JP2016104026A5 - - Google Patents
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- JP2016104026A5 JP2016104026A5 JP2016004910A JP2016004910A JP2016104026A5 JP 2016104026 A5 JP2016104026 A5 JP 2016104026A5 JP 2016004910 A JP2016004910 A JP 2016004910A JP 2016004910 A JP2016004910 A JP 2016004910A JP 2016104026 A5 JP2016104026 A5 JP 2016104026A5
- Authority
- JP
- Japan
- Prior art keywords
- amyloid
- antibody
- disease
- fragment
- disorder
- 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.)
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- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 35
- 239000012634 fragment Substances 0.000 claims 27
- 239000000203 mixture Substances 0.000 claims 24
- 102000013455 Amyloid beta-Peptides Human genes 0.000 claims 21
- 108010090849 Amyloid beta-Peptides Proteins 0.000 claims 21
- 201000010099 disease Diseases 0.000 claims 18
- 208000035475 disorder Diseases 0.000 claims 17
- 238000000034 method Methods 0.000 claims 12
- 102000009091 Amyloidogenic Proteins Human genes 0.000 claims 8
- 108010048112 Amyloidogenic Proteins Proteins 0.000 claims 8
- 241001465754 Metazoa Species 0.000 claims 8
- 206010002022 amyloidosis Diseases 0.000 claims 7
- 102000004169 proteins and genes Human genes 0.000 claims 7
- 108090000623 proteins and genes Proteins 0.000 claims 7
- 208000024827 Alzheimer disease Diseases 0.000 claims 6
- 108010047041 Complementarity Determining Regions Proteins 0.000 claims 6
- 241000124008 Mammalia Species 0.000 claims 4
- 206010002026 amyotrophic lateral sclerosis Diseases 0.000 claims 4
- 230000015572 biosynthetic process Effects 0.000 claims 4
- 210000004556 brain Anatomy 0.000 claims 4
- 208000010877 cognitive disease Diseases 0.000 claims 4
- 210000004408 hybridoma Anatomy 0.000 claims 4
- 201000008319 inclusion body myositis Diseases 0.000 claims 4
- 208000027061 mild cognitive impairment Diseases 0.000 claims 4
- 210000004027 cell Anatomy 0.000 claims 3
- 230000001149 cognitive effect Effects 0.000 claims 3
- 230000007087 memory ability Effects 0.000 claims 3
- 239000002157 polynucleotide Substances 0.000 claims 3
- 102000040430 polynucleotide Human genes 0.000 claims 3
- 108091033319 polynucleotide Proteins 0.000 claims 3
- LZXHHNKULPHARO-UHFFFAOYSA-M (3,4-dichlorophenyl)methyl-triphenylphosphanium;chloride Chemical compound [Cl-].C1=C(Cl)C(Cl)=CC=C1C[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 LZXHHNKULPHARO-UHFFFAOYSA-M 0.000 claims 2
- SNKZJIOFVMKAOJ-UHFFFAOYSA-N 3-Amino-1-propanesulfonic acid Natural products NCCCS(O)(=O)=O SNKZJIOFVMKAOJ-UHFFFAOYSA-N 0.000 claims 2
- 208000023769 AA amyloidosis Diseases 0.000 claims 2
- 208000018282 ACys amyloidosis Diseases 0.000 claims 2
- 206010065040 AIDS dementia complex Diseases 0.000 claims 2
- 206010007509 Cardiac amyloidosis Diseases 0.000 claims 2
- 208000005145 Cerebral amyloid angiopathy Diseases 0.000 claims 2
- 229940122041 Cholinesterase inhibitor Drugs 0.000 claims 2
- 208000020406 Creutzfeldt Jacob disease Diseases 0.000 claims 2
- 208000003407 Creutzfeldt-Jakob Syndrome Diseases 0.000 claims 2
- 208000010859 Creutzfeldt-Jakob disease Diseases 0.000 claims 2
- 206010012289 Dementia Diseases 0.000 claims 2
- 201000010374 Down Syndrome Diseases 0.000 claims 2
- 208000001976 Endocrine Gland Neoplasms Diseases 0.000 claims 2
- 208000007487 Familial Cerebral Amyloid Angiopathy Diseases 0.000 claims 2
- 208000032849 Hereditary cerebral hemorrhage with amyloidosis Diseases 0.000 claims 2
- 208000009829 Lewy Body Disease Diseases 0.000 claims 2
- 201000002832 Lewy body dementia Diseases 0.000 claims 2
- 208000018737 Parkinson disease Diseases 0.000 claims 2
- 208000007660 Residual Neoplasm Diseases 0.000 claims 2
- 206010039811 Secondary amyloidosis Diseases 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 2
- 230000000996 additive effect Effects 0.000 claims 2
- 125000003275 alpha amino acid group Chemical group 0.000 claims 2
- 230000000975 bioactive effect Effects 0.000 claims 2
- 239000000544 cholinesterase inhibitor Substances 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- ADEBPBSSDYVVLD-UHFFFAOYSA-N donepezil Chemical compound O=C1C=2C=C(OC)C(OC)=CC=2CC1CC(CC1)CCN1CC1=CC=CC=C1 ADEBPBSSDYVVLD-UHFFFAOYSA-N 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 230000000694 effects Effects 0.000 claims 2
- 201000011523 endocrine gland cancer Diseases 0.000 claims 2
- ASUTZQLVASHGKV-JDFRZJQESA-N galanthamine Chemical compound O1C(=C23)C(OC)=CC=C2CN(C)CC[C@]23[C@@H]1C[C@@H](O)C=C2 ASUTZQLVASHGKV-JDFRZJQESA-N 0.000 claims 2
- 208000002780 macular degeneration Diseases 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 201000006417 multiple sclerosis Diseases 0.000 claims 2
- 201000002212 progressive supranuclear palsy Diseases 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims 2
- 102000002659 Amyloid Precursor Protein Secretases Human genes 0.000 claims 1
- 108010043324 Amyloid Precursor Protein Secretases Proteins 0.000 claims 1
- 229940125373 Gamma-Secretase Inhibitor Drugs 0.000 claims 1
- PVNIIMVLHYAWGP-UHFFFAOYSA-N Niacin Chemical compound OC(=O)C1=CC=CN=C1 PVNIIMVLHYAWGP-UHFFFAOYSA-N 0.000 claims 1
- XSVMFMHYUFZWBK-NSHDSACASA-N Rivastigmine Chemical compound CCN(C)C(=O)OC1=CC=CC([C@H](C)N(C)C)=C1 XSVMFMHYUFZWBK-NSHDSACASA-N 0.000 claims 1
- 239000012190 activator Substances 0.000 claims 1
- 230000003942 amyloidogenic effect Effects 0.000 claims 1
- 230000003110 anti-inflammatory effect Effects 0.000 claims 1
- 239000002439 beta secretase inhibitor Substances 0.000 claims 1
- 229940088623 biologically active substance Drugs 0.000 claims 1
- 239000002738 chelating agent Substances 0.000 claims 1
- 238000012258 culturing Methods 0.000 claims 1
- 238000003745 diagnosis Methods 0.000 claims 1
- 235000015872 dietary supplement Nutrition 0.000 claims 1
- 208000037765 diseases and disorders Diseases 0.000 claims 1
- 229960003530 donepezil Drugs 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 230000001747 exhibiting effect Effects 0.000 claims 1
- 229960003980 galantamine Drugs 0.000 claims 1
- ASUTZQLVASHGKV-UHFFFAOYSA-N galanthamine hydrochloride Natural products O1C(=C23)C(OC)=CC=C2CN(C)CCC23C1CC(O)C=C2 ASUTZQLVASHGKV-UHFFFAOYSA-N 0.000 claims 1
- 239000003540 gamma secretase inhibitor Substances 0.000 claims 1
- 230000000977 initiatory effect Effects 0.000 claims 1
- 238000011835 investigation Methods 0.000 claims 1
- BUGYDGFZZOZRHP-UHFFFAOYSA-N memantine Chemical compound C1C(C2)CC3(C)CC1(C)CC2(N)C3 BUGYDGFZZOZRHP-UHFFFAOYSA-N 0.000 claims 1
- 229960004640 memantine Drugs 0.000 claims 1
- 239000002207 metabolite Substances 0.000 claims 1
- 239000002184 metal Substances 0.000 claims 1
- 238000012544 monitoring process Methods 0.000 claims 1
- 239000002858 neurotransmitter agent Substances 0.000 claims 1
- 229960003512 nicotinic acid Drugs 0.000 claims 1
- 235000001968 nicotinic acid Nutrition 0.000 claims 1
- 239000011664 nicotinic acid Substances 0.000 claims 1
- 239000002773 nucleotide Substances 0.000 claims 1
- 125000003729 nucleotide group Chemical group 0.000 claims 1
- 238000001050 pharmacotherapy Methods 0.000 claims 1
- RMHMFHUVIITRHF-UHFFFAOYSA-N pirenzepine Chemical compound C1CN(C)CCN1CC(=O)N1C2=NC=CC=C2NC(=O)C2=CC=CC=C21 RMHMFHUVIITRHF-UHFFFAOYSA-N 0.000 claims 1
- 229960004633 pirenzepine Drugs 0.000 claims 1
- MGNVWUDMMXZUDI-UHFFFAOYSA-N propane-1,3-disulfonic acid Chemical compound OS(=O)(=O)CCCS(O)(=O)=O MGNVWUDMMXZUDI-UHFFFAOYSA-N 0.000 claims 1
- 230000004043 responsiveness Effects 0.000 claims 1
- 229960004136 rivastigmine Drugs 0.000 claims 1
- 229960001685 tacrine Drugs 0.000 claims 1
- YLJREFDVOIBQDA-UHFFFAOYSA-N tacrine Chemical group C1=CC=C2C(N)=C(CCCC3)C3=NC2=C1 YLJREFDVOIBQDA-UHFFFAOYSA-N 0.000 claims 1
- 102000013498 tau Proteins Human genes 0.000 claims 1
- 108010026424 tau Proteins Proteins 0.000 claims 1
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05027092.5 | 2005-12-12 | ||
| EP05027092 | 2005-12-12 | ||
| EP06014729.5 | 2006-07-14 | ||
| EP06014729 | 2006-07-14 | ||
| EP06020766 | 2006-10-02 | ||
| EP06020766.9 | 2006-10-02 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013216451A Division JP2014039561A (ja) | 2005-12-12 | 2013-10-17 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017069675A Division JP2017153480A (ja) | 2005-12-12 | 2017-03-31 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016104026A JP2016104026A (ja) | 2016-06-09 |
| JP2016104026A5 true JP2016104026A5 (cg-RX-API-DMAC7.html) | 2016-08-18 |
| JP6174727B2 JP6174727B2 (ja) | 2017-08-02 |
Family
ID=37896141
Family Applications (5)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008544834A Active JP5419131B2 (ja) | 2005-12-12 | 2006-12-08 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
| JP2010039568A Withdrawn JP2010187674A (ja) | 2005-12-12 | 2010-02-25 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
| JP2013216451A Withdrawn JP2014039561A (ja) | 2005-12-12 | 2013-10-17 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
| JP2016004910A Active JP6174727B2 (ja) | 2005-12-12 | 2016-01-14 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
| JP2017069675A Ceased JP2017153480A (ja) | 2005-12-12 | 2017-03-31 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
Family Applications Before (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2008544834A Active JP5419131B2 (ja) | 2005-12-12 | 2006-12-08 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
| JP2010039568A Withdrawn JP2010187674A (ja) | 2005-12-12 | 2010-02-25 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
| JP2013216451A Withdrawn JP2014039561A (ja) | 2005-12-12 | 2013-10-17 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017069675A Ceased JP2017153480A (ja) | 2005-12-12 | 2017-03-31 | 治療的特性を有するβ１〜４２特異的モノクローナル抗体 |
Country Status (31)
Families Citing this family (100)
| Publication number | Priority date | Publication date | Assignee | Title |
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| DE10303974A1 (de) | 2003-01-31 | 2004-08-05 | Abbott Gmbh & Co. Kg | Amyloid-β(1-42)-Oligomere, Verfahren zu deren Herstellung und deren Verwendung |
| US8663650B2 (en) | 2003-02-21 | 2014-03-04 | Ac Immune Sa | Methods and compositions comprising supramolecular constructs |
| WO2004092197A2 (en) * | 2003-04-07 | 2004-10-28 | The Regents Of The University Of California | Amyloid-specific peptides and uses thereof |
| RU2432362C2 (ru) † | 2005-11-30 | 2011-10-27 | Эбботт Лэборетриз | Моноклональные антитела и их применения |
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| ES2407429T3 (es) | 2005-12-12 | 2013-06-12 | Ac Immune S.A. | Vacuna terapéurica |
| KR101591223B1 (ko) | 2005-12-12 | 2016-02-04 | 에이씨 이뮨 에스.에이. | 치료적 특성을 갖는 베타 1-42 특이적인 단일클론성 항체 |
| US7959949B2 (en) | 2006-04-27 | 2011-06-14 | University Of Central Florida Research Foundation, Inc. | Functionalized nanoceria composition for ophthalmic treatment |
| SG173385A1 (en) * | 2006-07-14 | 2011-08-29 | Ac Immune S A Ch | Humanized antibody against amyloid beta |
| KR20180043854A (ko) * | 2006-07-14 | 2018-04-30 | 에이씨 이뮨 에스.에이. | 아밀로이드 베타에 대해 인간화된 항체 |
| EP3988566A1 (en) * | 2006-07-14 | 2022-04-27 | AC Immune SA | Humanized antibody against amyloid beta |
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| US8455626B2 (en) | 2006-11-30 | 2013-06-04 | Abbott Laboratories | Aβ conformer selective anti-aβ globulomer monoclonal antibodies |
| SI2436696T1 (sl) | 2007-01-05 | 2017-10-30 | University Of Zurich | Anti-beta-amiloidno protitelo in načini njegove uporabe |
| HRP20140049T1 (hr) | 2007-01-05 | 2014-02-28 | University Of Zürich | Anti beta-amiloid antitijela i njihova upotreba |
| WO2008084402A2 (en) | 2007-01-11 | 2008-07-17 | Philipps-Universitaet Marburg | Diagnosis and treatment of alzheimer's and other neurodementing diseases |
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| US9656991B2 (en) | 2007-04-18 | 2017-05-23 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
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| AU2015200604B2 (en) * | 2007-10-05 | 2016-10-27 | Ac Immune S.A. | Use of anti-amyloid beta antibody in ocular diseases |
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| JO3076B1 (ar) | 2007-10-17 | 2017-03-15 | Janssen Alzheimer Immunotherap | نظم العلاج المناعي المعتمد على حالة apoe |
| WO2009104736A1 (ja) * | 2008-02-22 | 2009-08-27 | 財団法人ヒューマンサイエンス振興財団 | 組織アミロイドプラーク親和性抗体及びそれを用いた医薬組成物 |
| WO2009132277A1 (en) * | 2008-04-25 | 2009-10-29 | The Board Of Regents Of The University Of Oklahoma | Inhibition of neovascularization by cerium oxide nanoparticles |
| US8916199B1 (en) | 2008-04-25 | 2014-12-23 | University of Central Florida Research Foundation, Ind. | Inhibition of angiogenesis associated with ovarian cancer by nanoparticles of cerium oxide |
| AT509611B1 (de) * | 2008-06-12 | 2012-04-15 | Affiris Forschungs-Und Entwicklungs Gmbh | Vakzin |
| CA2730073A1 (en) * | 2008-07-09 | 2010-01-14 | University Of Zurich | Method of promoting neurogenesis |
| US9127202B1 (en) | 2008-07-18 | 2015-09-08 | University Of Central Florida Research Foundation, Inc. | Biocompatible nano rare earth oxide upconverters for imaging and therapeutics |
| EA028427B1 (ru) | 2008-07-21 | 2017-11-30 | Пробиодруг Аг | АНТИТЕЛО, СВЯЗЫВАЮЩЕЕСЯ С Aβ-ПЕПТИДАМИ ИЛИ ИХ ВАРИАНТАМИ, КОМПОЗИЦИЯ, СОДЕРЖАЩАЯ ЭТО АНТИТЕЛО, И ЕГО ПРИМЕНЕНИЕ |
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