Methods and compositions comprising desmopressin in combination with an alpha-adrenergic receptor antagonist
The invention provides methods and compositions for use of desmopressin in combination with an alpha-adrenergic receptor antagonist. The methods and compositions are useful in the treatment of nocturia and other urinary frequency disorders.
1. A method of inhibiting the urge to urinate in an adult human subject over an interval of about two hours to no more than about eight hours, comprising intranasally administering to an adult human subject in need thereof a composition comprising an alpha-adrenergic receptor antagonist and desmopressin so that both exert physiological activity during an overlapping time period, wherein the desmopressin is administered in an amount that delivers to the blood stream a concentration of desmopressin no more than 2 ng/kg.
2. The method of claim 1 , wherein the method inhibits the urge to urinate in a human subject over an interval of about 4 hours to about 7 hours.
3. The method of claim 1 , wherein an antidiuretic effect is achieved over an interval of about two hours to no more than about six hours.
4. The method of claim 1 , wherein an antidiuretic effect is achieved over an interval of about four hours to no more than about seven hours.
5. The method of claim 1 , wherein the administering achieves in the subject a blood plasma concentration of desmopressin that does not exceed 15 pg/mL.
6. The method of claim 1 , wherein the administering achieves in the subject a blood plasma concentration of desmopressin in the range of about 0.5 pg/mL to about 5 pg/mL.
7. The method of claim 1 , wherein the administering achieves in the human subject a blood plasma concentration of desmopressin in the range of about 0.5 pg/mL to about 2.5 pg/mL.
8. The method of claim 1 , wherein the alpha-adrenergic receptor antagonist is alfuzosin, amosulalol, arotinolol, dapiprazole, doxazosin, ergoloid mesylates, fenspiride, idazoxan, indoramin, labetalol, naftopidil, nicergoline, prazosin, silodosin, tamsulosin, terazosin, tolazoline, yohimbine, phenoxybenzamine, phentolamine, atipamezole, or a pharmaceutically acceptable salt thereof.
9. The method of claim 1 , wherein the alpha-adrenergic receptor antagonist is alfuzosin, doxazosin, idazoxan, prazosin, silodosin, tamsulosin, terazosin, tolazoline, yohimbine, or a pharmaceutically acceptable salt thereof.
10. The method of claim 1 , wherein the alpha-adrenergic receptor antagonist is alfuzosin, doxazosin, prazosin, silodosin, tamsulosin, terazosin, tolazoline, yohimbine, or a pharmaceutically acceptable salt thereof.
11. The method of claim 1 , wherein the subject suffers from nocturia, incontinence, enuresis, or diabetes insipidus.
12. The method of claim 1 , wherein the subject suffers from nocturia.
13. The method of claim 1 , wherein urine production in the human subject is restored within about two hours after administration of desmopressin has been terminated.
14. The method of claim 1 , wherein the method comprises administering to the adult human subject an alpha-adrenergic receptor antagonist on a daily basis for a period of at least a month and administering desmopressin before the subject retires to sleep.
15. The method of claim 1 , further comprising administering a 5-alpha reductase inhibitor.
16. The method of claim 15 , wherein the 5-alpha reductase inhibitor is dutasteride, epristeride, finasteride, izonsteride, turosteride, AS-601811, FK143, TF-505, or a pharmaceutically acceptable salt thereof.
17. The method of claim 1 , wherein the adult human subject is an adult male human.
18. A pharmaceutical composition comprising desmopressin, an alpha-adrenergic receptor antagonist, and a pharmaceutically acceptable carrier, wherein the composition is formulated for intranasal administration.
19. The pharmaceutical composition of claim 18 , wherein the alpha-adrenergic receptor antagonist is alfuzosin, amosulalol, arotinolol, dapiprazole, doxazosin, ergoloid mesylates, fenspiride, idazoxan, indoramin, labetalol, naftopidil, nicergoline, prazosin, silodosin, tamsulosin, terazosin, tolazoline, yohimbine, phenoxybenzamine, phentolamine, atipamezole, or a pharmaceutically acceptable salt thereof.