IP Library Patent Application 13956287
Patent Application
App. No. 13/956,287

METHODS AND COMPOSITIONS FOR TREATING FLAVIVIRIDAE INFECTIONS

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Patent No.
US None
App. No.
13/956,287
Abstract

A method and composition for treating a host infected with flavivirus or pestivirus comprising administering an effective flavivirus or pestivirus treatment amount of a described 1′, 2′ or 3′-modified nucleoside or a pharmaceutically acceptable salt or prodrug thereof, is provided.

Claims (38)

1 - 30 . (canceled)

31 . A method for the treatment of a Flaviviridae infection in a host, comprising administering to said host an anti-virally effective amount of a β-D-2′-methyl-ribofuranosyl nucleoside or a phosphate thereof, or a pharmaceutically acceptable salt or ester thereof.

32 . The method of claim 31 , wherein an anti-virally effective amount of a β-D-2′-methyl-ribofuranosyl nucleoside or a phosphate thereof, or a pharmaceutically acceptable ester thereof is administered.

33 . The method of claim 32 , wherein the nucleoside is a pyrimidine nucleoside.

34 . The method of claim 33 , wherein the β-D-2′-methyl-ribofuranosyl pyrimidine nucleoside is administered in combination or alternation with a second anti-Flaviviridae agent.

35 . The method of claim 34 , wherein the second anti-Flaviviridae agent is an interferon.

36 . The method of claim 34 , wherein the second anti-Flaviviridae agent is ribavirin.

37 . The method of claim 34 , wherein the second anti-Flaviviridae agent is an interferon, ribavirin, or a combination thereof.

38 . The method of claim 31 , wherein the nucleoside is a pyrimidine nucleoside.

39 . The method of claim 38 , wherein the β-D-2′-methyl-ribofuranosyl pyrimidine nucleoside is administered in combination or alternation with a second anti-Flaviviridae agent.

40 . The method of claim 39 , wherein the second anti-Flaviviridae agent is an interferon.

41 . The method of claim 39 , wherein the second anti-Flaviviridae agent is ribavirin.

42 . The method of claim 39 , wherein the second anti-Flaviviridae agent is an interferon, ribavirin, or a combination thereof.

43 . The method of claim 31 , wherein the β-D-2′-methyl-ribofuranosyl nucleoside or a phosphate thereof, or a pharmaceutically acceptable salt or ester thereof is in a tablet or capsule.

44 . The method of claim 31 , wherein a unit dose of the β-D-2′-methyl-ribofuranosyl nucleoside or a phosphate thereof, or a pharmaceutically acceptable salt or ester thereof is administered.

45 . The method of claim 43 , wherein the tablet or capsule contains 50 to 1000 mg of the β-D-2′-methyl-ribofuranosyl nucleoside or a phosphate thereof, or a pharmaceutically acceptable salt or ester thereof.

46 . The method of claim 44 , wherein the unit dose contains 50 to 1000 mg of the β-D-2′-methyl-ribofuranosyl nucleoside or a phosphate thereof, or a pharmaceutically acceptable salt or ester thereof.

47 . The method of claim 31 , wherein the nucleoside is a β-D-2′-methyl-2′-halo-ribofuranosyl nucleoside or a phosphate thereof, or a pharmaceutically acceptable salt or ester thereof.

48 . The method of claim 47 , wherein an anti-virally effective amount of a β-D-2′-methyl-2′-halo-ribofuranosyl nucleoside, or a phosphate thereof, or a pharmaceutically acceptable ester thereof is administered.

49 . The method of claim 48 , wherein the nucleoside is a β-D-2′-methyl-2′-halo-ribofuranosyl pyrimidine nucleoside.

50 . A method for the treatment of a Flaviviridae infection in a host, comprising administering to the host an anti-virally effective amount of a compound of Formula XI:

or a pharmaceutically acceptable salt or ester thereof;

wherein:

Base is a pyrimidine base;

R 1 and R 2 are each independently H or phosphate;

R 6 is alkyl;

R 7 is halo; and

X is O.

51 . The method of claim 50 , wherein Base is uracil.

52 . The method of claim 51 , wherein R 6 is methyl.

53 . The method of claim 52 , wherein R 1 is phosphate.

54 . The method of claim 53 , wherein R 2 is H.

55 . The method of claim 50 , wherein the compound of Formula XI is administered in combination or alternation with a second anti-Flaviviridae agent.

56 . The method of claim 55 , wherein the second anti-Flaviviridae agent is an interferon.

57 . The method of claim 55 , wherein the second anti-Flaviviridae agent is ribavirin.

58 . The method of claim 55 , wherein the second anti-Flaviviridae agent is an interferon, ribavirin, or a combination thereof

59 . The method of claim 54 , wherein the compound of Formula XI is administered in combination or alternation with a second anti-Flaviviridae agent.

60 . The method of claim 59 , wherein the second anti-Flaviviridae agent is an interferon, ribavirin or a combination thereof.