Jochen G. Salfeld - North Grafton MA Deborah J. Allen - London, GB Hendricus R. J. M. Hoogenboom - Hasselt, BE Zehra Kaymakcalan - Westboro MA Boris Labkovsky - Framingham MA John A. Mankovich - Andover MA Brian T. McGuinness - Cambridge, GB Andrew J. Roberts - Cambridge, GB Paul Sakorafas - Shrewsbury MA David Schoenhaut - Clifton NJ Tristan J. Vaughan - Cambridge, GB Michael White - Framingham MA Alison J. Wilton - Cambridge, GB
Assignee:
BASF Aktiengesellschaft - Ludwigshafen
International Classification:
A61K 39395
US Classification:
4241421, 424 852, 4241451, 424800, 424810
Abstract:
Human antibodies, preferably recombinant human antibodies, that specifically bind to human tumor necrosis factor (hTNF) are disclosed. These antibodies have high affinity for hTNF (e. g. , K =10 M or less), a slow off rate for hTNF dissociation (e. g. , K =10 sec or less) and neutralize hTNF activity in vitro and in vivo. An antibody of the invention can be a full-length antibody or an antigen-binding portion thereof. The antibodies, or antibody portions, of the invention are useful for detecting hTNF and for inhibiting hTNF activity, e. g. , in a human subject suffering from a disorder in which hTNF activity is detrimental. Nucleic acids, vectors and host cells for expressing the recombinant human antibodies of the invention, and methods of synthesizing the recombinant human antibodies, are also encompassed by the invention.
Human Antibodies That Bind Human Il-12 And Methods For Producing
Jochen Salfeld - North Grafton MA, US Michael Roguska - Ashland MA, US Michael Paskind - Sterling MA, US Subhashis Banerjee - Shrewsbury MA, US Daniel Tracey - Harvard MA, US Michael White - Framingham MA, US Zehra Kaymakcalan - Westborough MA, US Boris Labkovsky - Marlborough MA, US Paul Sakorafas - Newton MA, US Geertruida M. Veldman - Sudbury MA, US Amy Venturini - Lexington MA, US Angela Widom - Acton MA, US Stuart Friedrich - Melrose MA, US Nicholas W. Warne - Andover MA, US Angela Myles - Andover MA, US John Gawain Elvin - Cambridge, GB Alexander Robert Duncan - Little Shelford, GB Elaine Joy Derbyshire - Royston, GB Sara Carmen - Cambridge, GB Thor Las Holtet - Royston, GB Sarah Leila Du Fou - Hitchen, GB Stephen Smith - Ely, GB
Human antibodies, preferably recombinant human antibodies, that specifically bind to human interleukin-12 (hIL-12) are disclosed. Preferred antibodies have high affinity for hIL-12 and neutralize hIL-12 activity in vitro and in vivo. An antibody of the invention can be a full-length antibody or an antigen-binding portion thereof. The antibodies, or antibody portions, of the invention are useful for detecting hIL-12 and for inhibiting hIL-12 activity, e. g. , in a human subject suffering from a disorder in which hIL-12 activity is detrimental. Nucleic acids, vectors and host cells for expressing the recombinant human antibodies of the invention, and methods of synthesizing the recombinant human antibodies, are also encompassed by the invention.
Jochen G. Salfeld - North Grafton MA, US Deborah J. Allen - Cambridge, GB Hendricus R. J. M. Hoogenboom - Maastricht, BE Zehra Kaymakcalan - Westboro MA, US Boris Labkovsky - Framingham MA, US John A. Mankovich - Andover MA, US Brian T. McGuinness - Comberton, GB Andrew J. Roberts - Cambridge, GB Paul Sakorafas - Newton MA, US David Schoenhaut - Garfield NJ, US Tristan J. Vaughan - Impington, GB Michael White - Framingham MA, US Alison J. Wilton - Cambridge, GB
Human antibodies, preferably recombinant human antibodies, that specifically bind to human tumor necrosis factor a (hTNFα) are disclosed. These antibodies have high affinity for hTNFα (e. g. , K=10M or less), a slow off rate for hTNFα dissociation (e. g. , K=10secor less) and neutralize hTNFα activity in vitro and in vivo. An antibody of the invention can be a full-length antibody or an antigen-binding portion thereof. The antibodies, or antibody portions, of the invention are useful for detecting hTNFα and for inhibiting hTNFα activity, e. g. , in a human subject suffering from a disorder in which hTNFα activity is detrimental. Nucleic acids, vectors and host cells for expressing the recombinant human antibodies of the invention, and methods of synthesizing the recombinant human antibodies, are also encompassed by the invention.
Jochen G. Salfeld - North Grafton MA, US Michael Roguska - Ashland MA, US Michael Paskind - Sterling MA, US Subhashis Banerjee - Shrewsbury MA, US Daniel Edward Tracey - Harvard MA, US Michael White - Framingham MA, US Zehra Kaymakcalan - Westborough MA, US Boris Labkovsky - Marlborough MA, US Paul Sakorafas - Newton MA, US Geertruida M. Veldman - Sudbury MA, US Amy Venturini - Lexington MA, US Angela Widom - Acton MA, US Stuart Friedrich - Cary NC, US Nicholas W. Warne - Andover MA, US Angela Myles - Andover MA, US John Gawain Elvin - Cambridge, GB Alexander Robert Duncan - Cambridge, GB Elaine J. Derbyshire - Royston, GB Sara Carmen - Cambridge, GB Stephen Smith - Ely, GB Thor Las Holtet - Royston, GB Sarah Leila Du Fou - Hitchen, GB
Assignee:
Abbott GmbH & Co., KG - Wiesbaden
International Classification:
C07K 16/24 A61K 39/395
US Classification:
53038823, 4241451
Abstract:
Human antibodies, preferably recombinant human antibodies, that specifically bind to human interleukin-12 (hIL-12) are disclosed. Preferred antibodies have high affinity for hIL-12 and neutralize hIL-12 activity in vitro and in vivo. An antibody of the invention can be a full-length antibody or an antigen-binding portion thereof. The antibodies, or antibody portions, of the invention are useful for detecting hIL-12 and for inhibiting hIL-12 activity, e. g. , in a human subject suffering from a disorder in which hIL-12 activity is detrimental. Nucleic acids, vectors and host cells for expressing the recombinant human antibodies of the invention, and methods of synthesizing the recombinant human antibodies, are also encompassed by the invention.
Methods For Treating Rheumatoid Arthritis Using Human Antibodies That Bind Human Tnfα
Jochen G. Salfeld - North Grafton MA, US Deborah J. Allen - London, GB Zehra Kaymakcalan - Westborough MA, US Boris Labkovsky - Marlborough MA, US John A. Mankovich - Andover MA, US Brian T. McGuinness - Cambridge, GB Andrew J. Roberts - Cambridge, GB Paul Sakorafas - Newton Highlands MA, US Hendricus R. J. M. Hoogenboom - Hasselt, BE David Schoenhaut - Clifton NJ, US Tristan J. Vaughan - Cambridge, GB Michael White - Framingham MA, US Alison J. Wilton - Cambridge, GB
Assignee:
Abbott Biotechnology Ltd.
International Classification:
A61K 39/395 A61K 31/495
US Classification:
4241421, 4241451, 4241581, 424810, 514249
Abstract:
Human antibodies, preferably recombinant human antibodies, that specifically bind to human tumor necrosis factor α (hTNFα) are disclosed. These antibodies have high affinity for hTNFα (e. g. , K=10M or less), a slow off rate for hTNFα dissociation (e. g. , K=10secor less) and neutralize hTNFα activity in vitro and in vivo. An antibody of the invention can be a full-length antibody or an antigen-binding portion thereof. The antibodies, or antibody portions, of the invention are useful for detecting hTNFα and for inhibiting hTNFα activity, e. g. , in a human subject suffering from a disorder in which hTNFα activity is detrimental. Nucleic acids, vectors and host cells for expressing the recombinant human antibodies of the invention, and methods of synthesizing the recombinant human antibodies, are also encompassed by the invention.
Jochen G. Salfeld - North Grafton MA, US Deborah J. Allen - London, GB Hendricus R. J. M. Hoogenboom - Hasselt, BE Zehra Kaymakcalan - Westborough MA, US Boris Labkovsky - Marlborough MA, US John A. Mankovich - Andover MA, US Brian T. McGuinness - Cambridge, GB Andrew J. Roberts - Cambridge, GB Paul Sakorafas - Newton MA, US David Schoenhaut - Clifton NJ, US Tristan J. Vaughan - Cambridge, GB Michael White - Framingham MA, US Alison J. Wilton - Cambridge MA, US
Human antibodies, preferably recombinant human antibodies, that specifically bind to human tumor necrosis factor α (hTNFα) are disclosed. These antibodies have high affinity for hTNFα (e. g. , K=10M or less), a slow off rate for hTNFα dissociation (e. g. , K=10secor less) and neutralize hTNFα activity in vitro and in vivo. An antibody of the invention can be a full-length antibody or an antigen-binding portion thereof. The antibodies, or antibody portions, of the invention are useful for detecting hTNFα and for inhibiting hTNFα activity, e. g. , in a human subject suffering from a disorder in which hTNFα activity is detrimental. Nucleic acids, vectors and host cells for expressing the recombinant human antibodies of the invention, and methods of synthesizing the recombinant human antibodies, are also encompassed by the invention.
Methods For Inhibiting The Activity Of The P40 Subunit Of Human Il-12
Jochen G. Salfeld - North Grafton MA, US Michael Roguska - Ashland MA, US Michael Paskind - Sterling MA, US Subhashis Banerjee - Hamden CT, US Daniel Edward Tracey - Harvard MA, US Michael White - Framingham MA, US Zehra Kaymakcalan - Westborough MA, US Boris Labkovsky - Marlborough MA, US Paul Sakorafas - Newton Highlands MA, US Geertruida M. Veldman - Sudbury MA, US Amy Venturini - Lexington MA, US Angela Widom - Acton MA, US Stuart Friedrich - Cary NC, US Nicholas W. Warne - Andover MA, US Angela Kantor - Pepperell MA, US John Gawain Elvin - Meldreth, GB Alexander Robert Duncan - Carton, GB Elaine Joy Derbyshire - Crowthorne, GB Sara Carmen - Cambridge, GB Stephen Smith - Ely, GB Thor Las Holtet - Rønde, DK Sarah Leila Du Fou - Hitchen, GB
Human antibodies, preferably recombinant human antibodies, that specifically bind to human interleukin-12 (hIL-12 ) are disclosed. Preferred antibodies have high affinity for hIL-12 and neutralize hIL-12 activity in vitro and in vivo. An antibody of the invention can be a full-length antibody or an antigen-binding portion thereof. The antibodies, or antibody portions, of the invention are useful for detecting hIL-12 and for inhibiting hIL-12 activity, e. g. , in a human subject suffering from a disorder in which hIL-12 activity is detrimental. Nucleic acids, vectors and host cells for expressing the recombinant human antibodies of the invention, and methods of synthesizing the recombinant human antibodies, are also encompassed by the invention.
Jochen G. Salfeld - North Grafton MA, US Deborah J. Allen - London, GB Hendricus R. J. M. Hoogenboom - Hasselt, BE Zehra Kaymakcalan - Westboro MA, US Boris Labkovsky - Framingham MA, US John A. Mankovich - Andover MA, US Brian T. McGuinness - Cambridge, GB Andrew J. Roberts - Cambridge, GB Paul Sakorafas - Shrewsbury MA, US David Schoenhaut - Clifton NJ, US Tristan J. Vaughan - Cambridge, GB Michael White - Framingham MA, US Alison J. Wilton - Cambridge, GB
Assignee:
Abbott Biotechnology Ltd. - Hamilton
International Classification:
A61K 39/395 C07K 16/24
US Classification:
4241421, 4241451, 4241581, 53038815, 53038823
Abstract:
Human antibodies, preferably recombinant human antibodies, that specifically bind to human tumor necrosis factor α (hTNFα) are disclosed. These antibodies have high affinity for hTNFα (e. g. , K=10M or less), a slow off rate for hTNFα dissociation (e. g. , K=10secor less) and neutralize hTNFα activity in vitro and in vivo. An antibody of the invention can be a full-length antibody or an antigen-binding portion thereof. The antibodies, or antibody portions, of the invention are useful for detecting hTNFα and for inhibiting hTNFα activity, e. g. , in a human subject suffering from a disorder in which hTNFα activity is detrimental. Nucleic acids, vectors and host cells for expressing the recombinant human antibodies of the invention, and methods of synthesizing the recombinant human antibodies, are also encompassed by the invention.
Pfizer - Andover, MA since Jan 2013
Senior Scientist
Biogen Idec - Waltham Apr 2007 - Mar 2012
Scientist
Abbott Bioresearch Center Apr 2002 - Feb 2007
Biacore Facility Manager
BASF Bioresesearch 1989 - 2001
Senior Research Associate
Children's Hospital Boston 1983 - 1994
Clinical Chemistry Technologist
Education:
Harvard University 1998 - 2002
Certificate, Administrative Management
Boston University 1983 - 1987
MA, Microbiology
Boston University 1977 - 1981
BA, Biology