Abstract: The present invention relates to methods for diagnosing multiple sclerosis in a subject, the method, comprising determining the level of phosphorylation of a marker in a biological sample from the subject, wherein the marker is selected from ?1-antitrypsin (a1AT) and vitamin D binding protein (VDBP); and comparing the level of phosphorylation of the marker in the sample to a reference value.
Type:
Application
Filed:
July 10, 2006
Publication date:
July 17, 2008
Applicant:
AstraZeneca AB
Inventors:
Bodil Eriksson, Bo Franzen, Jan Ottervald
Abstract: The present invention relates to new compounds or salts, solvates or solvated salts thereof, processes for their preparation and to new intermediates used in the preparation thereof, pharmaceutical compositions containing said compounds and to the use of said compounds in therapy.
Type:
Application
Filed:
December 21, 2006
Publication date:
July 17, 2008
Applicant:
AstraZeneca AB
Inventors:
Yevgeni Besidski, Martin Nylof, Inger Kers, Karin Skogholm, Shawn Johnston, Paul Jones, Denis Lebrecque, Andrew Griffin
Abstract: The invention relates to a novel group of compounds of Formula (I) or a salt thereof: wherein R1, A and HET-1 are as described in the specification, which may be useful in the treatment or prevention of a disease or medical condition mediated through glucokinase (GLK) such as type 2 diabetes. The invention also relates to pharmaceutical compositions comprising said compounds, methods of treatment of diseases mediated by GLK using said compounds and methods for preparing compounds of Formula (I).
Type:
Application
Filed:
October 22, 2007
Publication date:
July 17, 2008
Applicant:
AstraZeneca AB
Inventors:
Leonie Campbell, Kurt Gordon Pike, Abid Suleman, Michael James Waring
Abstract: A compound of formula (I) or a pharmaceutically acceptable salt thereof, processes for their preparation, pharmaceutical compositions containing them and their use in therapy, for example in the treatment of proliferative disease such as cancer and particularly in disease mediated by an mTOR kinase and/or one or more PI3K enzyme.
Type:
Application
Filed:
August 23, 2007
Publication date:
July 17, 2008
Applicant:
AstraZeneca AB
Inventors:
Maurice Raymond Verschoyle Finlay, Jeffrey Morris, Kurt Gordon Pike
Abstract: This invention relates to novel compounds having the structural formula I below: and to their pharmaceutically acceptable salt, compositions and methods of use. These novel compounds provide a treatment or prophylaxis of cognitive impairment, Alzheimer Disease, neurodegeneration and dementia.
Inventors:
James Arnold, Phil Edwards, Mark Sylvester, Stefan Berg, Jorg Holenz, Annika Kers, Karin Kolmodin, Laszlo Rakos, Liselotte Ohberg, Rotticci Didier, Gianni Chessari, Miles Congreve, Christopher Murray, Sahil Patel
Abstract: The present invention provides new compounds of formula Ia and Ib: as well as a process for their preparation and new intermediates used therein, pharmaceutical formulations containing said therapeutically active compounds and to the use of said active compounds in therapy.
Type:
Grant
Filed:
March 28, 2003
Date of Patent:
July 15, 2008
Assignee:
AstraZeneca AB
Inventors:
Stefan Berg, Sven Hellberg, Martin Nylöf, Yafeng Xue
Abstract: The present invention relates to the discovery of an association between the gene encoding FGF-BP1 (fibroblast growth factor-binding protein) and chronic obstructive pulmonary disease (COPD). The invention identifies a role for FGF-BP1 in COPD. The present invention therefore relates to diagnostic techniques for the detection of COPD by detecting all or part of this gene, its precursors or products (mRNA, cDNA, genomic DNA, or protein). The present invention also provides methods and as-says for identifying compounds which modulate FGF-BP1 and which may be used for treating respiratory diseases such as COPD. Furthermore, the invention relates to polymorphisms in the genes encoding FGF-BP1. The invention also relates to the use of polymorphisms in the FGF-BP1-encoding genes in assessing predisposition and/or susceptibility of an individual to chronic obstructive pulmonary disease (COPD).
Abstract: A compound of formula (I), wherein the substituents are as defined in the text for use in inhibiting insulin-like growth factor 1 receptor activity in a warm blooded animal such as man.
Abstract: Compounds of general formula: wherein R1 and R2 are as defined in the specification, as well as salts, enantiomers thereof and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.
Type:
Grant
Filed:
November 5, 2003
Date of Patent:
July 8, 2008
Assignee:
AstraZeneca AB
Inventors:
William Brown, Andrew Griffin, Niklas Plobeck, Christopher Walpole
Abstract: Compounds of the formula (I), or a pharmaceutically-acceptable salt, or an in-vivo-hydrolysable ester thereof, and compounds as shown in (I) wherein C is for example wherein A and B are independently selected from R2a to R3b are independently selected from hydrogen and fluorine; R1a and R1b are independently selected from, for example, hydroxy, —NHC(?W)R4, wherein W is O or S; R4 is, for example, hydrogen, amino, (1-4C)alkyl; HET-1 is, for example, a C-linked 5-membered heteroaryl ring; HET-2 is, for example, an N-linked 5-membered, fully or partially unsaturated heterocyclic ring; are useful as antibacterial agents; and processes for their manufacture and pharmaceutical compositions containing them are described.
Type:
Grant
Filed:
September 9, 2002
Date of Patent:
July 8, 2008
Assignee:
AstraZeneca AB
Inventors:
Michael Barry Gravestock, Neil James Hales, Michael Lingard Swain, Sheila Irene Hauck, Stuart Dennett Mills
Abstract: A compound of formula (I): wherein the substituents are as defined in the text for use in inhibiting insulin-like growth factor 1 receptor activity in a warm blooded animal such as man.
Abstract: The present invention relates to a method of treating a metastatic prostate cancer patient by administering to said patient an effective amount of a bicalutamide (4?-cyano-??,??,??-trifluoro-3-(4-fluorophenylsulphonyl)-2-hydroxy-2-methylpropiono-m-toluidide) containing formulation capable of delivering at least a mean steady state plasma level of (R)-bicalutamide enantiomer of 40 ?g/ml; and to bicalutamide containing products and formulations capable of delivering the at least mean steady state plasma level of (R)-bicalutamide enantiomer of 40 ?g/ml to a patient in need thereof.
Type:
Application
Filed:
February 21, 2006
Publication date:
July 3, 2008
Applicant:
ASTRAZENECA AB
Inventors:
Kevin Joseph Carroll, Thomas Meredydd Morris, Ian Derek Cockshott, Bo-Eric Persson, Paul Alfred Dickinson
Abstract: This invention relates to novel compounds having the structural formula I below: and to their pharmaceutically acceptable salt, compositions and methods of use. These novel compounds provide a treatment or prophylaxis of cognitive impairment, Alzheimer Disease, neurodegeneration and dementia.
Abstract: A compound of formula (I) wherein the substituents are as defined in the text for use in inhibiting insulin-like growth factor 1 receptor activity in a warm blooded animal such as man.
Abstract: The present invention provides a process for the preparation of a compound of formula (I): wherein R1 is C1-6 alkyl; R2 and R3 are, independently, C1-6 alkyl; and R4 is C1-6 alkyl or benzyl (wherein the phenyl ring of benzyl is optionally substituted by nitro, S(O)2(C1-4 alkyl), cyano, C1-4 alkyl, C1-4 alkoxy, C(O)(C1-4 alkyl), N(C1-6 alkyl)2, CF3 or OCF3); the process comprising reacting a compound of formula (II): wherein R2, R3 and R4 are as defined above, with a suitable base; and reacting the product so formed with R1OC(O)CH2X, wherein R1 is as defined above and X is chloro, bromo or iodo; wherein the process is carried out in a suitable solvent at a temperature in the range ?40° C. to ?5° C.; and wherein at least 0.2 moles of the compound of formula (II) are used in the process.
Abstract: The invention relates to thienopyrimidinediones of formula (I): wherein: R1, R2, Q are as defined in the specification, and Ar and Ar2 are selected from certain aromatic ring systems which may be optionally substituted, as defined in the specification. Processes for the preparation of compounds of formula (I), pharmaceutical compositions containing them and their use in therapy are also described and claimed.
Type:
Grant
Filed:
January 15, 2004
Date of Patent:
July 1, 2008
Assignee:
AstraZeneca AB
Inventors:
Simon David Guile, Anthony Howard Ingall
Abstract: The invention provides compounds of formula (I) pharmaceutically acceptable salt or solvate thereof, in which R1, A1, m and A are as defined in the specification; a process for their preparation; pharmaceutical compositions containing them; and their use in therapy.
Type:
Application
Filed:
August 29, 2005
Publication date:
June 26, 2008
Applicant:
AstraZeneca AB
Inventors:
Rhonan Ford, Barrie Martin, Toby Thompson, Nicholas Tomkinson, Paul Willis
Abstract: There is provided a compound of formula (I): or a pharmaceutically acceptable salt thereof. There are also provided processes for the manufacture of a compound of Formula 1, and the use of a compound of Formula 1 as a medicament and in the treatment of cancer.
Type:
Application
Filed:
December 18, 2007
Publication date:
June 26, 2008
Applicant:
ASTRAZENECA AB
Inventors:
David Buttar, Kevin Micheal Foote, Maria-Elena Theoclitou, Andrew Peter Thomas