IP Library Granted Patent US 10,870,673
Granted Patent B2
US 10,870,673 · App. 16/918,898 · Granted Dec 22, 2020

β-D-2′-deoxy-2′-α-fluoro-2′-β-C-substituted-2-modified-N

Inventors: Jean-Pierre Sommadossi (Boston, MA); Adel Moussa (Burlington, MA)
Assignee: Atea Pharmaceuticals, Inc.
C07H19/207A61K31/7076A61P31/14C07H19/16C07H19/20
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Quick Facts
Patent No.
US 10,870,673
App. No.
16/918,898
Granted
Dec 22, 2020
Kind
B2
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 (38)

1. A compound of the formula

or a pharmaceutically acceptable salt thereof.

2. A pharmaceutical composition comprising an effective therapeutic amount of a compound of claim 1 or a pharmaceutically acceptable salt thereof, in a pharmaceutically acceptable carrier.

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

4. The pharmaceutical composition of claim 3 , wherein the oral dosage form is a solid dosage form.

5. The pharmaceutical composition of claim 4 , wherein the solid dosage form is a tablet.

6. The pharmaceutical composition of claim 4 , wherein the solid dosage form is a capsule.

7. The pharmaceutical composition of claim 3 , wherein the oral dosage form is a liquid dosage form.

8. The pharmaceutical composition of claim 7 , wherein the liquid dosage form is a suspension or solution.

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

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

11. A compound of the formula

or a pharmaceutically acceptable salt thereof.

12. A pharmaceutical composition comprising an effective therapeutic amount of a compound of claim 11 or a pharmaceutically acceptable salt thereof, in a pharmaceutically acceptable carrier.

13. The pharmaceutical composition of claim 12 , in an oral dosage form.

14. The pharmaceutical composition of claim 13 , wherein the oral dosage form is a solid dosage form.

15. The pharmaceutical composition of claim 14 , wherein the solid dosage form is a tablet.

16. The pharmaceutical composition of claim 14 , wherein the solid dosage form is a capsule.

17. The pharmaceutical composition of claim 13 , wherein the oral dosage form is a liquid dosage form.

18. The pharmaceutical composition of claim 17 , wherein the liquid dosage form is a suspension or solution.

19. The pharmaceutical composition of claim 12 , in an intravenous formulation.

20. The pharmaceutical composition of claim 12 , in a parenteral formulation.

21. A compound of the formula:

or a pharmaceutically acceptable salt thereof, wherein the compound is at least 90% free of the opposite phosphorus R-enantiomer.

22. The compound of claim 21 , wherein the compound is at least 98% free of the opposite phosphorus R-enantiomer.

23. The compound of claim 21 , wherein the compound is at least 99% free of the opposite phosphorus R-enantiomer.

24. A pharmaceutical composition comprising an effective therapeutic amount of a compound of the formula

or a pharmaceutically acceptable salt thereof in a pharmaceutically acceptable carrier, wherein the compound is at least 90% free of the opposite phosphorus R-enantiomer.

25. The pharmaceutical composition of claim 24 , wherein the compound is at least 98% free of the opposite phosphorus R-enantiomer.

26. The pharmaceutical composition of claim 24 , wherein the compound is at least 99% free of the opposite phosphorus R-enantiomer.

27. The pharmaceutical composition of claim 24 , in an oral dosage form.

28. The pharmaceutical composition of claim 27 , wherein the oral dosage form is a solid dosage form.

29. The pharmaceutical composition of claim 28 , wherein the solid dosage form is a tablet.

30. The pharmaceutical composition of claim 28 , wherein the solid dosage form is a capsule.

31. The pharmaceutical composition of claim 27 , wherein the oral dosage form is a liquid dosage form.

32. The pharmaceutical composition of claim 31 , wherein the liquid dosage form is a suspension or solution.

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

34. The pharmaceutical composition of claim 24 , in a parenteral formulation.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE APPLICATION NUMBER 17028319 PREVIOUSLY RECORDED AT REEL: 053997 FRAME: 0501. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Nov 28, 2022
From: SOMMADOSSI, JEAN-PIERRE; MOUSSA, ADEL
To: ATEA PHARMACEUTICALS, INC.
Reel/Frame 062003/0409 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 7, 2020
From: SOMMADOSSI, JEAN-PIERRE; MOUSSA, ADEL
To: ATEA PHARMACEUTICALS, INC.
Reel/Frame 053997/0501 →
Continuity (9)
Continuation 16900397 · Jun 12, 2020
Continuation 16278621 · Feb 18, 2019
Continuation 16001549 · Jun 6, 2018
Continuation 15782628 · Oct 12, 2017
Continuation 15063461 · Mar 7, 2016
Provisional Application 62276597 · Jan 8, 2016
Provisional Application 62253958 · Nov 11, 2015
Provisional Application 62129319 · Mar 6, 2015
Related Publication 20200331955A1 · Oct 22, 2020
Cited By (2)
US 12,458,656 US 12,551,499