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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.
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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.
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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.
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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.
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公开(公告)号:US20220251117A1
公开(公告)日:2022-08-11
申请号:US17720621
申请日:2022-04-14
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Edward J. Olhava , Mihaela Diana Danca
IPC: C07F5/02 , A61K31/198 , A61K31/454 , A61K31/675 , A61K31/69 , C07C233/83 , C07F5/05
Abstract: The present invention provides novel compounds useful as proteasome inhibitors. The invention also provides pharmaceutical compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various diseases.
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公开(公告)号:US20220241413A1
公开(公告)日:2022-08-04
申请号:US17617811
申请日:2020-06-09
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Antonio Palumbo , Kristina Allikmets , Deborah Berg , Eric Fedyk
IPC: A61K39/395 , A61K31/454 , A61K31/573 , A61K31/69 , A61K31/135 , A61K31/47 , A61K31/167 , A61P35/00
Abstract: Methods of administering isolated anti-CD38 antibodies in combination with lenalidomide or pomobdomide, and dexamethasone and, optionally, bortezomib, for the treatment of multiple myeloma.
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公开(公告)号:US20220204525A1
公开(公告)日:2022-06-30
申请号:US17694635
申请日:2022-03-14
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Koichiro FUKUOKA , Kazuhiro MIWA , Tsuyoshi SASAKI , Fumiya KOMURA
IPC: C07D495/04 , C07D333/38 , C07D409/12
Abstract: The present invention provides a production method of a thienopyrimidine derivative or a salt thereof which has a gonadotropin releasing hormone (GnRH) antagonistic action with high quality in high yield. The present invention provides a method of producing a thienopyrirnidine derivative, which comprises reacting 6-(4-aminophenyl)-1-(2,6-difluorobenzyl)-5-dimethylaminomethyl-3-(6-methoxypyridazin-3-yl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione or salt thereof, 1,1′-carbonyldiimidazole or a salt thereof and methoxyamine or a salt thereof, and the like.
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公开(公告)号:USD956205S1
公开(公告)日:2022-06-28
申请号:US29759628
申请日:2020-11-24
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
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公开(公告)号:US20220168294A1
公开(公告)日:2022-06-02
申请号:US17673072
申请日:2022-02-16
Applicant: Takeda Pharmaceutical Company Limited
Inventor: Toshiya Nishi , Shinichi KONDO
IPC: A61K31/4545 , A61P25/08
Abstract: Aspects of the present invention relate to a method of treating an epileptic encephalopathy in a mammal in need thereof, comprising administering a composition comprising an effective amount of (4-benzyl-4-hydroxypiperidin-1-yl) (2,4′-bipyridin-3-yl)methanone or a pharmaceutically acceptable salt thereof to the mammal.
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公开(公告)号:US20220135638A1
公开(公告)日:2022-05-05
申请号:US17279266
申请日:2019-09-24
Applicant: TAKEDA PHARMACEUTICAL COMPANY LIMITED
Inventor: Hiroshi IMOTO , Mari ADACHI , Yoko KANEMATSU , Taiji ASAMI , Ayumu NIIDA , Naoki NISHIZAWA , Derek Cecil COLE , Mack FLINSPACH , Nick SCORAH , Abhijit Suresh BHAT
Abstract: The present disclosure provides GIP receptor agonist peptide compounds having an activating action on GIP receptors and use of the GIP receptor agonist peptide as a medicament for the treatment and/or prevention of diabetes, obesity, emesis, or a symptom or condition associated with diabetes, obesity, or emesis. Specifically, a GIP receptor agonist peptide containing a sequence represented by the formula (I) or a salt thereof, and a medicament comprising the same are provided. Formula I: P1-A1-A2-A3-A4-A5-A6-A7-A8-A9-A10-A11-A12-A13-A14-A15-A16-A17-A18-A19-A20-A21-A22-A23-A24-A25-A26-A27-A28-A29-A30-A341-A32-A33-A34-A35-A36-A37-A38-A39-A40-A41-P2 (SEQ ID NO: 4), or a salt thereof, wherein each symbol is as defined herein, with the proviso that the GIP receptor agonist peptide does not have an amino acid sequence as provided in SEQ ID NOs: 4-569 disclosed in PCT/JP2018/013540.
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