US2016095851A1PendingUtilityA1

Sublingual apomorphine

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Assignee: CYNAPSUS THERAPEUTICS INCPriority: Jun 12, 2009Filed: Dec 8, 2015Published: Apr 7, 2016
Est. expiryJun 12, 2029(~2.9 yrs left)· nominal 20-yr term from priority
A61P 25/16A61P 15/10A61K 31/485Y10T428/2982A61K 9/006A61K 31/473A61K 9/06A61K 9/0056A61K 9/70A61K 47/02A61K 9/2086A61K 9/7007A61K 31/44A61K 47/10A61K 47/183A61K 47/18
61
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Claims

Abstract

The invention features sublingual formulations of apomorphine and apomorphine prodrugs, and methods of treating Parkinson's disease, sexual dysfunction, and depressive disorders therewith.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 .- 2 . (canceled) 
     
     
         3 . A pharmaceutical composition in unit dosage form formulated for sublingual administration, wherein said unit dosage form is a film comprising from 2 mg to 40 mg of an acid addition salt of apomorphine present as a solid solution with a polymer, and wherein said film is impregnated with particles comprising a pH neutralizing agent. 
     
     
         4 . The pharmaceutical composition of  claim 3 , wherein said pH neutralizing agent is an inorganic base. 
     
     
         5 . The pharmaceutical composition of  claim 4 , wherein said inorganic base is sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, sodium phosphate monobasic, sodium phosphate dibasic, sodium phosphate tribasic, potassium phosphate monobasic, potassium phosphate dibasic, potassium phosphate tribasic, or a mixture thereof. 
     
     
         6 . The pharmaceutical composition of  claim 5 , wherein said inorganic base is sodium phosphate monobasic, sodium phosphate dibasic, sodium phosphate tribasic, potassium phosphate monobasic, potassium phosphate dibasic, potassium phosphate tribasic, or a mixture thereof. 
     
     
         7 . The pharmaceutical composition of  claim 3 , wherein said film further comprises an antioxidant. 
     
     
         8 . The pharmaceutical composition of  claim 7 , wherein said antioxidant is selected from the group consisting of thiols, sulphoximines, metal chelators, sodium metabisulfite, vitamins, phenols, benzoates, uric acid, mannose, propyl gallate, selenium, stilbenes, and combinations thereof. 
     
     
         9 . The pharmaceutical composition of  claim 8 , wherein said antioxidant is sodium metabisulfite. 
     
     
         10 . The pharmaceutical composition of  claim 8 , wherein said antioxidant is a metal chelator. 
     
     
         11 . The pharmaceutical composition of  claim 10 , wherein said metal chelators is EDTA. 
     
     
         12 . The pharmaceutical composition of  claim 3 , wherein said film further comprises a plasticizer selected from the group consisting of glycerol, propylene glycol, fatty acid esters, sorbitan esters, citric acid esters, PEG 400, polyvinyl methyl ether, triacetin; mannitol, xylitol, and sorbitol. 
     
     
         13 . The pharmaceutical composition of  claim 12 , wherein said plasticizer is glycerol. 
     
     
         14 . The pharmaceutical composition of  claim 3 , wherein said film comprises from 2 to 40 mg of said acid addition salt of apomorphine. 
     
     
         15 . The pharmaceutical composition of  claim 14 , wherein said mucoadhesive film comprises 10±3 mg of said acid addition salt of apomorphine. 
     
     
         16 . The pharmaceutical composition of  claim 14 , wherein said mucoadhesive film comprises 15±3 mg of said acid addition salt of apomorphine. 
     
     
         17 . The pharmaceutical composition of  claim 14 , wherein said mucoadhesive film comprises 22±4 mg of said acid addition salt of apomorphine. 
     
     
         18 . The pharmaceutical composition of  claim 14 , wherein said mucoadhesive film comprises 27±4 mg of said acid addition salt of apomorphine. 
     
     
         19 . The pharmaceutical composition of  claim 14 , wherein said mucoadhesive film comprises 30±5 mg of said acid addition salt of apomorphine. 
     
     
         20 . The pharmaceutical composition of  claim 14 , wherein said mucoadhesive film comprises 35±5 mg of said acid addition salt of apomorphine. 
     
     
         21 . A method of treating a patient having Parkinson's disease comprising administering to said patient an effective amount of the pharmaceutical composition of  claim 3 . 
     
     
         22 . The method of  claim 21 , wherein said administering alleviates “off” symptoms of Parkinson's disease.

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