Abstract: The invention provides compositions containing hydroxyethyl starch and polypeptides, including therapeutic polypeptides such as interleukin-11, that provide for enhanced stability of the polypeptide following storage at room temperature or elevated temperatures.
Type:
Grant
Filed:
March 17, 2003
Date of Patent:
January 3, 2006
Assignees:
Wyeth, The Regents of the University of Colorado
Inventors:
Nicholas W. Warne, Rebecca L. Koval, John Carpenter, Theodore W. Randolph, Suchart Chongpraset
Abstract: The invention is a process for the preparation of compounds of the Formula I: where R1, R2, R3, R4 and R5 are defined in the specification, which are intermediates useful for the preparation of tubulin inhibitors which are useful in the treatment of cancer.
Abstract: The invention provides compounds of formula Wherein R1, R2, R3, R4, R5, R6a, R6b, R6c, R6d, R6e and R7 are defined in the specification. These compounds are useful as antibiotic agents.
Abstract: The present invention provides probe arrays for expression profiling of rat genes. Each probe array comprises a plurality of probes, each of which is directed to a rat gene that encodes a sequence selected from SEQ ID NOs: 1-8,192. Suitable probes for the present invention include polynucleotides that can hybridize under stringent or nucleic acid array hybridization conditions to the RNA transcripts, or the complements thereof, of the corresponding rat genes. Suitable probes also include antibodies or other protein-binding molecules that can bind to the protein products of the corresponding rat genes. In one embodiment, a probe array of the present invention includes one or more probes, each of which is directed to a rat gene that encodes a sequence selected from SEQ ID NOs: 7622 and 8084-8124.
Abstract: An injectable or implantable rod-shaped formulation is disclosed for delivery of osteogenic proteins. The formulation comprises hyaluronic acid derivatives and osteogenic proteins, and optional excipients and active ingredients such as a bone resorption inhibitor. Methods of making injectable rod-shaped pharmaceutical compositions and methods of using the osteogenic compositions to treat osteoporotic and/or osteopenic bone are also disclosed.
Abstract: The present invention provides a compound of formula I and the use thereof for the therapeutic treatment, prevention or amelioration of a disease or disorder characterized by elevated ?-amyloid deposits or ?-amyloid levels in a patient.
Type:
Application
Filed:
June 15, 2005
Publication date:
December 22, 2005
Applicant:
Wyeth
Inventors:
Michael Malamas, James Erdei, Iwan Gunawan, Ping Zhou, Yinfa Yan, Dominick Quagliato
Abstract: The present invention provides a compound of formula I and the use thereof for the therapeutic treatment, prevention or amelioration of a disease or disorder characterized by elevated ?-amyloid deposits or ?-amyloid levels in a patient.
Type:
Application
Filed:
June 15, 2005
Publication date:
December 22, 2005
Applicant:
Wyeth
Inventors:
Michael Malamas, James Erdei, Iwan Gunawan, Keith Barnes, Matthew Johnson, Yu Hui
Abstract: A process to excystate protozoal sporocysts involves treatment of an infected tissue sample with a sodium hypochlorite solution to stimulate excystation of the sporocysts from the tissue. Thereafter, removal of the sodium hypochlorite solution and treatment of the sample with a cell culture media as the excystation fluid eliminates incubation and subsequent washing steps using expensive reagents. The excystation fluid contains substantially no chelating agents, proteins, enzymes or bile acids.
Abstract: Human cell surface molecules CD70 and CD203c are expressed at higher levels in kidney carcinomas, particularly renal cell carcinomas and clear cell renal cell carcinomas, yet are expressed at low levels in normal kidney and other diseased kidney tissue, and at low levels in other tissues. CD70 and CD203c show specificity towards kidney carcinomas, particularly renal cell carcinomas and clear cell renal cell carcinomas and thus can be used as diagnostic markers and therapeutic targets for these diseases. In addition, antibodies or small molecules against these molecules could be used in treatments towards these diseases.
Type:
Application
Filed:
September 29, 2003
Publication date:
December 22, 2005
Applicant:
Wyeth
Inventors:
Wei Liu, Maryann Whitley, Donna Slonim, Steven Howes
Abstract: The present invention relates to methods of making Gonadotropin Releasing Hormone (“GnRH”) (also known as Leutinizing Hormone Releasing Hormone) receptor antagonists.
Type:
Application
Filed:
June 16, 2005
Publication date:
December 22, 2005
Applicant:
Wyeth
Inventors:
Alexander Gontcharov, Gulnaz Khafizova, John Potoski, Donna Huryn
Abstract: The present invention provides substituted 10,11-Dihydro-5H-benzo[e]-pyrrolo[1,2-a][1,4]diazepine and 9,10-Dihydro-4H-3a,5,9-triaza-benzo[f]azulene compounds as well as methods and pharmaceutical compositions utilizing these compounds for the treatment and/or prevention and/or suppression of disorders which may be remedied or alleviated by oxytocin antagonist activity, including prevention and/or suppression of preterm labor, suppression labor at term prior to caesarean deliver, and for the treatment of dysmenorrhea. These compounds are also useful in enhancing fertility rates, enhancing survival rates and synchronizing estrus in farm animals.
Type:
Grant
Filed:
April 10, 2002
Date of Patent:
December 20, 2005
Assignee:
Wyeth
Inventors:
Amedeo Arturo Failli, William Jennings Sanders, Eugene John Trybulski
Abstract: The present invention provides processes for the preparation of compounds of Formula III that are useful in the preparation of pharmaceuticals for the treatment of inflammatory diseases.
Type:
Application
Filed:
June 9, 2005
Publication date:
December 15, 2005
Applicant:
Wyeth
Inventors:
Weiguo Liu, John Considine, Zhixian Ding, John Potoski
Abstract: The invention provides truncated biologically active ADAMTS polypeptides, particularly those with hyalectenase activity, and more particularly those with aggrecanase activity, that exhibit greater stability and homogeneity and higher expression yields than their full-length counterparts. The invention also provides nucleic acid molecules encoding such truncated biologically active ADAMTS polypeptides and methods for producing the truncated biologically active ADAMTS polypeptides. In addition, the invention provides methods for identifying compounds capable of modulating biologically active ADAMTS polypeptides, particularly those compounds that inhibit aggrecanase activity.
Type:
Application
Filed:
April 18, 2005
Publication date:
December 15, 2005
Applicant:
WYETH
Inventors:
Edward LaVallie, Lisa Collins-Racie, Christopher Corcoran, Natalie Twine, Michael Agostino
Abstract: The present invention provides processes for the preparation of compounds of Formula I, which are useful in the preparation of pharmaceuticals for the treatment of inflammatory diseases. The compounds of Formula I are also useful as pharmaceuticals.
Type:
Application
Filed:
June 9, 2005
Publication date:
December 15, 2005
Applicant:
Wyeth
Inventors:
Weiguo Liu, John Considine, Zhixian Ding, John Potoski
Abstract: A convenient preparation of boron-containing compounds, borate salts, pyrrolecarbonitrile boron-containing compounds, N-substituted-pyrrole-2-carbonitrile boron-containing compounds, and derivatives thereof is provided. The present invention also provides for the use of these boron-containing compounds and derivatives thereof in coupling reactions to provide bi-aryl compounds.
Type:
Application
Filed:
April 25, 2005
Publication date:
December 8, 2005
Applicant:
Wyeth
Inventors:
Bogdan Wilk, Arkadiy Rubezhov, Jean Helom
Abstract: Processes for using a compound of formula III: to make compounds of formulae I and II: and processes for making the compound of formula III, where R1-5 and J are as defined herein.
Type:
Application
Filed:
June 7, 2005
Publication date:
December 8, 2005
Applicant:
Wyeth
Inventors:
Ting-Zhong Wang, Lalitha Krishnan, Joseph Zeldis, Jeremy Levin, Jean Schmid, Mellard Jennings, Huan-Qiu Li, Zhixin Wen
Abstract: A process for preparing the compound of formula II by reacting the compound of formula I with an enzyme that can hydrolyze the ester bond: where * indicates a chiral center, R1 and R2 each independently represent H, C1-C6alkyl, —CN or —CCH, and R3 and R4 each independently represent H or C1-C6alkyl.
Abstract: This invention provides estrogen receptor modulators of formula 1, having the structure wherein, A is wherein R1, R2, R3, and R4, and X as defined in the specification, or a pharmaceutically acceptable salt thereof.
Type:
Application
Filed:
March 30, 2005
Publication date:
December 8, 2005
Applicant:
Wyeth
Inventors:
Michael Malamas, Iwan Gunawan, Heather Harris, James Keith, Leo Albert
Abstract: Compositions particularly useful as coatings for solid dosage forms of therapeutic agents are provided, as are solid dosage forms comprising such coatings, processes for preparing such solid dosage forms, and the products of those processes. The coating compositions generally provide excellent strength and resistance to cracking, even when applied to flexible/swellable tablet cores such as hydrogel-type cores. The compositions also exhibit excellent odor-blocking characteristics.
Type:
Application
Filed:
June 7, 2005
Publication date:
December 8, 2005
Applicant:
Wyeth
Inventors:
John Clark, John Michelucci, Deborah Sherman