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Tissue anchor system |
| The invention claimed is: 1. An adjustable tissue anchor comprising: a. an anchor body having a ... |
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Ribozyme mediated inactivation of the androgen receptor |
| The present invention describes inactivation of AR gene expression by engineering hammerhead ... |
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Thyrotropin-releasing hormone analogues and their therapeutic applications |
| The present invention pertains to novel TRH analogues, compositions, and methods for the controlled ... |
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Probiotics in primary prevention of atopic diseases |
| What is claimed is: 1. A method for prevention of atopic diseases selected from the group ... |
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Humanin-like peptide and use thereof |
| The invention claimed is: 1. A polypeptide comprising an amino acid sequence as shown in SEQ ID NO: ... |
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Method of treating cardiovascular diseases |
| OF PREFERRED EMBODIMENTS As examples of the diseases which the method according to the invention ... |
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Rapid production of autologous tumor vaccines |
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Pharmaceutical compositions comprising an adenosine receptor agonist or antagonist |
| OF THE INVENTION In accordance with the invention novel therapeutic use is provided for certain ... |
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Ribavirin-interferon alfa combination therapy for eradicating detectable HCV-RNA in patients having chronic hepatitis C infection
| Details |
Inventors: Ganguly, Ashit K.; McCormick, Jinping; Lovey, Raymond G.; Bennett, Frank; Saksena, Anil K.; Girijavallabhan, Viyyoor M.;
Assignee: Schering Corporation (Kenilworth, NJ)
Primary Examiner: Lewis; Patrick
Assistant Examiner:
Attorney, Agent or Firm: Henderson; Melodie W.
Ribavirin derivatives represented by the formula V, pharmaceutical compositions containing them as well as the use of the ribavirin derivatives represented by the formula V for the preparation of a medicament for the treatment of susceptible viral infections, for example, chronic hepatitis C infections administrating, the ribavirin derivatives being represented by formula V ##STR00001## are disclosed. |
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DETAILED DESCRIPTION The term "alkyl" as used herein means straight and branched carbon chains of one to twenty carbons, preferably one to six carbons and more preferably one to three carbons. The term "alkenyl" as used herein means straight and branched chain alkyl groups containing at least one carbon-carbon double bond and two to twenty carbons, preferably two to eight carbons. The term "alkynyl" as used herein means straight and branched chain alkyl groups containing at least one carbon-carbon triple bond and two to twenty carbons, and preferably two to six carbons containing at least one carbon-carbon triple bond. The term "cycloalkyl" as used herein means carbocyclic rings of three to twelve carbons, preferably three to seven carbons and more preferably three to six carbons optionally substituted by one double bond. The term "alkanoyl" as used herein means straight and branched chain alkanoyl groups of one to twenty carbons, preferably two to twelve, more preferably two to ten and most preferably two to six carbons. The term "alkenoyl" as used herein means straight and branched chain alkenoyl groups of one to twenty carbons containing at least one carbon-carbon double bond, preferably two to twelve, or more preferably two to ten and most preferably two to six carbons containing at least one carbon-carbon double bond. The term "halo" as used herein means fluroro, chloro or bromo, preferably fluroro or chloro. The term "alkynoyl" as used herein means straight and branched chain alkenoyl groups of one to twenty carbons containing at least one carbon-carbon triple bond, preferably two to twelve, or more preferably two to ten and most preferably two to six carbons containing at least one carbon-carbon triple bond. The term "alkoxy" as used herein means straight and branched chain alkyl groups containing one bond to oxygen at the one carbon and one to ten carbons. Typically suitable alkoxy includes methoxy, ethoxy and tert-butoxy. The term "aryl" as used herein (including the aryl portion of aryloxy and aralkyl, e
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