US2005130944A1PendingUtilityA1

Method of making and using 7alpha,11beta-dimethyl-17beta-hydroxyestr-4-en-3-one 17-undecanoate

Assignee: US GOV HEALTH & HUMAN SERVPriority: Mar 31, 2000Filed: Jan 21, 2005Published: Jun 16, 2005
Est. expiryMar 31, 2020(expired)· nominal 20-yr term from priority
A61P 5/24C07J 1/0074C07J 21/006C07J 1/007C07J 1/0059A61K 31/56C07J 71/001A61P 15/16
55
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Claims

Abstract

Disclosed are methods of using 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate (II) for various hormonal therapies, dosage forms comprising 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate, and processes for its preparation.

Claims

exact text as granted — not AI-modified
1 - 38 . (canceled)  
     
     
         39 . A crystalline compound of formula 10 
       
         
           
           
               
               
           
         
       
       having a melting point of 155-157° C.  
     
     
         40 . A compound of formula 5 
       
         
           
           
               
               
           
         
       
     
     
         41 . A compound of formula 6 
       
         
           
           
               
               
           
         
       
     
     
         42 . A compound of formula 7 
       
         
           
           
               
               
           
         
       
     
     
         43 . A compound of formula 9 
       
         
           
           
               
               
           
         
       
     
     
         44 - 45 . (canceled)  
     
     
         46 . A method for providing hormonal therapy to a patient comprising the oral administration of up to about 75 mg/day of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate to a patient in need thereof.  
     
     
         47 . The method of  claim 46 , wherein the hormonal therapy continues at least 3 months.  
     
     
         48 . The method of  claim 46 , wherein the hormonal therapy is the treatment of hypogonadism in a male patient.  
     
     
         49 . The method of  claim 48 , wherein up to about 50 mg/day of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is administered to the patient.  
     
     
         50 . The method of  claim 49 , wherein up to about 25 mg/day of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is administered to the patient.  
     
     
         51 . The method of  claim 46 , wherein hormonal therapy is male contraception.  
     
     
         52 . The method of  claim 51 , wherein the therapy continues for at least 3 months.  
     
     
         53 . The method of  claim 51 , wherein up to about 50 mg/day 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is administered to the patient.  
     
     
         54 . The method of  claim 51 , wherein up to about 30 mg/day of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is administered to the patient.  
     
     
         55 . The method of  claim 51 , further comprising the administration of estrogen, a progestin, or both.  
     
     
         56 . The method of  claim 46 , wherein the hormone therapy is the promotion and maintenance of muscle mass in a patient.  
     
     
         57 . The method of  claim 56 , wherein the therapy continues for at least 3 months.  
     
     
         58 . The method of  claim 46 , wherein the hormonal therapy is the pilliative treatment of breast cancer in women.  
     
     
         59 . The method of  claim 47 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is administered as a formulation comprising 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate and an oily carrier.  
     
     
         60 . A method for providing hormonal therapy to a patient comprising administering parenterally to the patient an average dosage of up to about 600 mg/month of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate during the treatment period.  
     
     
         61 . The method of  claim 60 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is parenterally administered as a formulation comprising 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate as a solid and an aqueous carrier, with the amount of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate administered at each interval being selected so that the average amount of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate administered during the period of hormonal treatment averages up to about 50 mg/week.  
     
     
         62 . The method of  claim 61 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is crystalline and the formulation comprises a suspension of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate in the aqueous carrier.  
     
     
         63 . The method of  claim 60 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is parenterally administered as a formulation comprising 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate and an aqueous carrier, with up to about 600 mg of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate being administered once over a period of at least about 1 month.  
     
     
         64 . The method of  claim 60 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is parenterally administered as a formulation comprising 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate and an aqueous carrier, with up to about 450 mg of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate being administered once over a period of at least about 2 months.  
     
     
         65 . The method of  claim 60 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is parenterally administered as a formulation comprising 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate and an aqueous carrier, with up to about 300 mg of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate being administered once over a period of at least about 3 months.  
     
     
         66 . The method of  claim 60 , wherein the hormonal treatment is the treatment of hypogonadism in male patients.  
     
     
         67 . The method of  claim 61 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is administered in a parenteral formulation comprising 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate and an aqueous carrier.  
     
     
         68 . The method of  claim 67 , wherein from about 150 mg to about 450 mg of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is patenterally administered once over a period of at least about 1 month.  
     
     
         69 . The method of  claim 68 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is parenterally administered once over a period of at least about 2 months.  
     
     
         70 . The method of  claim 67 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is parenterally administered once over a period of at least about 3 months.  
     
     
         71 . The method of  claim 60 , wherein the hormonal treatment is male contraception.  
     
     
         72 . The method of  claim 71 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is parenterally administered at an average dosage of up to about 200 mg/week.  
     
     
         73 . The method of  claim 71 , further comprising the administration of contraception-effective amounts of estrogen, progestins or mixtures thereof, wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is parenterally administered up to about 100 mg at intervals of at least about 2 weeks.  
     
     
         74 . The method of  claim 73 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is parenterally administered up to about 75 mg at intervals of at least about 1 month.  
     
     
         75 . An oral dosage formulation comprising 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate and a pharmaceutically-acceptable carrier.  
     
     
         76 . The oral dosage formulation of  claim 75 , wherein the pharmaceutically-acceptable carrier comprises an oil.  
     
     
         77 . The oral dosage formulation of  claim 76 , wherein the formulation comprises up to about 25 mg of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate  
     
     
         78 . The oral dosage formulation of  claim 77 , wherein the formulation comprises up to about 15 mg of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate.  
     
     
         79 . An aqueous formulation for parenteral administration comprising 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate and water.  
     
     
         80 . The aqueous formulation of  claim 79 , wherein 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is in crystalline form.  
     
     
         81 . A method for preparing 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate (Compound II) comprising the steps of: 
 (a) converting the ether group of Compound 1                         to a carbonyl group, providing Compound 2                         (b) ketalizing the carbonyl group of Compound 2 to provide Compound 4;                          (c) epoxidizing Compound 4 to provide the epoxide of Compound 5;                          (d) opening the epoxide ring in Compound 5 and substituting an alkyl group at C 11  to provide Compound 6 (comprising a mixture of 7α- and 7β-methyl isomers, Compounds 6a and 6b, respectively) by use of a Grignard reagent;                          (e) deketalizing and dehydrating Compound 6 to provide Compound 7;                          (f) converting Compound 7a to Compound 9;                          (g) converting Compound 9 to Compound 10; and                          (h) esterifying Compound 10 to provide Compound II                          
     
     
         82 . 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate (Compound II) in crystalline form.  
     
     
         83 . The compound of  claim 82 , having a m.p. of 62-64° C.  
     
     
         84 . The compound of  claim 82 , wherein the purity of the crystalline 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate is at least 99%.  
     
     
         85 . The oral dosage form of  claim 75 , wherein the formulation comprises up to about 75 mg of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate.  
     
     
         86 . The aqueous formulation of  claim 79 , wherein the formulation comprises up to about 600 mg of 7α,11β-dimethyl-17β-hydroxyestr-4-en-3-one 17-undecanoate.

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