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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
发明人: Naoyuki MURATA , Sayan CHUANOI , Shigeo YANAI
摘要: 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
IPC分类号: C07F5/02 , A61K31/198 , A61K31/454 , A61K31/675 , A61K31/69 , C07C233/83 , C07F5/05
摘要: 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
发明人: Antonio Palumbo , Kristina Allikmets , Deborah Berg , Eric Fedyk
IPC分类号: A61K39/395 , A61K31/454 , A61K31/573 , A61K31/69 , A61K31/135 , A61K31/47 , A61K31/167 , A61P35/00
摘要: 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
IPC分类号: C07D495/04 , C07D333/38 , C07D409/12
摘要: 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
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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
发明人: Toshiya Nishi , Shinichi KONDO
IPC分类号: A61K31/4545 , A61P25/08
摘要: 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
发明人: Hiroshi IMOTO , Mari ADACHI , Yoko KANEMATSU , Taiji ASAMI , Ayumu NIIDA , Naoki NISHIZAWA , Derek Cecil COLE , Mack FLINSPACH , Nick SCORAH , Abhijit Suresh BHAT
摘要: 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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公开(公告)号:US11299553B2
公开(公告)日:2022-04-12
申请号:US16199453
申请日:2018-11-26
摘要: Disclosed herein are antibodies capable of binding to plasma kallikrein and inhibit its activity. Such antibodies interact with one or more critical residues in the catalytic domain of the plasma kallikrein. The antibodies may also contain specific heavy chain complementarity determining region 3 (CDRs) motifs and optionally specific residues at certain positions within both the heavy chain variable region and the light chain variable region.
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公开(公告)号:US20220106357A1
公开(公告)日:2022-04-07
申请号:US17492256
申请日:2021-10-01
IPC分类号: C07K1/14 , C07K14/745 , C07K16/00 , C07K14/765 , C07K14/81 , C07K14/755
摘要: The present invention provides a method of fractionating human plasma, in some embodiments, using the Cohn fractionation procedure. The improvement comprises the use of physiologically active reconstituted spray dried human plasma as the starting material for the fractionation procedure.
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公开(公告)号:US20220099670A1
公开(公告)日:2022-03-31
申请号:US17427222
申请日:2021-01-31
发明人: Shin KANEKO , Shoichi IRIGUCHI , Keiko SEKIYA , Yoshiaki KASSAI
IPC分类号: G01N33/567 , C12N5/00 , C12N5/0784 , G01N33/50
摘要: Disclosed is a method for detecting regulatory dendritic cells, the method comprising step a: detecting the presence or absence of one or more types of molecules on a cell surface in a cell population that comprises regulatory dendritic cells; and step b: identifying regulatory dendritic cells on the basis of the presence or absence of the one or more types of molecules. Also disclosed is a method for producing a cell population enriched for regulatory dendritic cells, the method comprising step 1: detecting the presence or absence of one or more types of molecules on a cell surface in a cell population that comprises regulatory dendritic cells; and step 2: obtaining a cell population enriched for regulatory dendritic cells on the basis of the presence or absence of the one or more types of molecules. Further disclosed is a cell population enriched for regulatory dendritic cells obtained by the method.
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