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公开(公告)号:US11628223B2
公开(公告)日:2023-04-18
申请号:US16651501
申请日:2018-09-28
发明人: Narihiro Toda , Yusuke Ota , Fuminao Doi , Masaki Meguro , Ichiro Hayakawa , Shinji Ashida , Takeshi Masuda , Takashi Nakada , Mitsuhiro Iwamoto , Naoya Harada , Tomoko Terauchi , Daisuke Okajima , Kensuke Nakamura , Hiroaki Uchida , Hirofumi Hamada
IPC分类号: C07D487/04 , C07D487/20 , A61K47/68 , A61P35/00 , C07K16/30
摘要: A novel antibody-pyrrolodiazepine derivative and a novel antibody-pyrrolodiazepine derivative conjugate using the same, comprising substituted benzo[e]pyrrolo[1,2-a][1,4]diazepines represented by the [Formula 24], [Formula 25], [Formula 26], and/or [Formula 27].
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公开(公告)号:US20230084707A1
公开(公告)日:2023-03-16
申请号:US17714032
申请日:2022-04-05
发明人: Narihiro TODA , Yusuke OTA , Fuminao DOI , Masaki MEGURO , Ichiro HAYAKAWA , Shinji ASHIDA , Takeshi MASUDA , Takashi NAKADA , Mitsuhiro IWAMOTO , Naoya HARADA , Tomoko TERAUCHI , Daisuke OKAJIMA , Kensuke NAKAMURA , Hiroaki UCHIDA , Hirofumi HAMADA
IPC分类号: A61K47/68 , A61P35/00 , C07K16/30 , C07D487/04
摘要: The present invention provides a novel antibody-pyrrolodiazepine derivative and a novel antibody-pyrrolodiazepine derivative conjugate using the same, and a novel CLDN6 and/or CLDN9 antibody.
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3.
公开(公告)号:US20230061732A1
公开(公告)日:2023-03-02
申请号:US17616430
申请日:2020-06-04
发明人: Masatora FUKUDA , Makoto KOIZUMI , Shinzo IWASHITA
IPC分类号: C12N15/113 , A61K31/7115 , A61K31/7125 , A61P43/00
摘要: An oligonucleotide that induces a site-specific editing for a target RNA, the oligonucleotide including a first oligonucleotide that specifies the target RNA, a second oligonucleotide that is linked to the 3′-side of the first oligonucleotide, a third oligonucleotide that is capable of forming a complementary pair together with the second oligonucleotide, and a first linking portion that links the second oligonucleotide and the third oligonucleotide. The first oligonucleotide is composed of a target-corresponding nucleotide residue that corresponds to an adenosine residue in the target RNA; an oligonucleotide of 10 to 30 residues linked to the 5′-side of the target-corresponding nucleotide residue and having a base sequence complementary to the target RNA; and an oligonucleotide of 3-6 residues linked to the 3′-side of the target-corresponding nucleotide residue and having a base sequence complementary to the target RNA. The second oligonucleotide consists of 5 to 8 residues and the third oligonucleotide consists of 5 to 8 residues. At least one residue selected from a counter region composed of the target-corresponding nucleotide residue and two respective residues on the 3′- and 5′-sides thereof is a nucleotide residue other than a natural ribonucleotide residue.
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公开(公告)号:US11584800B2
公开(公告)日:2023-02-21
申请号:US16997613
申请日:2020-08-19
发明人: Hiroyuki Naito , Yusuke Ogitani , Takeshi Masuda , Takashi Nakada , Masao Yoshida , Shinji Ashida , Koji Morita , Hideki Miyazaki , Yuji Kasuya , Ichiro Hayakawa , Yuki Abe
IPC分类号: A61K47/68 , A61K39/395 , A61K31/4745 , A61K39/00 , C07K16/32 , C07D491/22 , C07K16/28 , C07K16/30 , C07D491/052
摘要: As an antitumor drug which is excellent in terms of antitumor effect and safety and has an excellent therapeutic effect, there is provided an antibody-drug conjugate in which an antitumor compound represented by the following formula is conjugated to an anti-HER2 antibody via a linker having a structure represented by the following formula: -L1-L2-LP-NH—(CH2)n1-La-(CH2)n2-C(═O)— wherein the anti-HER2 antibody is connected to the terminal L1, and the antitumor compound is connected to the carbonyl group of the —(CH2)n2-C(═O)— moiety with the nitrogen atom of the amino group at position 1 as the connecting position.
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5.
公开(公告)号:US11583590B2
公开(公告)日:2023-02-21
申请号:US17543697
申请日:2021-12-06
发明人: Narihiro Toda , Yusuke Ota , Fuminao Doi , Masaki Meguro , Ichiro Hayakawa , Shinji Ashida , Takeshi Masuda , Takashi Nakada , Mitsuhiro Iwamoto , Naoya Harada , Tomoko Terauchi , Daisuke Okajima , Kensuke Nakamura , Hiroaki Uchida , Hirofumi Hamada
IPC分类号: A61K47/68 , A61P35/00 , C07D487/04 , C07K16/30
摘要: The present invention provides a novel antibody-pyrrolodiazepine derivative and a novel antibody-pyrrolodiazepine derivative conjugate using the same, and a novel CLDN6 and/or CLDN9 antibody.
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公开(公告)号:US11555204B2
公开(公告)日:2023-01-17
申请号:US16338941
申请日:2017-10-02
发明人: Kenji Masuda , Koichi Nonaka , Hiroki Tanemura
IPC分类号: C12N15/85 , C12P21/02 , C12N15/113 , C12N15/09 , C12N5/10
摘要: The present invention provides an approach to enhancing the production of a foreign protein serving as a protein-based pharmaceutical product in host cells such as cultured cells derived from a mammal. The present invention provides transformed cells having a novel Hspa5 gene promoter, and a method for secreting and producing a foreign protein at high levels using the transformed host cells.
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公开(公告)号:US20220409540A1
公开(公告)日:2022-12-29
申请号:US17776743
申请日:2020-11-13
申请人: DAIICHI SANKYO COMPANY, LIMITED , NATIONAL INSTITUTES OF BIOMEDICAL INNOVATION, HEALTH AND NUTRTION
发明人: Takako NIWA , Takashi SUZUKI , Makoto KOIZUMI , Nao JONAI , Yoshikuni ONODERA , Fumihiko TAKESHITA , Ken ISHII
摘要: The present invention provides a vaccine for preventing and/or treating infections with human papillomavirus. The present invention relates to a lipid particle encapsulating a nucleic acid molecule capable of expressing the E6 and E7 antigens of human papillomavirus, wherein the lipid comprises a cationic lipid represented by general formula (Ia) or a pharmaceutically acceptable salt thereof: wherein R1 and R2 each independently represent a C1-C3 alkyl group; L1 represents a C17-C19 alkenyl group which may have one or a plurality of C2-C4 alkanoyloxy groups; L2 represents a C10-C19 alkyl group which may have one or a plurality of C2-C4 alkanoyloxy groups or a C10-C19 alkenyl group which may have one or a plurality of C2-C4 alkanoyloxy groups; and p is 3 or 4.
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公开(公告)号:US11530211B2
公开(公告)日:2022-12-20
申请号:US16960308
申请日:2019-01-18
发明人: Toshihiro Kiho , Tatsuya Yano , Satoshi Komoriya , Taisaku Tanaka
IPC分类号: C07D471/04 , A61P3/10 , C07D487/04 , C12N5/071
摘要: It is an object of the present invention to provide a new compound capable of efficiently inducing differentiation from pluripotent stem cells into insulin-producing cells. The object of the present invention is achieved by a compound represented by formula (I): wherein R1, R2, R3, n and A have the same meanings as defined in the description, respectively, or a salt thereof.
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公开(公告)号:US11447554B2
公开(公告)日:2022-09-20
申请号:US17511357
申请日:2021-10-26
发明人: Takenobu Katagiri , Kenji Osawa , Sho Tsukamoto , Shinnosuke Tsuji , Yoshirou Kawaguchi , Kensuke Nakamura
摘要: This application provides: an antibody which specifically binds to an ALK2 protein and has an activity of inhibiting BMP signal transduction mediated by ALK2; a method for producing the antibody; and a pharmaceutical composition comprising the antibody, for treating and/or preventing ectopic ossification and/or bone dysplasia, anemia, or diffuse intrinsic pontine glioma (DIPG).
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公开(公告)号:US20220267453A1
公开(公告)日:2022-08-25
申请号:US17629715
申请日:2020-07-22
发明人: Takenobu KATAGIRI , Sho TSUKAMOTO , Mai KURATANI
IPC分类号: C07K16/28
摘要: This application provides: an antibody or an antigen-binding fragment thereof which can be used not only as a therapeutic drug but as a tool of immunological and immunohistological analysis such as immunostaining or Western blot, specifically recognizes an extracellular region polypeptide of human, mouse and rat ALK2, and inhibits BMP signal transduction, and an antibody or an antigen-binding fragment thereof which has a property of specifically binding to an extracellular region of ALK2 to form an ALK2 homodimer and a property of inhibiting the formation of an ALK2-type II receptor heterodimer, and inhibits the activation of ALK2 kinase, or inhibits BMP signal transduction; and a method for inhibiting the activation of ALK2 kinase or a method for inhibiting BMP signal transduction using the antibody or the antigen-binding fragment thereof.
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