JP2011516420A5 - - Google Patents
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- Publication number
- JP2011516420A5 JP2011516420A5 JP2011502011A JP2011502011A JP2011516420A5 JP 2011516420 A5 JP2011516420 A5 JP 2011516420A5 JP 2011502011 A JP2011502011 A JP 2011502011A JP 2011502011 A JP2011502011 A JP 2011502011A JP 2011516420 A5 JP2011516420 A5 JP 2011516420A5
- Authority
- JP
- Japan
- Prior art keywords
- pharmaceutically acceptable
- acceptable salt
- compound
- aryl
- independently
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 150000001875 compounds Chemical class 0.000 claims description 80
- 150000003839 salts Chemical class 0.000 claims description 43
- 125000003118 aryl group Chemical group 0.000 claims description 34
- 125000000217 alkyl group Chemical group 0.000 claims description 28
- 125000001072 heteroaryl group Chemical group 0.000 claims description 28
- 125000005843 halogen group Chemical group 0.000 claims description 22
- 125000000623 heterocyclic group Chemical group 0.000 claims description 22
- 125000002723 alicyclic group Chemical group 0.000 claims description 18
- 125000004429 atom Chemical group 0.000 claims description 16
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 14
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 14
- 239000000203 mixture Substances 0.000 claims description 14
- 108010006533 ATP-Binding Cassette Transporters Proteins 0.000 claims description 13
- 102000005416 ATP-Binding Cassette Transporters Human genes 0.000 claims description 13
- 201000010099 disease Diseases 0.000 claims description 10
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 125000004104 aryloxy group Chemical group 0.000 claims description 8
- 230000000694 effects Effects 0.000 claims description 8
- -1 heteroalicyclic Chemical group 0.000 claims description 8
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 8
- 125000001931 aliphatic group Chemical group 0.000 claims description 6
- 125000001118 alkylidene group Chemical group 0.000 claims description 6
- 230000007812 deficiency Effects 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 125000004001 thioalkyl group Chemical group 0.000 claims description 6
- 206010014561 Emphysema Diseases 0.000 claims description 4
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 4
- 239000012472 biological sample Substances 0.000 claims description 4
- 208000035475 disorder Diseases 0.000 claims description 4
- 239000012634 fragment Substances 0.000 claims description 4
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 4
- 125000002015 acyclic group Chemical group 0.000 claims description 3
- 208000024827 Alzheimer disease Diseases 0.000 claims description 2
- 102000014461 Ataxins Human genes 0.000 claims description 2
- 108010078286 Ataxins Proteins 0.000 claims description 2
- 102100022548 Beta-hexosaminidase subunit alpha Human genes 0.000 claims description 2
- 208000014644 Brain disease Diseases 0.000 claims description 2
- 206010008025 Cerebellar ataxia Diseases 0.000 claims description 2
- 208000010693 Charcot-Marie-Tooth Disease Diseases 0.000 claims description 2
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 2
- 208000035473 Communicable disease Diseases 0.000 claims description 2
- 206010062264 Congenital hyperthyroidism Diseases 0.000 claims description 2
- 208000020406 Creutzfeldt Jacob disease Diseases 0.000 claims description 2
- 208000003407 Creutzfeldt-Jakob Syndrome Diseases 0.000 claims description 2
- 208000010859 Creutzfeldt-Jakob disease Diseases 0.000 claims description 2
- 201000003883 Cystic fibrosis Diseases 0.000 claims description 2
- 208000003556 Dry Eye Syndromes Diseases 0.000 claims description 2
- 206010013883 Dwarfism Diseases 0.000 claims description 2
- 208000024720 Fabry Disease Diseases 0.000 claims description 2
- 201000011240 Frontotemporal dementia Diseases 0.000 claims description 2
- 206010019860 Hereditary angioedema Diseases 0.000 claims description 2
- 208000033981 Hereditary haemochromatosis Diseases 0.000 claims description 2
- 208000023105 Huntington disease Diseases 0.000 claims description 2
- 206010060378 Hyperinsulinaemia Diseases 0.000 claims description 2
- 208000000563 Hyperlipoproteinemia Type II Diseases 0.000 claims description 2
- 206010051125 Hypofibrinogenaemia Diseases 0.000 claims description 2
- 208000000038 Hypoparathyroidism Diseases 0.000 claims description 2
- 102100024640 Low-density lipoprotein receptor Human genes 0.000 claims description 2
- 208000015439 Lysosomal storage disease Diseases 0.000 claims description 2
- 208000008955 Mucolipidoses Diseases 0.000 claims description 2
- 206010072928 Mucolipidosis type II Diseases 0.000 claims description 2
- 208000002678 Mucopolysaccharidoses Diseases 0.000 claims description 2
- 206010068871 Myotonic dystrophy Diseases 0.000 claims description 2
- 206010031243 Osteogenesis imperfecta Diseases 0.000 claims description 2
- 208000018737 Parkinson disease Diseases 0.000 claims description 2
- 208000000609 Pick Disease of the Brain Diseases 0.000 claims description 2
- 201000005660 Protein C Deficiency Diseases 0.000 claims description 2
- 208000021386 Sjogren Syndrome Diseases 0.000 claims description 2
- 208000009415 Spinocerebellar Ataxias Diseases 0.000 claims description 2
- 208000022292 Tay-Sachs disease Diseases 0.000 claims description 2
- 206010045261 Type IIa hyperlipidaemia Diseases 0.000 claims description 2
- 102100026383 Vasopressin-neurophysin 2-copeptin Human genes 0.000 claims description 2
- 208000004622 abetalipoproteinemia Diseases 0.000 claims description 2
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 2
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims description 2
- 239000003242 anti bacterial agent Substances 0.000 claims description 2
- 239000002260 anti-inflammatory agent Substances 0.000 claims description 2
- 229940121363 anti-inflammatory agent Drugs 0.000 claims description 2
- 229960005475 antiinfective agent Drugs 0.000 claims description 2
- 239000004599 antimicrobial Substances 0.000 claims description 2
- 201000004562 autosomal dominant cerebellar ataxia Diseases 0.000 claims description 2
- 230000015572 biosynthetic process Effects 0.000 claims description 2
- 229940124630 bronchodilator Drugs 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 201000010064 diabetes insipidus Diseases 0.000 claims description 2
- 206010012601 diabetes mellitus Diseases 0.000 claims description 2
- 239000003937 drug carrier Substances 0.000 claims description 2
- 230000002124 endocrine Effects 0.000 claims description 2
- 239000003172 expectorant agent Substances 0.000 claims description 2
- 201000001386 familial hypercholesterolemia Diseases 0.000 claims description 2
- 208000013746 hereditary thrombophilia due to congenital protein C deficiency Diseases 0.000 claims description 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 2
- 230000003451 hyperinsulinaemic effect Effects 0.000 claims description 2
- 201000008980 hyperinsulinism Diseases 0.000 claims description 2
- 238000000338 in vitro Methods 0.000 claims description 2
- 238000001727 in vivo Methods 0.000 claims description 2
- 208000015181 infectious disease Diseases 0.000 claims description 2
- 150000002632 lipids Chemical class 0.000 claims description 2
- 201000001441 melanoma Diseases 0.000 claims description 2
- 125000002950 monocyclic group Chemical group 0.000 claims description 2
- 208000020460 mucolipidosis II alpha/beta Diseases 0.000 claims description 2
- 229940066491 mucolytics Drugs 0.000 claims description 2
- 206010028093 mucopolysaccharidosis Diseases 0.000 claims description 2
- 201000000585 muscular atrophy Diseases 0.000 claims description 2
- 208000000638 myeloperoxidase deficiency Diseases 0.000 claims description 2
- 230000004770 neurodegeneration Effects 0.000 claims description 2
- 208000015122 neurodegenerative disease Diseases 0.000 claims description 2
- 230000007823 neuropathy Effects 0.000 claims description 2
- 201000001119 neuropathy Diseases 0.000 claims description 2
- 235000015097 nutrients Nutrition 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- 108010040003 polyglutamine Proteins 0.000 claims description 2
- 229920000155 polyglutamine Polymers 0.000 claims description 2
- 230000000750 progressive effect Effects 0.000 claims description 2
- 208000011580 syndromic disease Diseases 0.000 claims description 2
- 150000001260 acyclic compounds Chemical group 0.000 claims 1
- 229940088710 antibiotic agent Drugs 0.000 claims 1
- 239000000168 bronchodilator agent Substances 0.000 claims 1
- 210000000170 cell membrane Anatomy 0.000 claims 1
- 0 C*1C2C(C)(C)CCC12 Chemical compound C*1C2C(C)(C)CCC12 0.000 description 9
- 238000000034 method Methods 0.000 description 5
- 102000012605 Cystic Fibrosis Transmembrane Conductance Regulator Human genes 0.000 description 4
- 108010079245 Cystic Fibrosis Transmembrane Conductance Regulator Proteins 0.000 description 4
- DYQQZIVYJMLWTD-UHFFFAOYSA-N CC(C)N(CCOC(C)c(cccc1)c1OC)C(C)C Chemical compound CC(C)N(CCOC(C)c(cccc1)c1OC)C(C)C DYQQZIVYJMLWTD-UHFFFAOYSA-N 0.000 description 1
- ITAXXPAEDHHVDK-UHFFFAOYSA-N CC(c(cccc1)c1OC)OCCN1CCCCC1 Chemical compound CC(c(cccc1)c1OC)OCCN1CCCCC1 ITAXXPAEDHHVDK-UHFFFAOYSA-N 0.000 description 1
- ODENTAMIJLBWSF-UHFFFAOYSA-N CC(c1ccccc1OC)N1CC(C)OC(C)C1 Chemical compound CC(c1ccccc1OC)N1CC(C)OC(C)C1 ODENTAMIJLBWSF-UHFFFAOYSA-N 0.000 description 1
- IPEOALIFMRMNRT-UHFFFAOYSA-N CC(c1ccccc1OC)N1CCCC1 Chemical compound CC(c1ccccc1OC)N1CCCC1 IPEOALIFMRMNRT-UHFFFAOYSA-N 0.000 description 1
- YUMRNIILPQNWDO-UHFFFAOYSA-N CC(c1ccccc1OC)N1CCN(CCO)CC1 Chemical compound CC(c1ccccc1OC)N1CCN(CCO)CC1 YUMRNIILPQNWDO-UHFFFAOYSA-N 0.000 description 1
- CBVDDSUFZQULQL-UHFFFAOYSA-N CC(c1ccccc1OC)N1CCN(CCOC)CC1 Chemical compound CC(c1ccccc1OC)N1CCN(CCOC)CC1 CBVDDSUFZQULQL-UHFFFAOYSA-N 0.000 description 1
- WSDVHWASCHELJA-UHFFFAOYSA-N CC(c1ccccc1OC)N1CCOCC1 Chemical compound CC(c1ccccc1OC)N1CCOCC1 WSDVHWASCHELJA-UHFFFAOYSA-N 0.000 description 1
- PYGFIGLUHGUOGN-UHFFFAOYSA-N CCN(CC)C(C)c(cccc1)c1OC Chemical compound CCN(CC)C(C)c(cccc1)c1OC PYGFIGLUHGUOGN-UHFFFAOYSA-N 0.000 description 1
- NUDVJQOVBFONPG-UHFFFAOYSA-N CCc(c(Cl)ccc1)c1Cl Chemical compound CCc(c(Cl)ccc1)c1Cl NUDVJQOVBFONPG-UHFFFAOYSA-N 0.000 description 1
- HYFLWBNQFMXCPA-UHFFFAOYSA-N CCc1ccccc1C Chemical compound CCc1ccccc1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
- CVGAWKYSRYXQOI-UHFFFAOYSA-N CCc1ccccc1Cl Chemical compound CCc1ccccc1Cl CVGAWKYSRYXQOI-UHFFFAOYSA-N 0.000 description 1
- XQFJDFIHJKPUEL-UHFFFAOYSA-N CN(C)c(cccc1)c1OC Chemical compound CN(C)c(cccc1)c1OC XQFJDFIHJKPUEL-UHFFFAOYSA-N 0.000 description 1
- RIWRFSMVIUAEBX-UHFFFAOYSA-N CNCc1ccccc1 Chemical compound CNCc1ccccc1 RIWRFSMVIUAEBX-UHFFFAOYSA-N 0.000 description 1
- KNZWULOUXYKBLH-UHFFFAOYSA-N CNc(cccc1)c1OC Chemical compound CNc(cccc1)c1OC KNZWULOUXYKBLH-UHFFFAOYSA-N 0.000 description 1
- WFWDIWPWCNUWLM-UHFFFAOYSA-N COc1ccccc1C(N1CCCCC1)I Chemical compound COc1ccccc1C(N1CCCCC1)I WFWDIWPWCNUWLM-UHFFFAOYSA-N 0.000 description 1
- WGRPQCFFBRDZFV-UHFFFAOYSA-N Cc1cccc(C(N)=O)c1 Chemical compound Cc1cccc(C(N)=O)c1 WGRPQCFFBRDZFV-UHFFFAOYSA-N 0.000 description 1
- ZDBWNRRPANCKMV-UHFFFAOYSA-N IOCc1ccccc1 Chemical compound IOCc1ccccc1 ZDBWNRRPANCKMV-UHFFFAOYSA-N 0.000 description 1
- POHJRJNCZQENQG-UHFFFAOYSA-N O=C1NC=CC(I)=C1 Chemical compound O=C1NC=CC(I)=C1 POHJRJNCZQENQG-UHFFFAOYSA-N 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US4077608P | 2008-03-31 | 2008-03-31 | |
| US61/040,776 | 2008-03-31 | ||
| PCT/US2009/038203 WO2009123896A1 (en) | 2008-03-31 | 2009-03-25 | Pyridyl derivatives as cftr modulators |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014018199A Division JP5930487B2 (ja) | 2008-03-31 | 2014-02-03 | Ｃｆｔｒモジュレーターとしてのピリジル誘導体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2011516420A JP2011516420A (ja) | 2011-05-26 |
| JP2011516420A5 true JP2011516420A5 (https=) | 2013-03-21 |
| JP5622285B2 JP5622285B2 (ja) | 2014-11-12 |
Family
ID=40790781
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011502011A Active JP5622285B2 (ja) | 2008-03-31 | 2009-03-25 | Ｃｆｔｒモジュレーターとしてのピリジル誘導体 |
| JP2014018199A Active JP5930487B2 (ja) | 2008-03-31 | 2014-02-03 | Ｃｆｔｒモジュレーターとしてのピリジル誘導体 |
| JP2015088075A Withdrawn JP2015131860A (ja) | 2008-03-31 | 2015-04-23 | Ｃｆｔｒモジュレーターとしてのピリジル誘導体 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2014018199A Active JP5930487B2 (ja) | 2008-03-31 | 2014-02-03 | Ｃｆｔｒモジュレーターとしてのピリジル誘導体 |
| JP2015088075A Withdrawn JP2015131860A (ja) | 2008-03-31 | 2015-04-23 | Ｃｆｔｒモジュレーターとしてのピリジル誘導体 |
Country Status (17)
| Country | Link |
|---|---|
| US (3) | US8227615B2 (https=) |
| EP (3) | EP2615085B1 (https=) |
| JP (3) | JP5622285B2 (https=) |
| CN (2) | CN101981011B (https=) |
| AU (1) | AU2009231993B2 (https=) |
| CA (1) | CA2718310C (https=) |
| CY (1) | CY1116953T1 (https=) |
| DK (1) | DK2615085T3 (https=) |
| ES (2) | ES2442945T3 (https=) |
| HK (1) | HK1198537A1 (https=) |
| HR (1) | HRP20151141T1 (https=) |
| HU (1) | HUE026220T2 (https=) |
| NZ (3) | NZ616097A (https=) |
| PL (1) | PL2615085T3 (https=) |
| PT (1) | PT2615085E (https=) |
| SI (1) | SI2615085T1 (https=) |
| WO (1) | WO2009123896A1 (https=) |
Families Citing this family (137)
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| RU2006111093A (ru) | 2003-09-06 | 2007-10-27 | Вертекс Фармасьютикалз Инкорпорейтед (Us) | Модуляторы атр-связывающих кассетных транспортеров |
| CN101675928A (zh) * | 2003-11-14 | 2010-03-24 | 沃泰克斯药物股份有限公司 | 可用作atp-结合弹夹转运蛋白调控剂的噻唑和噁唑 |
| BRPI0507278A (pt) * | 2004-01-30 | 2007-06-26 | Vertex Pharma | moduladores dos transportadores do cassete de ligação ao atp |
| US7977322B2 (en) | 2004-08-20 | 2011-07-12 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-binding cassette transporters |
| RS56037B1 (sr) | 2004-06-24 | 2017-09-29 | Vertex Pharma | Modulatori atp-vezujućih kasetnih transportera |
| US7999113B2 (en) | 2005-08-11 | 2011-08-16 | Vertex Pharmaceuticals Incorporated | Modulators of cystic fibrosis transmembrane conductance regulator |
| CN102775396B (zh) | 2005-11-08 | 2014-10-08 | 沃泰克斯药物股份有限公司 | Atp-结合弹夹转运蛋白的杂环调控剂 |
| CA2856037C (en) | 2005-12-28 | 2017-03-07 | Vertex Pharmaceuticals Incorporated | Modulators of atp-binding cassette transporters |
| EP3219705B1 (en) | 2005-12-28 | 2020-03-11 | Vertex Pharmaceuticals Incorporated | Pharmaceutical compositions of the amorphous form of n-[2,4-bis(1,1-dimethylethyl)-5-hydroxyphenyl]-1,4-dihydro-4-oxoquinoline-3-carboxamide |
| US7671221B2 (en) * | 2005-12-28 | 2010-03-02 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-Binding Cassette transporters |
| USRE50453E1 (en) | 2006-04-07 | 2025-06-10 | Vertex Pharmaceuticals Incorporated | Indole derivatives as CFTR modulators |
| EP2674428B1 (en) | 2006-04-07 | 2016-04-06 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-binding cassette transporters |
| US7645789B2 (en) | 2006-04-07 | 2010-01-12 | Vertex Pharmaceuticals Incorporated | Indole derivatives as CFTR modulators |
| US10022352B2 (en) | 2006-04-07 | 2018-07-17 | Vertex Pharmaceuticals Incorporated | Modulators of ATP-binding cassette transporters |
| US8563573B2 (en) | 2007-11-02 | 2013-10-22 | Vertex Pharmaceuticals Incorporated | Azaindole derivatives as CFTR modulators |
| CN104447716A (zh) * | 2007-05-09 | 2015-03-25 | 沃泰克斯药物股份有限公司 | Cftr调节剂 |
| AU2008256937A1 (en) * | 2007-05-25 | 2008-12-04 | Vertex Pharmaceuticals Incorporated | Ion channel modulators and methods of use |
| JP5389030B2 (ja) | 2007-08-24 | 2014-01-15 | バーテックス ファーマシューティカルズ インコーポレイテッド | （特に）嚢胞性線維症の処置に有用なイソチアゾロピリジノン |
| CA2702094C (en) | 2007-10-10 | 2018-05-01 | Parion Sciences, Inc. | Delivering osmolytes by nasal cannula |
| SI2578571T1 (sl) | 2007-11-16 | 2016-01-29 | Vertex Pharmaceuticals Incorporated | Izokinolinski modulatorji prenašalcev z atp-vezavno kaseto |
| MX365732B (es) * | 2007-12-07 | 2019-06-12 | Vertex Pharma | Procesos para producir acidos cicloalquilcarboxamido-piridin benzoicos. |
| EP3683218B1 (en) | 2007-12-07 | 2024-09-18 | Vertex Pharmaceuticals Incorporated | Solid forms of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl) benzoic acid |
| US20100036130A1 (en) | 2007-12-07 | 2010-02-11 | Vertex Pharmaceuticals Incorporated | Processes for producing cycloalkylcarboxamido-pyridine benzoic acids |
| CN101998854A (zh) * | 2007-12-07 | 2011-03-30 | 沃泰克斯药物股份有限公司 | 3-(6-(1-(2,2-二氟苯并[d][1,3]间二氧杂环戊烯-5-基)环丙烷甲酰氨基)-3-甲基吡啶-2-基)苯甲酸的制剂 |
| NZ720282A (en) | 2008-02-28 | 2017-12-22 | Vertex Pharma | Heteroaryl derivatives as cftr modulators |
| NZ616097A (en) | 2008-03-31 | 2015-04-24 | Vertex Pharma | Pyridyl derivatives as cftr modulators |
| US12458635B2 (en) | 2008-08-13 | 2025-11-04 | Vertex Pharmaceuticals Incorporated | Pharmaceutical composition and administrations thereof |
| US20100074949A1 (en) | 2008-08-13 | 2010-03-25 | William Rowe | Pharmaceutical composition and administration thereof |
| AR073709A1 (es) | 2008-09-29 | 2010-11-24 | Vertex Pharma | Unidades de dosis de acido 3-(6-(1-(2,2-difluorobenzeno (d) (1,3) dioxol-5-il) ciclopropancarboxamido)-3-metilpiridin-2-il) benzoico |
| EP2349263B1 (en) * | 2008-10-23 | 2014-04-23 | Vertex Pharmaceuticals Inc. | Modulators of cystic fibrosis transmembrane conductance regulator |
| PL2408750T3 (pl) | 2009-03-20 | 2016-02-29 | Vertex Pharma | Sposób otrzymywania modulatorów błonowego regulatora przewodnictwa swoistego dla mukowiscydozy |
| US8247436B2 (en) | 2010-03-19 | 2012-08-21 | Novartis Ag | Pyridine and pyrazine derivative for the treatment of CF |
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| MX2012011655A (es) | 2010-04-07 | 2012-11-23 | Vertex Pharma | Formas solidas de acido 3-(6-(1-(2,2-difluorobenzo [d][1-3]dioxol-5-il]ciclopropanocarboxamido)-3-metilpiridin-2-il) benzoico. |
| JP2013523833A (ja) | 2010-04-07 | 2013-06-17 | バーテックス ファーマシューティカルズ インコーポレイテッド | ３−（６−（１−（２，２−ジフルオロベンゾ［ｄ］［１，３］ジオキソール−５−イル）シクロプロパンカルボキサミド）−３−メチルピリジン−２−イル）安息香酸の医薬組成物およびその投与 |
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- 2009-03-25 DK DK12188920.8T patent/DK2615085T3/en active
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- 2009-03-25 PL PL12188920T patent/PL2615085T3/pl unknown
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- 2009-03-25 WO PCT/US2009/038203 patent/WO2009123896A1/en not_active Ceased
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- 2009-03-25 EP EP15182081.8A patent/EP2980077B1/en active Active
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