COMPOSITION COMPRISING A PDE4 INHIBITOR AND A PDE5 INHIBITOR
The claimed subject matter relates to pharmaceutical compositions comprising a PDE4 inhibitor and a PDE5 inhibitor and the treatment of a disease in which phosphodiesterase 4 (PDE4) and/or phosphodiesterase 5 (PDE5) is detrimental.
1 .- 24 . (canceled)
25 . A pharmaceutical composition comprising in a single dosage form
(a) an effective amount of a PDE4 inhibitor and
(b) an effective amount of a PDE5 inhibitor, and optionally
(c) a pharmaceutically acceptable carrier.
26 . The pharmaceutical composition according to claim 25 , wherein the single dosage form is an oral dosage form.
27 . A pharmaceutical composition comprising
(a) in a first dosage form an effective amount of a PDE4 inhibitor and optionally a pharmaceutically acceptable carrier and
(b) in a second dosage form an effective amount of a PDE5 inhibitor and optionally a pharmaceutically acceptable carrier.
28 .- 46 . (canceled)
47 . The pharmaceutical composition according to claim 27 , wherein the first and the second dosage forms are oral dosage forms.
48 . The pharmaceutical composition according to claim 25 , wherein the PDE4 inhibitor is 3-cyclopropylmethoxy-4-difluoromethoxy-N-(3,5-dichloropyrid-4-yl)-benzamide (Roflumilast) or a pharmaceutically acceptable salt, N-oxide, or a pharmaceutically acceptable salt of the N-oxide thereof and wherein the PDE5 inhibitor is selected from the group consisting of 5-[2-ethoxy-5-(4-methyl-1-piperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (SILDENAFIL), a pharmaceutically acceptable salt of SILDENAFIL, (6R,12aR)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-methylenedioxy-phenyl)-pyrazino[2′,1′:6,1]pyrido[3,4-b]indole-1,4-dione (TADALAFIL), a pharmaceutically acceptable salt of TADALAFIL, 2-[2-ethoxy-5-(4-ethylpiperazin-1-ylsulfonyl)phenyl]-5-methyl-7-propylimidazo[5,1-f][1,2,4]triazin-4(3H)-one (VARDENAFIL) and a pharmaceutically acceptable salt of VARDENAFIL.
49 . The pharmaceutical composition according to claim 48 , wherein the PDE4 inhibitor is 3-cyclopropylmethoxy-4-difluoromethoxy-N-(3,5-dichloropyrid-4-yl)-benzamide (Roflumilast) and wherein the PDE5 inhibitor is selected from the group consisting of 5-[2-ethoxy-5-(4-methyl-1-piperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (SILDENAFIL) and a pharmaceutically acceptable salt of SILDENAFIL.
50 . The pharmaceutical composition according to claim 26 , wherein the PDE4 inhibitor is 3-cyclopropylmethoxy-4-difluoromethoxy-N-(3,5-dichloropyrid-4-yl)-benzamide (Roflumilast) or a pharmaceutically acceptable salt, N-oxide, or a pharmaceutically acceptable salt of the N-oxide thereof and wherein the PDE5 inhibitor is selected from the group consisting of 5-[2-ethoxy-5-(4-methyl-1-piperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (SILDENAFIL), a pharmaceutically acceptable salt of SILDENAFIL, (6R,12aR)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-methylenedioxy-phenyl)-pyrazino[2′,1′:6,1]pyrido[3,4-b]indole-1,4-dione (TADALAFIL), a pharmaceutically acceptable salt of TADALAFIL, 2-[2-ethoxy-5-(4-ethylpiperazin-1-ylsulfonyl)phenyl]-5-methyl-7-propylimidazo[5,1-f][1,2,4]triazin-4(3H)-one (VARDENAFIL) and a pharmaceutically acceptable salt of VARDENAFIL.
51 . The pharmaceutical composition according to claim 50 , wherein the PDE4 inhibitor is 3-cyclopropylmethoxy-4-difluoromethoxy-N-(3,5-dichloropyrid-4-yl)-benzamide (Roflumilast) and wherein the PDE5 inhibitor is selected from the group consisting of 5-[2-ethoxy-5-(4-methyl-1-piperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (SILDENAFIL) and a pharmaceutically acceptable salt of SILDENAFIL.
52 . The pharmaceutical composition according to claim 27 , wherein the PDE4 inhibitor is 3-cyclopropylmethoxy-4-difluoromethoxy-N-(3,5-dichloropyrid-4-yl)-benzamide (Roflumilast) or a pharmaceutically acceptable salt, N-oxide, or a pharmaceutically acceptable salt of the N-oxide thereof and wherein the PDE5 inhibitor is selected from the group consisting of 5-[2-ethoxy-5-(4-methyl-1-piperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (SILDENAFIL), a pharmaceutically acceptable salt of SILDENAFIL, (6R,12aR)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-methylenedioxy-phenyl)-pyrazino[2′,1′:6,1]pyrido[3,4-b]indole-1,4-dione (TADALAFIL), a pharmaceutically acceptable salt of TADALAFIL, 2-[2-ethoxy-5-(4-ethylpiperazin-1-ylsulfonyl)phenyl]-5-methyl-7-propylimidazo[5,1-f][1,2,4]triazin-4(3H)-one (VARDENAFIL) and a pharmaceutically acceptable salt of VARDENAFIL.
53 . The pharmaceutical composition according to claim 52 , wherein the PDE4 inhibitor is 3-cyclopropylmethoxy-4-difluoromethoxy-N-(3,5-dichloropyrid-4-yl)-benzamide (Roflumilast) and wherein the PDE5 inhibitor is selected from the group consisting of 5-[2-ethoxy-5-(4-methyl-1-piperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (SILDENAFIL) and a pharmaceutically acceptable salt of SILDENAFIL.
54 . The pharmaceutical composition according to claim 47 , wherein the PDE4 inhibitor is 3-cyclopropylmethoxy-4-difluoromethoxy-N-(3,5-dichloropyrid-4-yl)-benzamide (Roflumilast) or a pharmaceutically acceptable salt, N-oxide, or a pharmaceutically acceptable salt of the N-oxide thereof and wherein the PDE5 inhibitor is selected from the group consisting of 5-[2-ethoxy-5-(4-methyl-1-piperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (SILDENAFIL), a pharmaceutically acceptable salt of SILDENAFIL, (6R,12aR)-2,3,6,7,12,12a-hexahydro-2-methyl-6-(3,4-methylenedioxy-phenyl)-pyrazino[2′,1′:6,1]pyrido[3,4-b]indole-1,4-dione (TADALAFIL), a pharmaceutically acceptable salt of TADALAFIL, 2-[2-ethoxy-5-(4-ethylpiperazin-1-ylsulfonyl)phenyl]-5-methyl-7-propylimidazo[5,1-f][1,2,4]triazin-4(3H)-one (VARDENAFIL) and a pharmaceutically acceptable salt of VARDENAFIL.
55 . The pharmaceutical composition according to claim 54 , wherein the PDE4 inhibitor is 3-cyclopropylmethoxy-4-difluoromethoxy-N-(3,5-dichloropyrid-4-yl)-benzamide (Roflumilast) and wherein the PDE5 inhibitor is selected from the group consisting of 5-[2-ethoxy-5-(4-methyl-1-piperazinylsulfonyl)phenyl]-1-methyl-3-n-propyl-1,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (SILDENAFIL) and a pharmaceutically acceptable salt of SILDENAFIL.
56 . A method of treating COPD in a patient comprising administering to a patient in need thereof the pharmaceutical composition according to claim 48 .
57 . A method of treating COPD in a patient comprising administering to a patient in need thereof the pharmaceutical composition according to claim 50 .
58 . A method of treating COPD in a patient comprising administering to a patient in need thereof the pharmaceutical composition according to claim 52 .
59 . A method of treating COPD in a patient comprising administering to a patient in need thereof the pharmaceutical composition according to claim 54 .