JP2016525516A5 - - Google Patents

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Publication number
JP2016525516A5
JP2016525516A5 JP2016526515A JP2016526515A JP2016525516A5 JP 2016525516 A5 JP2016525516 A5 JP 2016525516A5 JP 2016526515 A JP2016526515 A JP 2016526515A JP 2016526515 A JP2016526515 A JP 2016526515A JP 2016525516 A5 JP2016525516 A5 JP 2016525516A5
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JP
Japan
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composition
mutation
cytokine
mutated
leptin
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JP2016526515A
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English (en)
Japanese (ja)
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JP6580037B2 (ja
JP2016525516A (ja
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Priority claimed from PCT/EP2014/064227 external-priority patent/WO2015007536A2/en
Publication of JP2016525516A publication Critical patent/JP2016525516A/ja
Publication of JP2016525516A5 publication Critical patent/JP2016525516A5/ja
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JP2016526515A 2013-07-18 2014-07-03 高度に低下された受容体結合親和性を有するサイトカインを含むフソカイン Active JP6580037B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP13306034 2013-07-18
EP13306034.3 2013-07-18
PCT/EP2014/064227 WO2015007536A2 (en) 2013-07-18 2014-07-03 Fusokines involving cytokines with strongly reduced receptor binding affinities

Related Child Applications (1)

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JP2019154901A Division JP6853317B2 (ja) 2013-07-18 2019-08-27 高度に低下された受容体結合親和性を有するサイトカインを含むフソカイン

Publications (3)

Publication Number Publication Date
JP2016525516A JP2016525516A (ja) 2016-08-25
JP2016525516A5 true JP2016525516A5 (cg-RX-API-DMAC7.html) 2017-08-10
JP6580037B2 JP6580037B2 (ja) 2019-09-25

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ID=48906191

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JP2016526515A Active JP6580037B2 (ja) 2013-07-18 2014-07-03 高度に低下された受容体結合親和性を有するサイトカインを含むフソカイン
JP2019154901A Active JP6853317B2 (ja) 2013-07-18 2019-08-27 高度に低下された受容体結合親和性を有するサイトカインを含むフソカイン

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JP2019154901A Active JP6853317B2 (ja) 2013-07-18 2019-08-27 高度に低下された受容体結合親和性を有するサイトカインを含むフソカイン

Country Status (14)

Country Link
US (3) US10640542B2 (cg-RX-API-DMAC7.html)
EP (2) EP3299466B1 (cg-RX-API-DMAC7.html)
JP (2) JP6580037B2 (cg-RX-API-DMAC7.html)
KR (1) KR102322510B1 (cg-RX-API-DMAC7.html)
CN (2) CN110835376B (cg-RX-API-DMAC7.html)
AU (2) AU2014292371B2 (cg-RX-API-DMAC7.html)
BR (1) BR112016001036B1 (cg-RX-API-DMAC7.html)
CA (1) CA2917937C (cg-RX-API-DMAC7.html)
DK (1) DK3299466T3 (cg-RX-API-DMAC7.html)
ES (2) ES2757501T3 (cg-RX-API-DMAC7.html)
IL (1) IL243451B (cg-RX-API-DMAC7.html)
MX (1) MX375441B (cg-RX-API-DMAC7.html)
SG (2) SG11201600163VA (cg-RX-API-DMAC7.html)
WO (1) WO2015007536A2 (cg-RX-API-DMAC7.html)

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WO2017134301A1 (en) 2016-02-05 2017-08-10 Orionis Biosciences Nv Clec9a binding agents
CN109069573B (zh) 2016-03-07 2022-04-05 弗拉芒区生物技术研究所 结合cd20的单结构域抗体
EP3455245A2 (en) 2016-05-13 2019-03-20 Orionis Biosciences NV Therapeutic targeting of non-cellular structures
CN109689087B (zh) 2016-05-13 2023-04-04 奥里尼斯生物科学私人有限公司 靶向性突变干扰素-β及其用途
ES2917000T3 (es) 2016-10-24 2022-07-06 Orionis Biosciences BV Interferón-gamma mutante diana y usos del mismo
JP7586579B2 (ja) 2017-02-06 2024-11-19 オリオンズ バイオサイエンス インコーポレイテッド 標的化改変型インターフェロン及びその使用
CN110546160A (zh) 2017-02-06 2019-12-06 奥里尼斯生物科学公司 靶向嵌合蛋白及其用途
US11246911B2 (en) 2017-02-07 2022-02-15 Vib Vzw Immune-cell targeted bispecific chimeric proteins and uses thereof
CA3069994A1 (en) 2017-08-09 2019-02-14 Orionis Biosciences Inc. Pd-1 and pd-l1 binding agents
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CN111511764B (zh) 2017-08-09 2024-02-06 奥里尼斯生物科学有限公司 Clec9a结合剂及其用途
EP3973973A1 (en) 2017-10-31 2022-03-30 KaliVir Immunotherapeutics, Inc. Platform oncolytic vector for systemic delivery
US20200354424A1 (en) 2018-01-26 2020-11-12 Orionis Biosciences, Inc. Xcr1 binding agents and uses thereof
AU2019215440B2 (en) 2018-02-05 2025-12-04 Orionis Biosciences, Inc. Fibroblast binding agents and use thereof
US12084497B2 (en) 2018-08-08 2024-09-10 Orionis Biosciences, Inc. SIRP1α targeted chimeric proteins and uses thereof
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KR20220012227A (ko) 2019-03-28 2022-02-03 오리오니스 바이오사이언시즈 인코포레이티드 Clec9a-기반 키메라 단백질 복합체
CN113767115B (zh) 2019-03-28 2025-05-02 奥里尼斯生物科学股份有限公司 治疗性干扰素α1蛋白
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CR20230551A (es) 2021-04-30 2024-05-07 Kalivir Immunotherapeutics Inc Virus oncolíticos para la expresión modificada del mhc
EP4622660A1 (en) * 2022-11-21 2025-10-01 Wisconsin Alumni Research Foundation Synthetic il6-il1 beta fusion cytokine for promoting t cell cytotoxic function, t cell proliferation, and tumoricidal activity

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