IP Library Granted Patent US 10,201,584
Granted Patent B1
US 10,201,584 · App. 14/247,975 · Granted Feb 12, 2019

Compositions and methods for treating HCV

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Quick Facts
Patent No.
US 10,201,584
App. No.
14/247,975
Granted
Feb 12, 2019
Kind
B1
Abstract

This disclosure is directed to pharmaceutical compositions that comprise two or more therapeutic agents that, inter alia, are useful for inhibiting hepatitis C virus (HCV) and methods for inhibiting HCV by co-administering two or more anti-HCV therapeutic agents.

Claims (15)

1. A method for treating a subject infected with hepatitis C virus (HCV) genotype 1, said method comprising administering to said subject an amount of therapeutic agent A and an amount of therapeutic agent B, wherein therapeutic agent A is compound A or a salt thereof:

wherein therapeutic agent B is compound B or a salt thereof:

wherein the molar ratio of therapeutic agent A to therapeutic agent B is about 1:20 to about 1:2000, and wherein therapeutic agent A and therapeutic agent B are administered to the subject from the same pharmaceutical composition.

2. The method of claim 1 , wherein the subject is a human.

3. The method of claim 1 , wherein the total daily dosage amount of therapeutic agent A administered to the subject is about 25 mg.

4. The method of claim 1 , wherein therapeutic agent B is a sodium salt of compound B.

5. The method of claim 1 , wherein the method further comprises administering one or more additional therapeutic agents selected from the group consisting of interferon, ribavirin, taribavirin, and HCV inhibitor.

6. The method of claim 5 , wherein the additional therapeutic agent is an HCV inhibitor.

7. The method of claim 6 , wherein the HCV inhibitor is an HCV protease inhibitor.

8. The method of claim 5 , wherein therapeutic agent A, therapeutic agent B, and the additional therapeutic agent are administered to the subject from the same pharmaceutical composition.

9. The method of claim 3 , wherein the pharmaceutical composition is administered to the subject once is a 24-hour period.

10. The method of claim 7 , wherein the method further comprises administering a cytochrome P-450 inhibitor.

11. The method of claim 10 , wherein the cytochrome P-450 inhibitor is ritonavir.

12. The method of claim 1 , wherein the total daily dosage of both therapeutic agent A and therapeutic agent B are administered to the subject within a twenty-four hour period.

13. The method of claim 12 , wherein the pharmaceutical composition is administered once or twice daily.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED ON REEL 041248 FRAME 0945. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 9, 2017
From: ABBOTT LABORATORIES
To: ABBVIE INC.
Reel/Frame 042251/0951 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2017
From: COLLINS, CHRISTINE A.; COHEN, DANIEL E.; KOEV, GENNADIY; KRISHNAN, PREETHI; PILOT-MATIAS, TAMI J.
To: ABBOTT LABORATORIES
Reel/Frame 040845/0075 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 4, 2017
From: ABBOTT LABORATORIES
To: ABBVIE INC.
Reel/Frame 041248/0945 →