Abstract: The present invention relates to compositions and methods of preventing or reducing the risk or incidence of skeletal injuries in horses. The present invention further relates to compositions and methods for alleviating pain associated with skeletal injuries in horses and to treating skeletal injuries in horses.
Abstract: The present invention relates to novel cysteine protease inhibitors of Formula I:
the pharmaceutically acceptable salts and N-oxide derivatives thereof, their use as therapeutic agents and methods of making them.
Type:
Grant
Filed:
January 5, 2001
Date of Patent:
February 25, 2003
Assignee:
Merck & Co., Inc.
Inventors:
Renata Marcella Oballa, Petpiboon Prasit, Joel Stephane Robichaud, Elise Isabel, Eduardo Setti, Dan-Xiong Wang, Rohan V. Mendonca, Shankar Venkatraman
Abstract: Compounds of general structural formula I such as that shown in structural formula II
are selective NPY Y5 receptor antagonists, useful in the treatment of obesity and the complications associated therewith.
Type:
Grant
Filed:
June 29, 2001
Date of Patent:
December 17, 2002
Assignees:
Merck & Co., Inc., Banyu Pharmaceutical Co., Ltd.
Inventors:
Ying-Duo Gao, Douglas J. MacNeil, Lihu Yang, Nancy R. Morin, Takehiro Fukami, Akio Kanatani, Takahiro Fukuroda, Yasuyuki Ishii, Masaki Ihara
Abstract: This invention relates to a novel estrogen receptor and to the polynucleotide sequences encoding this receptor. This invention also relates to methods for identifying ligands which bind to this receptor, to the ligands so identified, and to pharmaceutical compositions comprising such ligands. This invention also relates to pharmaceutical compositions useful for treating or preventing estrogen receptor mediated diseases or conditions, such as abnormal bone resorption, cardiovascular diseases, cancer, or central nervous system disorders.
Abstract: The present invention relates to methods of identifying compounds useful as modulators of certain stress responsive kinases. More particularly, the compounds so identified are useful for treating or preventing diseases or conditions that are mediated by, for example, abnormal bone resorption or angiogenesis. These compounds are useful for treating or preventing osteoporosis, and inhibiting vascular restenosis, diabetic retinopathy, macular degeneration, angiogenesis, atherosclerosis, inflammation, and tumor growth.
Abstract: The present invention relates to methods for inhibiting bone resorption in a mammal comprising administering to a mammal in need thereof a therapeutically effective amount of an EP4 receptor subtype antagonist.
Type:
Grant
Filed:
October 13, 1999
Date of Patent:
July 2, 2002
Assignees:
Merck Frosst Canada & Co., Merck & Co., Inc.
Inventors:
Shun-ichi Harada, Gideon A. Rodan, Mohamed Machwate, Marc LaBelle, Kathleen Metters, Robert N. Young
Abstract: Disclosed is a combination therapy for treating and for preventing bone loss by the use of estrogen and a bisphosphonate selected from: alendronate, clodronate, tiludronate, YM175, BM 210995, or mixture thereof. Also described is a pharmaceutical composition of the above for carrying out the therapeutic method.
Abstract: The inhibition of natural bone formation experienced in the prophylaxis and/or treatment of bone resorption disease with a bisphosphonic acid or a pharmaceutically acceptable salt thereof is overcome by the concommitant administration of an agent that binds to the androgen receptor.
Abstract: The present invention relates to a whole cell assay for cathepsin K. The present invention is useful for determining cathepsin K activity in a mammalian cell systems and for identifying and evaluating inhibitors of cathepsin K.
Type:
Grant
Filed:
April 20, 2000
Date of Patent:
February 12, 2002
Assignee:
Merck Frosst Canada & Co.,
Inventors:
Joseph Mancini, Denis Riendeau, David Claveau
Abstract: The present invention relates to a method for inhibiting dental resorptive lesions and other disease states associated with dental resorptive lesions in a mammal by administering a therapeutically effective amount of a bisphosphonate or a pharmaceutically acceptable salt thereof to a mammal in need thereof. This invention also relates methods of alleviating of pain and reducing the risk of tooth loss associated with dental resorptive lesions in mammals.
Abstract: Compounds of general structural formula I such as that shown in structural formula II
are selective NPY Y5 receptor antagonists, useful in the treatment of obesity and the complications associated therewith.
Type:
Grant
Filed:
September 7, 2000
Date of Patent:
November 6, 2001
Assignee:
Merck & Co., Inc.
Inventors:
Ying-Duo Gao, Lihu Yang, Douglas J. MacNeil, Nancy R. Morin, Takehiro Fukami, Takahiro Fukuroda, Akio Kanatani, Yasuyuki Ishii, Masaki Ihara
Abstract: Compounds of the general structural formula I
are selective NPY Y5 receptor antagonists. The compounds and compositions of the present invention are useful in the treatment of obesity and complications associated therewith.
Type:
Grant
Filed:
November 8, 1999
Date of Patent:
February 20, 2001
Assignees:
Merck & Co., Inc., Banyu Pharmaceutical Co., Ltd.
Inventors:
Ying-Duo Gao, Douglas J. MacNeil, Lihu Yang, Nancy R. Morin, Takehiro Fukami, Akio Kanatani, Takahiro Fukuroda, Yasuyuki Ishii, Masaki Ihara