HRP20140073T1 - Kombinacija rosuvastatina inhibitora reduktaze hmg-coa s inhibitorom fosfodiesteraze-4, kao što je roflumilast, roflumilast-n-oksid, za lijeäśenje pluä†nih bolesti - Google Patents
Kombinacija rosuvastatina inhibitora reduktaze hmg-coa s inhibitorom fosfodiesteraze-4, kao što je roflumilast, roflumilast-n-oksid, za lijeäśenje pluä†nih bolesti Download PDFInfo
- Publication number
- HRP20140073T1 HRP20140073T1 HRP20140073TT HRP20140073T HRP20140073T1 HR P20140073 T1 HRP20140073 T1 HR P20140073T1 HR P20140073T T HRP20140073T T HR P20140073TT HR P20140073 T HRP20140073 T HR P20140073T HR P20140073 T1 HRP20140073 T1 HR P20140073T1
- Authority
- HR
- Croatia
- Prior art keywords
- roflumilast
- inhibitor
- hmg
- coa reductase
- pharmaceutically acceptable
- Prior art date
Links
- 229940121710 HMGCoA reductase inhibitor Drugs 0.000 title claims abstract 25
- 239000002471 hydroxymethylglutaryl coenzyme A reductase inhibitor Substances 0.000 title claims abstract 25
- 229940123932 Phosphodiesterase 4 inhibitor Drugs 0.000 title claims abstract 21
- 239000002587 phosphodiesterase IV inhibitor Substances 0.000 title claims abstract 21
- 208000019693 Lung disease Diseases 0.000 title claims abstract 15
- 230000002757 inflammatory effect Effects 0.000 title claims abstract 15
- MNDBXUUTURYVHR-UHFFFAOYSA-N roflumilast Chemical compound FC(F)OC1=CC=C(C(=O)NC=2C(=CN=CC=2Cl)Cl)C=C1OCC1CC1 MNDBXUUTURYVHR-UHFFFAOYSA-N 0.000 title claims 15
- 229960002586 roflumilast Drugs 0.000 title claims 15
- PCGSQNPMMSALEJ-UHFFFAOYSA-N roflumilast n-oxide Chemical compound ClC1=C[N+]([O-])=CC(Cl)=C1NC(=O)C1=CC=C(OC(F)F)C(OCC2CC2)=C1 PCGSQNPMMSALEJ-UHFFFAOYSA-N 0.000 title claims 15
- 229960000672 rosuvastatin Drugs 0.000 title claims 10
- BPRHUIZQVSMCRT-VEUZHWNKSA-N rosuvastatin Chemical compound CC(C)C1=NC(N(C)S(C)(=O)=O)=NC(C=2C=CC(F)=CC=2)=C1\C=C\[C@@H](O)C[C@@H](O)CC(O)=O BPRHUIZQVSMCRT-VEUZHWNKSA-N 0.000 title claims 10
- 150000003839 salts Chemical class 0.000 claims 17
- 239000008194 pharmaceutical composition Substances 0.000 claims 13
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 8
- 239000000047 product Substances 0.000 claims 8
- 230000002265 prevention Effects 0.000 claims 5
- 206010001889 Alveolitis Diseases 0.000 claims 4
- 208000004248 Familial Primary Pulmonary Hypertension Diseases 0.000 claims 4
- 201000009794 Idiopathic Pulmonary Fibrosis Diseases 0.000 claims 4
- 208000034189 Sclerosis Diseases 0.000 claims 4
- 208000006673 asthma Diseases 0.000 claims 4
- 201000001155 extrinsic allergic alveolitis Diseases 0.000 claims 4
- 208000022098 hypersensitivity pneumonitis Diseases 0.000 claims 4
- 208000036971 interstitial lung disease 2 Diseases 0.000 claims 4
- LALFOYNTGMUKGG-BGRFNVSISA-L rosuvastatin calcium Chemical group [Ca+2].CC(C)C1=NC(N(C)S(C)(=O)=O)=NC(C=2C=CC(F)=CC=2)=C1\C=C\[C@@H](O)C[C@@H](O)CC([O-])=O.CC(C)C1=NC(N(C)S(C)(=O)=O)=NC(C=2C=CC(F)=CC=2)=C1\C=C\[C@@H](O)C[C@@H](O)CC([O-])=O LALFOYNTGMUKGG-BGRFNVSISA-L 0.000 claims 4
- 201000000306 sarcoidosis Diseases 0.000 claims 4
- RGEBGDYYHAFODH-DHMAKVBVSA-M sodium;(e,3r,5s)-7-[4-(4-fluorophenyl)-2-[methyl(methylsulfonyl)amino]-6-propan-2-ylpyrimidin-5-yl]-3,5-dihydroxyhept-6-enoate Chemical group [Na+].CC(C)C1=NC(N(C)S(C)(=O)=O)=NC(C=2C=CC(F)=CC=2)=C1\C=C\[C@@H](O)C[C@@H](O)CC([O-])=O RGEBGDYYHAFODH-DHMAKVBVSA-M 0.000 claims 4
- 229940079593 drug Drugs 0.000 claims 3
- 239000003814 drug Substances 0.000 claims 3
- 239000004615 ingredient Substances 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 239000000546 pharmaceutical excipient Substances 0.000 claims 3
- 229940096701 plain lipid modifying drug hmg coa reductase inhibitors Drugs 0.000 claims 2
- 239000012752 auxiliary agent Substances 0.000 claims 1
- 239000013066 combination product Substances 0.000 claims 1
- 229940127555 combination product Drugs 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 238000009109 curative therapy Methods 0.000 abstract 1
- 230000003449 preventive effect Effects 0.000 abstract 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/275—Nitriles; Isonitriles
- A61K31/277—Nitriles; Isonitriles having a ring, e.g. verapamil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/35—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom
- A61K31/352—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having six-membered rings with one oxygen as the only ring hetero atom condensed with carbocyclic rings, e.g. methantheline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/335—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
- A61K31/365—Lactones
- A61K31/366—Lactones having six-membered rings, e.g. delta-lactones
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
- A61K31/405—Indole-alkanecarboxylic acids; Derivatives thereof, e.g. tryptophan, indomethacin
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/437—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4425—Pyridinium derivatives, e.g. pralidoxime, pyridostigmine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/4439—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/453—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with oxygen as a ring hetero atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/502—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with carbocyclic ring systems, e.g. cinnoline, phthalazine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/04—Drugs for disorders of the respiratory system for throat disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Claims (34)
1. Farmaceutski sastav, naznačen time, da obuhvaća farmaceutsku formulaciju koja uključuje jednu količinu PDE4-inhibitora, jednu količinu inhibitora reduktaze HMG-CoA i barem jedno farmaceutski prihvatljivo pomoćno sredstvo, pri čemu je PDE4-inhibitor odabran iz skupine koju čine: ROFLUMILAST, farmaceutski prihvatljiva sol od ROFLUMILASTA, ROFLUMILAST-N-oksid i farmaceutski prihvatljiva sol od ROFLUMILAST-N-oksida, dok inhibitor reduktaze HMG-CoA je ROSUVASTATIN ili njegova farmaceutski prihvatljiva sol, te pritom prva količina i druga količina zajedno sastavljaju učinkovitu količinu za prevenciju ili liječenje upalne plućne bolesti.
2. Kombinirani proizvod, naznačen time, da sadrži sljedeće sastojke: (A) jednu količinu PDE4-inhibitora; (B) jednu količinu inhibitora reduktaze HMG-CoA; pri čemu prva količina i druga količina zajedno sastavljaju učinkovitu količinu za prevenciju ili liječenje upalne plućne bolesti, gdje svaki od sastojaka (A) i (B) je formuliran u mješavini s barem jednim farmaceutski prihvatljivim pomoćnim sredstvom, dok je PDE4-inhibitor odabran iz skupine koju čine: ROFLUMILAST, farmaceutski prihvatljiva sol od ROFLUMILASTA, ROFLUMILAST-N-oksid i farmaceutski prihvatljiva sol od ROFLUMILAST-N-oksida, a inhibitor reduktaze HMG-CoA je ROSUVASTATIN ili njegova farmaceutski prihvatljiva sol.
3. Garnitura, naznačena time, da sadrži sljedeće sastojke: (A) farmaceutska formulacija koja uključuje jednu količinu PDE4-inhibitora u mješavini s barem jednim farmaceutski prihvatljivim pomoćnim sredstvom; (B) farmaceutska formulacija koja uključuje jednu količinu inhibitora reduktaze HMG-CoA u mješavini s barem jednim farmaceutski prihvatljivim pomoćnim sredstvom; pri čemu prva količina i druga količina zajedno sastavljaju učinkovitu količinu za prevenciju ili liječenje upalne plućne bolesti, dok je PDE4-inhibitor odabran iz skupine koju čine: ROFLUMILAST, farmaceutski prihvatljiva sol od ROFLUMILASTA, ROFLUMILAST-N-oksid i farmaceutski prihvatljiva sol od ROFLUMILAST-N-oksida, a inhibitor reduktaze HMG-CoA je ROSUVASTATIN ili njegova farmaceutski prihvatljiva sol.
4. Farmaceutski sastav prema zahtjevu 1, naznačen time, da PDE4-inhibitor je ROFLUMILAST.
5. Farmaceutski sastav prema zahtjevu 1, naznačen time, da PDE4-inhibitor je ROFLUMILAST-N-oksid.
6. Farmaceutski sastav prema bilo kojem od zahtjeva 1, 4 ili 5, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN hemi-kalcij.
7. Farmaceutski sastav prema bilo kojem od zahtjeva 1, 4 ili 5, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN natrij.
8. Farmaceutski sastav prema bilo kojem od zahtjeva 1, 4 ili 5, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN.
9. Kombinirani proizvod prema zahtjevu 2, naznačen time, da PDE4-inhibitor je ROFLUMILAST.
10. Kombinirani proizvod prema zahtjevu 2, naznačen time, da PDE4-inhibitor je ROFLUMILAST-N-oksid.
11. Kombinirani proizvod prema bilo kojem od zahtjeva 2, 9 ili 10, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN hemi-kalcij.
12. Kombinirani proizvod prema bilo kojem od zahtjeva 2, 9 ili 10, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN natrij.
13. Kombinirani proizvod prema bilo kojem od zahtjeva 2, 9 ili 10, naznačen time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN.
14. Garnitura prema zahtjevu 3, naznačena time, da PDE4-inhibitor je ROFLUMILAST.
15. Garnitura prema zahtjevu 3, naznačena time, da PDE4-inhibitor je ROFLUMILAST-N-oksid.
16. Garnitura prema bilo kojem od zahtjeva 3, 14 ili 15, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN hemi-kalcij.
17. Garnitura prema bilo kojem od zahtjeva 3, 14 ili 15, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN natrij.
18. Garnitura prema bilo kojem od zahtjeva 3, 14 ili 15, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN.
19. Farmaceutski sastav prema bilo kojem od zahtjeva 1, 4, 5, 6, 7 ili 8, naznačen time, da je upalna plućna bolest odabrana iz skupine koju čine: astma, COPD, skleroza, alveolitis, sarkoidoza, idiopatska plućna fibroza i plućna hipertenzija.
20. Farmaceutski sastav prema bilo kojem od zahtjeva 1, 4, 5, 6, 7 ili 8, naznačen time, da upalna plućna bolest je COPD.
21. Kombinirani proizvod prema bilo kojem od zahtjeva 2, 9, 10, 11, 12 ili 13, naznačen time, da je upalna plućna bolest odabrana iz skupine koju čine: astma, COPD, skleroza, alveolitis, sarkoidoza, idiopatska plućna fibroza i plućna hipertenzija.
22. Kombinirani proizvod prema bilo kojem od zahtjeva 2, 9, 10, 11, 12 ili 13, naznačen time, da upalna plućna bolest je COPD.
23. Garnitura prema bilo kojem od zahtjeva 3, 14, 15, 16, 17 ili 18, naznačena time, da je upalna plućna bolest odabrana iz skupine koju čine: astma, COPD, skleroza, alveolitis, sarkoidoza, idiopatska plućna fibroza i plućna hipertenzija.
24. Garnitura prema bilo kojem od zahtjeva 3, 14, 15, 16, 17 ili 18, naznačena time, da upalna plućna bolest je COPD.
25. Uporaba PDE4-inhibitora i inhibitora reduktaze HMG-CoA, naznačena time, da je za proizvodnju lijeka, posebno farmacetskog sastava prema izumu, za prevenciju ili liječenje upalne plućne bolesti, pri čemu je PDE4-inhibitor odabran iz skupine koju čine: ROFLUMILAST, farmaceutski prihvatljiva sol od ROFLUMILASTA, ROFLUMILAST-N-oksid i farmaceutski prihvatljiva sol od ROFLUMILAST-N-oksida, a inhibitor reduktaze HMG-CoA je ROSUVASTATIN ili njegova farmaceutski prihvatljiva sol.
26. Uporaba PDE4-inhibitora i inhibitora reduktaze HMG-CoA, naznačena time, da je za proizvodnju dodatnog lijeka koji se daje uzastopno ili odvojeno uz prvi lijek, posebno kombiniranog proizvoda ili garniture prema izumu, za prevenciju ili liječenje upalne plućne bolesti, pri čemu je PDE4-inhibitor odabran iz skupine koju čine: ROFLUMILAST, farmaceutski prihvatljiva sol od ROFLUMILASTA, ROFLUMILAST-N-oksid i farmaceutski prihvatljiva sol od ROFLUMILAST-N-oksida, a inhibitor reduktaze HMG-CoA je ROSUVASTATIN ili njegova farmaceutski prihvatljiva sol.
27. Uporaba prema zahtjevu 25 ili 26, naznačena time, da PDE4-inhibitor je ROFLUMILAST.
28. Uporaba prema zahtjevu 25 ili 26, naznačena time, da PDE4-inhibitor je ROFLUMILAST-N-oksid.
29. Uporaba prema bilo kojem od zahtjeva 25, 26, 27 ili 28, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN hemi-kalcij.
30. Uporaba prema bilo kojem od zahtjeva 25, 26, 27 ili 28, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN natrij.
31. Uporaba prema bilo kojem od zahtjeva 25, 26, 27 ili 28, naznačena time, da inhibitor reduktaze HMG-CoA je ROSUVASTATIN.
32. Uporaba prema bilo kojem od zahtjeva 25 do 31, naznačena time, da je upalna plućna bolest odabrana iz skupine koju čine: astma, COPD, skleroza, alveolitis, sarkoidoza, idiopatska plućna fibroza i plućna hipertenzija.
33. Uporaba prema bilo kojem od zahtjeva 25 do 31, naznačena time, da upalna plućna bolest je COPD.
34. Postupak za proizvodnju farmaceutskog sastava prema bilo kojem od zahtjeva 1, 4, 5, 6, 7, 8, 19 ili 20, naznačen time, da obuhvaća miješanje PDE4-inhibitora ili njegove farmaceutski prihvatljive soli s inhibitorom reduktaze HMG-CoA ili s njegovom farmaceutski prihvatljivom soli.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP06116625 | 2006-07-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
HRP20140073T1 true HRP20140073T1 (hr) | 2014-02-28 |
Family
ID=37311957
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HRP20140073TT HRP20140073T1 (hr) | 2006-07-05 | 2014-01-21 | Kombinacija rosuvastatina inhibitora reduktaze hmg-coa s inhibitorom fosfodiesteraze-4, kao što je roflumilast, roflumilast-n-oksid, za lijeäśenje pluä†nih bolesti |
HRP20140707TT HRP20140707T1 (hr) | 2006-07-05 | 2014-07-22 | KOMBINACIJA ATORVASTATINA ILI SIMVASTATINA KAO INHIBITORA REDUKTAZE HMG-CoA S INHIBITOROM FOSFODIESTERAZE 4 KOJI JE ROFLUMILAST, ZA LIJEČENJE UPALNIH BOLESTI PLUĆA |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HRP20140707TT HRP20140707T1 (hr) | 2006-07-05 | 2014-07-22 | KOMBINACIJA ATORVASTATINA ILI SIMVASTATINA KAO INHIBITORA REDUKTAZE HMG-CoA S INHIBITOROM FOSFODIESTERAZE 4 KOJI JE ROFLUMILAST, ZA LIJEČENJE UPALNIH BOLESTI PLUĆA |
Country Status (26)
Country | Link |
---|---|
US (2) | US20100069392A1 (hr) |
EP (3) | EP2359826B1 (hr) |
JP (3) | JP5349302B2 (hr) |
KR (1) | KR101433394B1 (hr) |
CN (3) | CN101484166B (hr) |
AT (1) | ATE535244T1 (hr) |
AU (1) | AU2007271186C1 (hr) |
BR (1) | BRPI0713768A2 (hr) |
CA (1) | CA2656366A1 (hr) |
CY (2) | CY1114742T1 (hr) |
DK (2) | DK2363130T3 (hr) |
EA (2) | EA032476B1 (hr) |
ES (3) | ES2489265T3 (hr) |
HR (2) | HRP20140073T1 (hr) |
IL (3) | IL195433A (hr) |
ME (2) | ME01648B (hr) |
MX (1) | MX2008016123A (hr) |
NO (1) | NO342590B1 (hr) |
NZ (3) | NZ594369A (hr) |
PL (2) | PL2363130T3 (hr) |
PT (2) | PT2359826E (hr) |
RS (2) | RS53084B (hr) |
SI (2) | SI2363130T1 (hr) |
UA (3) | UA106422C2 (hr) |
WO (1) | WO2008003701A2 (hr) |
ZA (1) | ZA200809905B (hr) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI436767B (zh) * | 2008-03-14 | 2014-05-11 | Otsuka Pharma Co Ltd | 基質金屬蛋白酶-2(mmp-2)及/或基質金屬蛋白酶-9(mmp-9)抑制劑 |
CN102671198A (zh) * | 2011-12-17 | 2012-09-19 | 东莞达信生物技术有限公司 | 一种降压降脂复方药及其制备方法 |
CA2953209A1 (en) * | 2014-06-05 | 2015-12-10 | Transgenion-International Institute For Regenerative Translational Medicine Gmbh | Methods of diagnosing chronic obstructive pulmonary disease (copd) using novel molecular biomarkers |
JP6755242B2 (ja) * | 2014-06-05 | 2020-09-16 | トランスゲニオン−インターナショナル インスティテュート フォー リジェネレイティヴ トランスレイショナル メディシン ゲーエムベーハー | 新規分子バイオマーカーを使用して慢性閉塞性肺疾患(copd)を診断する方法 |
JP6755241B2 (ja) * | 2014-06-05 | 2020-09-16 | トランスゲニオン−インターナショナル インスティテュート フォー リジェネレイティヴ トランスレイショナル メディシン ゲーエムベーハー | 新規分子バイオマーカーを使用して慢性閉塞性肺疾患(copd)を診断する方法 |
US20210031012A1 (en) | 2018-01-26 | 2021-02-04 | Progenity, Inc. | Treatment of a disease of the gastrointestinal tract with a pde4 inhibitor |
WO2020106757A1 (en) | 2018-11-19 | 2020-05-28 | Progenity, Inc. | Ingestible device for delivery of therapeutic agent to the gastrointestinal tract |
US11707610B2 (en) | 2019-12-13 | 2023-07-25 | Biora Therapeutics, Inc. | Ingestible device for delivery of therapeutic agent to the gastrointestinal tract |
WO2021218988A1 (zh) * | 2020-04-30 | 2021-11-04 | 中国科学院上海药物研究所 | Prdx1激动剂及其用途 |
WO2024028388A1 (en) * | 2022-08-03 | 2024-02-08 | Chiesi Farmaceutici S.P.A. | Dry powder inhaler |
Family Cites Families (60)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IL60219A (en) | 1979-06-15 | 1985-05-31 | Merck & Co Inc | Hypocholesteremic fermentation products of the hmg-coa reductase inhibitor type,their preparation and pharmaceutical compositions containing them |
AU548996B2 (en) | 1980-02-04 | 1986-01-09 | Merck & Co., Inc. | Tetrahydro-2h-pyran-2-one derivatives |
MX7065E (es) | 1980-06-06 | 1987-04-10 | Sankyo Co | Un procedimiento microbiologico para preparar derivados de ml-236b |
AU570021B2 (en) | 1982-11-22 | 1988-03-03 | Novartis Ag | Analogs of mevalolactone |
US4681893A (en) | 1986-05-30 | 1987-07-21 | Warner-Lambert Company | Trans-6-[2-(3- or 4-carboxamido-substituted pyrrol-1-yl)alkyl]-4-hydroxypyran-2-one inhibitors of cholesterol synthesis |
EP0307342B1 (de) | 1987-07-10 | 1996-01-03 | Hoechst Aktiengesellschaft | 3-Desmethyl-mevalonsäurederivate, Verfahren zu ihrer Herstellung, pharmazeutische Präparate auf Basis dieser Verbindungen, ihre Verwendung sowie Zwischenprodukte |
CA1336714C (en) | 1987-08-20 | 1995-08-15 | Yoshihiro Fujikawa | Quinoline type mevalonolactone inhibitors of cholesterol biosynthesis |
US4863957A (en) | 1987-12-21 | 1989-09-05 | Rorer Pharmaceutical Corporation | Novel HMG-CoA reductase inhibitors |
FR2642065B1 (fr) | 1989-01-24 | 1991-05-24 | Lipha | Derives d'acides benzocycloalcenyl dihydroxy alcanoiques, procede de preparation et medicaments les contenant |
CA2396738C (en) | 1990-11-30 | 2006-08-29 | Masatoshi Chihiro | Thiazole derivatives as active superoxide radical inhibitors |
JP2648897B2 (ja) | 1991-07-01 | 1997-09-03 | 塩野義製薬株式会社 | ピリミジン誘導体 |
EP1380571A1 (en) * | 1992-04-02 | 2004-01-14 | Smithkline Beecham Corporation | Compounds useful for treating allergic and inflammatory diseases |
US5552438A (en) | 1992-04-02 | 1996-09-03 | Smithkline Beecham Corporation | Compounds useful for treating allergic and inflammatory diseases |
CZ290266B6 (cs) * | 1993-07-02 | 2002-06-12 | Byk Gulden Lomberg Chemische Fabrik Gmbh | Substituované benzamidy, způsob jejich výroby a farmaceutické prostředky s jejich obsahem |
GB9504460D0 (en) | 1995-03-06 | 1995-04-26 | Bayer Ag | N-(3-Benzofuranyl)urea-derivatives |
US6004974A (en) | 1995-06-06 | 1999-12-21 | Pfizer Inc | Tricyclic 5,6-dihydro-9h-pyrazolo[3,4-c]-1,2,4-triazolo[4,3-α]pyridines |
DE19636150A1 (de) | 1996-09-06 | 1998-03-12 | Asta Medica Ag | N-substituierte Indol-3-glyoxylamide mit antiasthmatischer, antiallergischer und immunsuppressiver/immunmodulierender Wirkung |
UA59443C2 (uk) | 1998-04-28 | 2003-09-15 | Арцнайміттельверк Дрезден Гмбх | Гідроксііндол, спосіб його одержання, лікарська форма на його основі та спосіб її одержання |
US20010006656A1 (en) * | 1999-02-17 | 2001-07-05 | University Of Washington | Methods and compositions for inhibiting inflammation associated with pulmonary disease |
DE19944161A1 (de) | 1999-09-15 | 2001-03-22 | Bayer Ag | Neue Kombination zur Behandlung von sexueller Dysfunktion |
MY134008A (en) | 1999-12-22 | 2007-11-30 | Merck Frosst Canada Inc | Subtituted 8-arylquinoline phospohodiestrase-4 inhibitors |
US6410563B1 (en) * | 1999-12-22 | 2002-06-25 | Merck Frosst Canada & Co. | Substituted 8-arylquinoline phosphodiesterase-4 inhibitors |
JP2001294526A (ja) * | 2000-02-10 | 2001-10-23 | Takeda Chem Ind Ltd | TNF−α抑制剤 |
AU2001232245A1 (en) | 2000-02-10 | 2001-08-20 | Takeda Chemical Industries Ltd. | Tnf- alpha inhibitors |
MY123585A (en) | 2000-03-23 | 2006-05-31 | Merck Canada Inc | Tri-aryl-substituted-ethane pde4 inhibitors. |
US20050102317A1 (en) * | 2000-07-21 | 2005-05-12 | Ali Kamarei | System and method for event calendaring using a customizable rules subset |
CA2422820A1 (en) | 2000-09-19 | 2002-03-28 | Novimmune S.A. | Use of statins (hmg-coa reductase inhibitors) for the preparation of medicament as a novel type of immunomodulator, immunosuppressor and anti-inflammatory agent |
US6740666B2 (en) * | 2000-12-20 | 2004-05-25 | Merck & Co., Inc. | Substituted 8-arylquinoline phosphodiesterase-4 inhibitors |
EA200300836A1 (ru) * | 2001-02-15 | 2004-02-26 | Алтана Фарма Аг | Производные фталазинон-пиперидина в качестве ингибиторов pde4 |
KR20100036390A (ko) * | 2001-03-06 | 2010-04-07 | 셀러지 파마세우티칼스, 인크 | 비뇨생식기 장애 치료용 화합물 및 그 방법 |
JP4193435B2 (ja) * | 2002-07-23 | 2008-12-10 | ブラザー工業株式会社 | インクカートリッジ、および、そのインク充填方法 |
AU2002257459B2 (en) * | 2001-05-24 | 2006-12-14 | Merck Frosst Canada Ltd | 1-biaryl-1,8-napthyridin-4-one phosphodiesterase-4 inhibitors |
CA2450686A1 (en) * | 2001-06-27 | 2003-01-09 | Merck Frosst Canada & Co./Merck Frosst Canada & Cie | Substituted 8-arylquinoline pde4 inhibitors |
US20030114469A1 (en) | 2001-09-27 | 2003-06-19 | Cohen David Saul | Combinations |
MY140561A (en) | 2002-02-20 | 2009-12-31 | Nycomed Gmbh | Dosage form containing pde 4 inhibitor as active ingredient |
EP1519922A1 (en) * | 2002-07-02 | 2005-04-06 | Merck Frosst Canada & Co. | Di-aryl-substituted ethane pyridone pde4 inhibitors |
BR0316256A (pt) * | 2002-11-18 | 2005-10-04 | Celgene Corp | Métodos de inibir a produção de tnf-alfa e a atividade de pde4, de tratar ou prevenir uma doença ou um distúrbio, de controlar os nìveis de camp em uma célula e de produzir um composto, composição farmacêutica e composto |
IS7839A (is) | 2002-11-22 | 2004-05-23 | Merck Frosst Canada Ltd. | 4-oxó-1-(3-setið fenýl-1,4-díhýdró-1,8-naftýridín-3-karboxamíð fosfódíesterasa-4 hindrar |
WO2004047829A1 (en) * | 2002-11-27 | 2004-06-10 | Altana Pharma Ag | New synergistic combination comprising roflumilast and formoterol |
US20050119330A1 (en) * | 2003-03-17 | 2005-06-02 | Kao Peter N. | Use of antiproliferative agents in the treatment and prevention of pulmonary proliferative vascular diseases |
US20040254238A1 (en) * | 2003-04-07 | 2004-12-16 | Osteoscreen | Bone growth stimulation with NO/statin and other NO modulating combinations |
DE602004020332D1 (de) | 2003-04-11 | 2009-05-14 | Glenmark Pharmaceuticals Sa | Neue heterozyklische verbindungen, die sich für die behandlung von entzündlichen und allergischen erkrankungen eignen: verfahren zu deren herstellung und pharmazeutische zusammensetzungen, die diese enthalten |
CN100441185C (zh) * | 2003-04-30 | 2008-12-10 | 麦克弗罗斯特加拿大有限公司 | 8-(3-联芳基)苯基喹啉磷酸二酯酶-4抑制剂 |
WO2004098578A2 (en) * | 2003-05-12 | 2004-11-18 | Altana Pharma Ag | Composition comprising a pde4 inhibitor and a tnf-alfa antagonist selected from infliximab, adalimumab, cdp870 and cdp517 |
WO2004103407A2 (en) * | 2003-05-22 | 2004-12-02 | Altana Pharma Ag | Composition comprising a pde4 inhibitor and a pde5 inhibitor |
WO2004110368A2 (en) * | 2003-06-06 | 2004-12-23 | Merck & Co., Inc. | Combination therapy for the treatment of hypertension |
US20060148721A1 (en) * | 2003-06-06 | 2006-07-06 | Erondu Ngozi E | Combination therapy for the treatment of dyslipidemia |
DE10348646A1 (de) | 2003-10-15 | 2005-05-25 | Gkn Driveline International Gmbh | Rollbalg mit großem Krümmungsradius |
CA2563693C (en) * | 2004-04-19 | 2010-07-06 | Loma Linda University | Composition and method of decreasing renal ischemic damage |
ZA200609228B (en) * | 2004-04-23 | 2008-05-28 | Celgene Corp | Methods of using and compositions comprising PDE4 modulators for the treatment and management of pulmonary hypertension |
ES2257152B1 (es) * | 2004-05-31 | 2007-07-01 | Laboratorios Almirall S.A. | Combinaciones que comprenden agentes antimuscarinicos y agonistas beta-adrenergicos. |
GB0415789D0 (en) * | 2004-07-15 | 2004-08-18 | Astrazeneca Ab | Novel combination |
DE102004046236A1 (de) | 2004-09-22 | 2006-03-30 | Altana Pharma Ag | Arzneimittelzubereitung |
GB0508924D0 (en) | 2005-04-30 | 2005-06-08 | Astrazeneca Ab | New use |
GB0510207D0 (en) | 2005-05-19 | 2005-06-22 | Astrazeneca Ab | Novel combination |
EP1894576B1 (en) | 2005-06-08 | 2011-05-25 | Kowa Company, Ltd. | Novel triglyceride reducing agent |
AU2006304787A1 (en) | 2005-10-21 | 2007-04-26 | Braincells, Inc. | Modulation of neurogenesis by PDE inhibition |
AR057555A1 (es) | 2005-10-27 | 2007-12-05 | Merck Frosst Canada Ltd | Un inhibidor de fosfodiesterasa-4 4-oxo-1-(3-sustituido fenil-1,4-dihidro-1,8-naftiridin-3-carboxamida y un procedimiento de preparacion del mismo |
AU2006313430B2 (en) | 2005-11-08 | 2012-09-06 | Ranbaxy Laboratories Limited | Process for (3R,5R)-7-[2-(4-fluorophenyl)-5-isopropyl-3-phenyl-4- [(4-hydroxy methyl phenyl amino) carbonyl]-pyrrol-1-yl]-3, 5-dihydroxy-heptanoic acid hemi calcium salt |
WO2008036846A2 (en) * | 2006-09-22 | 2008-03-27 | Braincells, Inc. | Combination comprising an hmg-coa reductase inhibitor and a second neurogenic agent for treating a nervous system disorder and increasing neurogenesis |
-
2007
- 2007-07-03 EA EA201401042A patent/EA032476B1/ru not_active IP Right Cessation
- 2007-07-03 NZ NZ594369A patent/NZ594369A/xx not_active IP Right Cessation
- 2007-07-03 CA CA002656366A patent/CA2656366A1/en not_active Abandoned
- 2007-07-03 NZ NZ603207A patent/NZ603207A/en not_active IP Right Cessation
- 2007-07-03 ES ES11164518.0T patent/ES2489265T3/es active Active
- 2007-07-03 ES ES07787007T patent/ES2378281T3/es active Active
- 2007-07-03 ES ES11164516.4T patent/ES2443342T3/es active Active
- 2007-07-03 AT AT07787007T patent/ATE535244T1/de active
- 2007-07-03 KR KR1020097001868A patent/KR101433394B1/ko active IP Right Grant
- 2007-07-03 UA UAA201212837A patent/UA106422C2/uk unknown
- 2007-07-03 JP JP2009517256A patent/JP5349302B2/ja not_active Expired - Fee Related
- 2007-07-03 PL PL11164518T patent/PL2363130T3/pl unknown
- 2007-07-03 ME MEP-2014-9A patent/ME01648B/me unknown
- 2007-07-03 SI SI200731492T patent/SI2363130T1/sl unknown
- 2007-07-03 EP EP11164516.4A patent/EP2359826B1/en active Active
- 2007-07-03 UA UAA200900759A patent/UA98466C2/uk unknown
- 2007-07-03 CN CN2007800252405A patent/CN101484166B/zh not_active Expired - Fee Related
- 2007-07-03 PL PL11164516T patent/PL2359826T3/pl unknown
- 2007-07-03 SI SI200731395T patent/SI2359826T1/sl unknown
- 2007-07-03 US US12/308,878 patent/US20100069392A1/en not_active Abandoned
- 2007-07-03 AU AU2007271186A patent/AU2007271186C1/en not_active Ceased
- 2007-07-03 CN CN2012102488576A patent/CN102772411A/zh active Pending
- 2007-07-03 CN CN2012102495122A patent/CN102764440A/zh active Pending
- 2007-07-03 EA EA200900073A patent/EA021461B1/ru not_active IP Right Cessation
- 2007-07-03 UA UAA201111256A patent/UA101556C2/uk unknown
- 2007-07-03 NZ NZ573378A patent/NZ573378A/en not_active IP Right Cessation
- 2007-07-03 EP EP11164518.0A patent/EP2363130B1/en active Active
- 2007-07-03 ME MEP-2014-91A patent/ME01901B/me unknown
- 2007-07-03 EP EP07787007A patent/EP2040707B1/en active Active
- 2007-07-03 RS RS20130560A patent/RS53084B/en unknown
- 2007-07-03 DK DK11164518.0T patent/DK2363130T3/da active
- 2007-07-03 DK DK11164516.4T patent/DK2359826T3/da active
- 2007-07-03 MX MX2008016123A patent/MX2008016123A/es active IP Right Grant
- 2007-07-03 PT PT111645164T patent/PT2359826E/pt unknown
- 2007-07-03 WO PCT/EP2007/056683 patent/WO2008003701A2/en active Application Filing
- 2007-07-03 RS RS20140402A patent/RS53461B/en unknown
- 2007-07-03 BR BRPI0713768-0A patent/BRPI0713768A2/pt not_active Application Discontinuation
- 2007-07-03 PT PT111645180T patent/PT2363130E/pt unknown
-
2008
- 2008-11-20 ZA ZA200809905A patent/ZA200809905B/xx unknown
- 2008-11-23 IL IL195433A patent/IL195433A/en active IP Right Grant
-
2009
- 2009-01-27 NO NO20090370A patent/NO342590B1/no not_active IP Right Cessation
-
2012
- 2012-08-05 IL IL221309A patent/IL221309A/en active IP Right Grant
- 2012-08-05 IL IL221307A patent/IL221307A/en active IP Right Grant
- 2012-10-11 JP JP2012225891A patent/JP2013035870A/ja active Pending
- 2012-10-11 JP JP2012225892A patent/JP2013035871A/ja active Pending
-
2014
- 2014-01-07 CY CY20141100008T patent/CY1114742T1/el unknown
- 2014-01-21 HR HRP20140073TT patent/HRP20140073T1/hr unknown
- 2014-07-22 HR HRP20140707TT patent/HRP20140707T1/hr unknown
- 2014-08-07 CY CY20141100621T patent/CY1115462T1/el unknown
-
2015
- 2015-05-22 US US14/719,948 patent/US9713614B2/en not_active Expired - Fee Related
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
HRP20140073T1 (hr) | Kombinacija rosuvastatina inhibitora reduktaze hmg-coa s inhibitorom fosfodiesteraze-4, kao što je roflumilast, roflumilast-n-oksid, za lijeäśenje pluä†nih bolesti | |
UY28958A1 (es) | Nuevos derivados de piridazin-3(2h)-ona | |
HRP20120286T1 (hr) | Kombinacija antikolinergika i inhibitora fosfodiesteraze tip 4 za liječenje respiratornih bolesti | |
NZ600790A (en) | Combination therapy for copd | |
HRP20131233T1 (hr) | Terapeutski sastav koji obuhvaä†a specifiäśni antagonist receptora endotelina i pde5-inhibitor | |
WO2006018182A8 (en) | Combinations for the treatment of diseases involving cell proliferation | |
TW200602051A (en) | Pyrazolo[3,4-b]pyridine compound, and its use as a PDE4 inhibitor | |
NO20045219L (no) | Kalsitonin-gen-relaterte peptid-reseptor-antagonister | |
GEP20084452B (en) | Sulfonamide derivatives for the treatment of diseases | |
JP2008540486A5 (hr) | ||
JP2009518415A5 (hr) | ||
WO2009109616A3 (en) | 1-benzyl-3-hydroxymethylindazole derivatives and use thereof in the treatment of diseases based on the expression of mcp-1, cxrl and p40 | |
WO2003065987A3 (en) | Granzyme b inhibitors | |
WO2009109654A3 (en) | 1-benzyl-3-hydr0xymethylindaz0le derivatives and use thereof in the treatment of diseases based on the expression of mcp-1, cxcr1 and p40 | |
WO2005079766A3 (en) | Therapeutic combination comprising a tissue factor antagonist and anti-cancer compounds | |
WO2005032470A3 (en) | Compositions and methods for treating burns | |
EP1750703A4 (en) | METHOD FOR REDUCING GASTROINTESTINAL TOXICITY BY ADMINISTRATION OF TEGAFUR | |
AU2020278236A8 (en) | Methods of treating Sjögren's Syndrome using a Bruton's tyrosine kinase inhibitor | |
MX2007000967A (es) | Composiciones de risedronato y metodos para su uso. | |
UY30847A1 (es) | Uso de derivados de mononitrato de dianhidrohexita como agentes para el tratamiento de trastornos intestinales | |
WO2005011594A3 (en) | Combination of dehydroepiandrosterone or dehydroepiandrosterone-sulfate with a tyrosine kinase inhibitor, delta opioid receptor antagonist, neurokinin receptor antagonist, or vcam inhibitor for treatment of asthma or chronic obstructive pulmonary disease | |
SE0303480D0 (sv) | Benzofuranes | |
WO2005120148A3 (en) | Compounds derived from lidocaine, pharmaceutical compositions, use and method of treatment, prevention or inhibition of diseases | |
WO2009049648A3 (en) | Improved pharmaceutical composition containing antiviral agent and method for the preparation thereof | |
MX2018014425A (es) | Beta-horquilla peptidomimetica con actividad inhibidora de elastasa y formas de dosificacion en aerosol de la misma. |