Antengene Corporation
Founder and Chief Executive Officer
Celgene Oct 1, 2008 - Apr 2017
Executive Director, Clinical Development, Hematology and Oncology
Novartis Apr 2006 - Oct 2008
Senior Director and Global Clinical Program Head; Clinical Development
Novartis Apr 2006 - Oct 2008
Senior Director, Oncology Clinical Development
Novartis Apr 2006 - Oct 2008
Director
Education:
University of Maryland - Baltimore 1989 - 1993
Doctorates, Doctor of Philosophy
Xiang - Ya Medical College 1983 - 1989
Doctor of Medicine, Doctorates, Medicine
Skills:
Oncology Clinical Development Clinical Trials Drug Development Cro Regulatory Submissions Drug Discovery Pharmacology Neurology Clinical Research
Executive Director, Clinical Development at Celgene
Location:
United States
Industry:
Pharmaceuticals
Work:
Celgene since Oct 2008
Executive Director, Clinical Development
Novartis Oncology Apr 2006 - Oct 2008
Senior Director/Global Clinical Program Head; Clinical Development
Us Patents
N-Substituted Tricyclic 1-Aminopyrazoles As Inhibitors For The Treatment Of Cell Proliferative Disorders
Chih Yung Ho - Lansdale PA, US Bengt Anders Brunmark - LaJolla CA, US Stuart Emanuel - Doylestown PA, US Dana L. Johnson - Upper Black Eddy PA, US Donald W. Ludovici - Quakertown PA, US Umar Maharoof - North Wales PA, US Jay M. Mei - North Wales PA, US Jan L. Sechler - Doylestown PA, US Eric D. Strobel - Hatboro PA, US Robert W. Tuman - Chalfont PA, US Hwa Kwo Yen - Malvern PA, US
Assignee:
Janssen Pharmaceutica NV
International Classification:
A61K 31/416 A61K 31/4439 C07D 401/12
US Classification:
5462757, 5483595, 514338, 514405
Abstract:
The invention is directed to N-substituted tricyclic 3-AMINOPYRAZOLE derivatives, which are useful as inhibitors of platelet-derived growth factor receptor (PDGF-R) kinase, and methods for the preparation of said derivatives. The present invention is further directed to pharmaceutical compositions comprising the compounds of the present invention and to methods for treating conditions such as tumors and other cell proliferative disorders.
N-Substituted Tricyclic 3-Aminopyrazoles As Anti-Mitotic Tubulin Polymerization Inhibitors
Robert A. Galemmo - Paoli PA, US Dana L. Johnson - Upper Black Eddy PA, US Umar S. M. Maharoof - North Wales PA, US Jay M. Mei - North Wales PA, US Robert W. Tuman - Chalfont PA, US
Assignee:
Janssen Pharmaceutica NV
International Classification:
A61K 31/416 C07D 231/54
US Classification:
514405, 5483591
Abstract:
The invention is directed to compounds having the following structures:.
N-Substituted Tricyclic 3-Aminopyrazoles As Inhibitors For The Treatment Of Cell Proliferative Disorders
Chih Ho - Lansdale PA, US Bengt Brunmark - LaJolla CA, US Stuart Emanuel - Doylestown PA, US Robert Galemmo - Collegeville PA, US Dana Johnson - Upper Black Eddy PA, US Donald Ludovici - Quakertown PA, US Umar Maharoof - North Wales PA, US Jay Mei - North Wales PA, US Jan Sechler - Doylestown PA, US Eric Strobel - Hatboro PA, US Robert Tuman - Chalfont PA, US Hwa Yen - Malvern PA, US
International Classification:
A61K031/415 C07D231/56 C07D231/54
US Classification:
514/405000, 548/359100, 548/360100
Abstract:
The invention is directed to N-substituted tricyclic 3-AMINOPYRAZOLE derivatives, which are useful as inhibitors of platelet-derived growth factor receptor (PDGF-R) kinase, and methods for the preparation of said derivatives. The present invention is further directed to pharmaceutical compositions comprising the compounds of the present invention and to methods for treating conditions such as tumors and other cell proliferative disorders.
Immobilized N-Substituted Tricyclic 3-Aminopyrazoles For The Identification Of Biomolecular Targets
Chih Ho - Lansdale PA, US Robert Galemmo - Paoli PA, US Dana Johnson - Upper Black Eddy PA, US Jay Mei - North Wales PA, US Stanley Belkowski - Norristown PA, US Richard Connors - Harleysville PA, US
The present invention relates to immobilized N-substituted tricyclic 3-aminopyrazole compounds of Formula 1 as tools for the identification of bimolecular targets in cells of therapeutic significance, profiling the selectivity of compounds, prediction of possible related toxicities and exploration of mechanisms of action in biological systems for therapeutic indications related to compounds. These agents can be used to identify biomolecules with the potential to interact with the immobilized reagent. The identified biomolecule may be then be used as a therapeutic target, serve as a marker of drug action, or alternatively describe an untoward or toxic potential of the immobilized agent.
Methods Of Treating A Bruton's Tyrosine Kinase Disease Or Disorder
- Cambridge MA, US Heather Lounsbury - Framingham MA, US Kathryn Stiede - Hollis NH, US Bruce A. Silver - Dunkirk MD, US Jay M. Mei - North Wales PA, US
International Classification:
A61K 31/506 A61K 9/48 A61K 9/00
Abstract:
The present invention provides methods of treating, stabilizing or lessening the severity or progression of a disease or disorder associated with BTK.
Methods Of Treating A Disease Or Disorder Associated With Bruton's Tyrosine Kinase