 , wherein the targeting lipid comprises N-acetyl galactosamine. 
     
     
         19 . The formulation of  claim 18 , wherein the N-acetyl galactosamide comprises at least a mono-, bi- or a triantennary sugar unit. 
     
     
         20 . The formulation of  claim 17 , wherein said targeting lipid is present in the formulation in a molar amount of from about 0.001% to about 5%. 
     
     
         21 . The formulation of  claim 17 , wherein said targeting lipid is the compound selected from the group consisting of Formula II, Formula III, Formula VI and Formula VII: 
       
         
           
           
               
               
           
         
       
     
     
         22 . The lipid formulation of  claim 3 , comprising about 50% of cationic lipid of formula I, about 10% of the neutral lipid, about 38.5% of the sterol, and about 1.5% of the PEG or PEG-modified lipid. 
     
     
         23 . The lipid formulation of  claim 3 , comprising about 50% of cationic lipid of formula I, about 10% of the neutral lipid, about 35% of the sterol, and about 5% of the PEG or PEG-modified lipid. 
     
     
         24 . The lipid formulation of  claim 3 , comprising about 57.2% of cationic lipid of formula I, about 7.1% of the neutral lipid, about 34.3% of the sterol, and about 1.4% of the PEG or PEG-modified lipid. 
     
     
         25 . A method of delivering a therapeutic agent to a cell comprising administering to a subject the lipid formulation of  claim 2 . 
     
     
         26 - 29 . (canceled) 
     
     
         30 . A method of modulationg the expression of a target gene in a cell, the method comprising providing to a cell the lipid formulation of  claim 3 .

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