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公开(公告)号:US11524992B2
公开(公告)日:2022-12-13
申请号:US16751788
申请日:2020-01-24
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Dasa Lipovsek , Joseph Toth , Ginger C. Rakestraw , Irvith M. Carvajal , Stanley Richard Krystek, Jr. , Steven R. O'Neil , Guodong Chen , Richard Y. Huang , Bryan C. Barnhart , John Thomas Loffredo , Christina Terragni
Abstract: Provided herein are polypeptides which include tenth fibronectin type III domains (10Fn3) that bind to glypican-3. Also provided are fusion molecules comprising a 10Fn3 domain that bind to glypican-3 for use in diagnostic and therapeutic applications. Glypican-3 10Fn3 drug conjugates are also provided.
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52.
公开(公告)号:US20220185856A1
公开(公告)日:2022-06-16
申请号:US17555633
申请日:2021-12-20
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Paul E. Morin , Daniel Cohen , Ranjan Mukherjee , Timothy P. Reilly , Rose C. Christian , Dasa Lipovsek , Ray Camphausen , John Krupinski
Abstract: Modified FGF-21 polypeptides and uses thereof are provided, for example, for the treatment of diseases associated with fibrosis. Modified FGF-21 polypeptides are disclosed that contain an internal deletion and optionally replacement peptide, optionally modified with at least one non-naturally-encoded amino acid, and/or optionally fused to a fusion partner.
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公开(公告)号:US11344639B2
公开(公告)日:2022-05-31
申请号:US16305284
申请日:2017-05-31
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Paul E. Morin , David Donnelly , Dasa Lipovsek , Jochem Gokemeijer , Maria Jure-Kunkel , David Fabrizio , Martin C. Wright , Douglas Dischino , Samuel J. Bonacorsi, Jr. , Ralph Adam Smith , Virginie Lafont , Daniel Cohen , David K. Leung
Abstract: Provided herein are novel 10Fn3 domains which specifically bind to PD-L1, as well as imaging agents based on the same for diagnostics.
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公开(公告)号:US11060085B2
公开(公告)日:2021-07-13
申请号:US16195295
申请日:2018-11-19
Applicant: Bristol-Myers Squibb Company
Inventor: Dasa Lipovsek
Abstract: This application provides an improved screening method for the selection of target-binding proteins having desirable biophysical properties. The method combines mRNA display and yeast surface display in a way that takes advantage of the desirable attributes of both processes.
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公开(公告)号:US20200247873A1
公开(公告)日:2020-08-06
申请号:US16740248
申请日:2020-01-10
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Dasa Lipovsek , Jonathan H. Davis
Abstract: Fibronectin type III (10Fn3) binding domains having novel designs that are associated with reduced immunogenicity are provided. The application describes alternative 10Fn3 binding domains in which certain immunogenic regions are not modified when producing a binder in order to maintain recognition as a self antigen by the host organism. The application also describes 10Fn3 binding domains in which HLA anchor regions have been destroyed thereby reducing the immunogenic contribution of the adjoining region. Also provided are 10Fn3 domains having novel combinations of modified regions that can bind to a desired target with high affinity.
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公开(公告)号:US10604556B2
公开(公告)日:2020-03-31
申请号:US15341623
申请日:2016-11-02
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Jonathan Davis , Dasa Lipovsek , Ray Camphausen
Abstract: Fibronectin type III (10Fn3) binding domains having novel designs that are associated with reduced immunogenicity are provided. The application describes alternative 10Fn3 binding domains in which certain immunogenic regions are not modified when producing a binder in order to maintain recognition as a self antigen by the host organism. The application also describes 10Fn3 binding domains in which HLA anchor regions have been destroyed thereby reducing the immunogenic contribution of the adjoining region. Also provided are 10Fn3 domains having novel combinations of modified regions that can bind to a desired target with high affinity.
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公开(公告)号:US10442851B2
公开(公告)日:2019-10-15
申请号:US15127166
申请日:2015-03-19
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Tracy S. Mitchell , Michael L. Gosselin , Dasa Lipovsek , Rex Parker , Ray Camphausen , Jonathan Davis , David Fabrizio
Abstract: The present invention relates to polypeptides which include tenth fibronectin type III domains (10Fn3) that binds to serum albumin, with south pole loop substitutions. The invention further relates to fusion molecules comprising a serum albumin-binding 10Fn3 joined to a heterologous protein for use in diagnostic and therapeutic applications.
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公开(公告)号:US10406251B2
公开(公告)日:2019-09-10
申请号:US15529260
申请日:2015-11-24
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Paul E. Morin , David Donnelly , Dasa Lipovsek , Jochem Gokemeijer , Maria N. Jure-Kunkel , David Fabrizio , Martin C. Wright , Douglas Dischino , Samuel J. Bonacorsi, Jr. , Ralph Adam Smith , Virginie Lafont , Daniel Cohen
IPC: A61K51/08 , C07K14/78 , G01N33/60 , G01N33/68 , G01N33/574
Abstract: Provided herein are novel polypeptides comprising fibronectin type III tenth (10Fn3) domains which specifically bind to Programmed Death Ligand-1 (PD-L1), as well as imaging agents based on the same for diagnostics.
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公开(公告)号:US20190256570A1
公开(公告)日:2019-08-22
申请号:US16287342
申请日:2019-02-27
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Gene M. Dubowchik , Olafur S. Gudmundsson , Xiaojun Han , R. Michael Lawrence , Dasa Lipovsek , Cort S. Madsen , Claudio Mapelli , Paul E. Morin , Michael C. Myers
Abstract: The present disclosure generally relates to modified relaxin polypeptides, such as modified human relaxin 2 polypeptides, comprising a non-naturally encoded amino acid which is linked to a pharmacokinetic enhancer, and therapeutic uses of such polypeptides, such as for the treatment of cardiovascular conditions (such as heart failure) and/or conditions relating to fibrosis.
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60.
公开(公告)号:US10377806B2
公开(公告)日:2019-08-13
申请号:US15979881
申请日:2018-05-15
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Paul E. Morin , Daniel Cohen , Ranjan Mukherjee , Timothy P. Reilly , Rose C. Christian , Dasa Lipovsek , Ray Camphausen , John Krupinski
Abstract: Modified FGF-21 polypeptides and uses thereof are provided, for example, for the treatment of diseases associated with fibrosis. Modified FGF-21 polypeptides are disclosed that contain an internal deletion and optionally replacement peptide, optionally modified with at least one non-naturally-encoded amino acid, and/or optionally fused to a fusion partner.
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