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Medivir AB

Medivir AB Patent applications
Patent application numberTitlePublished
20120123119ACYCLIC NUCLEOSIDE DERIVATIVES - Methods and novel intermediates for the preparation of and the treatment with acyclic nucleoside derivatives of the formula:05-17-2012
20120115807COMBINATION OF ALOVUDINE AND ZIDOVUDINE IN A MOLAR RATIO OF 1:100 TO 1:350 - Co-administration of alovudine and zidovudine at ratios considerably in excess of the prior art completely or substantially abolishes the mitochondrial toxicity of alovudine in mitochondrial DNA depletion experiments. The invention thus provides pharmaceutical compositions comprising alovudine and zidovudine in a molar ratio in the range 1:100 to 1:350 and methods for the treatment or prophylaxis of multiply resistant HIV comprising the simultaneous or consequential administration of alovudine and zidovudine in the characteristic molar ratio.05-10-2012
20120015994(2,5-DIOXOIMIDAZOLIDIN-I-YL)-N-HYDROXY-ACETAMIDES AS METALLOPROTEINASE INHIBITORS - The invention provides compounds of the formula (I)01-19-2012
20110230436Uracyl Cyclopropyl Nucleotides - Compounds of the formula I:09-22-2011
20110172410ANTIVIRAL NUCLEOSIDES - 4-Amino-1-((2R,3S,4S,5R)-5-azido-4-hydroxy-5-hydroxymethyl-3-methyl-tetrahydro-furan-2-yl)-1H-pyrimidin-2-one (22) and prodrugs thereof are hepatitis C(HCV) polymerase inhibitors. Also disclosed are compositions and methods for inhibiting HCV and treating HCV-mediated diseases, processes for making the compounds and synthetic intermediates employed in the process.07-14-2011
201101122941-[2', 3' -DIDEOXY-3' C- (HYDROXYMETHYL) - BETA-D-ERYTHRO-PENTOFURANOSYL] CYTOSINE DERIVATIVES AS HIV INHIBITORS - Compounds of the formula I05-12-2011
20110112089Cysteine Protease Inhibitors - A compound of the formula II05-12-2011
20110105524CYSTEINE PROTEASE INHIBITORS - Compounds of the formula II:05-05-2011
20110092460CYCLOPROPYL POLYMERASE INHIBITORS - Compounds of formula I:04-21-2011
20110039862Protease Inhibitors - Compounds of the formula II:02-17-2011
20110021459DUTPASE INHIBITORS - Deoxyuridine derivatives of the formula01-27-2011
20110015148ANTIVIRAL NUCLEOSIDES - 4-Amino-1-((2R,3S,4S,5R)-5-azido-4-hydroxy-5-hydroxymethyl-3-methyl-tetrahydro-furan-2-yl)-1H-pyrimidin-2-one (22) and prodrugs thereof are hepatitis C (HCV) polymerase inhibitors. Also disclosed are compositions and methods for inhibiting HCV and treating HCV-mediated diseases, processes for making the compounds and synthetic intermediates employed in the process.01-20-2011
20100166706HCV NS-3 SERINE PROTEASE INHIBITORS - Methods drawn to peptidomimetic compounds which inhibit the NS3 protease of the hepatitis C virus (HCV), are described. The compounds have the formula (VI) where the variable definitions are as provided in the specification. The compounds comprise a carbocyclic P2 unit in conjunction with a novel linkage to those portions of the inhibitor more distal to the nominal cleavage site of the native substrate, which linkage reverses the orientation of peptidic bonds on the distal side relative to those proximal to the cleavage site.07-01-2010
20100130735ANTIVIRAL NUCLEOSIDES - 4-Amino-1-((2R,3S,4S,5R)-5-azido-4-hydroxy-5-hydroxymethyl-3-methyl-tetrahydro-furan-2-yl)-1H-pyrimidin-2-one (22) and prodrugs thereof are hepatitis C(HCV) polymerase inhibitors. Also disclosed are compositions and methods for inhibiting HCV and treating HCV-mediated diseases, processes for making the compounds and synthetic intermediates employed in the process.05-27-2010
20100075924DUTPASE INHIBITORS - Deoxyuridine derivatives of the formula03-25-2010
20100041728HCV INHIBITING MACROCYCLIC PHENYLCARBAMATES - Compounds of the formula 1:02-18-2010
20100003216HCV NS-3 Serine Protease Inhibitors - Compounds of the formula01-07-2010
20090281140Macrocyclic inhibitors of hepatitis c virus - Inhibitors of HCV replication of formula (I)11-12-2009
20090270429ANTIVIRAL FORMULATION - A topical antiviral composition comprising acyclovir, penciclovir and/or omaciclovir in a glucocorticoid-free pharmaceutical carrier comprising 15 to 25 weight % propylene glycol and 10 to 25 weight % isopropyl C10-29-2009
20090215846(2,5-DIOXOIMIDAZOLIDIN-I-YL)-N-HYDROXY-ACETAMIDES AS METALLOPROTEINASE INHIBITORS - The invention provides compounds of the formula (I) wherein the variables are as defined in the specification. The compounds of the invention are inhibitors of metalloproteinase MMP-12 and are among other things useful for the treatment of obstructive airway diseases, such as chronic obstructive pulmonary disease (COPD).08-27-2009
20090076041ACYCLIC NUCLEOSIDE DERIVATIVES - Methods and novel intermediates for the preparation of and the treatment with acyclic nucleoside derivatives of the formula:03-19-2009
20090023758Macrocyclic Inhibitors of Hepatitis C Virus - Compounds of the formula (I): and N-oxides, salts and stereoisomers thereof wherein A is OR01-22-2009

Patent applications by Medivir AB