Abstract: Compounds of formula I wherein X is or Y; and wherein A, Y, R1, R2, R3, R4 and R5 are as defined in the specification as a base or a pharmaceutically acceptable salt, solvate or solvate of salt thereof, processes for their preparation, new intermediates used therein, pharmaceutical formulations containing said compounds and to the use of said compounds in therapy.
Type:
Application
Filed:
October 2, 2006
Publication date:
October 16, 2008
Applicant:
ASTRAZENECA AB
Inventors:
Per I Arvidsson, Erwan Arzel, Jeremy Burrows, Martina Claesson, Colin Ray, Tobias Rein, Didier Rotticci, Peter Soderman
Abstract: This invention relates to novel compounds having the structural formula I below: (I) and to their pharmaceutically acceptable salts, compositions and methods of use. These novel compounds provide a treatment or prophylaxis of cognitive impairment, Alzheimer Disease, neurodegeneration and dementia.
Type:
Application
Filed:
November 13, 2006
Publication date:
October 16, 2008
Applicant:
ASTRAZENECA AB
Inventors:
Jeffrey Albert, Donald Andisik, Phil Edwards, Mark Sylvester
Abstract: The present invention relates to slow release anastrozole formulations, more particularly to biodegradable polymers, typically a polylactide or poly(lactide-co-glycolide) co-polymer, in which anastrozole is incorporated, including microparticle formulations and monolithic implant formulations. The invention also relates to methods of treatment using said formulations, particularly methods for the treatment of breast cancer.
Type:
Application
Filed:
August 29, 2006
Publication date:
October 9, 2008
Applicant:
ASTRAZENECA AB
Inventors:
Paul Richard Gellert, Balvinder Singh Matharu
Abstract: The invention relates to a pharmaceutical composition comprising an interleukin-13 antibody, more particularly a monoclonal interleukin-13 antibody, especially a human interleukin-13 monoclonal antibody, to a process for purifying said antibody and to the use of said composition in treating interleukin-13 related disorders, such as asthma, atopic dermatitis, allergic rhinitis, fibrosis, chronic obstructive pulmonary disease, scleroderma, inflammatory bowel disease and Hodgkin's lymphoma, particularly asthma.
Type:
Application
Filed:
September 29, 2006
Publication date:
October 9, 2008
Applicant:
ASTRAZENECA AB
Inventors:
Brendan Cormick Fish, Jeanette Elizabeth Langstone, Karen Bannister, Claire Louise Hope
Abstract: There is provided compounds of formula I, wherein R1, R2, R4, R41 to R46, A, B and G have meanings given in the description, which are useful in the prophylaxis and in the treatment of arrhythmias, in particular atrial and ventricular arrhythmias.
Type:
Application
Filed:
February 11, 2008
Publication date:
October 9, 2008
Applicant:
ASTRAZENECA AB
Inventors:
Annika Bjore, Ulrik Gran, Gert Strandlund
Abstract: The present invention relates to certain novel compounds of the Formula I to processes for preparing such compounds, to their the utility in modulation of nuclear hormone receptors Liver X Receptor (LXR)?(NR1H3) and/or ?(NR1H2) and in treating and/or preventing clinical conditions including cardiovascular diseases such as atherosclerosis; inflammatory diseases, Alzheimer's disease, lipid disorders (dyslipidemias) whether or not associated with insulin resistance, type 2 diabetes and other manifestations of the metabolic syndrome, to methods for their therapeutic use and to pharmaceutical compositions containing them.
Type:
Grant
Filed:
July 8, 2004
Date of Patent:
October 7, 2008
Assignee:
AstraZeneca AB
Inventors:
Jonas Boström, Kay Brickmann, Patrik Holm, Pernilla Sandberg, Marianne Swanson, Christer Westerlund
Abstract: The invention concerns compounds of Formula I, or a pharmaceutically acceptable salt thereof, where R1, n, R2, R3, and R4 are as defined in the description. The present invention also relates to processes for the preparation of such compounds, pharmaceutical compositions containing them and their use in the manufacture of a medicament for use as an antiproliferative agent in the prevention or treatment of tumours or other proliferative conditions which are sensitive to the inhibition of EphB4 kinases.
Type:
Application
Filed:
February 28, 2008
Publication date:
October 2, 2008
Applicant:
ASTRAZENECA AB
Inventors:
Susan Elizabeth Ashton, Darren Anthony Edward Cross, Simon John East, Jason Grant Kettle, Mark Andrew Pearson, Stephen Robert Wedge, Bernard Christophe Barlaam, Richard Ducray, Stuart Charles Purkiss
Abstract: The present invention relates fusion proteins and their use in enzymatic treatment of Alzheimer's disease patients. Said fusion protein has the formula M-A, capable of degrading amyloid beta peptide at one or more cleavage sites in its amino acid sequence, wherein M is a protein component that prolongs the half-life of the fusion protein, and A is a protein component that cleaves the amyloid beta peptide.
Abstract: Methods of treatment and pharmaceutical compositions for providing improved cognition in subjects suffering from schizophrenia, Alzheimer's disease or other conditions with impaired cognitive function.
Type:
Application
Filed:
March 17, 2008
Publication date:
October 2, 2008
Applicant:
ASTRAZENECA AB
Inventors:
Stacy A. Castner, Thomas Hudzik, Donna L. Maier, Ladislav Mrzljak, Timothy Piser, Jeff S. Smith, Dan Widzowski, Graham V. Williams
Abstract: The present invention provides a process for the preparation of substantially racemic 2-{[2-(4-hydroxyphenyl)ethyl]thio}-3-[4-(2-{4-[(methylsulfonyl)oxy]phenoxy}ethyl)phenyl]-propanoic acid which comprises reacting 2-{[2-(4-hydroxyphenyl)ethyl]thio}-3-[4-(2-{4-[(methylsulfonyl)oxy]phenoxy}ethyl)phenyl]propanoic acid enriched in one enantiomer with a base in an inert solvent.
Type:
Grant
Filed:
June 16, 2004
Date of Patent:
September 30, 2008
Assignee:
AstraZeneca AB
Inventors:
Eva-Lotte Lindstedt-Alstermark, Kjell Andersson, Henrik Sorensen
Abstract: Compounds of the following formula (I) wherein R1R2, n, Ar1 and A2 are as defined in the specification, in vivo-hydrolysable precursors thereof, pharmaceutically acceptable salts thereof, the use in therapy and pharmaceutical compositions and methods of treatment using the same. The example compounds are 1-(2-(naphthylmethoxy)-1-phenylethyl)piperazine derivatives. The compounds are neurokinin 1 (NK1) receptor antagonist and/or serotonin reuptake inhibitors, with medical indications for depression and other disorders.
Abstract: The present invention relates to a pyrimidine compound (I) useful as a pharmaceutical intermediate, to a process for preparing said pyrimidine compound, to intermediates used in said process, and to the use of said pyrimidine compound in the preparation of pharmaceuticals.
Type:
Application
Filed:
April 28, 2008
Publication date:
September 25, 2008
Applicant:
AstraZeneca AB
Inventors:
Ulf Larsson, Mattias Magnusson, Tibor Musil, Andreas Palmgren
Abstract: Compounds of Formula I wherein R1, A, R2, R3, R4, R5, n, m and q are as described in the specification, pharmaceutically-acceptable salts, methods of making, pharmaceutical compositions containing and methods for using the same.
Type:
Application
Filed:
September 19, 2006
Publication date:
September 25, 2008
Applicant:
ASTRAZENECA AB
Inventors:
James B. Campbell, Jeffrey S. Albert, Cristobal Alhambra, James Kang, Gerard M. Koether, Thomas R. Simpson, James Woods, Yan Li
Abstract: The present invention relates to compounds and compositions for treating diseases associated with cysteine protease activity. The compounds are reversible inhibitors of cysteine proteases S, K, F, L and B. Of particular interest are diseases associated with Cathepsin S. In addition this invention also discloses processes for the preparation of such inhibitors.
Type:
Application
Filed:
June 3, 2008
Publication date:
September 25, 2008
Applicant:
ASTRAZENECA AB
Inventors:
Andrew Bailey, Garry Pairaudeau, Anil Patel, Stephen Thom
Abstract: Compounds of the formula (I), and pharmaceutically acceptable salts and in vivo hydrolysable esters thereof are described. Also described are processes for their preparation and their use as medicaments, particularly medicaments for producing a cell cycle inhibitory (anti cell proliferation) effect in a warm blooded animal, such as man.
Abstract: A compound of the Formula (I), wherein A together with the carbon atoms to which it is attached forms a fused 5-membered heteroaryl ring, wherein said heteroaryl ring contains 1 or 2 heteroatoms selected from O, N and S, and wherein the 5-membered ring containing G is linked to the ring formed by A in the meta position to the bridgehead carbon marked # in Formula (I): G is selected from O, S and NR5; Z is selected from N and CR6; Q1 is selected from optionally substituted aryl and heteroaryl, and the substituents R1 to R6 are as defined in the text for use in the production of an anti-angiogenic effect in a warm blooded animal such as man.
Type:
Grant
Filed:
August 1, 2003
Date of Patent:
September 23, 2008
Assignee:
AstraZeneca AB
Inventors:
Richard William Arthur Luke, Clifford David Jones, William McCoull, Barry Raymond Hayter
Abstract: The present invention is directed to novel compounds of formula (I)/(II)/(III), their use in therapy and pharmaceutical compositions comprising said novel compounds.
Type:
Application
Filed:
September 20, 2006
Publication date:
September 18, 2008
Applicant:
Astrazeneca AB
Inventors:
Alexander Minidis, David Wensbo, Abdelmalik Slassi, Methvin Isaac, Caroline Ericsson, Veronica Profir, Per-Olov Bergstrom, Louise Edwards, Jalaj Arora, Tao Xin
Abstract: The present invention provides a compound of a formula (I): [Chemical formula should be inserted here. Please see paper copy] wherein the variables are defined herein; to a process for preparing such a compound; and to the use of such a compound in the treatment of a PDE4 mediated disease state.
Type:
Application
Filed:
July 3, 2006
Publication date:
September 18, 2008
Applicant:
ASTRAZENECA AB
Inventors:
Annea Lisius, Grigorios Nikitidis, Peter Sjo