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公开(公告)号:US20220002428A1
公开(公告)日:2022-01-06
申请号:US17373965
申请日:2021-07-13
Applicant: Pfizer Inc. , Bristol-Myers Squibb Company
Inventor: Jing MIN , Yanli WU , Rory F. FINN , Barrett R. THIELE , Wei LIAO , Ronald P. GLADUE , Arvind RAJPAL , Timothy J. PARADIS , Peter BRAMS , Brigitte DEVAUX , Yi WU , Kristopher TOY , Heidi N. LEBLANC , Haichun HUANG
IPC: C07K16/28
Abstract: The present disclosure provides isolated binding molecules that bind to the human OX40R, nucleic acid molecules encoding an amino acid sequence of the binding molecules, vectors comprising the nucleic acid molecules, host cells containing the vectors, methods of making the binding molecules, pharmaceutical compositions containing the binding molecules, and methods of using the binding molecules or compositions.
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公开(公告)号:US20180171018A1
公开(公告)日:2018-06-21
申请号:US15878344
申请日:2018-01-23
Applicant: PFIZER INC.
Inventor: Tracy Chia-Chien KUO , Javier Fernando CHAPARRO RIGGERS , Wei CHEN , Amy Shaw-Ru CHEN , Edward Derrick PASCUA , Thomas John VAN BLARCOM , Leila Marie BOUSTANY , Weihsien HO , Yik Andy YEUNG , Pavel STROP , Arvind RAJPAL
IPC: C07K16/28 , A61K39/395 , A61K47/68 , A61K31/454 , A61K31/69 , A61K31/704 , A61K39/00
CPC classification number: C07K16/2878 , A61K31/454 , A61K31/69 , A61K31/704 , A61K39/3955 , A61K39/39558 , A61K47/6801 , A61K47/6849 , A61K2039/505 , C07K16/2803 , C07K16/2809 , C07K2317/21 , C07K2317/31 , C07K2317/56 , C07K2317/565 , C07K2317/73 , C07K2317/732 , C07K2317/92 , A61K2300/00
Abstract: The present invention relates to antibodies, e.g., full length antibodies or antigen binding fragments thereof, that specifically bind to BCMA (B-Cell Maturation Antigen) and/or CD3 (Cluster of Differentiation 3). The invention also relates to antibody conjugates (e.g., antibody-drug-conjugates) comprising the BCMA antibodies, compositions comprising the BCMA antibodies, and methods of using the BCMA antibodies and their conjugates for treating conditions associated with cells expressing BCMA (e.g., cancer or autoimmune disease). The invention further relates to heteromultimeric antibodies that specifically bind to CD3 and a tumor cell antigen, (e.g., bispecific antibodies that specifically bind to CD3 and BCMA). Compositions comprising such heteromultimeric antibodies, methods for producing and purifying such heterodimeric antibodies, and their use in diagnostics and therapeutics are also provided.
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公开(公告)号:US20210188991A1
公开(公告)日:2021-06-24
申请号:US17129833
申请日:2020-12-21
Applicant: PFIZER INC.
Inventor: Tracy Chia-Chien KUO , Javier Fernando CHAPARRO RIGGERS , Wei CHEN , Amy Shaw-Ru CHEN , Edward Derrick PASCUA , Thomas John VAN BLARCOM , Leila Marie BOUSTANY , Weihsien HO , Yik Andy YEUNG , Pavel STROP , Arvind RAJPAL
IPC: C07K16/28 , A61K39/395 , A61K31/454 , A61K31/704 , A61K31/69 , A61K47/68
Abstract: The present invention relates bispecific antibodies that specific binds to BCMA (B-Cell Maturation Antigen) and CD3 (Cluster of Differentiation 3). Method of making the bispecific antibodies and method of using the bispecific antibodies for the treatment of multiple myeloma are also provided.
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公开(公告)号:US20170313787A1
公开(公告)日:2017-11-02
申请号:US15593259
申请日:2017-05-11
Applicant: PFIZER INC. , RINAT NEUROSCIENCE CORP.
Inventor: Pavel STROP , Magdalena Grazyna DORYWALSKA , Arvind RAJPAL , David SHELTON , Shu-Hui LIU , Jaume PONS , Russell DUSHIN
CPC classification number: C07K17/02 , A61K47/68 , A61K47/6803 , A61K47/6851 , A61K47/6889 , C07K16/30 , C07K2317/31 , C07K2317/73
Abstract: The present invention provides engineered polypeptide conjugates (e.g., antibody-drug-conjugates, toxin-(biocompatible polymer) conjugates, antibody-(biocompatible polymer) conjugates, and bispecific antibodies) comprising acyl donor glutamine-containing tags and amine donor agents. In one aspect, the invention provides an engineered Fc-containing polypeptide conjugate comprising the formula (Fc-containing polypeptide)-T-A, wherein T is an acyl donor glutamine-containing tag engineered at a specific site or comprises an endogenous glutamine made reactive by the Fc-containing polypeptide engineering, wherein A is an amine donor agent, and wherein the amine donor agent is site-specifically conjugated to the acyl donor glutamine-containing tag or the endogenous glutamine. The invention also provides methods of making engineered polypeptide conjugates using transglutaminase.
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公开(公告)号:US20210115159A1
公开(公告)日:2021-04-22
申请号:US16951003
申请日:2020-11-18
Applicant: PFIZER INC. , RINAT NEUROSCIENCE CORP.
Inventor: Pavel STROP , Magdalena Grazyna DORYWALSKA , Arvind RAJPAL , David SHELTON , Shu-Hui LIU , Jaume PONS , Russell DUSHIN
Abstract: The present invention provides engineered polypeptide conjugates (e.g., antibody-drug-conjugates, toxin-(biocompatible polymer) conjugates, antibody-(biocompatible polymer) conjugates, and bispecific antibodies) comprising acyl donor glutamine-containing tags and amine donor agents. In one aspect, the invention provides an engineered Fc-containing polypeptide conjugate comprising the formula (Fc-containing polypeptide)-T-A, wherein T is an acyl donor glutamine-containing tag engineered at a specific site or comprises an endogenous glutamine made reactive by the Fc-containing polypeptide engineering, wherein A is an amine donor agent, and wherein the amine donor agent is site-specifically conjugated to the acyl donor glutamine-containing tag or the endogenous glutamine. The invention also provides methods of making engineered polypeptide conjugates using transglutaminase.
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公开(公告)号:US20190241669A1
公开(公告)日:2019-08-08
申请号:US16384719
申请日:2019-04-15
Applicant: Pfizer Inc.
Inventor: Tracy Chia-Chien KUO , Bijan Andre BOLDAJIPOUR , Javier Fernando CHAPARRO RIGGERS , Philippe DUCHATEAU , Roman Ariel GALETTO , Alexandre JUILLERAT , Thomas Charles PERTEL , Arvind RAJPAL , Barbra Johnson SASU , Cesar Adolfo SOMMER , Julien VALTON , Thomas John VAN BLARCOM
IPC: C07K16/28 , C07K14/705 , A61K31/7076 , A61K35/17 , C12N15/63 , C07K14/725 , A61K39/00
CPC classification number: C07K16/2878 , A61K31/7076 , A61K35/17 , A61K38/00 , A61K39/0011 , A61K2039/505 , A61K2039/5156 , C07K14/7051 , C07K14/70517 , C07K14/70578 , C07K16/2863 , C07K16/2896 , C07K2317/56 , C07K2317/565 , C07K2317/569 , C07K2317/622 , C07K2317/73 , C07K2317/92 , C07K2319/02 , C07K2319/03 , C07K2319/33 , C12N15/63
Abstract: The invention provides CARs (CARs) that specifically bind to BCMA (B-Cell Maturation Antigen). The invention further relates to engineered immune cells comprising such CARs, CAR-encoding nucleic acids, and methods of making such CARs, engineered immune cells, and nucleic acids. The invention further relates to therapeutic methods for use of these CARs and engineered immune cells for the treatment of a condition associated with malignant cells expressing BCMA (e.g., cancer).
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公开(公告)号:US20150266974A1
公开(公告)日:2015-09-24
申请号:US14677983
申请日:2015-04-03
Applicant: RINAT NEUROSCIENCE CORP. , PFIZER INC.
Inventor: Jaume PONS , Jeffrey Raymond CHABOT , Javier Fernando CHAPARRO RIGGERS , Bruce Charles GOMES , Hong LIANG , Kapil MAYAWALA , Jerome Thomas METTETAL, II , Arvind RAJPAL , David Louis SHELTON
CPC classification number: C07K16/4291 , C07K16/28 , C07K16/40 , C07K2317/56 , C07K2317/565 , C07K2317/70 , C07K2317/732 , C07K2317/734 , C07K2317/76 , C07K2317/92 , C07K2317/94 , C07K2319/21
Abstract: The present invention relates to antibodies with pH dependent binding to its antigen such that the affinity for antigen binding at physiological pH (i.e., pH 7.4) is greater than at endosomal pH (i.e., pH 6.0 or 5.5). In other words, the KD or koff ratio at pH 5.5/pH 7.4 or at pH 6.0/pH 7.4 is more than, or ranges between, 2, 3, 4, 8, 10, 16, 20, 30, 40, or 100 or more. Such pH dependent antibodies preferentially dissociate from the antigen in the endosome. This can increase antibody half life, as compared to antibodies with equivalent KDs at pH 7.4 but with no pH dependent binding, when the antigen is one that undergoes antigen-mediated clearance (e.g., PCSK9). Antibodies with pH dependent binding can decrease total antigen half life when the antigen undergoes reduced clearance when bound to antibody (e.g., IL6). Antibodies with pH dependent binding can also prolong the decrease in antigen which is not antibody-bound. This can be important when antagonizing a target antigen typically present at high levels (e.g., IgE, DKK1, C5 and SOST). In addition, such antibodies can increase antigen half life when the antigen is a receptor and the receptor has increased clearance when bound to antibody (e.g, GMCSF receptor).
Abstract translation: 本发明涉及与其抗原具有pH依赖性结合的抗体,使得在生理pH(即pH 7.4)下抗原结合的亲和力大于内体pH(即pH6.0或5.5)时的亲和力。 换句话说,pH5.5 / pH7.4或pH6.0 / pH7.4下的KD或koff比大于或等于2,3,4,8,10,16,20,30,40或100 或者更多。 这种pH依赖性抗体优先从内体中的抗原解离。 与抗原为经过抗原介导的清除(例如,PCSK9)的抗原相比,与具有pH 7.4但具有pH依赖性结合的等效KD的抗体相比,可以增加抗体半衰期。 当与抗体(例如IL6)结合时,当抗原经历减少的清除时,具有pH依赖性结合的抗体可降低总抗原半衰期。 具有pH依赖性结合的抗体也可以延长不抗体结合的抗原的降低。 当拮抗通常以高水平存在的靶抗原(例如IgE,DKK1,C5和SOST)时,这可能是重要的。 此外,当抗原是受体时,这种抗体可以增加抗原半衰期,并且当与抗体(例如,GMCSF受体)结合时,该受体具有增加的清除能力。
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公开(公告)号:US20240018252A1
公开(公告)日:2024-01-18
申请号:US18456399
申请日:2023-08-25
Applicant: PFIZER INC.
Inventor: Tracy Chia-Chien KUO , Javier Fernando CHAPARRO RIGGERS , Wei CHEN , Amy Shaw-Ru CHEN , Edward Derrick PASCUA , Thomas John VAN BLARCOM , Leila Marie BOUSTANY , Weihsien HO , Yik Andy YEUNG , Pavel STROP , Arvind RAJPAL
IPC: C07K16/28 , A61K31/454 , A61K39/395 , A61K38/07 , A61P35/00 , A61K31/704
CPC classification number: C07K16/2878 , C07K16/2809 , A61K31/454 , A61K39/3955 , A61K38/07 , A61P35/00 , A61K31/704 , C07K2317/31 , A61K39/00
Abstract: The present invention relates to antibodies, e.g., full length antibodies or antigen binding fragments thereof, that specifically bind to BCMA (B-Cell Maturation Antigen) and/or CD3 (Cluster of Differentiation 3). The invention also relates to antibody conjugates (e.g., antibody-drug-conjugates) comprising the BCMA antibodies, compositions comprising the BCMA antibodies, and methods of using the BCMA antibodies and their conjugates for treating conditions associated with cells expressing BCMA (e.g., cancer or autoimmune disease). The invention further relates to heteromultimeric antibodies that specifically bind to CD3 and a tumor cell antigen, (e.g., bispecific antibodies that specifically bind to CD3 and BCMA). Compositions comprising such heteromultimeric antibodies, methods for producing and purifying such heterodimeric antibodies, and their use in diagnostics and therapeutics are also provided.
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公开(公告)号:US20200024366A1
公开(公告)日:2020-01-23
申请号:US16296852
申请日:2019-03-08
Applicant: Pfizer Inc. , RINAT NEUROSCIENCE CORP.
Inventor: Jaume PONS , Jeffrey Raymond CHABOT , Javier Fernando CHAPARRO RIGGERS , Bruce Charles GOMES , Hong LIANG , KapiI MAYAWALA , Jerome Thomas METTETAL, II , Arvind RAJPAL , David Louis SHELTON
Abstract: The present invention relates to antibodies with pH dependent binding to its antigen such that the affinity for antigen binding at physiological pH (i.e., pH 7.4) is greater than at endosomal pH (i.e., pH 6.0 or 5.5). In other words, the KD or koff ratio at pH 5.5/pH 7.4 or at pH 6.0/pH 7.4 is more than, or ranges between, 2, 3, 4, 8, 10, 16, 20, 30, 40, or 100 or more. Such pH dependent antibodies preferentially dissociate from the antigen in the endosome. This can increase antibody half life, as compared to antibodies with equivalent KDs at pH 7.4 but with no pH dependent binding, when the antigen is one that undergoes antigen-mediated clearance (e.g., PCSK9). Antibodies with pH dependent binding can decrease total antigen half life when the antigen undergoes reduced clearance when bound to antibody (e.g., IL6). Antibodies with pH dependent binding can also prolong the decrease in antigen which is not antibody-bound. This can be important when antagonizing a target antigen typically present at high levels (e.g., IgE, DKK1, C5 and SOST). In addition, such antibodies can increase antigen half life when the antigen is a receptor and the receptor has increased clearance when bound to antibody (e.g., GMCSF receptor).
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公开(公告)号:US20190135932A1
公开(公告)日:2019-05-09
申请号:US16245816
申请日:2019-01-11
Applicant: Pfizer Inc. , Bristol-Myers Squibb Company
Inventor: Jing MIN , Yanli WU , Rory F. FINN , Barrett R. THIELE , Wei LIAO , Ronald P. GLADUE , Arvind RAJPAL , Timothy J. PARADIS , Peter BRAMS , Brigitte DEVAUX , Yi WU , Kristopher TOY , Heidi N. LEBLANC , Haichun HUANG
IPC: C07K16/28
Abstract: The present disclosure provides isolated binding molecules that bind to the human OX40R, nucleic acid molecules encoding an amino acid sequence of the binding molecules, vectors comprising the nucleic acid molecules, host cells containing the vectors, methods of making the binding molecules, pharmaceutical compositions containing the binding molecules, and methods of using the binding molecules or compositions.
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