-
公开(公告)号:US20220411413A1
公开(公告)日:2022-12-29
申请号:US17872680
申请日:2022-07-25
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Masami YAMADA , Shinkichi SUZUKI , Takahiro SUGIMOTO , Minoru NAKAMURA , Hiroki SAKAMOTO , Makoto KAMATA
IPC: C07D405/14 , C07D209/46 , C07D401/10 , C07D401/14 , C07D403/04 , C07D403/10 , C07D401/06 , C07D405/04 , A61K31/4035 , A61K31/4155 , A61K31/4439 , A61K31/13 , A61K31/325 , A61K31/445 , A61K31/55 , A61K31/045 , A61K31/4406
Abstract: The present invention provides a compound having a cholinergic muscarinic M1 receptor positive allosteric modulator activity and useful as an agent for the prophylaxis or treatment of Alzheimer's disease, schizophrenia, pain, sleep disorder, Parkinson's disease dementia, dementia with Lewy bodies, and the like.
The present invention relates to a compound represented by the formula (I) or a salt thereof. wherein each symbol is as described in the specification, or a salt thereof.-
公开(公告)号:US20220409734A1
公开(公告)日:2022-12-29
申请号:US17610391
申请日:2020-05-08
Applicant: Yutaka NISHIMOTO , Yumiko ISHII , TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Dylan Bradley ENGLAND , Steve P. LANGSTON , Hong Myung LEE , Liting MA , Zhan SHI , Stepan VYSKOCIL , Jianing WANG , He XU , Yutaka NISHIMOTO , Yumiko ISHII
Abstract: The present disclosure provides antibody drug conjugates comprising STING modulators. Also provided are compositions comprising the antibody drug conjugates. The compounds and compositions are useful for stimulating an immune response in a subject in need thereof. Formula (I):
-
公开(公告)号:US20220401443A1
公开(公告)日:2022-12-22
申请号:US17866203
申请日:2022-07-15
Inventor: Vijaykumar Reddy RAJASEKHAR , Brendan Mark JOHNSON , David B. MACLEAN , Lynn SEELY , Paul N. MUDD, JR.
IPC: A61K31/501 , A61P35/00 , A61K31/513 , A61K9/00 , A61K31/4166
Abstract: Methods for treating prostate cancer, including advanced prostate cancer, in a subject in need thereof, include administering once-daily to the subject, at least 80 mg of N-(4-(1-(2,6-difluorobenzyl)-5-((dimethylamino)methyl)-3-(6-methoxy-3-pyridazinyl)-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidin-6-yl)phenyl)-N′-methoxyurea, or a corresponding amount of a pharmaceutically acceptable salt thereof. Another method includes: administering once-daily to the subject in need thereof, an oral load dose formulation having from 240 mg to 480 mg of N-(4-(1-(2,6-difluorobenzyl)-5-((dimethylamino)methyl)-3-(6-methoxy-3-pyridazinyl)-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidin-6-yl)phenyl)-N′-methoxyurea, or a corresponding amount of a pharmaceutically acceptable salt thereof; and thereafter administering once-daily to the subject, an oral maintenance dose formulation having 80 mg to 160 mg of N-(4-(1-(2,6-difluorobenzyl)-5-((dimethylamino)methyl)-3-(6-methoxy-3-pyridazinyl)-2,4-dioxo-1,2,3,4-tetrahydrothieno[2,3-d]pyrimidin-6-yl)phenyl)-N′-methoxyurea, or a corresponding amount of a pharmaceutically acceptable salt thereof.
-
公开(公告)号:US11524957B2
公开(公告)日:2022-12-13
申请号:US17044366
申请日:2019-04-01
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Lei Zhu , John Daniel Bailey , Landon Durak , Joshua David Waetzig , Masahiro Mizuno , Kazuhiro Maeda , Tsuneo Yasuma , Hiroshi Yamaguchi , Koichiro Fukuoka , Kazuyuki Akiyama
IPC: C07D453/02 , C07D409/04
Abstract: The present invention provides processes and synthetic intermediates for the synthesis of 2-[(2S)-1-azabicyclo[2.2.2]oct-2-yl]-6-(3-methyl-1H-pyrazol-4-yl)thieno[3,2-d]pyrimidin-4 {3H)-one or a salt, hydrate, or tautomer thereof, or any combination thereof, which are Cdc7 kinase inhibitors, and are useful for the treatment of disorders of cell proliferation, particularly cancer, and other disorders associated with Cdc7 activity.
-
公开(公告)号:US20220331303A1
公开(公告)日:2022-10-20
申请号:US17642337
申请日:2020-09-12
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Deborah HARTMAN , Rebecca EVANS , Helene FAESSEL , Robert RUBENS , Shinichiro TANAKA
IPC: A61K31/445 , A61P25/26 , A61K45/06
Abstract: Described herein are methyl 3-((methylsulfonyl)amino)-2-(((4-phenylcyclohexyl)oxy)methyl)-piperidine-1-carboxylate (Compound (I)), compositions comprising Compound (I), and the use of Compound (I) for the treatment of excessive sleepiness in a subject in need thereof.
-
公开(公告)号:US20220323443A1
公开(公告)日:2022-10-13
申请号:US17627857
申请日:2020-07-17
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Akihiro Ohashi , Kenichi Iwai , Tadahiro Nambu , Jie Yu , Kurt Eng , Michael Joseph Kuranda , Kazuho Nishimura , Cong Li
IPC: A61K31/519 , A61K31/555 , A61K45/06 , A61P35/00
Abstract: The present disclosure relates to the treatment of cancer using a combination therapy comprising Compound 1 and/or tautomers thereof or a pharmaceutically acceptable salt or hydrate thereof, and a second therapy.
-
公开(公告)号:US20220313733A1
公开(公告)日:2022-10-06
申请号:US17618080
申请日:2020-06-10
Applicant: Kyoto University , Takeda Pharmaceutical Company Limited
Inventor: Makoto IKEYA , Daisuke KAMIYA
IPC: A61K35/12 , C12N5/0797 , C12N5/071
Abstract: A method for producing renal stromal cells, comprising a step (3) of culturing renal stromal precursors in a medium comprising a platelet derived growth factor receptor agonist to obtain renal stromal cells is provided as a technique for supplying renal stromal cells. This production method can further comprise a step (2) of inducing renal stromal precursors from neural crest cells, and a step (1) of culturing pluripotent stem cells in a medium comprising a GSK3β inhibitor, a TGFβ inhibitor, and retinoic acid and/or a derivative thereof to induce neural crest cells.
-
公开(公告)号:US11458477B2
公开(公告)日:2022-10-04
申请号:US17102509
申请日:2020-11-24
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Daniel J. Sexton , Ryan Faucette
IPC: B01L3/00 , A61B5/15 , A61B5/154 , C07K16/40 , G01N33/564 , G01N33/573 , G01N33/96
Abstract: Disclosed herein are evacuated blood collection tubes comprising protease inhibitor cocktails in liquid form and uses thereof for assessing features associated with the contact system in a subject, including the endogenous level of contact system activation, the endogenous level of a drug that targets a component of contact system during treatment, and/or the immunogenicity of such a drug.
-
公开(公告)号:US20220288042A1
公开(公告)日:2022-09-15
申请号:US17829439
申请日:2022-06-01
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Emil Chuang
IPC: A61K31/438 , A61P1/14
Abstract: Provided herein is a method of treating or alleviating one or more symptoms of a disorder, disease, or condition mediated by a dopamine D2 or D3 receptor with 3-((1-cyclohexyl-4-oxo-8-(4-oxo-4-phenylbutyl)-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoic acid or a pharmaceutically acceptable salt thereof. Also provided herein is a method of increasing the scrum prolactin level with 3-((1-cyclohexyl-4-oxo-8-(4-oxo-4-phenylbutyl)-1,3,8-triazaspiro[4.5]decan-3-yl)methyl)benzoic acid or a pharmaceutically acceptable salt thereof.
-
公开(公告)号:US20220251576A1
公开(公告)日:2022-08-11
申请号:US17622580
申请日:2020-06-25
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Naoyuki MURATA , Sayan CHUANOI , Shigeo YANAI
Abstract: A novel means for safely and efficiently introducing a target substance such as nucleic acid, protein, or the like into immune cells such as T cell and the like is provided by the present invention. Thus, a system for delivering a target substance into an immune cell, including ultrafine bubble water or ultrafine bubble aqueous solution containing ultrafine bubbles with an average diameter of not more than 200 nm and not containing phospholipid, and an ultrasound generator in combination; a method for increasing the delivery of a nucleic acid or a protein into an immune cell by using the ultrafine bubble water, etc. and ultrasound; and the like are provided.
-
-
-
-
-
-
-
-
-