JP2016507546A5 - - Google Patents

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Publication number
JP2016507546A5
JP2016507546A5 JP2015556537A JP2015556537A JP2016507546A5 JP 2016507546 A5 JP2016507546 A5 JP 2016507546A5 JP 2015556537 A JP2015556537 A JP 2015556537A JP 2015556537 A JP2015556537 A JP 2015556537A JP 2016507546 A5 JP2016507546 A5 JP 2016507546A5
Authority
JP
Japan
Prior art keywords
methyl
dose
aminosulfonyl
thiazol
pyridinyl
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.)
Withdrawn
Application number
JP2015556537A
Other languages
English (en)
Japanese (ja)
Other versions
JP2016507546A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2014/052743 external-priority patent/WO2014124978A2/en
Publication of JP2016507546A publication Critical patent/JP2016507546A/ja
Publication of JP2016507546A5 publication Critical patent/JP2016507546A5/ja
Withdrawn legal-status Critical Current

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JP2015556537A 2013-02-12 2014-02-12 アルツハイマー病を治療する方法において使用するためのヘリカーゼ/プライマーゼ阻害剤 Withdrawn JP2016507546A (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP13154982 2013-02-12
EP13154982.6 2013-02-12
PCT/EP2014/052743 WO2014124978A2 (en) 2013-02-12 2014-02-12 Helicase-primase inhibitors for use in a method of treating alzheimer's disease

Publications (2)

Publication Number Publication Date
JP2016507546A JP2016507546A (ja) 2016-03-10
JP2016507546A5 true JP2016507546A5 (enExample) 2016-04-21

Family

ID=47709982

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2015556537A Withdrawn JP2016507546A (ja) 2013-02-12 2014-02-12 アルツハイマー病を治療する方法において使用するためのヘリカーゼ/プライマーゼ阻害剤

Country Status (16)

Country Link
US (1) US20150374676A1 (enExample)
EP (1) EP2956134A2 (enExample)
JP (1) JP2016507546A (enExample)
KR (1) KR20150119089A (enExample)
CN (1) CN105101963A (enExample)
AU (1) AU2014217962A1 (enExample)
BR (1) BR112015019220A2 (enExample)
CA (1) CA2898798A1 (enExample)
CL (1) CL2015002241A1 (enExample)
EA (1) EA201500836A1 (enExample)
IL (1) IL240459A0 (enExample)
MX (1) MX2015010339A (enExample)
PH (1) PH12015501762A1 (enExample)
SG (1) SG11201506153TA (enExample)
WO (1) WO2014124978A2 (enExample)
ZA (1) ZA201505243B (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2573085A1 (en) 2011-09-26 2013-03-27 AiCuris GmbH & Co. KG N-[5-(aminosulfonyl)-4methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl] acetamide mesylate monohydrate having a specific particle size distribution range and a specific surface area range
WO2018096177A1 (en) * 2016-11-28 2018-05-31 Aicuris Anti-Infective Cures Gmbh A maleate salt of the free base of n-[5-(aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-n-methyl-2-[4-(2-pyridinyl)-phenyl]-acetamide, pharmaceutical formulations, methods of manufacture and uses thereof for the treatment of herpes viruses
US11439608B2 (en) 2017-09-25 2022-09-13 Qun Lu Roles of modulators of intersectin-CDC42 signaling in Alzheimer's disease
TW202038947A (zh) * 2018-11-28 2020-11-01 德商創新分子有限責任公司 在與溶瘤病毒之組合療法中治療癌症的解旋酶引子酶抑制劑
WO2022108381A1 (ko) 2020-11-19 2022-05-27 주식회사 오에이티씨 디다노신을 포함하는 신경염증성 질환 예방 또는 치료용 조성물
JP2025530762A (ja) * 2022-08-29 2025-09-17 アセンブリー・バイオサイエンシーズ・インコーポレイテッド ヘルペスウイルス用医薬組成物

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DOP2000000109A (es) * 1999-12-23 2002-08-30 Gerald Kleymann Derivados de tiazolilamida
DE102005014248A1 (de) * 2005-03-30 2006-10-05 Aicuris Gmbh & Co. Kg Pharmazeutische Zubereitung von N-[5-(Aminosulfonyl)-4-methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl]acetamid
US8299059B2 (en) * 2009-10-30 2012-10-30 Eli Lilly And Company Crystalline compound and a process for its preparation
EP2573085A1 (en) * 2011-09-26 2013-03-27 AiCuris GmbH & Co. KG N-[5-(aminosulfonyl)-4methyl-1,3-thiazol-2-yl]-N-methyl-2-[4-(2-pyridinyl)phenyl] acetamide mesylate monohydrate having a specific particle size distribution range and a specific surface area range

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