Abstract: The present invention relates to compounds of Formula I described herein and their pharmaceutically acceptable salts, and their use in medicine, in particular as Trk antagonists.
Abstract: The present invention relates to methods of treating and/or preventing acne in patients comprising the step of administering to patients in need of such treatment a therapeutically effective amount of an ACC inhibitor or a pharmaceutically acceptable salt thereof.
Type:
Application
Filed:
August 29, 2014
Publication date:
August 4, 2016
Applicant:
Pfizer Inc.
Inventors:
William Paul Esler, Gabriele Elisabeth Sonnenberg
Abstract: The present disclosure provides (a) vectors comprising a multi-antigen construct encoding two, three, or more immunogenic PAA polypeptides; (b) compositions comprising the vectors, (c) methods relating to uses of the vectors and compositions for eliciting an immune response or for treating prostate cancers.
Abstract: The present invention provides compounds of formula I, wherein the variables R1, R2, R5 and b are as defined in the specification. Corresponding pharmaceutical compositions, methods of treatment, methods of synthesis, and intermediates are also disclosed.
Type:
Grant
Filed:
December 4, 2013
Date of Patent:
August 2, 2016
Assignee:
Pfizer Inc.
Inventors:
Michael Aaron Brodney, Brian Thomas O'Neill, Christopher Ryan Butler, Erik Alphie LaChapelle
Abstract: Myeloperoxidase inhibitors, pharmaceutical compositions containing such inhibitors and the use of such inhibitors to treat, for example, cardiovascular conditions.
Type:
Grant
Filed:
June 9, 2014
Date of Patent:
July 26, 2016
Assignee:
Pfizer Inc.
Inventors:
Philip A. Carpino, Edward L. Conn, Robert L. Dow, Matthew S. Dowling, David Hepworth, Daniel Wei-Shung Kung, Suvi Orr, Benjamin N. Rocke, Roger B. Ruggeri, Matthew F. Sammons, Joseph S. Warmus, Yan Zhang
Abstract: A device for dispensing individual doses of powder from respective pockets of a disc-shaped carrier by outwardly rupturing a lidding foil by means of pressure on an opposite side surface, the device providing individual respective deaggregation flow paths for each pocket, split airstreams allowing improved entrainment of powder, a cam mechanism for outwardly rupturing the pockets, an indexing mechanism linked to the cam mechanism and a dose counter.
Type:
Grant
Filed:
August 18, 2014
Date of Patent:
July 26, 2016
Assignee:
PFIZER LIMITED
Inventors:
Peter John Houzego, John Kelshaw Conway, Martin Douglas Pearl, Andrew Mark Bryant
Abstract: The present invention relates to antibodies that bind brain-derived neurotrophic factor (BDNF). The invention further relates to nucleic acid sequences coding for such antibodies. The present invention also relates to immunoconjugates comprising the antibodies of the invention and pharmaceutical compositions comprising the antibodies and/or the immunoconjugates. The present invention further relates to methods for treating pain and medical uses relating thereto.
Type:
Application
Filed:
September 1, 2015
Publication date:
July 21, 2016
Applicant:
PFIZER INC.
Inventors:
Laird Bloom, Qingcong Lin, Heather Hongrong Shih, Ying Sun, Orla Margaret Cunningham, William James Jonathan Finlay
Abstract: Compounds of Formula (A) are described herein and the uses thereof for the treatment of diseases, conditions and/or disorders mediated by pharmaceutical compositions and the uses thereof as asialoglycoprotein receptor (ASGPR) targeting agents.
Type:
Application
Filed:
April 7, 2016
Publication date:
July 21, 2016
Applicant:
Pfizer Inc.
Inventors:
Spiros Liras, Vincent Mascitti, Benjamin Thuma
Abstract: The present invention relates to the use of ROS kinase inhibitors for treating abnormal cell growth in mammals. In particular, the invention provides methods of treating mammals suffering from cancer mediated by at least one genetically altered ROS. In particular, the invention provides methods of treating mammals suffering from cancer mediated by at least one genetically altered ROS by administration of crizotinib.
Abstract: The present invention relates to indole and indazole compounds of Formula (I) that activate 5? adenosine monophosphate-activated protein kinase (AMPK). The invention also encompasses pharmaceutical compositions containing these compounds and methods for treating or preventing diseases, conditions, or disorders ameliorated by activation of AMPK.
Type:
Grant
Filed:
September 24, 2013
Date of Patent:
July 19, 2016
Assignee:
Pfizer Inc.
Inventors:
Samit Kumar Bhattacharya, Kimberly O'Keefe Cameron, Matthew Scott Dowling, David Christopher Ebner, David James Edmonds, Dilinie Prasadhini Fernando, Kevin James Filipski, Daniel Wei-Shung Kung, Esther Cheng Yin Lee, Aaron Christopher Smith, Meihua Mike Tu
Abstract: The present invention provides, in part, compounds of Formula I: and pharmaceutically acceptable salts thereof; processes for the preparation of; intermediates used in the preparation of; and compositions containing such compounds or salts, and their uses for treating D1-mediated (or D1-associated) disorders including, e.g., schizophrenia (e.g., its cognitive and negative symptoms), schizotypal personality disorder, cognitive impairment (e.g., cognitive impairment associated with schizophrenia, AD, PD, or pharmacotherapy therapy), ADHD, Parkinson's disease, anxiety, and depression.
Type:
Application
Filed:
March 22, 2016
Publication date:
July 14, 2016
Applicant:
PFIZER INC.
Inventors:
DAVID LAWRENCE FIRMAN GRAY, LEI ZHANG, MICHALE AARON BRODNEY, MICHAEL ERIC GREEN, CHAKRAPANI SUBRAMANYAM
Abstract: This invention provides a nutritional supplement composition which is a vitamin mint that can be taken anytime or anywhere without water or other liquid which is usually required for swallowing a tablet. The present invention is a nutritional supplement composition which is a convenient, flavorful and enjoyable vitamin mint which can be ingested without water.
Abstract: The present invention provides a process for preparing a compound of formula: (Formula XI and XII) (XI) (XII) wherein X, Y, Z, A, B and E are as defined herein, by reacting a compound of formula: (Formula XIII) (XIII) with a compound of formula: (Formula XIV and XV) (XIV) (XV) respectively, in the presence of a transition metal catalyst, a ligand suitable for use with 15 the catalyst and a reducing agent. The invention also provides novel intermediates.
Type:
Grant
Filed:
October 8, 2013
Date of Patent:
July 12, 2016
Assignee:
Pfizer Ireland Pharmaceuticals
Inventors:
Adam James Musgrave Burrell, Padraig Mary O'Neill, Alan John Pettman
Abstract: Provided herein are antagonists of prostaglandin EP3 receptor, processes to make said antagonists, and methods comprising administering said antagonists to a mammal in need thereof.
Type:
Application
Filed:
December 16, 2015
Publication date:
June 23, 2016
Applicant:
Pfizer Inc.
Inventors:
Kevin Bahnck, Daniel Canterbury, David James Edmonds, Kentaro Futatsugi, Esther Cheng Yin Lee, Elnaz Menhaji-Klotz, Jana Polivkova, Robert Vernon Stanton
Abstract: The present invention relates to methods of treating sleep disorders in patients comprising administration of a ghrelin receptor inverse agonist or antagonist. The invention also includes methods of treating sleep disorders comprising the administration of a pharmaceutical composition comprising a ghrelin receptor inverse agonist or antagonist and at least one pharmaceutically acceptable carrier, diluent, or excipient.
Type:
Grant
Filed:
May 21, 2013
Date of Patent:
June 21, 2016
Assignee:
Pfizer Inc.
Inventors:
William S. Denney, Margaret Jackson, Gabriele Sonnenberg
Abstract: Processes and intermediates for the preparation of compounds of the Formula I and the pharmaceutically acceptable salts, prodrugs, solvates and hydrates thereof, wherein R1, R2, and R3 have the definitions provided herein.
Abstract: Methods for treating cancer in a patient in need thereof, with a therapeutically effective amount of an anti-4-1BB antibody in combination with a therapeutically effective amount of an ADCC-inducing antibody, are disclosed.
Type:
Application
Filed:
February 1, 2016
Publication date:
June 2, 2016
Applicant:
Pfizer Inc.
Inventors:
Leslie Lynne Sharp, Timothy Scott Fisher, Mark William Elliott
Abstract: The present invention concerns dosages for the treatment of human patients susceptible to or diagnosed with a disorder characterized by marked elevations of low density lipoprotein particles in the plasma with a PCSK9 antagonist antiboyd alone or in combination with a statin.