US2012114697A1PendingUtilityA1

Treatment of holocrine gland dysfunction with clostridia neurotoxins

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Assignee: SANDERS IRAPriority: Aug 19, 2002Filed: Aug 27, 2010Published: May 10, 2012
Est. expiryAug 19, 2022(expired)· nominal 20-yr term from priority
A61P 43/00A61K 39/08A61K 38/4893A61P 15/14A61K 38/4813Y02A50/30
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Claims

Abstract

Methods of using clostridial toxins and other biological agents to control holocrine gland dysfunction in humans is provided. In preferred embodiments the methods provide beneficial effects in humans.

Claims

exact text as granted — not AI-modified
1 - 12 . (canceled) 
     
     
         13 - 28 . (canceled) 
     
     
         29 . A method of treating unwanted lactation or mammalian hypertrophy in a subject in need of such treatment which comprises administering to a breast of said subject a therapeutically effective amount of Botulinum toxin. 
     
     
         30 . The method of  claim 29 , wherein the administration is topical. 
     
     
         31 . The method of  claim 29 , wherein the Botulinum toxin is Botulinum toxin A. 
     
     
         32 . The method of  claim 29 , wherein the administration is by injection into the breast. 
     
     
         33 . The method of  claim 32 , comprising injection at multiple sites, wherein the sites of adjacent injections are separated by about 0.5 to 10 cm. 
     
     
         34 . The method of  claim 33 , wherein the sites of adjacent injections are separated by about 1.5 to about 3 cm. 
     
     
         35 . The method of  claim 29 , wherein the amount administered is between 0.1 and 1000 U of Botulinum toxin. 
     
     
         36 . The method of  claim 29 , wherein the amount administered is between 1 and 100 U of Botulinum toxin. 
     
     
         37 . The method of  claim 29 , wherein the amount administered is between 2 and 3 U of Botulinum toxin. 
     
     
         38 . The method of  claim 29 , wherein said method is repeated at intervals of from about 3 to about 6 months to inhibit said recurrence. 
     
     
         39 . The method of  claim 29 , wherein said method is repeated at intervals of about 4 months to inhibit said recurrence. 
     
     
         40 . The method of  claim 29 , wherein the Botulinum toxin is chosen from the group consisting of Botulinum toxin B, Botulinum toxin C, Botulinum toxin D, Botulinum toxin E, Botulinum toxin F and Botulinum toxin G.

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