US2016279143A1PendingUtilityA1

Topical treatment for chemotherapy induced eyelash loss or hypotrichosis using prostamide f2 alpha agonists

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Assignee: ALLERGAN INCPriority: Feb 4, 2002Filed: Nov 12, 2015Published: Sep 29, 2016
Est. expiryFeb 4, 2022(expired)· nominal 20-yr term from priority
A61K 9/0048A61K 8/63A61K 9/0014A61K 9/08A61Q 7/00A61Q 1/10A61K 31/165A61K 2800/10A61K 8/4953A61K 8/42A61K 31/5575
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Claims

Abstract

The present invention is directed to compositions and methods for the treatment of post-chemotherapeutic hypotrichosis. More specifically, the present invention is directed to the use of compositions comprising bimatoprost for the treatment of post-chemotherapeutic hypotrichosis which may be applied before, during and after receiving chemotherapeutic treatment.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 ) A method of growing eyelashes in chemotherapy patients, the method comprising applying 0.03% w/v bimatoprost at least once a day to the eyelids of a chemotherapy patient from at least one selected from the group consisting of before, during, and after chemotherapeutic treatment wherein patients receiving 0.03% w/v bimatoprost resulted in greater eyelash growth as compared to patients not receiving 0.03% w/v bimatoprost. 
     
     
         2 ) The method of  claim 1 , wherein 0.03% w/v bimatoprost is applied after chemotherapeutic treatment and results in greater eyelash growth in patients as compared to patients not receiving 0.03% w/v bimatoprost. 
     
     
         3 ) The method of  claim 2 , wherein the method results in eyelashes which are longer or thicker as compared to patients not receiving 0.03% w/v bimatoprost. 
     
     
         4 ) The method of  claim 1 , wherein the patients receiving 0.03% w/v bimatoprost before starting chemotherapeutic treatment resulted in greater eyelash growth as compared to patients receiving 0.03% w/v bimatoprost during or after chemotherapeutic treatment. 
     
     
         5 ) The method of  claim 1 , wherein 0.03% w/v bimatoprost is applied to the upper eyelid. 
     
     
         6 ) The method of  claim 1 , wherein 0.03% w/v bimatoprost is applied to the lower eyelid. 
     
     
         7 ) The method of  claim 1 , wherein the bimatoprost is added before, during and after chemotherapeutic treatment. 
     
     
         8 ) A method of treating eyelashes loss in chemotherapy patients, the method comprising applying 0.03% w/v bimatoprost at least once a day to the eyelids of a chemotherapy patient from at least one selected from the group consisting of before, during, and after chemotherapeutic treatment wherein patients receiving 0.03% w/v bimatoprost resulted in greater eyelash growth as compared to patients not receiving 0.03% w/v bimatoprost. 
     
     
         9 ) The method of  claim 8 , wherein 0.03% w/v bimatoprost is applied after chemotherapeutic treatment and results in greater eyelash growth in patients as compared to patients not receiving 0.03% w/v bimatoprost. 
     
     
         10 ) The method of  claim 9 , wherein the method results in eyelashes which are longer or thicker as compared to patients not receiving 0.03% w/v bimatoprost. 
     
     
         11 ) The method of  claim 8 , wherein the patients receiving 0.03% w/v bimatoprost before starting chemotherapeutic treatment resulted in greater eyelash growth as compared to patients receiving 0.03% w/v bimatoprost during or after chemotherapeutic treatment. 
     
     
         12 ) The method of  claim 8 , wherein 0.03% w/v bimatoprost is applied to the upper eyelid. 
     
     
         13 ) The method of  claim 8 , wherein 0.03% w/v bimatoprost is applied to the lower eyelid. 
     
     
         14 ) The method of  claim 8 , wherein the bimatoprost is applied after completing chemotherapeutic treatment. 
     
     
         15 ) The method of  claim 14 , wherein the method is applied for at least 12 months after completing chemotherapeutic treatment. 
     
     
         16 ) The method of  claim 12  wherein the method is applied prior to receiving chemotherapeutic treatment. 
     
     
         17 ) The method of  claim 16 , wherein the method is applied for six months after receiving chemotherapeutic treatment. 
     
     
         18 ) The method of  claim 8  wherein the bimatoprost is in the form of a solution or an emulsion. 
     
     
         19 ) The method of  claim 8  wherein the bimatoprost is applied to the upper eyelid or both the upper and lower eyelid. 
     
     
         20 ) The method of  claim 8  wherein the method is applied after the patient completes chemotherapeutic treatment.

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