US2008287459A1PendingUtilityA1

Pharmaceutical Composition for Treating Hair Loss and Benign Prostatic Hyperplasia

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Assignee: LEE EUN-JOOPriority: Apr 14, 2004Filed: Apr 13, 2005Published: Nov 20, 2008
Est. expiryApr 14, 2024(expired)· nominal 20-yr term from priority
Inventors:Eun Joo Lee
A61P 35/00A61P 13/08A61K 8/494A61P 17/14A61K 31/495A61Q 7/00A61K 8/30
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Claims

Abstract

The present invention is related to an orally administered pharmaceutical composition for the prevention of hair loss; having the effects of epilation, hair toning, and hair growth; and for the treatment of female hirsutism and benign prostatic hyperplasia. The composition of the present invention is non-steroidal and is advantageous in that it has no side effects such as lowering of sexual function, etc. shown in the conventional oral treatment agents of related diseases.

Claims

exact text as granted — not AI-modified
1 . A pharmaceutical composition for the prevention of hair loss; and having the effects of epilation, hair toning, and hair growth; and for the treatment of female hirsutism and benign prostatic hyperplasia, which comprises as an active ingredient 2-[2-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]-acetic acid, or its pharmaceutically acceptable salt, hydrate, or solvate. 
   
   
       2 . The pharmaceutical composition of  claim 1 , wherein said active ingredient is a racemate or optical isomer of 2-[2-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]-acetic acid. 
   
   
       3 . The pharmaceutical composition of  claim 2 , wherein said active ingredient is 2-[2-[4-[(4-chlorophenyl)phenylmethyl]-1-piperazinyl]ethoxy]-acetic acid dihydrochloride. 
   
   
       4 . The pharmaceutical composition of  claim 3 , wherein said composition is for oral administration or local administration. 
   
   
       5 . The pharmaceutical composition of  claim 4 , wherein said composition is in the form of a tablet, a powder, a dried syrup, a chewable tablet, a granule, a chewing tablet, a capsule, a soft capsule, a pill, a drink, or a sublingual tablet. 
   
   
       6 . The pharmaceutical composition of  claim 4 , wherein said composition is administered orally once to three times a day in a dosage amount of 1 to 2,000 mg/day based on the amount of the effective component. 
   
   
       7 . The pharmaceutical composition of  claim 6 , wherein said composition is administered orally once to three times a day in a dosage amount of 5 to 300 mg/day based on the amount of the effective component.

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