SGC stimulators in combination with additional treatment for the therapy of cystic fibrosis
The present invention relates to soluble guanylate cyclase (sGC) and to phosphodiesterases (PDEs) and the pharmacology of sGC stimulators, sGC activators and PDE inhibitors (PDE5i) in combination with a) treatments, leading to increased cGMP mobilization, and/or b) tretaments correcting and/or potentiatiating CFTR function, and/or c) treatments currently used as standard of care in Cystic Fibrosis, and/or d) antinflammatory treatments for the preparation of medicaments for the treatment of Cystic Fibrosis (CF) with improved efficacy over methods of treatments already known.
1. A method of treating cystic fibrosis comprising administering a therapeutically effective amount of
(a) at least one compound selected from the group consisting of methyl-4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-5-pyrimidinyl¬(methyl)carbamate (3), methyl-{4,6-diamino-2-[5-fluor-1-(2-fluorbenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]pyrimidine-5-yl}carbamate (3a), methyl-4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-5-pyrimidinyl¬carbamate (4), and 3-(4-amino-5-cyclopropylpyrimidine-2-yl)-1-(2-fluorbenzyl) 1H-pyrazolo[3,4-b]pyridine (4a), and
(b) at least one other pharmacological compound selected from the group consisting of VX-809, VX-770, and VX-661
to a patient in need thereof.
2. The method of treating cystic fibrosis according to claim 1 , wherein a therapeutically effective amount of (a) methyl-4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-5-pyrimidinyl¬(methyl)carbamate (3) and (b) at least one other pharmacological compound selected from the group consisting of VX-809, VX-770, and VX-661 is administered.
3. The method of claim 1 , wherein a therapeutically effective amount of methyl-4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-5-pyrimidinyl-(methyl)carbamate (3), VX-809 and VX-770 is administered.
4. The method of treating cystic fibrosis according to claim 1 , wherein a therapeutically effective amount of methyl-4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-5-pyrimidinyl¬(methyl)carbamate (3), VX-661 and VX-770 is administered.
5. A method of treating cystic fibrosis comprising administering a synergistically effective amount of
(a) at least one compound selected from the group consisting of methyl-4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-5-pyrimidinyl¬(methyl)carbamate (3), methyl-{4,6-diamino-2-[5-fluor-1-(2-fluorbenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]pyrimidine-5-yl}carbamate (3a), methyl-4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-5-pyrimidinyl¬carbamate (4), and 3-(4-amino-5-cyclopropylpyrimidine-2-yl)-1-(2-fluorbenzyl)1H-pyrazolo[3,4-b]pyridine (4a), and
(b) at least one other pharmacological compound selected from the group consisting of VX-809, VX-770, and VX-661
to a patient in need thereof.
6. The method of treating cystic fibrosis according to claim 5 , wherein a synergistically effective amount of (a) methyl-4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-5-pyrimidinyl¬(methyl)carbamate (3) and (b) at least one other pharmacological compound selected from the group consisting of VX-809, VX-770, and VX-661 is administered.
7. The method of claim 5 , wherein a synergistically effective amount of methyl-4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-5-pyrimidinyl-(methyl)carbamate (3), VX-809 and VX-770 is administered.
8. The method of treating cystic fibrosis according to claim 5 , wherein a synergistically effective amount of methyl-4,6-diamino-2-[1-(2-fluorobenzyl)-1H-pyrazolo[3,4-b]pyridine-3-yl]-5-pyrimidinyl¬(methyl)carbamate (3), VX-661 and VX-770 is administered.