IP Library Patent Application 17306643
Patent Application
App. No. 17/306,643

BETA-D-2'-DEOXY-2'-ALPHA-FLUORO-2'-BETA-C-SUBSTITUTED-2-MODIFIED-N6-SUBSTITUTED PURINE NUCLEOTIDES FOR HCV TREATMENT

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Quick Facts
Patent No.
US None
App. No.
17/306,643
Abstract

A compound of the structure: or a pharmaceutically acceptable salt or composition thereof for the treatment of a host infected with or exposed to an HCV virus or other disorders more fully described herein.

Claims (39)

1 . A pharmaceutical composition comprising an effective amount of a compound of the formula:

or a pharmaceutically acceptable salt thereof and an effective amount of an additional anti-viral compound selected from a protease inhibitor, a NS5B polymerase inhibitor, and a NS5A inhibitor in a pharmaceutically acceptable carrier.

2 . The pharmaceutical composition of claim 1 comprising a compound of the formula:

or a pharmaceutically acceptable salt thereof.

3 . The pharmaceutical composition of claim 1 comprising a compound of the formula:

or a pharmaceutically acceptable salt thereof.

4 . The pharmaceutical composition of claim 1 , wherein the additional anti-viral compound is a protease inhibitor.

5 . The pharmaceutical composition of claim 4 , wherein the protease inhibitor is a NS3/4A protease inhibitor.

6 . The pharmaceutical composition of claim 1 , wherein the additional anti-viral compound is a NS5A inhibitor.

7 . The pharmaceutical composition of claim 1 , wherein the additional anti-viral compound is a NS5B polymerase inhibitor.

8 . The pharmaceutical composition of claim 1 , in an oral dosage form.

9 . The pharmaceutical composition of claim 8 , wherein the oral dosage form is a solid dosage form.

10 . The pharmaceutical composition of claim 9 , wherein the solid dosage form is a tablet or capsule.

11 . The pharmaceutical composition of claim 8 , wherein the oral dosage form is a liquid dosage form.

12 . The pharmaceutical composition of claim 11 , wherein the liquid dosage form is a suspension or solution.

13 . The pharmaceutical composition of claim 1 , in an intravenous formulation.

14 . The pharmaceutical composition of claim 1 , in a parenteral formulation.

15 . The pharmaceutical composition of claim 2 , wherein the additional anti-viral compound is a protease inhibitor.

16 . The pharmaceutical composition of claim 15 , wherein the protease inhibitor is a NS3/4A protease inhibitor.

17 . The pharmaceutical composition of claim 2 , wherein the additional anti-viral compound is a NS5A inhibitor.

18 . The pharmaceutical composition of claim 2 , wherein the additional anti-viral compound is a NS5B polymerase inhibitor.

19 . The pharmaceutical composition of claim 2 , in an oral dosage form.

20 . The pharmaceutical composition of claim 19 , wherein the oral dosage form is a solid dosage form.

21 . The pharmaceutical composition of claim 20 , wherein the solid dosage form is a tablet or capsule.

22 . The pharmaceutical composition of claim 19 , wherein the oral dosage form is a liquid dosage form.

23 . The pharmaceutical composition of claim 22 , wherein the liquid dosage form is a suspension or solution.

24 . The pharmaceutical composition of claim 2 , in an intravenous formulation.

25 . The pharmaceutical composition of claim 2 , in a parenteral formulation.

26 . The pharmaceutical composition of claim 3 , wherein the additional anti-viral compound is a protease inhibitor.

27 . The pharmaceutical composition of claim 26 , wherein the protease inhibitor is a NS3/4A protease inhibitor.

28 . The pharmaceutical composition of claim 3 , wherein the additional anti-viral compound is a NS5A inhibitor.

29 . The pharmaceutical composition of claim 3 , wherein the additional anti-viral compound is a NS5B polymerase inhibitor.

30 . The pharmaceutical composition of claim 3 , in an oral dosage form.

31 . The pharmaceutical composition of claim 30 , wherein the oral dosage form is a solid dosage form.

32 . The pharmaceutical composition of claim 31 , wherein the solid dosage form is a tablet or capsule.

33 . The pharmaceutical composition of claim 30 , wherein the oral dosage form is a liquid dosage form.

34 . The pharmaceutical composition of claim 33 , wherein the liquid dosage form is a suspension or solution.

35 . The pharmaceutical composition of claim 3 , in an intravenous formulation.

36 . The pharmaceutical composition of claim 3 , in a parenteral formulation.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 12, 2021
From: SOMMADOSSI, JEAN-PIERRE; MOUSSA, ADEL
To: ATEA PHARMACEUTICALS, INC.
Reel/Frame 057161/0092 →