Abstract: Compounds of formula I or pharmaceutically acceptable salts thereof: wherein R1, R2, R3, R4, and R5 and are as defined in the specification as well as salts and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.
Abstract: This invention relates to novel compounds having the structural formula (I) and to their pharmaceutical compositions and to their methods of use. These novel compounds provide a treatment or prophylaxis of cancer.
Type:
Application
Filed:
December 22, 2008
Publication date:
April 16, 2009
Applicant:
ASTRAZENECA AB
Inventors:
Brian Aquila, Michael Howard Block, Audrey Davies, Jayachandran Ezhuthachan, Sandra Ann Filla, Timothy Pontz, Daniel John Russell, Maria-Elena Theoclitou, XiaoLan Zheng
Abstract: The present invention relates to new compounds of formula (I), wherein R1 to R12, P, X, Q and n are as defined as in formula I, or salts, solvates or solvated salts thereof, processes for their preparation and to new intermediates used in the preparation thereof, pharmaceutical formulations containing said compounds and to the use of said compounds in therapy.
Type:
Application
Filed:
May 22, 2006
Publication date:
April 16, 2009
Applicant:
AstraZeneca AB
Inventors:
Gunnar Nordvall, Carl Petersson, Laszlo Rakos, Daniel Sohn
Abstract: A pharmaceutical composition which comprises N-(3-methoxy-5-methylpyrazin-2-yl)-2-(4-[1,3,4-oxadiazol-2-yl]phenyl)pyridine-3-sulphonamide with mannitol and/or microcrystalline cellulose is described.
Type:
Application
Filed:
October 10, 2008
Publication date:
April 16, 2009
Applicant:
ASTRAZENECA AB
Inventors:
John David Blyth, Andrew John Day, Kieran James Lennon
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:
April 16, 2009
Applicant:
AstraZeneca AB
Inventors:
Annika Bjore, Ulrik Gran, Gert Strandlund
Abstract: Compounds of formula (I) or pharmaceutically acceptable salts thereof: wherein R1, R2, R3, R4 and Z are as defined in the specification as well as salts and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.
Type:
Grant
Filed:
June 9, 2004
Date of Patent:
April 14, 2009
Assignee:
AstraZeneca AB
Inventors:
Ziping Liu, Daniel Pagé, Christopher Walpole, Hua Yang
Abstract: The present invention provides a compound of formula (I), wherein: Z is (A) OR (B) and wherein the remaining variables are defined herein; to a process for preparing such a compound; and to the use of such a compound in the treatment of achemokine (such as CCR3) or H1 mediated disease state.
Type:
Grant
Filed:
March 17, 2003
Date of Patent:
April 14, 2009
Assignee:
AstraZeneca AB
Inventors:
Christopher Luckhurst, Matthew Perry, Hitesh Sanganee, Brian Springthorpe
Abstract: An environmental sensor device for detecting environmental conditions within a pharmaceutical product package is described. The sensor device is a stand alone device that includes: a housing defining the outer dimensions of the sensor device, a humidity sensor, a temperature sensor, a control circuit, a memory circuit, a power source and a communications interface. The housing has outer dimensions that allow it to fit inside a pharmaceutical product package. A system and method for evaluating best before date for pharmaceutical products are also described.
Type:
Application
Filed:
June 28, 2006
Publication date:
April 9, 2009
Applicant:
ASTRAZENECA AB
Inventors:
Helen Brown, Darren Hodson, Rachel Jury, Simon Newey, Aziz-ur Rehman
Abstract: Pharmaceutical compositions, oral pharmaceutical compositions, and solid dosage forms comprising up to about 750 mg of 11-piperazin-1-yldibenzo[b,f] [1,4]thiazepine, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier or diluent are provided.
Type:
Application
Filed:
June 13, 2008
Publication date:
April 9, 2009
Applicant:
AstraZeneca AB
Inventors:
Patricia C. Davis, Jeffrey M. Goldstein, Scott W. Grimm, Raymond F. Suckow, Helen R. Winter
Abstract: Methods of treating at least one symptom or condition associated with Anxiety Disorders and/or Mood Disorders comprising administering an effective amount of a compound of Formula I or its pharmaceutically acceptable salt are provided herein.
Type:
Application
Filed:
June 13, 2008
Publication date:
April 9, 2009
Applicant:
ASTRAZENECA AB
Inventors:
Patricia C. Davis, Jeffrey Goldstein, Scott W. Grimm, Raymond F. Suckow, Helen R. Winter
Abstract: Compounds of formula (I) or a pharmaceutically acceptable salt thereof; compositions comprising them, processes for preparing them and their use in medical therapy (for example modulating the glucocorticoid receptor in a warm blooded animal).
Type:
Application
Filed:
October 26, 2005
Publication date:
April 9, 2009
Applicant:
ASTRAZENECA AB
Inventors:
Hakan Bladh, Krister Henriksson, Vijaykumar Hulikal, Matti Lepisto
Abstract: Compounds of formula I: and pharmaceutically-acceptable salts thereof, wherein Q, Ar1, A and Ar2 are as defined in the specification, pharmaceutical compositions and formulations containing them, methods of using them to treat diseases and conditions either alone or in combination with other therapeutically-active compounds or substances, processes and intermediates used to prepare them, uses of them as medicaments for therapy, uses of them in the manufacture of medicaments and uses of them for diagnostic and analytic purposes.
Abstract: The present invention provides the S enantiomer of a compound of formula (I) wherein n is 1 or 2 as well as pharmaceutically acceptable salts, solvates, crystalline forms and prodrugs thereof, to processes for preparing such compounds, to their the utility in treating clinical conditions including lipid disorders (dyslipidemias) whether or not associated with insulin resistance, to methods for their therapeutic use and to pharmaceutical compositions containing them.
Type:
Grant
Filed:
December 18, 2002
Date of Patent:
April 7, 2009
Assignee:
AstraZeneca AB
Inventors:
Eva-Lotte Alstermark Lindstedt, Anna Christina Olsson, Lanna Li
Abstract: The invention relates to a group of novel pyrazole compounds of Formula (I): wherein: R1, R2, R3, M and R5 are as defined in the specification, which are useful as gonadotrophin releasing hormone antagonists. The invention also relates to pharmaceutical formulations of said compounds, methods of treatment using said compounds and to processes for the preparation of said compounds.
Type:
Grant
Filed:
August 19, 2003
Date of Patent:
April 7, 2009
Assignee:
AstraZeneca AB
Inventors:
Thomas Geoffrey Colerick Bird, Mickael Louis Pierre Maudet, Matthias Ferdinand Herdemann
Abstract: The present invention relates to a novel crystalline form of 5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole, known under the generic name omeprazole. Further, the present invention also relates to the use of the novel crystalline form of 5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H -benzimidazole for the treatment of gastrointestinal disorders, pharmaceutical compositions containing it as well as processes for the preparation of the novel crystalline form of 5-methoxy-2-[[(4-methoxy-3,5-dimethyl-2-pyridinyl)methyl]sulfinyl]-1H-benzimidazole.
Type:
Grant
Filed:
May 4, 2006
Date of Patent:
April 7, 2009
Assignee:
AstraZeneca AB
Inventors:
Karin Lövqvist, Gunnel Sundén, David Noreland, Ingvar Ymén
Abstract: An improved process for manufacture of (E)-7-[4-(4-fluorophenyl)-6-isopropyl-2-[methyl)(methylsulfonyl)amino]pyrimidin-5-yl](3R,5S)-3,5-dihydroxyhept-6-enoic acid calcium salt, which is useful for the production of a pharmaceutical useful in the treatment of, inter alia, hypercholesterolemia, hyperlipoproteinemia and atherosclerosis, is described.
Abstract: A pharmaceutical composition comprising a compound of formula wherein n, m, p, X, Y, W, A, G and D are as defined in the specification, enantiomers thereof, or pharmaceutically acceptable salts thereof, its use in therapy, especially in the treatment or prophylaxis of psychotic disorders and intellectual impairment disorders.
Type:
Grant
Filed:
March 15, 2004
Date of Patent:
March 24, 2009
Assignee:
AstraZeneca AB
Inventors:
Eifion Phillips, Robert Mack, John Macor, Simon Semus
Abstract: Disclosed herein is at least one cyclopropyl amide derivative, at least one pharmaceutical composition comprising at least one cyclopropyl amide derivative disclosed herein, and at least one method of using at least one cyclopropyl amide derivative disclosed herein for treating at least one histamine H3 receptor associated condition therewith.
Type:
Application
Filed:
August 21, 2008
Publication date:
March 19, 2009
Applicant:
ASTRAZENECA AB
Inventors:
James Arnold, Todd Andrew Brugel, Scott Throner, Steven Wesolowski, Phil Edwards, Andrew Griffin, Thierry Groblewski, Denis Labrecque
Abstract: Disclosed are compounds of Formula (I) wherein G, R2, A, D and E are as described in the specification, or pharmaceutically-acceptable salts, or in vivo-hydrolysable precursors thereof. Also disclosed herein is at least one method of making, at least one pharmaceutical composition containing, and at least one method for using at least one compound in accordance with Formula I.
Type:
Application
Filed:
January 3, 2007
Publication date:
March 19, 2009
Applicant:
ASTRAZENECA AB
Inventors:
Rebecca Urbanek, Dean Brown, Gary Steelman, William Blackwell, Steven Wesolowski, Xia Wang