US2019030032A1PendingUtilityA1

Depot formulations

72
Assignee: DURECT CORPPriority: May 18, 2007Filed: Jun 25, 2018Published: Jan 31, 2019
Est. expiryMay 18, 2027(~0.8 yrs left)· nominal 20-yr term from priority
Inventors:Jeremy C. WrightFelix TheeuwesJohn W. GibsonKeith E. BranhamStefania Sjobeck
A61K 9/10A61K 47/26A61K 9/0024A61K 9/0019A61K 31/519A61K 9/08A61K 47/34A61K 47/22A61P 25/18
72
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Claims

Abstract

Disclosed are formulations and related methods that comprise a non-polymeric, non-water soluble high viscosity liquid carrier material having a viscosity of at least 5,000 cP at 37° C. that does not crystallize neat under ambient or physiological conditions; a specified linear polymer comprising lactide repeat units; and one or more solvents that have a solvent capacity.

Claims

exact text as granted — not AI-modified
1 .- 40 . (canceled) 
     
     
         41 . A formulation comprising:
 a biologically active substance; and   a vehicle comprising:   (i) sucrose acetate isobutyrate (SAIB) in an amount of from 25 to 85 wt % based on total weight of the vehicle;   (ii) a linear poly(lactide-co-glycolide) in an amount of from 10 to 45 wt % based on total weight of the vehicle, wherein the linear poly(lactide-co-glycolide) possesses a ratio R of lactide repeat units to total repeat units in the linear poly(lactide-co-glycolide); and   (iii) one or more solvents that have a solvent capacity, wherein the one or more solvents dissolve the SAIB and the linear poly(lactide-co-glycolide), and wherein the SAIB, linear poly(lactide-co-glycolide), and one or more solvents are monophasic when maintained at approximately 25° C. for a one-week period;   wherein the linear poly(lactide-co-glycolide) has a weight average molecular weight less than or equal to 15 kilodaltons, and wherein   (a) R satisfies the following: 0.55≤R≤about 0.95;   (b) when R satisfies the following: 0.55≤R≤0.85, the solvent capacity of the one or more solvents is greater than or equal to 25%; and   (c) when R satisfies the following: greater than 0.85 to about 0.95, the solvent capacity of the one or more solvents is greater than or equal to about 10%.   
     
     
         42 . The formulation of  claim 41 , wherein the biologically active substance comprises an atypical antipsychotic. 
     
     
         43 . The formulation of  claim 41 , wherein the biologically active substance comprises an antiviral. 
     
     
         44 . The formulation of  claim 41 , wherein the linear poly(lactide-co-glycolide) is present in an amount ranging from about 15 wt % to 45 wt %, based on the total weight of the vehicle. 
     
     
         45 . The formulation of  claim 41 , wherein the linear poly(lactide-co-glycolide) has a weight average molecular weight less than 12.5 kilodaltons. 
     
     
         46 . The formulation of  claim 41 , wherein when R satisfies the following: greater than 0.85 to about 0.95, the solvent capacity of the one or more solvents is greater than or equal to about 15%. 
     
     
         47 . The formulation of  claim 41 , wherein when R satisfies the following: greater than 0.85 to about 0.95, the solvent capacity of the one or more solvents is greater than 20%. 
     
     
         48 . A method of administering a biologically active substance comprising administering the formulation of  claim 41 . 
     
     
         49 . A formulation comprising:
 a biologically active substance; and   a vehicle comprising:   (i) sucrose acetate isobutyrate (SAIB) in an amount of from 25 to 85 wt % based on total weight of the vehicle;   (ii) a linear poly(lactide-co-glycolide) in an amount of from 10 to 45 wt % based on total weight of the vehicle, wherein the linear poly(lactide-co-glycolide) possesses a ratio R of lactide repeat units to total repeat units in the linear poly(lactide-co-glycolide); and   (iii) one or more solvents that have a solvent capacity, wherein the one or more solvents dissolve the SAIB and the linear poly(lactide-co-glycolide), and wherein the SAIB, linear poly(lactide-co-glycolide), and one or more solvents are monophasic when maintained at approximately 25° C. for a one-week period;   wherein the linear poly(lactide-co-glycolide) has a weight average molecular weight less than or equal to 15 kilodaltons, and   wherein:   (a) R satisfies the following: 0.55≤R≤0.85; and   (b) the solvent capacity of the one or more solvents is greater than or equal to 25%.   
     
     
         50 . The formulation of  claim 49 , wherein the biologically active substance comprises an atypical antipsychotic. 
     
     
         51 . The formulation of  claim 49 , wherein the biologically active substance comprises an antiviral. 
     
     
         52 . The formulation of  claim 49 , wherein the linear poly(lactide-co-glycolide) is present in an amount ranging from about 15 wt % to 45 wt %, based on the total weight of the vehicle. 
     
     
         53 . The formulation of  claim 49 , wherein the linear poly(lactide-co-glycolide) has a weight average molecular weight less than 12.5 kilodaltons. 
     
     
         54 . A method of administering a biologically active substance comprising administering the formulation of  claim 49 . 
     
     
         55 . A formulation comprising:
 a biologically active substance; and   a vehicle comprising:   (i) sucrose acetate isobutyrate (SAIB) in an amount of from 25 to 85 wt % based on total weight of the vehicle;   (ii) a linear poly(lactide-co-glycolide) in an amount of from 10 to 45 wt % based on total weight of the vehicle, wherein the linear poly(lactide-co-glycolide) possesses a ratio R of lactide repeat units to total repeat units in the linear poly(lactide-co-glycolide); and   (iii) one or more solvents that have a solvent capacity, wherein the one or more solvents dissolve the SAIB and the linear poly(lactide-co-glycolide), and wherein the SAIB, linear poly(lactide-co-glycolide), and one or more solvents are monophasic when maintained at approximately 25° C. for a one-week period;   wherein the linear poly(lactide-co-glycolide) has a weight average molecular weight less than or equal to 15 kilodaltons, and wherein   R satisfies the following: greater than 0.85 to about 0.95; and   the solvent capacity of the one or more solvents is greater than or equal to about 10%.   
     
     
         56 . The formulation of  claim 55 , wherein the biologically active substance comprises an atypical antipsychotic. 
     
     
         57 . The formulation of  claim 55 , wherein the biologically active substance comprises an antiviral. 
     
     
         58 . The formulation of  claim 55 , wherein the linear poly(lactide-co-glycolide) is present in an amount ranging from about 15 wt % to 45 wt %, based on the total weight of the vehicle. 
     
     
         59 . The formulation of  claim 55 , wherein the linear poly(lactide-co-glycolide) has a weight average molecular weight less than 12.5 kilodaltons. 
     
     
         60 . The formulation of  claim 55 , wherein the solvent capacity of the one or more solvents is greater than or equal to about 15%. 
     
     
         61 . The formulation of  claim 55 , wherein the solvent capacity is greater than 20%. 
     
     
         62 . The formulation of  claim 55 , wherein the solvent capacity of the one or more solvents is greater than or equal to about 25%. 
     
     
         63 . A method of administering a biologically active substance comprising administering the formulation of  claim 55 . 
     
     
         64 . A formulation comprising:
 a biologically active substance; and   a vehicle comprising:   (i) sucrose acetate isobutyrate (SAIB) in an amount of from 25 to 85 wt % based on total weight of the vehicle;   (ii) a linear poly(lactide-co-glycolide) in an amount of from 10 to 45 wt % based on total weight of the vehicle, wherein the linear poly(lactide-co-glycolide) possesses a ratio R of lactide repeat units to total repeat units in the linear poly(lactide-co-glycolide), wherein R satisfies the following: 0.55≤R≤about 0.95; and   (iii) one or more solvents present in an amount ranging from 25 weight percent up to about 43 weight percent, based on total weight of the vehicle, wherein the one or more solvents dissolve the SAIB and the linear poly(lactide-co-glycolide), and wherein the SAIB, linear poly(lactide-co-glycolide), and one or more solvents are monophasic when maintained at approximately 25° C. for a one-week period;   wherein the linear poly(lactide-co-glycolide) has a weight average molecular weight less than or equal to 15 kilodaltons, and   wherein the one or more solvents comprise ethanol, ethyl lactate, propylene carbonate, glycofurol, N-methylpyrrolidone, 2-pyrrolidone, benzyl benzoate, caprylic/capric triglyceride, propylene glycol, acetone, methyl acetate, ethyl acetate, methyl ethyl ketone, benzyl alcohol, triacetin, dimethylformamide, dimethylsulfoxide, tetrahydrofuran, caprolactam, decylmethylsulfoxide, oleic acid, 1-dodecylazacycloheptan-2-one, and combinations thereof.   
     
     
         65 . The formulation of  claim 64 , wherein the biologically active substance comprises an atypical antipsychotic. 
     
     
         66 . The formulation of  claim 64 , wherein the biologically active substance comprises an antiviral. 
     
     
         67 . The formulation of  claim 64 , wherein the linear poly(lactide-co-glycolide) is present in an amount ranging from about 15 wt % to 45 wt %, based on the total weight of the vehicle. 
     
     
         68 . The formulation of  claim 64 , wherein the linear poly(lactide-co-glycolide) has a weight average molecular weight less than 12.5 kilodaltons. 
     
     
         69 . The formulation of  claim 64 , wherein the one or more solvents is present in an amount ranging from 25 weight percent up to about 35 weight percent, based on the total weight of the vehicle. 
     
     
         70 . A method of administering a biologically active substance comprising administering the formulation of  claim 64 .

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