Abstract: Compounds having the formula are angiogenesis inhibitors. Also disclosed are compositions containing the compounds, methods of making the compounds, and methods of treatment using the compounds.
Type:
Grant
Filed:
October 8, 2004
Date of Patent:
September 22, 2009
Assignee:
Abbott Laboratories
Inventors:
Fortuna Haviv, Michael F. Bradley, Daryl R. Sauer
Abstract: Compounds of Formula (I) inhibit the PARP enzyme and are useful for treating a disease or a disorder associated with PARP. Also disclosed are pharmaceutical compositions comprising compounds of Formula (I), methods of treatment comprising compounds of Formula (I), and methods of inhibiting the PARP enzyme comprising compounds of Formula (I).
Type:
Grant
Filed:
April 11, 2006
Date of Patent:
June 23, 2009
Assignee:
Abbott Laboratories Inc.
Inventors:
Gui-Dong Zhu, Jianchun Gong, Virajkumar B. Gandhi, Thomas D. Penning, Vincent L. Giranda
Abstract: In one aspect, the present invention relates to a formulation in the form of molecular dispersion comprising i) fenofibric acid, a physiologically acceptable salt or derivative thereof and optionally other active substances, ii) a binder component comprising at least one enteric binder, and optionally iii) other physiologically acceptable excipients. In a second aspect, the present invention relates to novel salts of fenofibric acid that are photostable when compared to other salts of fenofibric acid.
Type:
Grant
Filed:
June 30, 2004
Date of Patent:
August 21, 2007
Assignee:
Abbott Laboratories
Inventors:
Russell Drew Cink, Joseph B. Paterson, Jr., Yi Gao, Geoff G. Z. Zhang, Michelle A. Long, John B. Morris, Joerg Rosenberg
Abstract: The present invention is directed to a formulation comprising a lipid-regulating agent dissolved in at least one structured lipid as the primary solvent medium for said agent. One or more emulsifiers may be added to the formulation.
Type:
Grant
Filed:
December 18, 1998
Date of Patent:
March 21, 2006
Assignee:
Abbott Laboratories
Inventors:
John M. Lipari, Dawn M. Raymond, Tom Reiland
Abstract: The present invention is directed to a formulation comprising a lipid-regulating agent dissolved in at least one monoglyceride as the primary solvent medium for said agent. One or more emulsifiers may be added to the formulation.
Type:
Grant
Filed:
December 18, 1998
Date of Patent:
January 4, 2005
Assignee:
Abbott Laboratories
Inventors:
John M. Lipari, Dawn M. Raymond, Tom Reiland, Yeshwant D. Sanzgiri
Abstract: Compounds having the formula
are useful for inhibiting protein kinases. Also disclosed are compositions which inhibit protein kinases and methods of inhibiting protein kinases in a patient.
Type:
Grant
Filed:
December 12, 2002
Date of Patent:
December 14, 2004
Assignee:
Abbott Laboratories
Inventors:
Qun Li, Keith W. Woods, Gui-Dong Zhu, John P. Fischer, Jianchun Gong, Tongmei Li, Virajkumar Gandhi, Sheela A. Thomas, Garrick K. Packard, Xiaohong Song, Jason N. Abrams, Robert B. Diebold, Jürgen Dinges, Charles W. Hutchins, Vincent S. Stoll, Saul H. Rosenberg, Vincent L. Giranda
Abstract: The present invention is directed to a formulation comprising a lipid-regulating agent dissolved in at least one medium chain glycerol ester of a fatty acid as the primary solvent medium for said agent. One or more emulsifiers may be added to the formulation.
Type:
Grant
Filed:
December 18, 1998
Date of Patent:
November 9, 2004
Assignee:
Abbott Laboratories
Inventors:
John M. Lipari, Dawn M. Raymond, Tom Reiland
Abstract: Compounds having the formula
or therapeutically acceptable salts thereof, are protein kinase inhibitors. Preparation of the compounds, compositions containing the compounds, and treatment of diseases using the compounds are disclosed.
Abstract: N-Alkylated peptides of formula (I)
Xaa1-Xaa2-Xaa3-Xaa4-Xaa5-Xaa6-Xaa7-Xaa8-Xaa9-Xaa10-Xaa11 (I),
are useful for inhibiting angiogenesis. Also disclosed are angiogenesis-inhibiting compositions and methods of inhibiting angiogenesis in a mammal.
Type:
Grant
Filed:
October 31, 2000
Date of Patent:
August 17, 2004
Assignee:
Abbott Laboratories
Inventors:
Fortuna Haviv, Jack Henkin, Douglas M. Kalvin, Michael F. Bradley
Abstract: Peptides having the formula:
A0-A1-A2-A3-A4-A5-A6-A7-A8-A9-A10
wherein A0 is selected from hydrogen or an acyl group; A10 is a hydroxyl group or an amino acid amide; and A1, A2, A3, A4, A5, A6, A7, A8, and A9 are amino acyl residues as defined herein.
Type:
Grant
Filed:
April 11, 2001
Date of Patent:
August 10, 2004
Assignee:
Abbott Laboratories
Inventors:
Jack Henkin, Fortuna Haviv, Michael F. Bradley, Douglas M. Kalvin, Andrew J. Schneider
Abstract: N-Benzoyl arylsulfonamides having the formula:
are BCL-X1 inhibitors and are useful for promoting apoptosis. Also disclosed are BCL-X1 inhibiting compositions and methods of promoting apoptosis in a mammal.
Type:
Grant
Filed:
September 20, 2001
Date of Patent:
April 13, 2004
Assignee:
Abbott Laboratories
Inventors:
David J. Augeri, Steven A. Baumeister, Milan Bruncko, Daniel A. Dickman, Hong Ding, Jurgen Dinges, Stephen W. Fesik, Philip J. Hajduk, Aaron R. Kunzer, William McClellan, David G. Nettesheim, Thorsten Oost, Andrew M. Petros, Saul H. Rosenberg, Wang Shen, Sheela A. Thomas, Xilu Wang, Michael D. Wendt
Abstract: Peptides having the formula:
A0-A1-A2-A3-A4-A5-A6-A7-A8-A9-A10
wherein A0 is selected from hydrogen or an acyl group; A10 is a hydroxyl group or an amino acid amide; and A1, A2, A3, A4, A5, A6, A7, A8, and A9 are amino acyl residues as defined herein.
Type:
Grant
Filed:
November 22, 1999
Date of Patent:
April 6, 2004
Assignee:
Abbott Laboratories
Inventors:
Jack Henkin, Fortuna Haviv, Michael F. Bradley, Douglas M. Kalvin, Andrew J. Schneider
Abstract: Mammalian kringle 5 fragments and kringle 5 fusion proteins are disclosed as a compounds for treating angiogenic diseases. Methods and compositions for inhibiting angiogenic diseases are also disclosed.
Abstract: Compounds having Formula I
or pharmaceutically acceptable salts or prodrugs thereof, are useful for treating pathological states which arise from or are exacerbated by angiogenesis. The invention also relates to pharmaceutical compositions comprising these compounds and to methods of inhibiting angiogenesis in a mammal.
Type:
Grant
Filed:
May 21, 1999
Date of Patent:
October 14, 2003
Assignee:
Abbott Laboratories
Inventors:
Megumi Kawai, Jack Henkin, George S. Sheppard, Richard A. Craig
Abstract: Compounds having the formula
are inhibitors of urokinase and are useful in the treatment of diseases in which urokinase plays a role. Also disclosed are urokinase-inhibiting compositions, methods for the preparation of urokinase-inhibitors, and a method of inhibiting urokinase in a mammal.
Type:
Grant
Filed:
April 25, 2001
Date of Patent:
December 17, 2002
Assignee:
Abbott Laboratories
Inventors:
Milan Bruncko, Christopher Robin Dalton, Vincent Louis Giranda, Jianchun Gong, Willian J. McClellan, Vicki L. Nienaber, Todd Warren Rockway, Daryl Richard Sauer, Moshe Weitzberg
Abstract: Compounds having the formula
are matrix metalloproteinase inhibitors. Also disclosed are matrix metalloproteinase-inhibiting compositions and methods of inhibiting matrix metalloproteinase in a mammal.
Type:
Grant
Filed:
January 27, 2000
Date of Patent:
September 25, 2001
Assignee:
Abbott Laboratories
Inventors:
Michael L. Curtin, Yujia Dai, Steven K. Davidsen, Joseph F. Dellaria, Jr., Alan S. Florjancic, Jianchun Gong, Yan Guo, Howard R. Heyman, James H. Holms, Michael R. Michaelides, Jamie R. Stacey, Douglas H. Steinman, Carol K. Wada, Lianhong Xu