US2009162441A1PendingUtilityA1

Pulmonary delivery in treating disorders of the central nervous system

64
Assignee: BARTUS RAYMOND TPriority: Sep 19, 2000Filed: Jul 2, 2008Published: Jun 25, 2009
Est. expirySep 19, 2020(expired)· nominal 20-yr term from priority
A61P 25/24A61P 25/18A61P 25/06A61P 25/22A61P 25/16A61P 25/00A61P 25/28A61P 25/08A61K 9/007A61K 9/14A61K 9/008A61K 9/16A61P 11/00A61K 31/4045A61K 9/0075
64
PatentIndex Score
0
Cited by
0
References
0
Claims

Abstract

A method for treating a disorder of the central nervous system includes administering to the respiratory tract of a patient a drug which is delivered to the pulmonary system, for instance to the alveoli or the deep lung. The drug is administered at a dose which is at least about two-fold less than the dose required by oral administration. Particles that include the drug can be employed. Preferred particles have a tap density of less than about 0.4 g/cm 3 . In addition to the medicament, the particles can include other materials such as, for example, phospholipids, amino acids, combinations thereof and others.

Claims

exact text as granted — not AI-modified
1 . A method for treating a disorder of the central nervous system comprising administering to the respiratory tract of a patient in need of treatment alprazolam for treating said disorder, wherein the alprazolam is administered in a dose that is at least about two times less than that required by oral administration and wherein delivery is to the pulmonary system. 
     
     
         2 . The method of  claim 1  wherein delivery is to the alveoli region of the pulmonary system. 
     
     
         3 . The method of  claim 1  wherein administering is for rescue therapy. 
     
     
         4 . The method of  claim 1  wherein the alprazolam is present in dry powder particles. 
     
     
         5 . The method of  claim 4  wherein the alprazolam is present in the dry powder particles in an amount of at least 20 weight percent. 
     
     
         6 . The method of  claim 4  wherein the alprazolam is present in the dry powder particles in an amount of at least 40 weight percent. 
     
     
         7 . The method of  claim 4  wherein the alprazolam is present in the dry powder particles in an amount of at least 50 weight percent. 
     
     
         8 . The method of  claim 4  wherein the particles have a tap density of less than about 0.4 g/cm 3 . 
     
     
         9 . The method of  claim 4  wherein the particles have a mass median aerodynamic diameter of less than about 5 microns. 
     
     
         10 . The method of  claim 4  wherein the particles have a mass median geometric diameter greater than about 5 microns. 
     
     
         11 . The method of  claim 4  wherein the particles have a mass median aerodynamic diameter of less than about 3 microns. 
     
     
         12 . The method of  claim 4  wherein the particles include a phospholipid. 
     
     
         13 . The method of  claim 4  wherein the particles include citrate and a multivalent salt. 
     
     
         14 . The method of  claim 4  wherein the particles include an amino acid. 
     
     
         15 . The method of  claim 14  wherein the amino acid is leucine. 
     
     
         16 . The method of  claim 4  wherein the particles are administered via a dry powder inhaler.

Cited by (0)

No later patents cite this yet.

References (0)

No backward citations on record.