JP2014502141A5 - - Google Patents
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- JP2014502141A5 JP2014502141A5 JP2013532226A JP2013532226A JP2014502141A5 JP 2014502141 A5 JP2014502141 A5 JP 2014502141A5 JP 2013532226 A JP2013532226 A JP 2013532226A JP 2013532226 A JP2013532226 A JP 2013532226A JP 2014502141 A5 JP2014502141 A5 JP 2014502141A5
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- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 30
- 102000013498 tau Proteins Human genes 0.000 claims description 22
- 108010026424 tau Proteins Proteins 0.000 claims description 22
- 201000010099 disease Diseases 0.000 claims description 20
- 206010012289 Dementia Diseases 0.000 claims description 12
- 208000015122 neurodegenerative disease Diseases 0.000 claims description 11
- 210000002682 neurofibrillary tangle Anatomy 0.000 claims description 11
- 208000035475 disorder Diseases 0.000 claims description 10
- 201000011240 Frontotemporal dementia Diseases 0.000 claims description 8
- 230000007170 pathology Effects 0.000 claims description 7
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- 238000003745 diagnosis Methods 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 230000004770 neurodegeneration Effects 0.000 claims description 6
- 239000008194 pharmaceutical composition Substances 0.000 claims description 6
- 210000000349 chromosome Anatomy 0.000 claims description 5
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- 208000024827 Alzheimer disease Diseases 0.000 claims description 4
- 208000011990 Corticobasal Degeneration Diseases 0.000 claims description 4
- 208000020406 Creutzfeldt Jacob disease Diseases 0.000 claims description 4
- 208000003407 Creutzfeldt-Jakob Syndrome Diseases 0.000 claims description 4
- 208000010859 Creutzfeldt-Jakob disease Diseases 0.000 claims description 4
- 201000010374 Down Syndrome Diseases 0.000 claims description 4
- 208000026072 Motor neurone disease Diseases 0.000 claims description 4
- 208000001089 Multiple system atrophy Diseases 0.000 claims description 4
- 206010068871 Myotonic dystrophy Diseases 0.000 claims description 4
- 208000000609 Pick Disease of the Brain Diseases 0.000 claims description 4
- 208000036757 Postencephalitic parkinsonism Diseases 0.000 claims description 4
- 108091000054 Prion Proteins 0.000 claims description 4
- 208000037065 Subacute sclerosing leukoencephalitis Diseases 0.000 claims description 4
- 206010042297 Subacute sclerosing panencephalitis Diseases 0.000 claims description 4
- 208000034799 Tauopathies Diseases 0.000 claims description 4
- 208000030886 Traumatic Brain injury Diseases 0.000 claims description 4
- 206010044688 Trisomy 21 Diseases 0.000 claims description 4
- 208000007930 Type C Niemann-Pick Disease Diseases 0.000 claims description 4
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims description 4
- 230000003796 beauty Effects 0.000 claims description 4
- 230000002308 calcification Effects 0.000 claims description 4
- 208000017004 dementia pugilistica Diseases 0.000 claims description 4
- 201000008319 inclusion body myositis Diseases 0.000 claims description 4
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- 208000005264 motor neuron disease Diseases 0.000 claims description 4
- 208000000170 postencephalitic Parkinson disease Diseases 0.000 claims description 4
- 230000002739 subcortical effect Effects 0.000 claims description 4
- 230000009529 traumatic brain injury Effects 0.000 claims description 4
- 208000033556 type C1 Niemann-Pick disease Diseases 0.000 claims description 4
- 206010018341 Gliosis Diseases 0.000 claims description 3
- 230000007387 gliosis Effects 0.000 claims description 3
- 102000040430 polynucleotide Human genes 0.000 claims description 3
- 108091033319 polynucleotide Proteins 0.000 claims description 3
- 239000002157 polynucleotide Substances 0.000 claims description 3
- 208000005145 Cerebral amyloid angiopathy Diseases 0.000 claims description 2
- 241000124008 Mammalia Species 0.000 claims description 2
- 206010033799 Paralysis Diseases 0.000 claims description 2
- 125000003275 alpha amino acid group Chemical group 0.000 claims 41
- 102100035360 Cerebellar degeneration-related antigen 1 Human genes 0.000 claims 10
- 101000737793 Homo sapiens Cerebellar degeneration-related antigen 1 Proteins 0.000 claims 10
- 210000004408 hybridoma Anatomy 0.000 claims 7
- 210000004027 cell Anatomy 0.000 claims 3
- 208000010877 cognitive disease Diseases 0.000 claims 3
- 208000028698 Cognitive impairment Diseases 0.000 claims 2
- 101000891579 Homo sapiens Microtubule-associated protein tau Proteins 0.000 claims 2
- 230000007812 deficiency Effects 0.000 claims 2
- 238000010494 dissociation reaction Methods 0.000 claims 2
- 230000005593 dissociations Effects 0.000 claims 2
- 102000057063 human MAPT Human genes 0.000 claims 2
- FWMNVWWHGCHHJJ-SKKKGAJSSA-N 4-amino-1-[(2r)-6-amino-2-[[(2r)-2-[[(2r)-2-[[(2r)-2-amino-3-phenylpropanoyl]amino]-3-phenylpropanoyl]amino]-4-methylpentanoyl]amino]hexanoyl]piperidine-4-carboxylic acid Chemical compound C([C@H](C(=O)N[C@H](CC(C)C)C(=O)N[C@H](CCCCN)C(=O)N1CCC(N)(CC1)C(O)=O)NC(=O)[C@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 FWMNVWWHGCHHJJ-SKKKGAJSSA-N 0.000 claims 1
- 102100034452 Alternative prion protein Human genes 0.000 claims 1
- 150000001413 amino acids Chemical class 0.000 claims 1
- 230000001149 cognitive effect Effects 0.000 claims 1
- 230000002596 correlated effect Effects 0.000 claims 1
- 230000000875 corresponding effect Effects 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 238000011065 in-situ storage Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- 230000001898 pallidal effect Effects 0.000 claims 1
- BZQFBWGGLXLEPQ-REOHCLBHSA-N phosphoserine Chemical compound OC(=O)[C@@H](N)COP(O)(O)=O BZQFBWGGLXLEPQ-REOHCLBHSA-N 0.000 claims 1
- 238000011084 recovery Methods 0.000 claims 1
- 208000024891 symptom Diseases 0.000 claims 1
- 210000004556 brain Anatomy 0.000 description 5
- 208000004434 Calcinosis Diseases 0.000 description 3
- 102000029797 Prion Human genes 0.000 description 3
- 206010059245 Angiopathy Diseases 0.000 description 2
- 208000037765 diseases and disorders Diseases 0.000 description 2
- 108090000765 processed proteins & peptides Proteins 0.000 description 2
- 201000002212 progressive supranuclear palsy Diseases 0.000 description 2
- 208000032612 Glial tumor Diseases 0.000 description 1
- 206010018338 Glioma Diseases 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 208000024571 Pick disease Diseases 0.000 description 1
- 230000005856 abnormality Effects 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 230000001575 pathological effect Effects 0.000 description 1
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10186810 | 2010-10-07 | ||
| EP10186810.7 | 2010-10-07 | ||
| EP11174248 | 2011-07-15 | ||
| EP11174248.2 | 2011-07-15 | ||
| PCT/EP2011/067604 WO2012045882A2 (en) | 2010-10-07 | 2011-10-07 | Pharmaceutical composition |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017008740A Division JP2017113004A (ja) | 2010-10-07 | 2017-01-20 | 薬学的組成物 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014502141A JP2014502141A (ja) | 2014-01-30 |
| JP2014502141A5 true JP2014502141A5 (https=) | 2016-06-23 |
| JP6371526B2 JP6371526B2 (ja) | 2018-08-08 |
Family
ID=44947048
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013532226A Active JP6371526B2 (ja) | 2010-10-07 | 2011-10-07 | タウを認識するリン酸化部位特異的抗体 |
| JP2017008740A Pending JP2017113004A (ja) | 2010-10-07 | 2017-01-20 | 薬学的組成物 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017008740A Pending JP2017113004A (ja) | 2010-10-07 | 2017-01-20 | 薬学的組成物 |
Country Status (29)
| Country | Link |
|---|---|
| US (2) | US9304138B2 (https=) |
| EP (2) | EP2625198B1 (https=) |
| JP (2) | JP6371526B2 (https=) |
| KR (1) | KR101988672B1 (https=) |
| CN (1) | CN103502272B (https=) |
| AR (1) | AR085198A1 (https=) |
| AU (1) | AU2011311516B2 (https=) |
| BR (1) | BR112013008333B1 (https=) |
| CA (1) | CA2812865C (https=) |
| CL (1) | CL2013000951A1 (https=) |
| CO (1) | CO6710903A2 (https=) |
| CR (1) | CR20130160A (https=) |
| DK (1) | DK2625198T3 (https=) |
| EC (1) | ECSP13012609A (https=) |
| ES (1) | ES2548686T3 (https=) |
| HK (1) | HK1216897A1 (https=) |
| HU (1) | HUE027649T2 (https=) |
| IL (1) | IL225568A (https=) |
| MX (1) | MX338421B (https=) |
| MY (1) | MY164376A (https=) |
| PE (1) | PE20140218A1 (https=) |
| PH (1) | PH12013500615A1 (https=) |
| PL (1) | PL2625198T3 (https=) |
| RU (1) | RU2603078C2 (https=) |
| SG (1) | SG189136A1 (https=) |
| SI (1) | SI2625198T1 (https=) |
| TW (1) | TW201216985A (https=) |
| WO (1) | WO2012045882A2 (https=) |
| ZA (1) | ZA201302432B (https=) |
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| US20120244174A1 (en) | 2011-01-31 | 2012-09-27 | Intellect Neurosciences Inc. | Treatment of tauopathies |
| GB201112056D0 (en) * | 2011-07-14 | 2011-08-31 | Univ Leuven Kath | Antibodies |
| US10813630B2 (en) | 2011-08-09 | 2020-10-27 | Corquest Medical, Inc. | Closure system for atrial wall |
| US10314594B2 (en) | 2012-12-14 | 2019-06-11 | Corquest Medical, Inc. | Assembly and method for left atrial appendage occlusion |
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| US12024568B2 (en) | 2012-09-13 | 2024-07-02 | Cornell University | Treatment of brain cancers using central nervous system mediated gene transfer of monoclonal antibodies |
| US20140142689A1 (en) | 2012-11-21 | 2014-05-22 | Didier De Canniere | Device and method of treating heart valve malfunction |
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