Mark E. Salvati - Lawrenceville NJ, US Marco M. Gottardis - Princeton NJ, US Ricardo M. Attar - Lawrenceville NJ, US John S. Sack - Lawrenceville NJ, US
Selective androgen receptor modulators (SARMs) having antagonist activity in hormone-dependent tumors while exhibiting no activity or agonist activity against other nontumor tissues containing the androgen receptor as well as methods for identifying, designing and using SARMs are provided.
Methods For Identifying Or Screening For Agents That Modulate 17Β-Hsd3
Matthew V. Lorenzi - Philadelphia PA, US Thomas Spires - Monroe NJ, US Dan You - Cranbury NJ, US Roberto Weinmann - Princeton NJ, US Marco Gottardis - Princeton NJ, US
Methods for determining whether a test agent inhibits a 17β-HSD3, the methods comprising: obtaining a recombinant host cell that expresses the 17β-HSD3; obtaining a reaction mixture comprising the 17β-HSD3, androstenedione, and the test agent; measuring the amount of testosterone in the reaction mixture by a scintillation proximity assay (SPA) using SPA beads conjugated with a testosterone-specific antibody, wherein when the amount of testosterone is lower in the presence of a test agent than in the absence of the test agent, the test agent is identified as an inhibitor of the 17β-HSD3.
Polynucleotides Encoding Human Histone Deacetylase Hdac9C
Donald G. Jackson - Lawrenceville NJ, US Matthew V. Lorenzi - Philadelphia PA, US Ricardo M. Attar - Lawrenceville NJ, US Marco Gottardis - Princeton NJ, US Liana M. Lee - San Francisco CA, US John N. Feder - Belle Mead NJ, US
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
C07H 21/04
US Classification:
536 231, 536 232, 4353201, 530350
Abstract:
The present invention relates to newly discovered human histone deacetylases (HDACs), also referred to as histone deacetylase-like polypeptides. The polynucleotide sequences and encoded polypeptides of the novel HDACs are encompassed by the invention, as well as vectors comprising these polynucleotides and host cells comprising these vectors. The invention also relates to antibodies that bind to the disclosed HDAC polypeptides, and methods employing these antibodies. Also related are methods of screening for modulators, such as inhibitors or antagonists, or agonists. The invention also relates to diagnostic and therapeutic applications which employ the disclosed HDAC polynucleotides, polypeptides, and antibodies, and HDAC modulators. Such applications can be used with diseases and disorders associated with abnormal cell growth or proliferation, cell differentiation, and cell survival, e. g. , neoplastic cell growth, and especially breast and prostate cancers or tumors.
Fused Cyclic Succinimide Compounds And Analogs Thereof, Modulators Of Nuclear Hormone Receptor Function
Mark E. Salvati - Lawrenceville NJ, US Ricardo M. Attar - Lawrenceville NJ, US Marco M. Gottardis - Princeton NJ, US James Aaron Balog - Scotch Plains NJ, US Dacia A. Pickering - Lawrenceville NJ, US Rogelio L. Martinez - Monmouth Junction NJ, US Chongqing Sun - East Windsor NJ, US
Fused cyclic compounds, methods of using such compounds in the treatment of nuclear hormone receptor-associated conditions such as cancer and immune disorders, and pharmaceutical compositions containing such compounds.
Multivalent Fibronectin Based Scaffold Domain Proteins
Ray Camphausen - Wayland MA, US Eric Furfine - Concord MA, US Irvith M. Carvajal - Brighton MA, US H. Nicholas Marsh - Charlestown MA, US Marco Gottardis - Princeton NJ, US Joan Carboni - Yardley PA, US Ricardo Attar - Lawrenceville NJ, US
The present invention relates to multivalent polypeptides comprising at least two fibronectin scaffold domains connected via a polypeptide linker. The invention also relates to multivalent polypeptides for use in diagnostic, research and therapeutic applications. The invention further relates to cells comprising such proteins, polynucleotide encoding such proteins or fragments thereof, and to vectors comprising the polynucleotides encoding the innovative proteins.
Stuart Emanuel - Doylestown PA, US Linda Engle - Framingham MA, US Ray Camphausen - Wayland MA, US Martin C. Wright - Boston MA, US Ginger Chao - Cambridge MA, US Marco Gottardis - Princeton NJ, US Joan Carboni - Yardley PA, US
The present invention relates to bispecific molecules comprising an EGFR binding domain and a distinct IGFIR binding domain for use in diagnostic, research and therapeutic applications. The invention further relates to cells comprising such proteins, polynucleotide encoding such proteins or fragments thereof, and vectors comprising the polynucleotides encoding the innovative proteins. Exemplary bispecific molecules include antibody-like protein dimers based on the tenth fibronectin type III domain.
Biomarkers And Methods For Determining Sensitivity To Insulin Growth Factor-1 Receptor Modulators
Fei Huang - Princeton NJ, US Xia Han - Pennington NJ, US Rameh Hafezi - Franklin Park NJ, US Jiwen Chen - Bridgewater NJ, US Douglas Michael Robinson - Hanover MA, US Gayle M. Wittenberg - Princeton NJ, US Ashok Ramesh Dongre - Newtown PA, US Joan M. Carboni - Yardley PA, US Ricardo M. Attar - Lawrenceville NJ, US Warren Hurlburt - Mount Laurel NJ, US Marco M. Gottardis - Princeton NJ, US
Assignee:
Bristol-Myers Squibb Company - Princeton NJ
International Classification:
A01N 61/00 G01N 33/53
US Classification:
514 1, 435 71
Abstract:
IGF1R biomarkers useful in a method for identifying and monitoring a mammal that will respond therapeutically to a method of treating cancer comprising administering an IGF1R modulator, wherein the method comprises (a) exposing the mammal to the IGF1R modulator and (b) measuring in the mammal the level of the at least one biomarker, wherein a difference in the level of the at least one biomarker measured in (b) compared to the level of the biomarker in a mammal that has not been exposed to the IGF1R modulator indicates that the mammal will respond therapeutically to the method of treating cancer and (c) wherein the level of the biomarker in a mammal after exposure to a IGF1R modulator indicates that the mammal has responded therapeutically to the method of treating cancer.
Transgenic Non-Human Mammals Expressing A Reporter Nucleic Acid Under The Regulation Of Androgen Response Elements
Ricardo Attar - Lawrenceville NJ, US David Bol - Gaithersburg MD, US Marco Gottardis - Princeton NJ, US Kasim Mookhtiar - Richboro PA, US Ronald Rowley - Guilford CT, US Jacek Ostrowski - Jamison PA, US
International Classification:
A01K067/027 C12N005/06
US Classification:
800/018000, 435/354000
Abstract:
A transgenic non-human mammal whose genome comprises a nucleic acid construct, wherein said construct comprises a reporter nucleic acid encoding a reporter operably linked to a promoter comprising an androgen response element (ARE), and said construct further comprises an androgen receptor nucleic acid encoding an androgen receptor, and wherein expression of said reporter nucleic acid is regulated by expression of said androgen receptor nucleic acid. The transgenic non-human mammals can be used as an in vivo model for the identification and development of selective androgen receptor modulators (SARMs) for the treatment of cancer or other disorders associated with defective androgen receptor function.
The Janssen Pharmaceutical Companies of Johnson & Johnson
Vice President of Oncology Innovation
The Janssen Pharmaceutical Companies of Johnson & Johnson
Vice President at Janssen, Pharmaceutical Companies of Johnson and Johnson
Bristol-Myers Squibb Jun 1998 - Aug 2012
Executive Director
Education:
University of Wisconsin - Madison
Doctorates, Doctor of Philosophy, Biology, Philosophy
Skills:
Oncology Pharmaceutical Industry Research Strategic Planning Drug Development Translational Medicine Biotechnology Drug Discovery Biomarkers Budgets Clinical Trials Public Speaking Leadership Negotiation Clinical Development Photoshop Admet Molecular Biology Microsoft Office Microsoft Excel Microsoft Word Powerpoint English Windows Outlook