NEW COMBINATION OF ACTIVE INGREDIENTS CONTAINING AN a1-ANTAGONIST AND A PDE 4 INHIBITOR
The subject of the present invention is a new combination of active ingredients consisting of alfuzosin and PDE 4 inhibitor, and pharmaceutical compositions containing them, for ameliorating and/or treating benign prostatic hyperplasia, urinary disorders, disorders related to bladder dysfunction, lower urinary tract symptoms associated or not associated with benign prostatic hyperplasia, urinary incontinence, bladder outlet obstruction associated or not associated with benign prostatic hyperplasia, interstitial cystitis and overactive bladder.
1 . A pharmaceutical composition comprising a combination of active ingredients, wherein said active ingredients are an α 1 -antagonist and a PDE 4 inhibitor and both active ingredients being present in the free state or in the form of a salt.
2 . The pharmaceutical composition according to claim 1 , wherein said α 1 -antagonist is chosen from doxazosin, terazosin, tamsulosin and alfuzosin, or a salt thereof.
3 . The pharmaceutical composition according to claim 1 , wherein said α 1 -antagonist is alfuzosin, or a salt thereof.
4 . The pharmaceutical composition according to claim 1 , wherein said PDE 4 inhibitor is chosen from rolipram, drotaverine, roflumilast, cilomilast and piclamilast, or a salt thereof.
5 . The pharmaceutical composition according to claim 1 , wherein said active ingredients are alfuzosin and drotaverine, each being present in the free state and/or in the form of a salt.
6 . The pharmaceutical composition according to claim 1 , wherein said active ingredients are alfuzosin hydrochloride and drotaverine hydrochloride.
7 . The pharmaceutical composition according to claim 1 , wherein said composition is in a form being able to be administered by the parenteral route or by the oral route.
8 . The pharmaceutical composition according to claim 1 , wherein said α 1 -antagonists and PDE 4 inhibitor are in a molar ratio of 0.6 to 800.
9 . A method of ameliorating and/or treating benign prostatic hyperplasia, urinary disorders, disorders related to bladder dysfunction, lower urinary tract symptoms associated or not associated with benign prostatic hyperplasia, urinary incontinence, bladder outlet obstruction associated or not associated with benign prostatic hyperplasia, interstitial cystitis and overactive bladder in a patient in need thereof comprising administering to said patient a therapeutically effective amount of the pharmaceutical composition of claim 1 .
10 . The pharmaceutical composition according to claim 1 , wherein said composition is a combined preparation of α 1 -antagonists and PDE 4 inhibitor for simultaneous use.
11 . The pharmaceutical composition according to claim 1 , wherein said composition is a combined preparation of α 1 -antagonists and PDE 4 inhibitor for separate or sequential use.
12 . (canceled)
13 . The method according to claim 9 , comprising administering by the parenteral and/or oral route 0.5 to 15 mg of alfuzosin per day and of 15 to 80 mg of PDE 4 inhibitor per day.
14 . The method according to claim 13 , wherein said PDE 4 inhibitor is chosen from rolipram, drotaverine, roflumilast, cilomilast and piclamilast, or a salt thereof.
15 . The method according to claim 13 , wherein said PDE 4 inhibitor is drotaverine, or a salt thereof.