IP Library Granted Patent US 11,077,092
Granted Patent B2
US 11,077,092 · App. 15/484,508 · Granted Aug 3, 2021

Methods of treating diabetes by administering a glucagon receptor antagonist in combination with a cholesterol absorption inhibitor

Inventors: Hong-Ping Guan (Scotch Plains, NJ); Jose M. Castro-Perez (New Providence, NJ); Harry R. Davis (Berkeley Heights, NJ); Samuel E. Engel (New York, NY); Douglas G. Johns (Ocean, NJ); Songnian Lin (Holmdel, NJ); Stephen F. Previs (Branchburg, NJ); Thomas P. Roddy (Whitehouse Station, NJ); Liangsu Wang (Hillsborough, NJ); Sheng-Ping Wang (Annandale, NJ); Yusheng Xiong (Plainsboro, NJ)
Assignee: Merck Sharp & Dohme Corp.
A61K31/397A61K9/209A61K31/194A61K31/403A61K31/404A61K31/415A61K31/4184A61K31/435A61K31/44A61K45/06
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Quick Facts
Patent No.
US 11,077,092
App. No.
15/484,508
Granted
Aug 3, 2021
Kind
B2
Abstract

Use of a glucagon receptor antagonist in combination with a cholesterol absorption inhibitor for the treatment of diabetes and related conditions is disclosed.

Claims (27)

1. A method of treating diabetes in a mammalian subject having an LDL cholesterol plasma level of less than 100 mg/dL, which comprises administering to said mammalian subject:

(a) a glucagon receptor antagonist, and

(b) a cholesterol absorption inhibitor,

wherein the subject is not further being treated with a statin.

2. The method of claim 1 wherein the glucagon receptor antagonist compound and the cholesterol absorption inhibitor compound are present in a single dosage form.

3. The method of claim 2 wherein the glucagon receptor antagonist compound and the cholesterol absorption inhibitor compound are in a bilayer tablet.

4. The method of claim 1 wherein the glucagon receptor antagonist compound and the cholesterol absorption inhibitor compound are present each in a separate dosage form for simultaneous or sequential administration.

5. The method of claim 1 for treating type 2 diabetes.

6. The method of claim 1 wherein the cholesterol absorption inhibitor compound is:

or a pharmaceutically acceptable salt thereof.

7. The method of claim 1 wherein the glucagon receptor antagonist compound is a compound selected from the following table of compounds:

or a pharmaceutically acceptable salt thereof.

8. The method of claim 1 wherein the mammalian subject is a human.

9. The method of claim 6 wherein the mammalian subject is a human.

10. The method of claim 7 wherein the mammalian subject is a human.

11. The method of claim 1 wherein the glucagon receptor antagonist compound is:

or a pharmaceutically acceptable salt thereof.

12. The method of claim 6 wherein the glucagon receptor antagonist compound is:

or a pharmaceutically acceptable salt thereof.

13. The method of claim 1 wherein the glucagon receptor antagonist compound is:

or a pharmaceutically acceptable salt thereof.

14. The method of claim 6 wherein the glucagon receptor antagonist compound is:

or a pharmaceutically acceptable salt thereof.

15. A method of reducing hyperglycemia in a mammalian subject having an LDL cholesterol plasma level of less than 100 mg/dL, which comprises administering to said mammalian subject:

(a) a glucagon receptor antagonist, and

(b) a cholesterol absorption inhibitor,

wherein the subject is not further being treated with a statin.

Assignments (2)
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 Apr 1, 2021
From: DAVIS, HARRY R; LIN, SONGNIAN; XIONG, YUSHENG; GUAN, HONG-PING; CASTRO-PEREZ, JOSE; JOHNS, DOUGLAS G.; PREVIS, STEPHEN F.; RODDY, THOMAS P.; WANG, LIANGSU; WANG, SHENG-PING; ENGEL, SAMUEL S.
To: MERCK SHARP & DOHME CORP.
Reel/Frame 055798/0538 →
Continuity (3)
Continuation 14649651
Provisional Application 61735304 · Dec 10, 2012
Related Publication 20170216250A1 · Aug 3, 2017