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公开(公告)号:EP4374877A3
公开(公告)日:2024-07-17
申请号:EP24161259.7
申请日:2015-09-11
发明人: Ohtake, Yoshihito , Okamoto, Naoki , Ono, Yoshiyuki , Kashiwagi, Hirotaka , Kimbara, Atsushi , Harada, Takeo , Hori, Nobuyuki , Murata, Yoshihisa , Tachibana, Kazutaka , Tanaka, Shota , Nomura, Kenichi , Ide, Mitsuaki , Mizuguchi, Eisaku , Ichida, Yasuhiro , Ohtomo, Shuichi , Horiba, Naoshi
IPC分类号: A61K31/50 , A61K31/19 , A61K31/4545 , A61K31/501 , A61K31/5025 , A61K31/503 , A61K31/506 , A61K31/537 , A61K31/5377 , A61K31/734 , A61K33/08 , A61K33/10 , A61K33/24 , A61K33/26 , A61K45/00 , A61P3/12 , A61P5/18 , A61P9/10 , A61P13/12 , A61P43/00
CPC分类号: C07D403/12 , C07D405/14 , C07D413/14 , A61K45/00 , A61K31/19 , A61K31/4545 , A61K31/50 , A61K31/501 , A61K31/5025 , A61K31/503 , A61K31/506 , A61K31/537 , A61K31/5377 , A61K31/734 , A61K33/08 , A61K33/10 , A61K33/24 , A61K33/26 , C07D401/06 , C07D401/12 , C07D237/04 , C07D403/14 , C07D471/04 , C07D487/04 , C07D487/08 , C07D498/08 , A61K33/244 , A61K45/06 , A61K31/24 , A61P13/12
摘要: The present invention provides a pharmaceutical composition containing, as an active ingredient, a dihydropyridazine-3,5-dione derivative or a salt thereof or a solvate of these, wherein the composition is administered in combination with a phosphorus adsorbent.
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公开(公告)号:EP4397663A1
公开(公告)日:2024-07-10
申请号:EP22864569.3
申请日:2022-08-30
申请人: Japan Tobacco, Inc.
发明人: OHBA, Yusuke , ADACHI, Kaoru , NISHIMARU, Tatsuya , SAKURAI, Kentaro , OGOSHI, Yosuke , SATO, Shimpei
IPC分类号: C07D487/04 , A61K31/519 , A61K31/5355 , A61K31/5377 , A61K31/5386 , A61K31/541 , A61K31/55 , A61K31/551 , A61K31/553 , A61P1/00 , A61P1/04 , A61P1/16 , A61P3/00 , A61P9/00 , A61P9/10 , A61P13/12 , A61P17/00 , A61P19/02 , A61P19/06 , A61P25/00 , A61P25/28
CPC分类号: A61K31/519 , A61K31/5355 , A61K31/5377 , A61K31/5386 , A61K31/541 , A61K31/55 , A61K31/551 , A61K31/553 , A61P1/00 , A61P1/04 , A61P1/16 , A61P3/00 , A61P9/00 , A61P9/10 , A61P13/12 , A61P17/00 , A61P19/02 , A61P19/06 , A61P21/02 , A61P25/00 , A61P25/16 , A61P25/28 , A61P27/04 , A61P29/00 , A61P37/02 , A61P37/04 , A61P37/06 , A61P37/08 , A61P43/00 , C07D487/04 , C07D519/00
摘要: A 6-aminopyrazolopyrimidine compound, or a pharmaceutically acceptable salt thereof, having NLRP3 inflammasome inhibitory activity, a pharmaceutical composition comprising the same, and their medical use, etc., are provided.
A compound of Formula [IA]:
or a pharmaceutically acceptable salt thereof,
wherein a partial structure:
is a structure of the following formula:
etc.
wherein R4 is hydrogen or C1-4 alkyl, in which the alkyl may be optionally substituted with hydroxy or cyano,
Ring group CyA is a group of the following formula:
etc.
wherein R6 and R7 are, each independently, hydrogen, hydroxy, cyano, C1-6 alkyl, etc., R8 and R9 are, each independently, hydrogen, C1-4 alkyl, or C1-4 haloalkyl, R10 is hydrogen, cyano, C1-6 alkyl, etc.),
R1 is hydrogen or C1-4 alkyl,
R2A and R3A are, each independently, hydrogen, C1-6 alkyl etc., alternatively, R2A and R3A may combine together with the nitrogen atom to which they attach and the -NR2AR3A group may form a 4- to 7-membered optionally-substituted heterocycloalkyl, etc.-
公开(公告)号:EP4397314A1
公开(公告)日:2024-07-10
申请号:EP24159638.6
申请日:2013-10-22
发明人: WILSON, Travis D. , SABBAH, Hani N
CPC分类号: A61K38/06 , A61P1/02 , A61P25/30 , A61P25/32 , A61P29/00 , A61P31/12 , A61P43/00 , A61P5/14 , A61P7/10 , A61P9/00 , A61P9/04 , A61P9/10 , A61P9/12
摘要: The disclosure provides methods of preventing or treating heart failure in a mammalian subject, reducing risk factors associated with heart failure, and/or reducing the likelihood or severity of heart failure. The disclosure also provides methods of preventing, or treating LV remodeling in a mammalian subject, and/or reducing the likelihood or severity of LV remodeling. The methods comprise administering to the subject an effective amount of an aromatic-cationic peptide. In some embodiments, the methods comprise administering to the subject an effective amount of an aromatic cationic peptide to reduce levels of C-reactive protein, tumor necrosis factor alpha, interleukin 6, reactive oxygen species, Nt-pro BNP, and/or cardiac troponin I, and/or reduce expression levels of MLCL AT1 and/or ALCAT 1 in subjects in need thereof. In some embodiments, the methods comprise administering to the subject an effective amount of an aromatic cationic peptide to increase expression of Taz1 and/or increase mK ATP activity in subjects in need thereof.
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24.
公开(公告)号:EP4392559A1
公开(公告)日:2024-07-03
申请号:EP22859731.6
申请日:2022-08-22
发明人: STEWART, Duncan , COURTMAN, David
IPC分类号: C12N15/113 , A61K35/12 , A61K38/44 , A61K48/00 , A61P9/00 , A61P9/10 , C12N9/02 , C12N15/10 , C12N15/53 , C12N15/85
CPC分类号: A61P9/00 , A61P9/10 , C12N15/85 , C12N9/0075 , C12Y114/13039 , C12N2830/00820130101 , C12N2830/00220130101 , A61K48/005 , A61K48/0058 , C12N2830/1520130101
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公开(公告)号:EP4382111A1
公开(公告)日:2024-06-12
申请号:EP22386089.1
申请日:2022-12-09
IPC分类号: A61K35/545 , A61P9/00 , A61K35/12 , A61K35/44 , A61L27/54 , A61P9/10 , A61P9/12 , A61P11/00 , A61P17/02 , B01D15/34
CPC分类号: A61K35/12 , A61K35/44 , A61K35/545 , A61L27/54 , B01D15/34 , A61P9/00 , A61P9/10 , A61P17/02 , A61P11/00 , A61P9/12 , A61L31/16 , A61L2300/62620130101 , A61L2300/6420130101
摘要: The present disclosure relates to extracellular vesicles (EVs) (and their contents) from a pluripotent stem-cell derived endothelial cell product (ECP); as well as their isolation; uses and methods employing the EVs in therapy, such as in promoting angiogenesis and/or neovascularisation.
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27.
公开(公告)号:EP3689344B1
公开(公告)日:2024-06-05
申请号:EP19218071.9
申请日:2016-04-13
IPC分类号: A61K31/277 , A61K9/08 , A61K9/00 , A61P25/06 , A61P9/00 , A61P9/06 , A61P9/10 , C07C255/42 , A61K47/20 , A61K47/18 , A61K47/12
CPC分类号: A61K9/08 , C07C255/42 , A61K9/0043 , A61K47/12 , A61K47/183 , A61K47/20 , A61K31/277 , A61P9/10 , A61P9/06 , A61P25/06
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公开(公告)号:EP4374914A1
公开(公告)日:2024-05-29
申请号:EP22845958.2
申请日:2022-07-20
申请人: Kyoto University
发明人: EIRAKU, Mototsugu
IPC分类号: A61P9/10 , A61P27/02 , C12M3/00 , C12N5/07 , C12N5/0735 , C12N5/10 , A61K35/30 , A61L27/38 , A61L27/40 , C07K14/78
CPC分类号: A61K35/30 , A61L27/38 , A61L27/40 , A61P9/10 , A61P27/02 , C07K14/78 , C12M3/00 , C12N5/06 , C12N5/10
摘要: The present disclosure includes a method of producing a retinal tissue, comprising inducing differentiation of pluripotent stem cells into a retinal tissue on a surface of a culture substrate, wherein the culture substrate comprises a region A and a region B on the surface, the differentiation is induced is the region A, the region A has cell adhesiveness, and the region B is adjacent to at least a part of the region A and has cell adhesiveness lower than the cell adhesiveness of the region A; a retinal tissue produced by the method; and a composition comprising the retinal tissue.
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29.
公开(公告)号:EP4331607A3
公开(公告)日:2024-05-29
申请号:EP23214939.3
申请日:2016-12-01
发明人: FURUTA, Shouji , MUKAI, Hironori
IPC分类号: A61K31/4965 , A61K9/16 , A61K9/20 , A61P7/02 , A61P9/10 , A61P9/12 , A61P11/00 , A61P13/12 , A61P11/06
CPC分类号: A61K9/1623 , A61K9/2018 , A61P9/10 , A61P11/00 , A61P7/02 , A61P13/12 , A61P11/06 , A61K9/1611 , A61K9/2059 , A61K31/4965 , A61P9/12 , A61K9/1652 , A61K9/2054 , A61K9/2013
摘要: A stabilized solid preparation containing 2-{4-[N-(5,6-diphenylpyrazin-2-yl)-N-isopropylamino]butylo xy}-N-(methylsulfonyl)acetamide is provided.
A solid preparation containing 2-{4-[N-(5,6-diphenylpyrazin-2-yl)-N-isopropylamino]butylo xy}-N-(methylsulfonyl)acetamide and D-mannitol having a specific surface area of 1.0 m2/g or less.-
30.
公开(公告)号:EP4342546A3
公开(公告)日:2024-05-22
申请号:EP24152348.9
申请日:2013-06-28
发明人: SONI, Paresh
IPC分类号: A61K31/232 , A61K31/397 , A61K45/06 , A61P9/10 , A61P9/00 , A61P3/04 , A61P3/06 , A61P9/04 , A61P9/06 , A61P43/00
CPC分类号: A61K31/397 , A61K31/232 , A61P3/04 , A61P3/06 , A61P43/00 , A61P9/00 , A61P9/04 , A61P9/06 , A61P9/10
摘要: In various embodiments, the present invention provides pharmaceutical compositions for use in methods of reducing a risk of a cardiovascular event in a subject on statin therapy and, in particular, a method of reducing the risk of a cardiovascular event in a subject on statin therapy having a fasting baseline triglyceride level of about 135 mg/dL to about 500 mg/dL, and administering to the subject a pharmaceutical composition comprising about 4 g of eicosapentaenoic acid ethyl ester per day.
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