US2009099232A1PendingUtilityA1

Injectable depot formulation comprising crystals of iloperidone

71
Assignee: WIECKHUSEN DIERKPriority: Jul 15, 2002Filed: Oct 21, 2008Published: Apr 16, 2009
Est. expiryJul 15, 2022(expired)· nominal 20-yr term from priority
A61K 9/0019A61K 47/26A61P 25/18A61P 25/28A61K 31/454A61K 47/10A61K 47/38
71
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Claims

Abstract

An injectable depot formulation comprising crystals having structure (I) wherein R is (FII) and the X50 value of the crystals is from 1 to 200 microns. Depot formulations containing crystals of iloperidone or its metabolites have the following advantages: (i) release of the crystals in plasma can be correlated with the size of the crystals; (ii) absorption of the crystals in plasma can be correlated with the size of the crystals; (iii) the particle size of the crystals can be controlled by crystal engineering and/or milling; and (iv) the crystals are stable upon storage, and stable to sterilization procedures, such as gamma irradiation.

Claims

exact text as granted — not AI-modified
1 . An injectable depot formulation comprising crystals of iloperidone or its metabolite or a pharmaceutically acceptable salt, hydrate, solvate, polymorph or stereoisomer of iloperidone or its metabolite, wherein the X 50  value of the crystals is from 1 to 200 microns. 
   
   
       2 . An injectable depot formulation comprising crystals having Structure (I) 
     
       
         
         
             
             
         
       
       wherein R is 
     
     
       
         
         
             
             
         
       
     
     and the X 50  value of the crystals is from 1 to 200 microns. 
   
   
       3 . The depot formulation according to  claim 2  wherein the crystals have Structure (II) 
     
       
         
         
             
             
         
       
     
   
   
       4 . The depot formulation according to  claim 2  wherein the crystals have Structure (III) 
     
       
         
         
             
             
         
       
     
   
   
       5 . The depot formulation according to  claim 2  wherein the crystals are a combination of crystals having Structure (II) 
     
       
         
         
             
             
         
       
     
     and crystals having Structure (III) 
     
       
         
         
             
             
         
       
     
   
   
       6 . The depot formulation according to  claim 1  wherein the X 50  value of the crystals is from 10 to 170 microns. 
   
   
       7 . The depot formulation according to  claim 6  wherein the X 50  value of the crystals is from 15 to 70 microns. 
   
   
       8 . The depot formulation according to  claim 1  wherein a suitable vehicle is used to form a suspension of the crystals. 
   
   
       9 . The depot formulation according to  claim 8  wherein the suitable vehicle is water. 
   
   
       10 . The depot formulation according to  claim 1  which additionally comprises an additional ingredient selected from the group consisting of a surfactant, solubilizer, emulsifier, preservative, isotonicity agent, dispersing agent, wetting agent, filler, solvent, buffer, stabilizer, lubricant, thickening agent, and combinations thereof. 
   
   
       11 . The depot formulation according to  claim 10  wherein the surfactant is selected from the group consisting of a sorbitan fatty acid ester, phosphatide, polyoxyethylated sorbitan monooleate, polyoxyalkylene derivatives of propylene glycol, polyoxyethylated fat, polyoxyethylated oleotriglyceride, linolizated oleotriglyceride, polyethylene oxide condensation products of fatty alcohol, and an alkylphenol. 
   
   
       12 . The depot formulation according to  claim 11  wherein the surfactant is a polyoxyalkylene derivative of propylene glycol. 
   
   
       13 . The depot formulation according to  claim 10  wherein the concentration of surfactant is in the range of about 0.5 to about 10 mg/mL. 
   
   
       14 . The depot formulation according to  claim 10  wherein the thickening agent is selected from the group consisting of sodium carboxymethyl cellulose, hydroxypropyl cellulose, calcium carboxymethyl cellulose, and crosslinked carboxymethyl cellulose. 
   
   
       15 . The depot formulation according to  claim 14  wherein the thickening agent is sodium carboxymethylcellulose. 
   
   
       16 . The depot formulation according to  claim 10  wherein the concentration of thickening agent is in the range of about 2 to about 25 mg/mL. 
   
   
       17 . The depot formulation according to  claim 10  wherein the isotonicity agent is selected from the group consisting of salts such as sodium chloride; sugars such as dextrose, mannitol, and lactose. 
   
   
       18 . The depot formulation according to  claim 17  wherein the isotonicity agent is mannitol. 
   
   
       19 . The depot formulation according to  claim 1  wherein the amount of iloperidone or its metabolite administered in one injection is from about 10 mg to about 1000 mg. 
   
   
       20 . The depot formulation according to  claim 19  wherein the amount of iloperidone or its metabolite administered in one injection is from about 100 mg to about 750 mg. 
   
   
       21 . A package comprising a container containing an injectable depot formulation comprising crystals of iloperidone or its metabolite or a pharmaceutically acceptable salt, hydrate, solvate, polymorph and stereoisomer of iloperidone or its metabolite, wherein the X 50  value of the crystals is from 1 to 200 microns. 
   
   
       22 . A package comprising a container containing an injectable depot formulation comprising crystals having Structure (I) 
     
       
         
         
             
             
         
       
       wherein R is 
     
     
       
         
         
             
             
         
       
     
     and the X 50  value of the crystals is from 1 to 200 microns. 
   
   
       23 . Crystals of iloperidone or its metabolite or a pharmaceutically acceptable salt, hydrate, solvate, polymorph and stereoisomer of iloperidone or its metabolite, wherein the X 50  value of the crystals is from 1 to 200 microns. 
   
   
       24 . Crystals having Structure (I) 
     
       
         
         
             
             
         
       
       wherein R is 
     
     
       
         
         
             
             
         
       
     
     and the X 50  value of the crystals is from 1 to 200 microns.

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