Abstract: The invention concerns quinazoline derivatives of Formula (I), wherein each of R1a, R1b, R2, R3 and a have any of the meanings defined in the description; processes for their preparation, 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 which are sensitive to inhibition of erbB receptor tyrosine kinases.
Type:
Grant
Filed:
September 22, 2004
Date of Patent:
November 23, 2010
Assignee:
AstraZeneca AB
Inventors:
Bernard Christophe Barlaam, Laurent Francois Andre Hennequin, Christopher Thomas Halsall
Abstract: The invention concerns bicyclic compounds of Formula (I) wherein, R1, R2, R3, R4, R5, X1, X2, Y, k, m, n and p 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 treatment of androgen-receptor associated conditions, particularly prostate cancer.
Type:
Application
Filed:
May 10, 2010
Publication date:
November 18, 2010
Applicant:
ASTRAZENECA AB
Inventors:
Robert Hugh Bradbury, Alfred Arthur Rabow
Abstract: The invention provides compounds of formula wherein R1, R2, R3, A and m are as defined in the specification and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together with processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The compounds are inhibitors of microsomal prostaglandin E synthase-1.
Type:
Application
Filed:
May 12, 2010
Publication date:
November 18, 2010
Applicant:
ASTRAZENECA AB
Inventors:
Johan Bylund, Maria E. Ek, Jörg Holenz, Annika Kers, Liselotte Öhberg
Abstract: The present invention relates to novel compounds of formulae I and II and therapeutically acceptable salts thereof, their pharmaceutical compositions processes for making them and their use in therapeutic methods for treatment and/or prevention of various diseases. In particular, the invention relates to compounds which interfere with ?-secretase and/or its substrate and hence modulate the formation of A? peptides.
Type:
Application
Filed:
May 11, 2010
Publication date:
November 18, 2010
Applicant:
AstraZeneca AB
Inventors:
Yvonne Lo-Alfredsson, Kim Paulsen, Laszlo Rakos, Didier Rotticci, Magnus Waldman
Abstract: A diagnostic system and method. In one embodiment, the invention is a diagnostic system comprising: a form comprising one or more diagnostic questions and one or more possible answers to each diagnostic question; a first overlay comprising one or more windows and one or more diagnostic fields, wherein when the first overlay is positioned over the form, the answers to the diagnostic questions that are indicative of the user having a first medical condition are visible through the windows of the first overlay; and wherein the one or more diagnostic fields contain criteria for diagnosing the user with the first medical condition based on the user's selection of answers on the form that are visible through the windows of the first overlay. In other embodiments, the invention is a computer-based version of the diagnostic system and a diagnostic method.
Abstract: Compounds of formula (I) and their pharmaceutically acceptable salts are described. Processes for their preparation, pharmaceutical compositions containing them, their use as medicaments and their use in the treatment of bacterial infections are also described.
Type:
Application
Filed:
August 16, 2007
Publication date:
November 11, 2010
Applicant:
ASTRAZENECA AB
Inventors:
Gregory Basarab, Pamela Hill, Kenneth Gregory Hull
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:
October 14, 2009
Publication date:
November 11, 2010
Applicant:
AstraZeneca AB
Inventors:
Yevgeni Besidski, Martin Nylöf, Inger Kers, Karin Skogholm, Shawn Johnstone, Paul Jones, Denis Labrecque, Andrew Griffin
Abstract: A process for preparing particles of a substance, such as a protein or polypeptide, comprising: (a) preparing a first liquid comprising water, the substance and a modulator, wherein the modulator has a solubility in water which decreases with increasing temperature; and (b) contacting the first liquid with a second liquid comprising a fluid gas and an organic solvent using an anti-solvent fluid gas technique under conditions of temperature and pressure which result in the precipitation of particles comprising the substance, wherein the temperature of the first liquid is at or above the cloud point temperature of the first liquid when the first liquid contacts the second liquid. Also claimed are particles obtained according to the process and compositions containing the particles.
Type:
Grant
Filed:
September 15, 2006
Date of Patent:
November 9, 2010
Assignee:
AstraZeneca AB
Inventors:
Goran Eric Sundholm, Mustafa Demirbuker, Saeed Moshashaee
Abstract: There are disclosed novel compounds of formula (I) wherein R1, R12, L, X and Y are as defined in the specification, and pharmaceutically acceptable salts thereof; together with processes for their preparation, compositions containing them and their use in therapy. The compounds are inhibitors of the enzyme MPO and are thereby particularly useful in the treatment or prophylaxis of neuroinflammatory disorders, cardiovascular disorders and respiratory disorders.
Type:
Grant
Filed:
December 5, 2005
Date of Patent:
November 9, 2010
Assignee:
AstraZeneca AB
Inventors:
Anders Bogevig, Yvonne Lo-Alfredsson, Donald Pivonka, Anna-Karin Tiden
Abstract: The invention concerns the use of a combination of an anti-angiogenic agent and an anti-hypertensive agent for use in the manufacture of a medicament for the treatment of a disease state associated with angiogenesis in a warm-blooded mammal, such as a human being. The invention also relates to pharmaceutical compositions comprising an anti-angiogenic agent and an anti-hypertensive agent, to kits thereof and to a method of treatment of a disease state associated with angiogenesis which comprises the administration of an effective amount of a combination of an anti-angiogenic agent and an anti-hypertensive agent to a warm-blooded animal, such as a human being.
Abstract: The invention provides certain novel 6-heteroaryl-5-methyl-3-oxo-4-[3(trifluoromethyl)phenyl]-3,4-dihydropyrazine-2-carboxamide derivatives and pharmaceutically acceptable salts thereof and particular Forms thereof; together with processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The compounds are inhibitors of human neutrophil elastase.
Type:
Application
Filed:
November 5, 2008
Publication date:
November 4, 2010
Applicant:
ASTRAZENECA R&D
Inventors:
Debra Ainge, David Chapman, Martin Lindsjo, Hans Lonn, Michael Lundkvist, Magnus Munck AF Rosen-Schold, Antonios Nikitidis, John Pavey
Abstract: The invention provides compounds of formula (I) wherein R1, R2, R3, R4, R5, R6, R7, R8, R9, R10, R11 and R12 are as defined in the specification, and optical isomers, racemates and tautomers thereof, and pharmaceutically acceptable salts thereof; together with processes for their preparation, pharmaceutical compositions containing them and their use in therapy. The compounds are useful in the treatment of respiratory syncytial virus (RSV).
Type:
Application
Filed:
March 9, 2010
Publication date:
November 4, 2010
Applicants:
ASTRAZENECA UK LIMITED, ARROW THERAPEUTICS LIMITED
Inventors:
Helen Blade, Heather Marie Jackson, Gary Peter Tomkinson, Elisa Ann Carron, James Andrew Lumley, Christopher John Pilkington, Alexander James Floyd Thomas, Justin Warne
Abstract: Compounds of Formula (I) wherein R1, R2, R3 R4 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:
June 5, 2008
Publication date:
November 4, 2010
Applicant:
AstraZeneca AB
Inventors:
Joshua Clayton, Ian Egle, James Empfield, James Folmer, Methvin Isaac, Fupeng Ma, Abdelmalik Slassi
Abstract: Disclosed herein are compounds of formula I in which R1, R2, R3, R4, R5, A, X, Y are as described in the specification, their use in pharmaceutical compositions and in methods of treatment or prophylaxis of a melanin-concentrating hormone related disease or condition.
Type:
Application
Filed:
April 30, 2010
Publication date:
November 4, 2010
Applicant:
AstraZeneca AB
Inventors:
Lars Anders Mikael JOHANSSON, Robert Andrew Judkins, Lanna Li, Bjorn Christian Ingvar Lofberg, Joachim Persson
Abstract: A method related to a process for treating pharmaceutical contents in a pharmaceutical processing vessel is provided. The contents have a number of predefined parameters of variable values. According to the method electromagnetic radiation of various frequencies is transmitted into the vessel and its contents. Electromagnetic radiation which has interacted with the contents is received. Based on the received electromagnetic radiation, a respective value of a physical quantity related to the contents is determining for a plurality of said frequencies. A combination of values of said predefined parameters which would, for said plurality of frequencies, approximately result in the determined values of said physical quantity is determined.
Abstract: The present invention is directed to novel compounds, to a process for their preparation, their use in therapy and pharmaceutical compositions comprising the novel compounds.
Abstract: There are provided crystalline forms of the compounds Ph(3-Cl)(5-OCHF2)—(R)CH(OH)C(O)-Aze-Pab(OMe) and Ph(3-Cl)(5-OCHF2)—(R)CH(OH)C(O)-Aze-Pab(OH), pharmaceutical compositions containing them, processes for obtaining them and their use in medical treatment.
Type:
Grant
Filed:
December 5, 2007
Date of Patent:
October 26, 2010
Assignee:
AstraZeneca AB
Inventors:
Bengt Leonard Åslund, Stefan Bengtsson, Gudrun Anita Bergman, Ursula Renata Maria Hohlneicher, Bo Ingvar Ymén
Abstract: The use of N-(3-methoxy-5-methylpyrazin-2-yl)-2-(4-[1,3,4-oxadiazol-2-yl]phenyl)pyridine-3-sulphonamide, or a pharmaceutically acceptable salt thereof, in the treatment of cancer and/or pain in a warm blooded animal such as man is described.
Type:
Grant
Filed:
August 20, 2003
Date of Patent:
October 26, 2010
Assignee:
AstraZeneca AB
Inventors:
David William Tonge, Sian Tomiko Taylor, Francis Thomas Boyle, Andrew Mark Hughes, Donna Johnstone, Marianne Bernice Ashford, Nigel Charles Barrass
Abstract: A quinazoline derivative of the Formula I: wherein the substituents are as defined in the text for use in the production of an anti-proliferative effect which effect is produced alone or in part by inhibiting erbB2 receptor tyrosine kinase in a warm-blooded animal such as man.
Type:
Grant
Filed:
September 14, 2006
Date of Patent:
October 26, 2010
Assignee:
AstraZeneca AB
Inventors:
Robert Hugh Bradbury, Bernard Christophe Barlaam, Richard Ducray
Abstract: Inhaler counter (20) comprising a counter housing (390), a rocker arm (200) with a pawl (210), the rocker arm being pivotally supported by the housing and arranged to perform a rocker movement in response to a linear actuation motion, a return spring (220) for resetting the rocker arm, a ratchet wheel (230) engagable with the pawl to convert the movement of the rocker arm into an incremental rotational motion of an axle arrangement (240) advancing a display means (60), the axle arrangement further comprising a back rotation prevention means (280) in the form of a spring loaded friction brake and a worm gear, the display means comprising rotatable indicator means (120) with teeth that engage the worm-gear and a stationary scale.
Type:
Grant
Filed:
September 8, 2009
Date of Patent:
October 26, 2010
Assignee:
AstraZeneca AB
Inventors:
Nic Bowman, Douglas Bradshaw, Lennart Sörby