US2019083484A1PendingUtilityA1

Formulations And Pharmacokinetics Of Deuterated Benzoquinoline Inhibitors Of Vesicular Monoamine Transporter 2

Assignee: AUSPEX PHARMACEUTICALS INCPriority: Sep 18, 2012Filed: Oct 17, 2018Published: Mar 21, 2019
Est. expirySep 18, 2032(~6.2 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 25/14A61K 9/2077A61K 9/2031C07B 2200/05A61K 9/5047A61K 9/2866A61K 9/288A61K 9/2027A61K 9/2013A61K 9/2846A61K 9/2072A61K 9/2095A61K 9/28A61K 9/1676A61K 9/284A61K 9/2018A61K 9/0053A61K 9/0065A61K 9/4808A61K 45/06C07D 455/06A61K 9/5073A61K 31/473A61K 31/4745A61K 9/5084A61K 9/2054A61K 9/5078
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Claims

Abstract

The present invention relates to new pharmaceutical compositions comprising benzoquinoline compounds, and methods to inhibit vesicular monoamine transporter 2 (VMAT2) activity in a subject for the treatment of chronic hyperkinetic movement disorders.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A solid d 6 -tetrabenazine oral dosage form comprising d 6 -tetrabenazine and a poly(ethylene oxide) polymer. 
     
     
         2 . A solid, extended-release d 6 -tetrabenazine oral dosage form comprising:
 about 1-15% by weight, based on the weight of the dosage form, of d 6 -tetrabenazine; and   about 5-20% by weight, based on the weight of the dosage form, of a poly(ethylene oxide) polymer.   
     
     
         3 . The oral dosage form according to  claim 2  in the form of a tablet comprising a tablet core and a coating, wherein the d 6 -tetrabenazine and poly(ethylene oxide) polymer are in the tablet core. 
     
     
         4 . The oral dosage form according to  claim 2  that releases the d 6 -tetrabenazine over a period of up to about 4 hours. 
     
     
         5 . The oral dosage form according to  claim 2  that releases the d 6 -tetrabenazine over a period of up to about 8 hours. 
     
     
         6 . The oral dosage form according to  claim 2  further comprising one or more of a filler, a lubricant, a binder, an absorbent, an antioxidant, a solubilizing agent, a dispersant, or a colorant. 
     
     
         7 . The oral dosage form according to  claim 2 , further comprising:
 about 60-70% by weight, based on the weight of the dosage form, of a filler;   about 15-25% by weight, based on the weight of the dosage form, of an absorbent;   about 1-10% by weight, based on the weight of the dosage form, of a dispersant;   about 0.5-2% by weight, based on the weight of the dosage form, of a solubilizing agent; and   about 0.5-2% by weight, based on the weight of the dosage form, of a lubricant.   
     
     
         8 . The oral dosage form according to  claim 7 , further comprising about 0.1-0.2% by weight, based on the weight of the dosage form, of an antioxidant. 
     
     
         9 . The oral dosage form according to  claim 8 , wherein the antioxidant is one or both of butylated hydroxyanisole and butylated hydroxytoluene. 
     
     
         10 . The oral dosage form according to  claim 9 , comprising
 about 60-70% by weight, based on the weight of the dosage form, of mannitol;   about 15-25%, based on the weight of the dosage form, by weight of microcrystalline cellulose;   about 1-10% by weight, based on the weight of the dosage form, of a polyvinylpyrrolidone;   about 0.5-2% by weight, based on the weight of the dosage form, of a polysorbate;   about 0.5-2% by weight, based on the weight of the dosage form, of magnesium stearate; and   about 0.1-0.2% by weight, based on the weight of the dosage form, of one or both of butylated hydroxyanisole and butylated hydroxytoluene.   
     
     
         11 . A method for treating a VMAT2-mediated disorder, comprising administering to a subject having or suspected of having such a disorder, a therapeutically effective amount of a composition of  claim 1 . 
     
     
         12 . The method of  claim 11 , wherein the VMAT2-mediated disorder is a chronic hyperkinetic movement disorder, Huntington's disease, hemiballismus, senile chorea, a tic disorder, tardive dyskinesia, dystonia, Tourette's syndrome, depression, cancer, rheumatoid arthritis, psychosis, multiple sclerosis, or asthma. 
     
     
         13 . A method for treating a VMAT2-mediated disorder, comprising administering to a subject having or suspected of having such a disorder, a therapeutically effective amount of a composition of  claim 2 . 
     
     
         14 . The method of  claim 13 , wherein the VMAT2-mediated disorder is a chronic hyperkinetic movement disorder, Huntington's disease, hemiballismus, senile chorea, a tic disorder, tardive dyskinesia, dystonia, Tourette's syndrome, depression, cancer, rheumatoid arthritis, psychosis, multiple sclerosis, or asthma.

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