IP Library Granted Patent US 9,555,038
Granted Patent B2
US 9,555,038 · App. 14/761,256 · Granted Jan 31, 2017

Heterocycle-substituted tetracyclic compounds and methods of use thereof for the treatment of viral diseases

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,555,038
App. No.
14/761,256
Granted
Jan 31, 2017
Kind
B2
Abstract

The present invention relates to novel Heterocycle-Substituted Tetracyclic Compounds of Formula (I): (I) and pharmaceutically acceptable salts thereof, wherein A, A′, R 2 R 3 , R 4 and R are as defined herein. The present invention also relates to compositions comprising at least one Heterocycle-Substituted Tetracyclic Compound, and methods of using the Heterocycle-Substituted Tetracyclic Compounds for treating or preventing HCV infection in a patient.

Claims (26)

1. A compound having the structure:

or a pharmaceutically acceptable salt thereof.

2. A compound having the structure:

or a pharmaceutically acceptable salt thereof.

3. A compound having the structure:

4. A pharmaceutically acceptable salt of the compound having the structure:

5. A pharmaceutical composition comprising an effective amount of the compound of claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

6. The pharmaceutical composition of claim 5 , further comprising one or more additional therapeutic agents, wherein the additional therapeutic agents are each independently selected from HCV protease inhibitors, HCV NS5A inhibitors and HCV NS5B polymerase inhibitors.

7. A pharmaceutical composition consisting essentially of the compound of claim 1 , or a pharmaceutically acceptable salt thereof, a HCV protease inhibitor, a HCV NS5B polymerase inhibitor and a pharmaceutically acceptable carrier, wherein the amounts of the compound of claim 1 , or a pharmaceutically acceptable salt thereof, the HCV protease inhibitor and the HCV NS5B polymerase inhibitor are together effective to treat HCV infection in a human patient.

8. The pharmaceutical composition of claim 7 , wherein the HCV protease inhibitor is the compound having the structure:

9. The pharmaceutical composition of claim 8 , wherein the HCV NS5B polymerase inhibitor is a nucleoside.

10. A method of treating a human patient infected with HCV, comprising the step of administering an amount of the compound of claim 1 , or a pharmaceutically acceptable salt thereof, effective to treat infection by HCV in said human patient.

11. The method of claim 10 , further comprising administering one or more additional therapeutic agents to said human patient, wherein the additional therapeutic agents are each independently selected from HCV protease inhibitors, HCV NS5A inhibitors and HCV NS5B polymerase inhibitors.

12. The method of claim 11 , wherein the one or more additional therapeutic agents comprise a HCV protease inhibitor and a HCV NS5B polymerase inhibitor.

13. The method of claim 12 , wherein the HCV protease inhibitor is the compound having the structure:

14. The method of claim 13 , wherein the HCV NS5B polymerase inhibitor is a nucleoside.

15. A pharmaceutical composition comprising an effective amount of the compound of claim 3 and a pharmaceutically acceptable carrier.

16. The pharmaceutical composition of claim 15 , further comprising one or more additional therapeutic agents, wherein the additional therapeutic agents are each independently selected from HCV protease inhibitors, HCV NS5A inhibitors and HCV NS5B polymerase inhibitors.

17. A pharmaceutical composition consisting essentially of the compound of claim 3 , a HCV protease inhibitor, a HCV NS5B polymerase inhibitor and a pharmaceutically acceptable carrier, wherein the amounts of the compound of claim 3 , the HCV protease inhibitor and the HCV NS5B polymerase inhibitor are together effective to treat HCV infection in a human patient.

18. The pharmaceutical composition of claim 17 , wherein the HCV protease inhibitor is the compound having the structure:

19. The pharmaceutical composition of claim 18 , wherein the HCV NS5B polymerase inhibitor is a nucleoside.

20. A method of treating a human patient infected with HCV, comprising the step of administering an amount of the compound of claim 3 effective to treat infection by HCV in said human patient.

21. The method of claim 20 , further comprising administering one or more additional therapeutic agents to said human patient, wherein the additional therapeutic agents are each independently selected from HCV protease inhibitors, HCV NS5A inhibitors and HCV NS5B polymerase inhibitors.

22. The method of claim 21 , wherein the one or more additional therapeutic agents comprise a HCV protease inhibitor and a HCV NS5B polymerase inhibitor.

23. The method of claim 22 , wherein the HCV protease inhibitor is the compound having the structure:

24. The method of claim 23 , wherein the HCV NS5B polymerase inhibitor is a nucleoside.

Assignments (4)
MERGER Recorded Aug 8, 2022
From: MERCK SHARP & DOHME CORP.
To: MERCK SHARP & DOHME LLC
Reel/Frame 061102/0145 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 1, 2015
From: SHANKAR, BANDARPALLE
To: MERCK SHARP & DOHME CORP.
Reel/Frame 037180/0440 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 1, 2015
From: HU, BIN; ZHONG, BIN; WANG, DAHAI; HAO, JINGLAI; WEI, WEI; JI, TAO; ZAN, SHUAI
To: WUXI APPTEC (SHANGHAI) CO., LTD.
Reel/Frame 037180/0863 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 1, 2015
From: WUXI APPTEC (SHANGHAI) CO., LTD.
To: MERCK SHARP & DOHME CORP.
Reel/Frame 037181/0060 →