HRP20100490T1 - Kombinacije koje sadrže antimuskarinska sredstva i pde4 inhibitore - Google Patents
Kombinacije koje sadrže antimuskarinska sredstva i pde4 inhibitore Download PDFInfo
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- HRP20100490T1 HRP20100490T1 HR20100490T HRP20100490T HRP20100490T1 HR P20100490 T1 HRP20100490 T1 HR P20100490T1 HR 20100490 T HR20100490 T HR 20100490T HR P20100490 T HRP20100490 T HR P20100490T HR P20100490 T1 HRP20100490 T1 HR P20100490T1
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- pde4 inhibitor
- combination
- receptor antagonist
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- 229940123932 Phosphodiesterase 4 inhibitor Drugs 0.000 title claims abstract 13
- 239000002587 phosphodiesterase IV inhibitor Substances 0.000 title claims abstract 13
- 239000003149 muscarinic antagonist Substances 0.000 title claims 8
- 239000002253 acid Substances 0.000 claims abstract 4
- 150000001450 anions Chemical class 0.000 claims abstract 4
- 150000003839 salts Chemical class 0.000 claims abstract 4
- 239000005557 antagonist Substances 0.000 claims abstract 3
- ZLLPOXZGRDWOKF-LBFFRULKSA-N [(3R)-1-(1-phenylethyl)-1-azoniabicyclo[2.2.2]octan-3-yl] 9H-xanthene-9-carboxylate Chemical compound C1CC([C@H](C2)OC(=O)C3C4=CC=CC=C4OC4=CC=CC=C43)CC[N+]12C(C)C1=CC=CC=C1 ZLLPOXZGRDWOKF-LBFFRULKSA-N 0.000 claims abstract 2
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 claims 7
- 150000001875 compounds Chemical class 0.000 claims 6
- 239000003814 drug Substances 0.000 claims 5
- 208000023504 respiratory system disease Diseases 0.000 claims 5
- 229940079593 drug Drugs 0.000 claims 4
- 101150015280 Cel gene Proteins 0.000 claims 3
- CFBUZOUXXHZCFB-OYOVHJISSA-N chembl511115 Chemical compound COC1=CC=C([C@@]2(CC[C@H](CC2)C(O)=O)C#N)C=C1OC1CCCC1 CFBUZOUXXHZCFB-OYOVHJISSA-N 0.000 claims 3
- 229950001653 cilomilast Drugs 0.000 claims 3
- 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 claims 3
- 229960002586 roflumilast Drugs 0.000 claims 3
- DDYUBCCTNHWSQM-UHFFFAOYSA-N 3-(3-cyclopentyloxy-4-methoxyphenyl)-3-(1,3-dioxoisoindol-2-yl)propanamide Chemical compound COC1=CC=C(C(CC(N)=O)N2C(C3=CC=CC=C3C2=O)=O)C=C1OC1CCCC1 DDYUBCCTNHWSQM-UHFFFAOYSA-N 0.000 claims 2
- XDBHURGONHZNJF-UHFFFAOYSA-N 6-[2-(3,4-diethoxyphenyl)-1,3-thiazol-4-yl]pyridine-2-carboxylic acid Chemical compound C1=C(OCC)C(OCC)=CC=C1C1=NC(C=2N=C(C=CC=2)C(O)=O)=CS1 XDBHURGONHZNJF-UHFFFAOYSA-N 0.000 claims 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims 2
- 208000018569 Respiratory Tract disease Diseases 0.000 claims 2
- 229940124748 beta 2 agonist Drugs 0.000 claims 2
- 239000003246 corticosteroid Substances 0.000 claims 2
- 229960001334 corticosteroids Drugs 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 229950002896 tetomilast Drugs 0.000 claims 2
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical group O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 claims 2
- VXYDHPDQMSVQCU-UHFFFAOYSA-N 2-[4-cyano-4-(3-cyclopentyloxy-4-methoxyphenyl)piperidin-1-yl]-n-hydroxyacetamide Chemical compound COC1=CC=C(C2(CCN(CC(=O)NO)CC2)C#N)C=C1OC1CCCC1 VXYDHPDQMSVQCU-UHFFFAOYSA-N 0.000 claims 1
- UTUUPXBCDMQYRR-HSZRJFAPSA-N 4-[(2r)-2-(3-cyclopentyloxy-4-methoxyphenyl)-2-phenylethyl]pyridine Chemical compound COC1=CC=C([C@H](CC=2C=CN=CC=2)C=2C=CC=CC=2)C=C1OC1CCCC1 UTUUPXBCDMQYRR-HSZRJFAPSA-N 0.000 claims 1
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims 1
- 102000010918 Cysteinyl leukotriene receptors Human genes 0.000 claims 1
- 108050001116 Cysteinyl leukotriene receptors Proteins 0.000 claims 1
- 102000007202 Muscarinic M3 Receptor Human genes 0.000 claims 1
- 108010008405 Muscarinic M3 Receptor Proteins 0.000 claims 1
- 108010040718 Neurokinin-1 Receptors Proteins 0.000 claims 1
- 102100037346 Substance-P receptor Human genes 0.000 claims 1
- DHCOPPHTVOXDKU-UHFFFAOYSA-N Tofimilast Chemical compound C1CN2C(C=3SC=CC=3)=NN=C2C2=C1C(CC)=NN2C1CCCC1 DHCOPPHTVOXDKU-UHFFFAOYSA-N 0.000 claims 1
- YPFLFUJKZDAXRA-UHFFFAOYSA-N [3-(carbamoylamino)-2-(2,4-dichlorobenzoyl)-1-benzofuran-6-yl] methanesulfonate Chemical compound O1C2=CC(OS(=O)(=O)C)=CC=C2C(NC(N)=O)=C1C(=O)C1=CC=C(Cl)C=C1Cl YPFLFUJKZDAXRA-UHFFFAOYSA-N 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 230000008485 antagonism Effects 0.000 claims 1
- 208000006673 asthma Diseases 0.000 claims 1
- -1 compound (3R)-1-phenethyl-3-(9H-xanthene-9-carbonyloxy)-1-azoniabicyclo [2.2.2 ]octane bromide Chemical class 0.000 claims 1
- PCCPERGCFKIYIS-AWEZNQCLSA-N daxalipram Chemical compound C1=C(OC)C(OCCC)=CC([C@@]2(C)OC(=O)NC2)=C1 PCCPERGCFKIYIS-AWEZNQCLSA-N 0.000 claims 1
- OMFNSKIUKYOYRG-MOSHPQCFSA-N drotaverine Chemical compound C1=C(OCC)C(OCC)=CC=C1\C=C/1C2=CC(OCC)=C(OCC)C=C2CCN\1 OMFNSKIUKYOYRG-MOSHPQCFSA-N 0.000 claims 1
- 229940121647 egfr inhibitor Drugs 0.000 claims 1
- STTRYQAGHGJXJJ-LICLKQGHSA-N filaminast Chemical compound COC1=CC=C(C(\C)=N\OC(N)=O)C=C1OC1CCCC1 STTRYQAGHGJXJJ-LICLKQGHSA-N 0.000 claims 1
- 229950006884 filaminast Drugs 0.000 claims 1
- 229940043355 kinase inhibitor Drugs 0.000 claims 1
- 229950008462 lirimilast Drugs 0.000 claims 1
- DPHDSIQHVGSITN-UHFFFAOYSA-N n-(3,5-dichloropyridin-4-yl)-2-[1-[(4-fluorophenyl)methyl]-5-hydroxyindol-3-yl]-2-oxoacetamide Chemical compound C1=C(C(=O)C(=O)NC=2C(=CN=CC=2Cl)Cl)C2=CC(O)=CC=C2N1CC1=CC=C(F)C=C1 DPHDSIQHVGSITN-UHFFFAOYSA-N 0.000 claims 1
- 102000002574 p38 Mitogen-Activated Protein Kinases Human genes 0.000 claims 1
- 238000004806 packaging method and process Methods 0.000 claims 1
- 239000000825 pharmaceutical preparation Substances 0.000 claims 1
- 239000003757 phosphotransferase inhibitor Substances 0.000 claims 1
- RRRUXBQSQLKHEL-UHFFFAOYSA-N piclamilast Chemical compound COC1=CC=C(C(=O)NC=2C(=CN=CC=2Cl)Cl)C=C1OC1CCCC1 RRRUXBQSQLKHEL-UHFFFAOYSA-N 0.000 claims 1
- 229950005184 piclamilast Drugs 0.000 claims 1
- 229940044601 receptor agonist Drugs 0.000 claims 1
- 239000000018 receptor agonist Substances 0.000 claims 1
- 229940044551 receptor antagonist Drugs 0.000 claims 1
- 239000002464 receptor antagonist Substances 0.000 claims 1
- HJORMJIFDVBMOB-UHFFFAOYSA-N rolipram Chemical compound COC1=CC=C(C2CC(=O)NC2)C=C1OC1CCCC1 HJORMJIFDVBMOB-UHFFFAOYSA-N 0.000 claims 1
- 229950005741 rolipram Drugs 0.000 claims 1
- 229960000278 theophylline Drugs 0.000 claims 1
- 229950003899 tofimilast Drugs 0.000 claims 1
- 102000014415 Muscarinic acetylcholine receptor Human genes 0.000 abstract 1
- 108050003473 Muscarinic acetylcholine receptor Proteins 0.000 abstract 1
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- 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
- A61K31/439—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 the ring forming part of a bridged ring system, e.g. quinuclidine
-
- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/13—Amines
- A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
- A61K31/137—Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
-
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/16—Amides, e.g. hydroxamic acids
- A61K31/165—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide
- A61K31/167—Amides, e.g. hydroxamic acids having aromatic rings, e.g. colchicine, atenolol, progabide having the nitrogen of a carboxamide group directly attached to the aromatic ring, e.g. lidocaine, paracetamol
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/56—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
- A61K31/57—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone
- A61K31/573—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids substituted in position 17 beta by a chain of two carbon atoms, e.g. pregnane or progesterone substituted in position 21, e.g. cortisone, dexamethasone, prednisone or aldosterone
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- A61K31/58—Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids containing heterocyclic rings, e.g. danazol, stanozolol, pancuronium or digitogenin
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Abstract
Kombinacija, naznačena time, da sadrži (a) inhibitor PDE4 i (b) antagonist muskarinskih receptora M3, koji antagonist je spoj (3R)-1-fenetil-3-(9H-ksanten-9-karboniloksi)-1-azoniabiciklo[2.2.2]oktan, u obliku soli koja sadrži anion X, koji je farmaceutski prihvatljiv anion mono ili polivalentne kiseline. Patent sadrži još 18 patentnih zahtjeva.
Claims (19)
1. Kombinacija, naznačena time, da sadrži (a) inhibitor PDE4 i (b) antagonist muskarinskih receptora M3, koji antagonist je spoj (3R)-1-fenetil-3-(9H-ksanten-9-karboniloksi)-1-azoniabiciklo[2.2.2]oktan, u obliku soli koja sadrži anion X, koji je farmaceutski prihvatljiv anion mono ili polivalentne kiseline.
2. Kombinacija u skladu s patentnim zahtjevom 1, naznačena time, da je antagonist M3 muskarinskih receptora (b) spoj (3R)-1-fenetil-3-(9H-ksanten-9-karboniloksi)-1-azoniabiciklo [2.2.2]oktan bromid.
3. Kombinacija u skladu s patentnim zahtjevom 1 ili 2, naznačena time, da je inhibitor PDE4 odabran iz skupine koju čine teofilin, drotaverin hidroklorid, cilomilast, roflumilast, denbufilin, rolipram, tetomilast, enprofilin, arofilin, cipamfilin, tofimilast, filaminast, piklamilast, (R)-(+)-4-[2-(3-ciklopentiloksi-4-metoksifenil)-2-feniletil]piridin, mesopram, N-(3,5-diklor-4-piridinil)-2-[1-(4-fluorobenzil)-5-hidroksi-1H-indol-3-il]-2-oksoacetamid, CDC-801 (ex. Celgene), CC-1088 (ex. Celgene), Lirimilast, ONO-6126 (ex. Ono), CC-10004 (ex. Celgene) i MN-001 (ex. Kvorin), po izboru u obliku njihovih racemata, enantiomera, dijastereomera i mješavina navedenog te, po izboru, njihovih farmakološki kompatibilnih adicijskih soli kiselina.
4. Kombinacija u skladu s patentnim zahtjevom 3, naznačena time, da je inhibitor PDE4 odabran iz skupine koju čine cilomilast, roflumilast, denbufilin i tetomilast, po izboru u obliku njihovih racemata, enantiomera, dijastereomera i mješavina navedenog, te, po izboru, njihovih farmakološki kompatibilnih adicijskih soli kiselina.
5. Kombinacija u skladu s patentnim zahtjevom 4, naznačena time, da je inhibitor PDE4 roflumilast.
6. Kombinacija u skladu s patentnim zahtjevom 4, naznačena time, da je inhibitor PDE4 cilomilast.
7. Kombinacija u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačena time, da su djelatne tvari (a) i (b) sadržane u jednom farmaceutskom pripravku.
8. Kombinacija u skladu s bilo kojim od prethodnih patentnih zahtjeva, naznačena time, da dodatno sadržava (c) dodatni djelatni spoj koji je odabran između: (a) β2-agonista, (b) kortikosteroida, (c) antagonista leukotrien-D4 receptora, (d) inhibitora egfr-kinaze, (e) inhibitora p38 kinaze i (f) agonista NK1 receptora.
9. Kombinacija u skladu s patentnim zahtjevom 8, naznačena time, da je djelatni spoj (c) odabran iz skupine koju čine (a) β2-agonisti i (b) kortikosteroidi.
10. Uporaba (a) inhibitora PDE4 kako se definira u bilo kojem od patentnih zahtjeva 1 i 3 do 6 i (b) antagonista muskarinskih receptora M3 kako se definiraju u patentnom zahtjevu 1 ili 2, naznačena time, da se koristi za pripravu lijeka za istovremenu, paralelnu, odvojenu ili sekvencijsku primjenu u liječenju bolesti dišnih putova koja reagira na M3 antagonizam kod bolesnika.
11. Uporaba u skladu s patentnim zahtjevom 10, naznačena time, da je bolest dišnih putova astma ili kronična opstruktivna bolest pluća (COPD).
12. Proizvedeni lijek, naznačen time, da sadrži (a) inhibitor PDE4 kako se definira u bilo kojem od patentnih zahtjeva 1 i 3 do 6 i (b) antagonist muskarinskih receptora M3 kako se definira u patentnom zahtjevu 1 ili 2, u obliku kombiniranog pripravka za istovremenu, paralelnu, odvojenu ili sekvencijsku primjenu u liječenju bolesnika koji boluje od ili je osjetljiv na bolest dišnih putova kako se definira u patentnom zahtjevu 10 ili 11.
13. Proizvedeni lijek u skladu s patentnim zahtjevom 12, naznačen time, da dodatno sadržava djelatni spoj (c) kako se definira u patentnom zahtjevu 8 ili 9.
14. Komplet dijelova, naznačen time, da sadrži (b) antagonist muskarinskih receptora M3 kako se definira u patentnom zahtjevu 1 ili 2 zajedno s uputama za istovremenu, paralelnu, odvojenu ili sekvencijsku primjenu u kombinaciji s (a) inhibitorom PDE4 kako se definira u bilo kojem od patentnih zahtjeva 1 i 3 do 6 za liječenje bolesnika koji boluje od ili je osjetljiv na bolest dišnih putova kako se definira u patentnom zahtjevu 10 ili 11.
15. Komplet u skladu s patentnim zahtjevom 14, naznačen time, da dodatno sadrži djelatni spoj (c) kako se definira u patentnom zahtjevu 8 ili 9.
16. Pakiranje, naznačeno time, da sadrži (b) antagonist muskarinskih receptora M3 kako se definira u patentnom zahtjevu 1 ili 2 i (a) inhibitor PDE4 kako se definira u bilo kojem od patentnih zahtjeva 1 i 3 do 6 za istovremenu, paralelnu, odvojenu ili sekvencijsku primjenu u liječenju bolesti dišnih putova kako se definira u patentnom zahtjevu 10 ili 11.
17. Pakiranje u skladu s patentnim zahtjevom 16, naznačeno time, da dodatno sadrži djelatni spoj (c) kako se definira u patentnom zahtjevu 8 ili 9.
18. Uporaba (b) antagonista muskarinskih receptora M3 kako se definira u patentnom zahtjevu 1 ili 2, naznačena time, da se koristi za pripravu lijeka za istovremenu, paralelnu, odvojenu ili sekvencijsku primjenu u kombinaciji s (a) inhibitorom PDE4 kako se definira u bilo kojem od patentnih zahtjeva 1 i 3 do 6 za liječenje bolesti dišnih putova kako se definira u patentnom zahtjevu 10 ili 11.
19. Uporaba (a) inhibitora PDE4 kako se definira u bilo kojem od patentnih zahtjeva 1 i 3 do 6, naznačena time, da se koristi za pripravu lijeka za istovremenu, paralelnu, odvojenu ili sekvencijsku primjenu u kombinaciji s (b) antagonistom muskarinskih receptora M3 kako se definira u patentnom zahtjevu 1 ili 2 za liječenje bolesti dišnih putova kako se definira u patentnom zahtjevu 10 ili 11.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ES200401312A ES2257152B1 (es) | 2004-05-31 | 2004-05-31 | Combinaciones que comprenden agentes antimuscarinicos y agonistas beta-adrenergicos. |
EP2005001969 | 2005-02-24 | ||
GB2005000740 | 2005-02-25 | ||
GB2005000722 | 2005-02-25 |
Publications (1)
Publication Number | Publication Date |
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HRP20100490T1 true HRP20100490T1 (hr) | 2010-10-31 |
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ID=34968792
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20090106T HRP20090106T3 (hr) | 2004-05-31 | 2009-02-20 | Kombinacije koje sadrže antimuskarinska sredstva i beta-adrenergičke agoniste |
HR20100104T HRP20100104T1 (hr) | 2004-05-31 | 2010-02-26 | Kombinacije koje sadrže antimuskarinska sredstva i kortikosteroide |
HR20100490T HRP20100490T1 (hr) | 2004-05-31 | 2010-09-03 | Kombinacije koje sadrže antimuskarinska sredstva i pde4 inhibitore |
Family Applications Before (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
HR20090106T HRP20090106T3 (hr) | 2004-05-31 | 2009-02-20 | Kombinacije koje sadrže antimuskarinska sredstva i beta-adrenergičke agoniste |
HR20100104T HRP20100104T1 (hr) | 2004-05-31 | 2010-02-26 | Kombinacije koje sadrže antimuskarinska sredstva i kortikosteroide |
Country Status (21)
Country | Link |
---|---|
US (2) | US20110224177A1 (hr) |
EP (5) | EP1905451B1 (hr) |
JP (1) | JP2012211183A (hr) |
AT (3) | ATE454904T1 (hr) |
AU (3) | AU2005247105B2 (hr) |
CA (3) | CA2568568C (hr) |
CY (1) | CY1110829T1 (hr) |
DE (3) | DE602005012102D1 (hr) |
DK (2) | DK1905451T3 (hr) |
ES (2) | ES2317245T3 (hr) |
HK (1) | HK1096605A1 (hr) |
HR (3) | HRP20090106T3 (hr) |
IL (3) | IL179686A0 (hr) |
MX (3) | MXPA06013850A (hr) |
NZ (3) | NZ551670A (hr) |
PL (2) | PL1891974T3 (hr) |
PT (3) | PT1905451E (hr) |
RS (3) | RS50786B (hr) |
RU (3) | RU2385156C2 (hr) |
SI (3) | SI1891974T1 (hr) |
WO (3) | WO2005115463A1 (hr) |
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EP2080523A1 (en) * | 2008-01-15 | 2009-07-22 | CHIESI FARMACEUTICI S.p.A. | Compositions comprising an antimuscarinic and a long-acting beta-agonist |
EP2100599A1 (en) * | 2008-03-13 | 2009-09-16 | Laboratorios Almirall, S.A. | Inhalation composition containing aclidinium for treatment of asthma and chronic obstructive pulmonary disease |
EP2100598A1 (en) | 2008-03-13 | 2009-09-16 | Laboratorios Almirall, S.A. | Inhalation composition containing aclidinium for treatment of asthma and chronic obstructive pulmonary disease |
GB0811100D0 (en) * | 2008-06-17 | 2008-07-23 | Astrazeneca Ab | New combination |
GB0814728D0 (en) * | 2008-08-12 | 2008-09-17 | Argenta Discovery Ltd | New combination |
WO2010097114A1 (en) * | 2009-02-26 | 2010-09-02 | Glaxo Group Limited | Novel combination of therapeutic agents |
EP4403231A2 (en) | 2009-02-26 | 2024-07-24 | Glaxo Group Limited | Pharmaceutical formulations comprising 4-{(1 r)-2-[(6-{2-[(2,6-dichlorobenzyl)oxy]ethoxy}hexyl)amino]-1-hydroxyethyl}-2-(hydroxymethyl)phenol |
CN107964016B (zh) | 2009-05-14 | 2021-10-01 | 天津合美医药科技有限公司 | 噻吩衍生物 |
GB0921075D0 (en) | 2009-12-01 | 2010-01-13 | Glaxo Group Ltd | Novel combination of the therapeutic agents |
EP2510928A1 (en) | 2011-04-15 | 2012-10-17 | Almirall, S.A. | Aclidinium for use in improving the quality of sleep in respiratory patients |
RU2666963C2 (ru) | 2012-04-13 | 2018-09-13 | Глаксосмитклайн Интеллекчуал Проперти Дивелопмент Лимитед | Агрегированные частицы |
GB201222679D0 (en) | 2012-12-17 | 2013-01-30 | Glaxo Group Ltd | Pharmaceutical combination products |
RS57075B1 (sr) * | 2013-03-15 | 2018-06-29 | Verona Pharma Plc | Kombinacija leka |
GB201308933D0 (en) * | 2013-05-17 | 2013-07-03 | Diurnal Ltd | Paediatric composition |
CN110592082A (zh) * | 2013-07-05 | 2019-12-20 | 柏业公司 | 呼吸疾病相关基因特异性siRNA、含有siRNA的双螺旋寡RNA结构及其用途 |
TW201542207A (zh) * | 2013-10-03 | 2015-11-16 | Otsuka Pharma Co Ltd | 嚴重氣喘治療劑 |
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2005
- 2005-05-31 AU AU2005247105A patent/AU2005247105B2/en not_active Ceased
- 2005-05-31 DE DE602005012102T patent/DE602005012102D1/de active Active
- 2005-05-31 ES ES05748688T patent/ES2317245T3/es active Active
- 2005-05-31 EP EP07023760A patent/EP1905451B1/en active Active
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- 2005-05-31 AU AU2005247104A patent/AU2005247104B2/en not_active Ceased
- 2005-05-31 MX MXPA06013850A patent/MXPA06013850A/es active IP Right Grant
- 2005-05-31 AT AT07023760T patent/ATE454904T1/de active
- 2005-05-31 AT AT07019646T patent/ATE474601T1/de active
- 2005-05-31 WO PCT/EP2005/005837 patent/WO2005115463A1/en active Application Filing
- 2005-05-31 MX MXPA06013846A patent/MXPA06013846A/es active IP Right Grant
- 2005-05-31 RU RU2006146813/15A patent/RU2385156C2/ru not_active IP Right Cessation
- 2005-05-31 SI SI200530959T patent/SI1905451T1/sl unknown
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- 2005-05-31 NZ NZ551670A patent/NZ551670A/en not_active IP Right Cessation
- 2005-05-31 RU RU2006146673/15A patent/RU2379033C2/ru not_active IP Right Cessation
- 2005-05-31 WO PCT/EP2005/005839 patent/WO2005115465A1/en not_active Application Discontinuation
- 2005-05-31 AU AU2005247106A patent/AU2005247106B2/en not_active Ceased
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- 2005-05-31 EP EP10003385A patent/EP2210614A1/en not_active Withdrawn
- 2005-05-31 DK DK07023760.7T patent/DK1905451T3/da active
- 2005-05-31 ES ES07023760T patent/ES2336144T3/es active Active
- 2005-05-31 RS RSP-2009/0075A patent/RS50786B/sr unknown
- 2005-05-31 EP EP05746222A patent/EP1761279A1/en not_active Withdrawn
- 2005-05-31 EP EP07019646A patent/EP1891974B1/en active Active
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- 2005-05-31 AT AT05748688T patent/ATE419011T1/de active
- 2005-05-31 NZ NZ551669A patent/NZ551669A/en not_active IP Right Cessation
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- 2005-05-31 DE DE602005018969T patent/DE602005018969D1/de active Active
- 2005-05-31 SI SI200530599T patent/SI1765404T1/sl unknown
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- 2005-05-31 MX MXPA06013849A patent/MXPA06013849A/es active IP Right Grant
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- 2005-05-31 RU RU2006147269/15A patent/RU2404772C2/ru not_active IP Right Cessation
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- 2005-05-31 CA CA2568571A patent/CA2568571C/en not_active Expired - Fee Related
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2007
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2009
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- 2010-10-11 CY CY20101100905T patent/CY1110829T1/el unknown
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2011
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