University of Michigan School of Dentistry
Adjunct Professor, Department of Periodontics and Oral Medicine
Amgen Mar 1, 1999 - Dec 2014
Scientific Director
Phylon Pharma Services Mar 1, 1999 - Dec 2014
Owner
Boston University Aug 1998 - Mar 1999
Instructor
Ucsf Feb 1996 - Aug 1998
Post-Doctoral Fellow
Education:
Mcmaster University 1989 - 1995
Doctorates, Doctor of Philosophy, Philosophy
University of Waterloo 1985 - 1989
Bachelors, Bachelor of Science, Kinesiology
Skills:
Metabolic Bone Disease Pharmacology Biomarkers Calcium Mineral Homeostasis Kidney Disease Osteoporosis Dental Research Cancer Biology Evolutionary Biology Rheumatoid Arthritis Implantology Research Orthopedic Research Vascular Biology Medical Imaging
Interests:
Children Education Poverty Alleviation Science and Technology Health
Paul Kostenuik - Newbury Park CA, US David Lacey - Newbury Park CA, US
Assignee:
Amgen Inc.
International Classification:
A61K039/395 A61K031/66 A61K038/17
US Classification:
424/178100, 514/012000, 514/102000
Abstract:
The present invention concerns therapeutic agents that modulate the activity of PTH and PTHrP. In accordance with the present invention, modulators of PTH and PTHrP comprise: (a) a PTH/PTHrP modulating domain; and (b) a vehicle, such as a polymer (e.g., PEG or dextran) or an Fc domain, which is preferred; wherein the vehicle is covalently attached to the C-terminus of the PTH/PTHrP modulating domain. The vehicle and the PTH/PTHrP modulating domain may be linked through the N- or C-terminus of the PTH/PTHrP modulating domain, as described further below. The preferred vehicle is an Fc domain, and the preferred Fc domain is an IgG Fc domain. Preferred PTH/PTHrP modulating domains comprise the PTH and PTHrP-derived amino acid sequences described hereinafter. Other PTH/PTHrP modulating domains can be generated by phage display, RNA-peptide screening and the other techniques mentioned herein. Such peptides typically will be modulators of both PTH activity and PTHrP activity, although such techniques can be used to generate peptide sequences that serve as selective modulators (e.g., agonists of PTH activity but not PTHrP activity).
Modulators Of Receptors For Parathyroid Hormone And Parathyroid Hormone-Related Protein
Paul Kostenuik - Newbury Park CA, US David Lacey - Newbury Park CA, US
Assignee:
Amgen Inc.
International Classification:
C07K016/46
US Classification:
530/391100
Abstract:
The present invention concerns therapeutic agents that modulate the activity of PTH and PTHrP. In accordance with the present invention, modulators of PTH and PTHrP comprise: (a) a PTH/PTHrP modulating domain; and (b) a vehicle, such as a polymer (e.g., PEG or dextran) or an Fc domain, which is preferred; wherein the vehicle is covalently attached to the C-terminus of the PTH/PTHrP modulating domain. The vehicle and the PTH/PTHrP modulating domain may be linked through the N— or C-terminus of the PTH/PTHrP modulating domain, as described further below. The preferred vehicle is an Fc domain, and the preferred Fc domain is an IgG Fc domain. Preferred PTH/PTHrP modulating domains comprise the PTH and PTHrP-derived amino acid sequences described hereinafter. Other PTH/PTHrP modulating domains can be generated by phage display, RNA-peptide screening and the other techniques mentioned herein. Such peptides typically will be modulators of both PTH activity and PTHrP activity, although such techniques can be used to generate peptide sequences that serve as selective modulators (e.g., agonists of PTH activity but not PTHrP activity).
Modulators Of Receptors For Parathyroid Hormone And Parathyroid Hormone-Related Protein
Paul Kostenuik - Newbury Park CA, US Colin Gegg - Newbury Park CA, US Mark Jarosinski - Boulder CO, US Olaf Kinstler - Newbury Park CA, US
International Classification:
C07K014/635 A61K038/29
US Classification:
514012000, 530399000
Abstract:
The present invention concerns therapeutic agents that modulate the activity of PTH and PTHrP. In accordance with the present invention, modulators of PTH and PTHrP comprise: (a) a PTH/PTHrP modulating domain; and (b) a vehicle, such as a polymer (e.g., PEG or dextran) or an Fc domain, which is preferred; wherein the vehicle is covalently attached to the C-terminus of the PTH/PTHrP modulating domain or through a sidechain at any residue from residue 14 through the C-terminal residue. The vehicle and the PTH/PTHrP modulating domain may be linked through the N- or C-terminus of the PTH/PTHrP modulating domain, as described further below. The preferred vehicle is PEG. Preferred PTH/PTHrP modulating domains comprise the PTH and PTHrP-derived amino acid sequences described hereinafter. Other PTH/PTHrP modulating domains can be generated by phage display, RNA-peptide screening and the other techniques mentioned herein. Such peptides typically will be modulators of both PTH activity and PTHrP activity, although such techniques can be used to generate peptide sequences that serve as selective modulators (e.g., agonists of PTH activity but not PTHrP activity).
Paul Kostenuik - Newbury Park CA, US Wenyan Shen - Palo Alto CA, US Thomas Boone - Newbury Park CA, US
International Classification:
A61K 39/395 C07K 16/46 C07K 16/28
US Classification:
424145100, 424178100, 530388240, 530391100
Abstract:
Chimeric molecules comprising receptor activator of NF-κB ligand (RANKL) antibodies and parathyroid hormone/parathyroid hormone-related protein (PTH/PTHrP) peptides are described. Compositions and methods for the treatment of bone diseases are also described.