Abstract: The present invention relates to new 2-Phenyl-1-[4-(2-Aminoethoxy)-Benzyl]-Indole compounds which are useful as estrogenic agents, as well as pharmaceutical compositions and methods of treatment utilizing these compounds, which have the general structures below: 1
Type:
Application
Filed:
October 24, 2003
Publication date:
November 18, 2004
Applicant:
Wyeth
Inventors:
Chris P. Miller, Michael D. Collini, Bach D. Tran, Arthur A. Santilli
Abstract: This invention provides 3&bgr;-hydroxy-5,7,9-estratriene-17-one and a pharmaceutically acceptable salt of its 3-sulfate ester, which is useful as an estrogen.
Type:
Grant
Filed:
January 21, 2003
Date of Patent:
November 16, 2004
Assignee:
Wyeth
Inventors:
Syed M. Shah, Panolil Raveendranath, Michael Z. Kagan
Abstract: Compounds of the formula
are useful for treating the cognitive deficits due to aging, stroke, head trauma, Alzheimer's disease or other neurodegenerative diseases, or schizophrenia. The compounds of the invention are also useful for the treatment of disorders such as anxiety, aggression and stress, and for the control of various physiological phenomena, such as appetite, thermoregulation, sleep and sexual behavior.
Abstract: The present invention provides a compound of formula I and the use thereof for the therapeutic treatment of disorders relating to or affected by the 5-HT6 receptor.
Type:
Grant
Filed:
April 19, 2002
Date of Patent:
November 9, 2004
Assignee:
Wyeth
Inventors:
Ping Zhou, Boyd Lynn Harrison, Yanfang Li
Abstract: This invention relates to a new antibiotic designated P175-A, to production of fermentation of Micromonospora echinospora NRRL 30633, to methods for recovery and concentration from the crude solutions, and to a process for purification and to semisynthetic esters and ethers of P175-A.
Type:
Application
Filed:
April 28, 2004
Publication date:
November 4, 2004
Applicant:
Wyeth Holdings Corporation
Inventors:
Haiyin He, Hui Yu Yang, Scott William Luckman, Valerie S. Bernan
Abstract: The present invention is directed to processes and compositions for protecting host animals (e.g., chickens) from exposure to virulent infectious bronchitis virus. In ovo administration of live, avirulent strains of IB at appropriate dosage levels on a per egg basis provides an effective and efficient vaccination having acceptable safety and efficacy features.
Type:
Application
Filed:
June 1, 2004
Publication date:
November 4, 2004
Applicant:
Wyeth
Inventors:
Berend Jongsma, Frans Gerrit Davelaar, Marinus Wynand Weststrate
Abstract: Compounds of the formula:
are useful in treating disease conditions mediated by TNF-&agr;, such as rheumatoid arthritis, osteoarthritis, sepsis, AIDS, ulcerative colitis, multiple sclerosis, Crohn's disease and degenerative cartilage loss.
Type:
Grant
Filed:
February 27, 2003
Date of Patent:
November 2, 2004
Assignee:
Wyeth Holdings Corporation
Inventors:
Jeremy I. Levin, James M. Chen, Derek C. Cole, Mila T. Du, Leif M. Laakso
Abstract: The present invention relates to novel, low molecular weight broad spectrum compounds in particular to a class of 4-substituted or unsubstituted-7-hydro-1,4-thiazepine-7-[bicyclic or tricyclic heteroaryl] substituted-3,6-dicarboxylic acid or their derivatives which have &bgr;-lactamase inhibitory and antibacterial properties. The compounds are therefore useful in the treatment of antibacterial infections in humans or animals, either alone or in combination with other antibiotics.
Abstract: This invention provides compounds of Formula I having the structure 1
Type:
Application
Filed:
May 11, 2004
Publication date:
October 28, 2004
Applicant:
Wyeth
Inventors:
John A. Butera, Craig E. Caufield, Russell F. Graceffa, Alexander Greenfield, Eric G. Gundersen, Lisa Marie Havran, Alan H. Katz, Joseph R. Lennox, Scott C. Mayer, Robert E. McDevitt
Abstract: This invention relates to soluble derivatives of wortmannin that utilizes water-soluble polymers as carriers for a drug and includes compounds having the structures as described within the specification.
Abstract: This disclosure provides antibodies and antigen-binding fragments that can act as agonists and/or antagonists of PD-1 (Programmed Death 1), thereby modulating immune responses in general, and those mediated by TcR and CD28, in particular. The disclosed compositions and methods may be used for example, in treating autoimmune diseases, inflammatory disorders, allergies, transplant rejection, cancer, and other immune system disorders.
Type:
Application
Filed:
December 22, 2003
Publication date:
October 28, 2004
Applicants:
Wyeth, Cambridge Antibody Technology
Inventors:
Mary Collins, Clive R. Wood, Beatriz M. Carreno, Deborah Luxenberg, Jason Jussif, Laura L. Carter, Frances K. Bennett, Viia Valge-Archer, John Andrews, Caroline Russell
Abstract: The present invention provides a compound of formula I and the use thereof for the therapeutic treatment of disorders relating to or affected by the 5-HT6 receptor.
Type:
Application
Filed:
April 20, 2004
Publication date:
October 21, 2004
Applicant:
Wyeth
Inventors:
Derek Cecil Cole, Joseph Raymond Stock, William Joseph Lennox, Ping Zhou
Abstract: The present invention provides a new process and intermediates for the production of antiviral compound 4′,4-bis-{4,6-bis-[3-(bis-carbamoyl-methyl-1-sulfamoyl)-phenylamino]-[1,3,5]triazin-2-ylamino}-biphenyl-2,2′-disulfonic acid and its pharmaceutically acceptable salts.
Type:
Grant
Filed:
January 31, 2002
Date of Patent:
October 19, 2004
Assignee:
Wyeth
Inventors:
Silvio Iera, Christopher A. Demerson, Jacqueline F. Lunetta, Maria Papamichelakis, Michael F. MacEwan, Wayne G. McMahon, John R. Potoski, Arthur G. Mohan
Abstract: The invention pertains to pharmaceutical compositions of Zosyn® in the presence of a buffer, preferably citrate, a particulate formation inhibitor, preferably EDTA optionally an aminoglycoside which when frozen and thawed or lyophilized and reconstituted reform a solution which has decreased particulate formation.
Type:
Application
Filed:
April 14, 2003
Publication date:
October 14, 2004
Applicant:
Wyeth Holdings Corporation
Inventors:
Jonathan Marc Cohen, Syed M. Shah, Christian Luther Ofslager, Mahdi Fawzi
Abstract: There is provided a process for the preparation of 3-cyano-6-alkoxy-7-nitro-4-quinolone intermediates useful for the preparation of protein tyrosine kinase (PTK) inhibitors which are useful in the treatment of cancer of the formula: 1
Type:
Application
Filed:
April 7, 2004
Publication date:
October 14, 2004
Applicant:
Wyeth Holdings Corporation
Inventors:
Scott Mason Duncan, Miguel Angel Pagan, Middleton Brawner Floyd