JP2014506583A5 - - Google Patents
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- JP2014506583A5 JP2014506583A5 JP2013554652A JP2013554652A JP2014506583A5 JP 2014506583 A5 JP2014506583 A5 JP 2014506583A5 JP 2013554652 A JP2013554652 A JP 2013554652A JP 2013554652 A JP2013554652 A JP 2013554652A JP 2014506583 A5 JP2014506583 A5 JP 2014506583A5
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- JP
- Japan
- Prior art keywords
- pharmaceutical composition
- receptor modulator
- composition according
- neurotransmitter
- immunomodulator
- 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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- 229940075993 receptor modulator Drugs 0.000 claims description 67
- 102000004108 Neurotransmitter Receptors Human genes 0.000 claims description 49
- 108090000590 Neurotransmitter Receptors Proteins 0.000 claims description 49
- 238000000034 method Methods 0.000 claims description 35
- 208000016192 Demyelinating disease Diseases 0.000 claims description 31
- 239000002955 immunomodulating agent Substances 0.000 claims description 28
- 229940121354 immunomodulator Drugs 0.000 claims description 28
- 230000002584 immunomodulator Effects 0.000 claims description 28
- 150000003839 salts Chemical class 0.000 claims description 22
- 229960001081 benzatropine Drugs 0.000 claims description 16
- GIJXKZJWITVLHI-PMOLBWCYSA-N benzatropine Chemical group O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(C=1C=CC=CC=1)C1=CC=CC=C1 GIJXKZJWITVLHI-PMOLBWCYSA-N 0.000 claims description 16
- NDAUXUAQIAJITI-UHFFFAOYSA-N albuterol Chemical compound CC(C)(C)NCC(O)C1=CC=C(O)C(CO)=C1 NDAUXUAQIAJITI-UHFFFAOYSA-N 0.000 claims description 12
- 229960002052 salbutamol Drugs 0.000 claims description 12
- 102000003840 Opioid Receptors Human genes 0.000 claims description 10
- 108090000137 Opioid Receptors Proteins 0.000 claims description 10
- 230000001919 adrenal effect Effects 0.000 claims description 10
- 102000012740 beta Adrenergic Receptors Human genes 0.000 claims description 10
- 108010079452 beta Adrenergic Receptors Proteins 0.000 claims description 10
- YNNUSGIPVFPVBX-NHCUHLMSSA-N clemastine Chemical compound CN1CCC[C@@H]1CCO[C@@](C)(C=1C=CC(Cl)=CC=1)C1=CC=CC=C1 YNNUSGIPVFPVBX-NHCUHLMSSA-N 0.000 claims description 10
- 229960002881 clemastine Drugs 0.000 claims description 10
- 150000001875 compounds Chemical class 0.000 claims description 10
- 229960000556 fingolimod Drugs 0.000 claims description 10
- KKGQTZUTZRNORY-UHFFFAOYSA-N fingolimod Chemical compound CCCCCCCCC1=CC=C(CCC(N)(CO)CO)C=C1 KKGQTZUTZRNORY-UHFFFAOYSA-N 0.000 claims description 10
- 230000002757 inflammatory effect Effects 0.000 claims description 10
- 201000006417 multiple sclerosis Diseases 0.000 claims description 10
- 229940121891 Dopamine receptor antagonist Drugs 0.000 claims description 8
- 229940122236 Histamine receptor antagonist Drugs 0.000 claims description 8
- 229940121948 Muscarinic receptor antagonist Drugs 0.000 claims description 8
- GIIZNNXWQWCKIB-UHFFFAOYSA-N Serevent Chemical compound C1=C(O)C(CO)=CC(C(O)CNCCCCCCOCCCCC=2C=CC=CC=2)=C1 GIIZNNXWQWCKIB-UHFFFAOYSA-N 0.000 claims description 8
- 239000000739 antihistaminic agent Substances 0.000 claims description 8
- 239000003210 dopamine receptor blocking agent Substances 0.000 claims description 8
- 230000002519 immonomodulatory effect Effects 0.000 claims description 8
- 239000003149 muscarinic antagonist Substances 0.000 claims description 8
- 229960004017 salmeterol Drugs 0.000 claims description 8
- 239000000126 substance Substances 0.000 claims description 8
- 229960002324 trifluoperazine Drugs 0.000 claims description 8
- ZEWQUBUPAILYHI-UHFFFAOYSA-N trifluoperazine Chemical compound C1CN(C)CCN1CCCN1C2=CC(C(F)(F)F)=CC=C2SC2=CC=CC=C21 ZEWQUBUPAILYHI-UHFFFAOYSA-N 0.000 claims description 8
- 239000000674 adrenergic antagonist Substances 0.000 claims description 6
- 201000001119 neuropathy Diseases 0.000 claims description 6
- 230000007823 neuropathy Effects 0.000 claims description 6
- 208000033808 peripheral neuropathy Diseases 0.000 claims description 6
- 238000011287 therapeutic dose Methods 0.000 claims description 6
- 208000010693 Charcot-Marie-Tooth Disease Diseases 0.000 claims description 5
- 206010012305 Demyelination Diseases 0.000 claims description 5
- 108010072051 Glatiramer Acetate Proteins 0.000 claims description 5
- 208000035895 Guillain-Barré syndrome Diseases 0.000 claims description 5
- 241000598436 Human T-cell lymphotropic virus Species 0.000 claims description 5
- 108010005716 Interferon beta-1a Proteins 0.000 claims description 5
- 108010005714 Interferon beta-1b Proteins 0.000 claims description 5
- 206010049567 Miller Fisher syndrome Diseases 0.000 claims description 5
- 206010028570 Myelopathy Diseases 0.000 claims description 5
- 208000003435 Optic Neuritis Diseases 0.000 claims description 5
- 206010036105 Polyneuropathy Diseases 0.000 claims description 5
- FHEAIOHRHQGZPC-KIWGSFCNSA-N acetic acid;(2s)-2-amino-3-(4-hydroxyphenyl)propanoic acid;(2s)-2-aminopentanedioic acid;(2s)-2-aminopropanoic acid;(2s)-2,6-diaminohexanoic acid Chemical compound CC(O)=O.C[C@H](N)C(O)=O.NCCCC[C@H](N)C(O)=O.OC(=O)[C@@H](N)CCC(O)=O.OC(=O)[C@@H](N)CC1=CC=C(O)C=C1 FHEAIOHRHQGZPC-KIWGSFCNSA-N 0.000 claims description 5
- 208000002552 acute disseminated encephalomyelitis Diseases 0.000 claims description 5
- 201000004339 autoimmune neuropathy Diseases 0.000 claims description 5
- 201000005011 autoimmune peripheral neuropathy Diseases 0.000 claims description 5
- 230000001684 chronic effect Effects 0.000 claims description 5
- 201000010099 disease Diseases 0.000 claims description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 5
- 229960003776 glatiramer acetate Drugs 0.000 claims description 5
- 229960004461 interferon beta-1a Drugs 0.000 claims description 5
- 229960003161 interferon beta-1b Drugs 0.000 claims description 5
- 208000036546 leukodystrophy Diseases 0.000 claims description 5
- 229960001156 mitoxantrone Drugs 0.000 claims description 5
- KKZJGLLVHKMTCM-UHFFFAOYSA-N mitoxantrone Chemical compound O=C1C2=C(O)C=CC(O)=C2C(=O)C2=C1C(NCCNCCO)=CC=C2NCCNCCO KKZJGLLVHKMTCM-UHFFFAOYSA-N 0.000 claims description 5
- 229960005027 natalizumab Drugs 0.000 claims description 5
- 230000007824 polyneuropathy Effects 0.000 claims description 5
- 206010036807 progressive multifocal leukoencephalopathy Diseases 0.000 claims description 5
- 208000009174 transverse myelitis Diseases 0.000 claims description 5
- 210000004885 white matter Anatomy 0.000 claims description 5
- CFJMRBQWBDQYMK-UHFFFAOYSA-N 1-phenyl-1-cyclopentanecarboxylic acid 2-[2-(diethylamino)ethoxy]ethyl ester Chemical compound C=1C=CC=CC=1C1(C(=O)OCCOCCN(CC)CC)CCCC1 CFJMRBQWBDQYMK-UHFFFAOYSA-N 0.000 claims description 4
- 230000002708 enhancing effect Effects 0.000 claims description 4
- 208000014188 hereditary optic neuropathy Diseases 0.000 claims description 4
- 229960003436 pentoxyverine Drugs 0.000 claims description 4
- 230000001225 therapeutic effect Effects 0.000 claims description 4
- 230000023105 myelination Effects 0.000 claims description 3
- 230000001537 neural effect Effects 0.000 claims description 3
- 230000004936 stimulating effect Effects 0.000 claims description 3
- RAQPOZGWANIDQT-UHFFFAOYSA-N 1-[2-(benzhydryloxy)ethyl]-4-(3-phenylpropyl)piperazine Chemical compound C=1C=CC=CC=1CCCN(CC1)CCN1CCOC(C=1C=CC=CC=1)C1=CC=CC=C1 RAQPOZGWANIDQT-UHFFFAOYSA-N 0.000 claims description 2
- KQWVAUSXZDRQPZ-UMTXDNHDSA-N 4-[(R)-[(2S,5R)-2,5-dimethyl-4-prop-2-enyl-1-piperazinyl]-(3-methoxyphenyl)methyl]-N,N-diethylbenzamide Chemical compound C1=CC(C(=O)N(CC)CC)=CC=C1[C@H](C=1C=C(OC)C=CC=1)N1[C@@H](C)CN(CC=C)[C@H](C)C1 KQWVAUSXZDRQPZ-UMTXDNHDSA-N 0.000 claims description 2
- 229930003347 Atropine Natural products 0.000 claims description 2
- 102000015554 Dopamine receptor Human genes 0.000 claims description 2
- 108050004812 Dopamine receptor Proteins 0.000 claims description 2
- 102000000543 Histamine Receptors Human genes 0.000 claims description 2
- 108010002059 Histamine Receptors Proteins 0.000 claims description 2
- RKUNBYITZUJHSG-UHFFFAOYSA-N Hyosciamin-hydrochlorid Natural products CN1C(C2)CCC1CC2OC(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-UHFFFAOYSA-N 0.000 claims description 2
- 102000014415 Muscarinic acetylcholine receptor Human genes 0.000 claims description 2
- 108050003473 Muscarinic acetylcholine receptor Proteins 0.000 claims description 2
- MGVRNMUKTZOQOW-UHFFFAOYSA-N N'-[2-(3,4-dichlorophenyl)ethyl]-N,N,N'-trimethylethane-1,2-diamine Chemical compound CN(C)CCN(C)CCC1=CC=C(Cl)C(Cl)=C1 MGVRNMUKTZOQOW-UHFFFAOYSA-N 0.000 claims description 2
- RKUNBYITZUJHSG-SPUOUPEWSA-N atropine Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)N2C)C(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-SPUOUPEWSA-N 0.000 claims description 2
- 229960000396 atropine Drugs 0.000 claims description 2
- OEXHQOGQTVQTAT-JRNQLAHRSA-N ipratropium Chemical compound O([C@H]1C[C@H]2CC[C@@H](C1)[N@@+]2(C)C(C)C)C(=O)C(CO)C1=CC=CC=C1 OEXHQOGQTVQTAT-JRNQLAHRSA-N 0.000 claims description 2
- 229960001888 ipratropium Drugs 0.000 claims description 2
- 229960002508 pindolol Drugs 0.000 claims description 2
- PHUTUTUABXHXLW-UHFFFAOYSA-N pindolol Chemical group CC(C)NCC(O)COC1=CC=CC2=NC=C[C]12 PHUTUTUABXHXLW-UHFFFAOYSA-N 0.000 claims description 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 37
- 238000007910 systemic administration Methods 0.000 claims 1
- 239000000203 mixture Substances 0.000 description 12
- 238000009472 formulation Methods 0.000 description 2
- 206010061323 Optic neuropathy Diseases 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 208000020911 optic nerve disease Diseases 0.000 description 1
- 210000000278 spinal cord Anatomy 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161444666P | 2011-02-18 | 2011-02-18 | |
| US61/444,666 | 2011-02-18 | ||
| PCT/US2012/025712 WO2012112933A1 (en) | 2011-02-18 | 2012-02-17 | Directed differentiation of oligodendrocyte precursor cells to a myelinating cell fate |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017026806A Division JP2017132769A (ja) | 2011-02-18 | 2017-02-16 | ミエリン形成細胞運命へのオリゴデンドロサイト前駆細胞の定方向分化 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2014506583A JP2014506583A (ja) | 2014-03-17 |
| JP2014506583A5 true JP2014506583A5 (enExample) | 2015-04-09 |
| JP6133790B2 JP6133790B2 (ja) | 2017-05-24 |
Family
ID=46672968
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2013554652A Expired - Fee Related JP6133790B2 (ja) | 2011-02-18 | 2012-02-17 | ミエリン形成細胞運命へのオリゴデンドロサイト前駆細胞の定方向分化 |
| JP2017026806A Pending JP2017132769A (ja) | 2011-02-18 | 2017-02-16 | ミエリン形成細胞運命へのオリゴデンドロサイト前駆細胞の定方向分化 |
| JP2019211952A Pending JP2020040981A (ja) | 2011-02-18 | 2019-11-25 | ミエリン形成細胞運命へのオリゴデンドロサイト前駆細胞の定方向分化 |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2017026806A Pending JP2017132769A (ja) | 2011-02-18 | 2017-02-16 | ミエリン形成細胞運命へのオリゴデンドロサイト前駆細胞の定方向分化 |
| JP2019211952A Pending JP2020040981A (ja) | 2011-02-18 | 2019-11-25 | ミエリン形成細胞運命へのオリゴデンドロサイト前駆細胞の定方向分化 |
Country Status (6)
| Country | Link |
|---|---|
| US (4) | US9592288B2 (enExample) |
| EP (2) | EP3502236B1 (enExample) |
| JP (3) | JP6133790B2 (enExample) |
| DK (1) | DK2675893T3 (enExample) |
| ES (1) | ES2716865T3 (enExample) |
| WO (1) | WO2012112933A1 (enExample) |
Families Citing this family (42)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP3502236B1 (en) | 2011-02-18 | 2023-08-23 | The Scripps Research Institute | Directed differentiation of oligodendrocyte precursor cells to a myelinating cell fate |
| JP2014528706A (ja) * | 2011-08-07 | 2014-10-30 | カディマステム リミテッド | 成熟、生存及びミエリン形成に作用する薬剤を同定する方法 |
| EP2724723A1 (en) * | 2012-10-25 | 2014-04-30 | Universitätsklinikum Hamburg-Eppendorf | Tegaserod for use in the treatment of nerve injuries |
| WO2014110154A1 (en) * | 2013-01-08 | 2014-07-17 | Pathologica Llc | Methods and comp0stions for treatment of demyelinating diseases |
| US10905663B2 (en) | 2013-03-05 | 2021-02-02 | The University Of Chicago | Treatment of demyelinating disorders |
| BR112015022896B1 (pt) * | 2013-03-15 | 2022-08-23 | Chongxi Yu | Composto de fármacos de alta penetração, composição farmacêutica e seus usos para o tratamento de doenças de parkinson |
| CA3042642A1 (en) | 2013-08-12 | 2015-02-19 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded immediate release abuse deterrent pill |
| GB201317363D0 (en) | 2013-10-01 | 2013-11-13 | Eisai Ltd | Novel compounds |
| WO2015095391A1 (en) | 2013-12-17 | 2015-06-25 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded extended release abuse deterrent pill |
| US9492444B2 (en) | 2013-12-17 | 2016-11-15 | Pharmaceutical Manufacturing Research Services, Inc. | Extruded extended release abuse deterrent pill |
| EP3082845B1 (en) * | 2013-12-20 | 2021-02-17 | University Of Manitoba | Methods and compositions for treatment of peripheral neuropathies |
| EP3169315B1 (en) | 2014-07-17 | 2020-06-24 | Pharmaceutical Manufacturing Research Services, Inc. | Immediate release abuse deterrent liquid fill dosage form |
| WO2016064873A1 (en) | 2014-10-20 | 2016-04-28 | Pharmaceutical Manufacturing Research Services, Inc. | Extended release abuse deterrent liquid fill dosage form |
| FR3029113A1 (fr) | 2014-12-02 | 2016-06-03 | Univ Paris-Sud | Composes pour le traitement des maladies mitochondriales |
| EP3118621A1 (en) * | 2015-07-14 | 2017-01-18 | Fundació Institut d'Investigació Biomèdica de Bellvitge (IDIBELL) | Methods and compositions for the diagnosis and for the treatment of adrenoleukodystrophy |
| PT3344248T (pt) * | 2015-09-02 | 2022-06-29 | Trevena Inc | Compostos moduladores do recetor opioide delta contendo aza-heterocíclicos de 6 membros, composições compreendendo os mesmos e seus usos |
| CN107286031B (zh) * | 2016-04-05 | 2019-08-09 | 上海医药工业研究院 | 2-二乙氨基-1-甲基乙基-7-环己基-7-氧庚酸酯的制备方法 |
| CA3043226A1 (en) * | 2016-11-14 | 2018-05-17 | Memorial Sloan-Kettering Cancer Center | Methods for drug discovery using stem cell-derived schwann cells |
| WO2018152293A1 (en) | 2017-02-17 | 2018-08-23 | Trevena, Inc. | 5-membered aza-heterocyclic containing delta-opioid receptor modulating compounds, methods of using and making the same |
| BR112019016775A2 (pt) | 2017-02-17 | 2020-03-31 | Trevena, Inc. | Compostos moduladores de receptor delta-opioide contendo aza-heterocíclico com 7 membros, métodos de uso e produção dos mesmos |
| SG11201909501TA (en) * | 2017-04-13 | 2019-11-28 | Univ Leland Stanford Junior | Personalized 3d neural culture system for generating human oligodendrocytes and studying myelination in vitro |
| US11478467B2 (en) * | 2017-05-04 | 2022-10-25 | Sreenivasarao Vepachedu | Targeted drug rescue with novel compositions, combinations, and methods thereof |
| EP3412294A1 (en) * | 2017-06-08 | 2018-12-12 | Universite De Fribourg | Hdac1/2 activator for promoting and/or accelerating myelination and/or remyelination |
| WO2019171333A1 (en) | 2018-03-08 | 2019-09-12 | Victoria Link Ltd | Treatment of demyelinating diseases |
| AU2018411573A1 (en) * | 2018-03-08 | 2020-10-01 | The Scripps Research Institute | Methods for promoting myelination and for treating demyelinating diseases |
| US20190336490A1 (en) * | 2018-04-05 | 2019-11-07 | Frequency Therapeutics, Inc. | Compositions and methods for increasing remyelination |
| EP3773535A4 (en) * | 2018-04-13 | 2022-01-05 | Mordechai Chevion | COMPOSITIONS AND METHODS OF TREATING DEMYELINIZATION |
| CN108624560B (zh) * | 2018-06-01 | 2022-04-08 | 南京艾尔普再生医学科技有限公司 | 一种分化培养基及少突胶质前体细胞的制备方法 |
| WO2019241744A1 (en) * | 2018-06-14 | 2019-12-19 | Curasen Therapeutics, Inc. | Methods for diagnosing, monitoring and treating neurological diseases and disorders |
| CN112770748A (zh) * | 2018-10-09 | 2021-05-07 | 美迪诺亚公司 | 异丁司特和干扰素-β的组合及其使用方法 |
| CN111317754B (zh) * | 2018-12-13 | 2022-02-18 | 泰州医药城国科化物生物医药科技有限公司 | 一种北豆根总碱的制备方法及应用 |
| CN109942592B (zh) * | 2019-05-09 | 2020-07-14 | 江西中医药大学 | 一种新原阿片碱型生物碱及其制备方法和应用 |
| EP3797769A1 (fr) * | 2019-09-25 | 2021-03-31 | Fontès, M. Michel | Composition a usage therapeutique |
| US11752149B2 (en) | 2019-12-02 | 2023-09-12 | Pipeline Therapeutics, Inc. | Muscarinic acetylcholine M1 receptor antagonists |
| US20230346746A1 (en) * | 2020-01-22 | 2023-11-02 | Technophage, Investigaçäo E Desenvolvimento Em Biotecnologia, S.A. | Eletriptan hydrobromide for treatment of spinal cord injury and improvement of locomotor function |
| US20230167406A1 (en) * | 2020-05-01 | 2023-06-01 | The Children's Medical Center Corporation | Compositions and methods of promoting myelination |
| CN117177755A (zh) * | 2021-05-21 | 2023-12-05 | 成都文鼎科技发展有限公司 | 一种调节神经病变的方法 |
| AU2023231903A1 (en) | 2022-03-11 | 2024-09-19 | Teijin Pharma Limited | Medicine containing vitamin d derivative or pharmaceutically acceptable salt or solvate thereof, used in combination with immunomodulatory substance |
| WO2023225206A1 (en) | 2022-05-18 | 2023-11-23 | The Scripps Research Institute | Method for enhancing remyelination via co-administration of muscarinic receptor antagonists and vitamin d analogues |
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| WO2025049588A1 (en) * | 2023-08-29 | 2025-03-06 | The Trustees Of Indiana University | Novel treatments for optic neuropathies and glaucoma |
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2012
- 2012-02-17 EP EP18208362.6A patent/EP3502236B1/en active Active
- 2012-02-17 EP EP12747134.0A patent/EP2675893B1/en active Active
- 2012-02-17 WO PCT/US2012/025712 patent/WO2012112933A1/en not_active Ceased
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- 2012-02-17 ES ES12747134T patent/ES2716865T3/es active Active
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