IP Library Granted Patent US 7,601,735
Granted Patent B2
US 7,601,735 · App. 10/475,830 · Granted Oct 13, 2009

Antiviral compounds

Assignee: Virogen Ltd.
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Quick Facts
Patent No.
US 7,601,735
App. No.
10/475,830
Granted
Oct 13, 2009
Kind
B2
Abstract

Use of certain castanospermine esters in the treatment of diseases caused by flaviviruses, in particular in the treatment of disease caused by the hepatitis C virus (HCV) and compositions containing said esters in combination with adjunctive therapeutic agents.

Claims (12)

1. A method for treating a Hepacivirus infection, said method comprising the step of administering to a patient a therapeutic composition comprising (i) an agent that alters immune function, and (ii) a glucosidase inhibitor wherein the agent that alters immune function is an interferon and the glucosidase inhibitor is [1S-(1α,6β,7α,8β,8αβ)]-octahydro-1 6,7,8-indolizinetetrol 6-butanoate.

2. The method according to claim 1 wherein the patient is a human.

3. The method according to claim 1 wherein the interferon is an α-interferon.

4. The method according to claim 1 wherein said Hepacivirus is Hepatitis C virus.

5. The method according to claim 1 wherein the composition further comprises a pharmaceutically acceptable excipient.

6. A method for treating a Hepacivirus infection, said method comprising the step of administering to a patient a therapeutic composition comprising (i) an agent that alters viral replication, and (ii) a glucosidase inhibitor wherein the agent that alters replication is ribavirin and the glucosidase inhibitor is [1S-(1α,6β,7α,8β,8αβ)]-octahydro-1 6,7,8-indolizinetetrol 6-butanoate.

7. The method according to claim 6 wherein the patient is a human.

8. The method according to claim 6 wherein said Hepacivirus is Hepatitis C virus.

9. The method according to claim 6 wherein the composition further comprises a pharmaceutically acceptable excipient.

10. A method for treating a Hepacivirus infection, said method comprising the step of administering to a patient a therapeutic composition comprising a glucosidase inhibitor, wherein the glucosidase inhibitor is [1S-(1α,6β,7α,8β,8αβ)]-octahydro-1 6,7,8-indolizinetetrol 6-butanoate.

11. The method according to claim 10 wherein said Hepacivirus is Hepatitis C virus.

12. The method according to claim 10 wherein the composition further comprises a pharmaceutically acceptable excipient.

Assignments (3)
CHANGE OF NAME Recorded Aug 10, 2011
From: SANOFI-AVENTIS
To: SANOFI
Reel/Frame 026728/0773 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2011
From: VIROGEN LTD.
To: SANOFI-AVENTIS
Reel/Frame 026504/0921 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 9, 2004
From: TYMS, STANLEY ALBERT; TAYLOR, DEBRA LYNN
To: VIROGEN LTD.
Reel/Frame 015110/0194 →
Priority Claims (1)
GB 0110832.3 · May 3, 2001 · national
Continuity (1)
Related Publication 20040147549A1 · Jul 29, 2004