US2018221387A1PendingUtilityA1

Composition and method for oral delivery of androgen prodrugs

Assignee: LIPOCINE INCPriority: Jun 15, 2015Filed: Jan 3, 2018Published: Aug 9, 2018
Est. expiryJun 15, 2035(~8.8 yrs left)· nominal 20-yr term from priority
A61J 1/10A61K 31/568A61K 9/4866A61J 1/035A61K 9/4858A61K 9/0053A61J 1/06A61J 7/0076
59
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Claims

Abstract

Provided oral testosterone undecanoate compositions can be administered to hypogonadal males with a meal without the fat content of the meal substantially effecting bioavailability.

Claims

exact text as granted — not AI-modified
1 . A method for replacement therapy in a male for a condition associated with a deficiency or absence of endogenous testosterone, said method comprising: orally administering to a male having a condition associated with a deficiency or absence of endogenous testosterone, with a meal, a pharmaceutical composition comprising from about 50 mg to about 300 mg of testosterone undecanoate and a pharmaceutically acceptable carrier said pharmaceutical acceptable carrier being selected to provide bioequivalent amounts of serum testosterone, testosterone undecanoate, dihydrotestosterone, or dihydrotestosterone undecanoate levels to said male when administered with (1) meals containing standard fat as compared to low fat and high fat, (2) meals containing low fat as compared to high fat, or both (1) and (2). 
     
     
         2 . The method of  claim 1 , wherein said pharmaceutical composition has about 75 mg, about 112.5 mg, about 150 mg, about 225 mg, or 300 mg of testosterone undecanoate. 
     
     
         3 . The method of  claim 1 , wherein said pharmaceutically acceptable carrier selected to provide bioequivalent amounts of serum testosterone levels to said male for meals containing low, standard fat and high fat. 
     
     
         4 . The method of  claim 1 , wherein said method provides a serum testosterone Cavg in the range of 300 ng/dL to 1100 ng/dL. 
     
     
         5 . The method of  claim 1 , wherein said administering occurs twice-a-day. 
     
     
         6 . The method of  claim 1 , wherein said method comprises administering from 285 mg to about 625 mg of testosterone undecanoate per day. 
     
     
         7 . The method of  claim 1 , wherein said composition comprises a lipophilic additive. 
     
     
         8 . The method of  claim 1 , wherein said composition comprises a hydrophilic additive. 
     
     
         9 . The method of  claim 1 , wherein said pharmaceutical composition (1) is pharmaceutically equivalent to an oral pharmaceutical composition having about 75 mg or about 112.5 mg of testosterone undecanoate at about 15 wt % loading, about 63 wt % Maisine 35-1, about 16 wt % Cremophor RH 40, and about 6 wt % PEG 8000 or (2) has about 75 mg or about 112.5 mg of testosterone undecanoate at about 15 wt % loading, about 63 wt % Maisine 35-1, about 16 wt % Cremophor RH 40, and about 6 wt % PEG 8000. 
     
     
         10 . The method of  claim 1 , wherein said method comprises administering the pharmaceutical composition as 2, 3, 4, 5, 6, 7, or 8 unit dosage forms per day. 
     
     
         11 . A method for replacement therapy in a male for conditions associated with a deficiency or absence of endogenous testosterone, said method comprising: orally administering to a male having a condition associated with a deficiency or absence of endogenous testosterone, with a meal having about 10 wt % to 50 wt % fat, a pharmaceutical composition comprising from about 50 mg to about 300 mg of testosterone undecanoate and a pharmaceutically acceptable carrier said pharmaceutical acceptable carrier being selected to provide bioequivalent amounts of serum testosterone, testosterone undecanoate, dihydrotestosterone, or dihydrotestosterone undecanoate levels to said male when administered with meals containing (1) standard fat as compared to low fat and high fat, (2) low fat to high fat, or (3) a combination thereof. 
     
     
         12 . The method of  claim 11 , wherein said pharmaceutical composition (1) is pharmaceutically equivalent to an oral pharmaceutical composition having about 75 mg or about 112.5 mg of testosterone undecanoate at about 15 wt % loading, about 63 wt % Maisine 35-1, about 16 wt % Cremophor RH 40, and about 6 wt % PEG 8000 or (2) has about 75 mg or about 112.5 mg of testosterone undecanoate at about 15 wt % loading, about 63 wt % Maisine 35-1, about 16 wt % Cremophor RH 40, and about 6 wt % PEG 8000. 
     
     
         13 . The method of  claim 11 , wherein said method provides a serum testosterone Cavg in the range of 300 ng/dL to 1100 ng/dL. 
     
     
         14 . The method of  claim 11 , wherein said method comprises administering from 285 mg to about 625 mg of testosterone undecanoate per day. 
     
     
         15 . The method of  claim 11 , said administering occurs twice-a-day. 
     
     
         16 . A pharmaceutical composition for oral administration comprising testosterone undecanoate and a pharmaceutical acceptable carrier said pharmaceutical composition providing bioequivalent amounts of serum testosterone undecanoate, testosterone, dihydrotestosterone, dihydrotestosterone undecanoate or a combination thereof to a male for a condition associated with a deficiency or absence of endogenous testosterone when administered with a meal (1) containing medium fat as compared to high fat or low fat or (2) containing low, standard and high fat. 
     
     
         17 . The pharmaceutical composition of  claim 16 , wherein said pharmaceutical composition is pharmaceutically equivalent to an oral pharmaceutical composition having about 75 mg or about 112.5 mg of testosterone undecanoate at 15 wt % loading, 63 wt % Maisine 35-1, 16 wt % Cremophor RH 40, and 6 wt % PEG 8000. 
     
     
         18 . The pharmaceutical composition of  claim 16 , further comprising a monoglyceride, a diglyceride or a combination thereof in amount of greater than about 10 wt % and has less than about 50 wt % triglyceride. 
     
     
         19 . A pharmaceutical composition for oral administration that is hypogonadal male serum testosterone bioequivalent to a formulation comprising 15 wt % testosterone undecanoate, about 63 wt % Maisine 35-1, about 16 wt % Cremophor RH 40, and about 6 wt % polyethylene glycol 8000 under medium fat as compared to low fat and high fat with the proviso that the formulation does not comprise about 15 wt % testosterone undecanoate, about 63 wt % Maisine 35-1, about 16 wt % Cremophor RH 40, and about 6 wt % polyethylene glycol 8000. 
     
     
         20 . The pharmaceutical composition of  claim 19 , wherein said pharmaceutical composition is pharmaceutically equivalent to an oral pharmaceutical composition having about 75 mg or about 112.5 mg of testosterone undecanoate at 15 wt % loading, 63 wt % Maisine 35-1, 16 wt % Cremophor RH 40, and 6 wt % PEG 8000. 
     
     
         21 - 42 . (canceled)

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