US2006039868A1PendingUtilityA1

Inhalable powder containing tiotropium

Assignee: BOEHRINGER INGELHEIM PHARMAPriority: Oct 12, 2000Filed: Oct 20, 2005Published: Feb 23, 2006
Est. expiryOct 12, 2020(expired)· nominal 20-yr term from priority
A61P 43/00A61P 11/00A61P 11/08A61P 11/06A61K 9/14A61K 9/0075A61K 31/439
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Claims

Abstract

The invention relates to powdered preparations containing tiotropium for inhalation, processes for preparing them as well as their use in preparing a pharmaceutical composition for the treatment of respiratory complaints, particularly for the treatment of COPD (chronic obstructive pulmonary disease) and asthma.

Claims

exact text as granted — not AI-modified
1 . An inhalable powder comprising 0.04 to 0.8% of tiotropium in admixture with a physiologically acceptable excipient, characterised in that the excipient consists of a mixture of coarser excipient with an average particle size of 15 to 80 μm and finer excipient with an average particle size of 1 to 9 μm, the proportion of the finer excipient constituting 1 to 20% of the total amount of excipient.  
     
     
         2 . An inhalable powder according to  claim 1 , characterised in that the tiotropium is present in the form of the chloride, bromide, iodide, methanesulphonate, para-toluenesulphonate or methyl sulphate thereof.  
     
     
         3 . An inhalable powder comprising between 0.048 and 0.96% of tiotropium bromide in admixture with a physiologically acceptable excipient, characterised in that the excipient consists of a mixture of coarser excipient with an average particle size of 15 to 80 μm and finer excipient with an average particle size of 1 to 9 μm, the proportion of the finer excipient constituting 1 to 20% of the total amount of excipient.  
     
     
         4 . An inhalable powder comprising between 0.05 and 1% of tiotropium bromide monohydrate in admixture with a physiologically acceptable excipient, characterised in that the excipient consists of a mixture of coarser excipient with an average particle size of 15 to 80 μm and finer excipient with an average particle size of 1 to 9 μm, the proportion of the finer excipient constituting 1 to 20% of the total amount of excipient.  
     
     
         5 . An inhalable powder according to one of claims  1 ,  2 ,  3  or  4 , characterised in that the excipient consists of a mixture of coarser excipient with an average particle size of 17 to 50 μm and finer excipient with an average particle size of 2 to 8 μm.  
     
     
         6 . An inhalable powder according to one of claims  1 ,  2 ,  3  or  4 , characterised in that the proportion of finer excipient in the total amount of excipient is 3 to 15%.  
     
     
         7 . An inhalable powder according to one of claims  1 ,  2 ,  3  or  4 , characterised in that the tiotropium used has a mean particle size of 0.5 to 10 μm.  
     
     
         8 . An inhalable powder according to one of claims  1 ,  2 ,  3  or  4 , characterised in that one or more monosaccharides, disaccharides, oligo- or polysaccharides, polyalcohols, salts thereof, or mixtures thereof are used as the excipients.  
     
     
         9 . An inhalable powder according to  claim 8 , characterised in that glucose, arabinose, lactose, saccharose, maltose, dextrane, sorbitol, mannitol, xylitol, sodium chloride, calcium carbonate or mixtures thereof are used as the excipients.  
     
     
         10 . An inhalable powder according to  claim 9 , characterised in that glucose or lactose or mixtures thereof are used as the excipients.  
     
     
         11 . A process for preparing an inhalable powder according to one of  claims 1  to  4 , comprising: (a) mixing coarser excipient fractions with finer excipient fractions to obtain an excipient mixture, and (b) mixing the excipient mixture thus obtained with the tiotropium.  
     
     
         12 . An inhalable powder prepared by the process according to  claim 11 .  
     
     
         13 . A method of treating a disease that is responsive to the administration of tiotropium, comprising administering to a host in need thereof an inhalable powder according to one of  claims 1  to  4  or  12 .  
     
     
         14 . A method according to  claim 13 , wherein the disease is asthma or COPD.  
     
     
         15 . An inhalette capsule containing an inhalable powder according to one of  claims 1  to  4  or  12 .  
     
     
         16 . An inhalette capsule containing from 3 to 10 mg of inhalable powder according to one of  claims 1  to  4  or  12 .  
     
     
         17 . An inhalette capsule according to  claim 16 , containing between 1.2 and 80 μg of tiotropium.

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