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公开(公告)号:WO2023079137A1
公开(公告)日:2023-05-11
申请号:PCT/EP2022/080965
申请日:2022-11-07
Applicant: KATHOLIEKE UNIVERSITEIT LEUVEN , VIB VZW , UNIVERSITEIT GENT
Inventor: GEUKENS, Nick , DECLERCK, Paul , IMBRECHTS, Maya , AMPOFO, Louanne , MAES, Wim , NEYTS, Johan , ABDELNABI, Rana , EECKHAUT, Hannah , CALLEWAERT, Nico , FIJALKOWSKA, Daria
IPC: C07K16/10 , A61K39/395 , A61P31/14 , C12N15/13 , A61K2039/505 , A61K2039/53 , C07K2317/21 , C07K2317/34 , C07K2317/56 , C07K2317/565 , C07K2317/76 , C07K2317/92
Abstract: The invention relates to antibodies or antigen binding fragments thereof, specifically binding to the trimeric spike protein of Wuhan Covid-SARS-2 and specifically binding to the RBD domain of all of Wuhan, alpha, beta, gamma, delta and omicron variant of Covid-SARS-2 spike protein, characterized in that said antibody or antigen binding fragment thereof has an IC50 in a SARS-CoV-2 pseudovirus infection lower than 1 nm in a SARS-CoV-2 pseudovirus infection, and in that said antibody or antigen binding fragment thereof has an affinity for RBD domain Wuhan Covid-SARS-2 spike protein with a KD of less than 500 pM, and in that said antibody or antigen binding fragment thereof has an affinity for trimeric spike protein of Wuhan Covid-SARS-2 with a KD of less than 300 pM.
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公开(公告)号:WO2015118147A1
公开(公告)日:2015-08-13
申请号:PCT/EP2015/052624
申请日:2015-02-09
Applicant: KATHOLIEKE UNIVERSITEIT LEUVEN , INSERM (INSTITUT NATIONAL DE LA SANTÉ ET DE LA RECHERCHE MÉDICALE) , Université de Caen Basse Normandie , Centre Hospitalier Universitaire de Caen
Inventor: DECLERCK, Paul , DE MEYER, Simon , GEUKENS, Nick , GILS, Ann , RUBIO, Marina , VIVIEN, Denis , WYSEURE, Tine
CPC classification number: C07K16/38 , A61K2039/505 , C07K16/468 , C07K2317/24 , C07K2317/31 , C07K2317/56 , C07K2317/565 , C07K2317/622 , C07K2317/626 , C07K2317/76 , G01N2800/22
Abstract: Disclosed herein is a bispecific inhibitor for use in treating thrombotic disorders, such as acute thrombotic disorders like stroke and thromboembolism. The bispecific inhibitor is based on monoclonal antibodies targeting TAFI and PAI-1, and shows efficacy in the presence or the absence of plasminogen activators such as tissue-type plasminogen activator (tPA).
Abstract translation: 本文公开了用于治疗血栓形成障碍的双特异性抑制剂,例如急性血栓形成障碍如中风和血栓栓塞。 双特异性抑制剂基于靶向TAFI和PAI-1的单克隆抗体,并且在纤溶酶原激活剂如组织型纤溶酶原激活物(tPA)的存在或不存在下显示有效性。
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