IP Library Granted Patent US 9,855,266
Granted Patent B2
US 9,855,266 · App. 15/467,129 · Granted Jan 2, 2018

Treatment for osteoarthritis by intra-articular administration of a cis-imidazoline

Inventors: Remi-Martin Laberge (San Francisco, CA); Judith Campisi (Berkeley, CA); Albert Davalos (San Rafael, CA); Marco Demaria (Groningen, NL); Nathaniel David (San Francisco, CA); Alain Philippe Vasserot (Carlsbad, CA); James L. Kirkland (Rochester, MN); Tamar Tchkonia (Rochester, MN); Jennifer Elisseeff (Baltimore, MD); Chaekyu Kim (Pikesville, MD); Okhee Jeon (Baltimore, MD); Yi Zhu (Rochester, MN)
Assignees: Unity Biotechnology, Inc.; Buck Institute for Research on Aging; Mayo Foundation for Medical Education and Research; The John Hopkins University
A61K31/496A61K31/4178A61K47/36
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Quick Facts
Patent No.
US 9,855,266
App. No.
15/467,129
Granted
Jan 2, 2018
Kind
B2
Abstract

Methods are provided herein for selectively killing senescent cells and for treating senescence-associated diseases and disorders by administering a senolytic agent. Senescence-associated diseases and disorders treatable by the methods using the senolytic agents described herein include cardiovascular diseases and disorders associated with or caused by arteriosclerosis, such as atherosclerosis; idiopathic pulmonary fibrosis; chronic obstructive pulmonary disease; osteoarthritis; senescence-associated ophthalmic diseases and disorders; and senescence-associated dermatological diseases and disorders.

Claims (18)

1. A method of treating osteoarthritis, comprising administering to a subject in need thereof a therapeutically effective amount of a compound according to Formula (I), or a pharmaceutically acceptable salt thereof:

wherein R is selected from saturated and unsaturated 5- and 6-membered rings containing at least one hetero atom, wherein the hetero atom is selected from S, N and O and is optionally substituted with a group selected from lower alkyl, cycloalkyl, —C═O—R 1 , hydroxy, lower alkyl substituted with hydroxy, lower alkyl substituted with lower alkoxy, lower alkyl substituted with —NH 2 , lower alkyl substituted with —C═O—R 1 , N-lower alkyl, —SO 2 CH 3 , ═O and —CH 2 C═OCH 3 ;

R 1 is selected from hydrogen, lower alkyl, —NH 2 , —N-lower alkyl, lower alkyl substituted with hydroxy, lower alkyl substituted with —NH 2 , and a 5- or 6-membered saturated ring containing at least one hetero atom selected from S, N and O;

X 1 and X 2 are each independently selected from hydrogen, lower alkoxy, —CH 2 OCH 3 , —CH 2 OCH 2 CH 3 , —OCH 2 CF 3 , and —OCH 2 CH 2 F; and

Y 1 and Y 2 are each independently selected from —Cl, —Br, —NO 2 , —C≡N, and —C≡CH.

2. The method of claim 1 , wherein R is piperazin-2-one.

3. The method of claim 1 , wherein Y 1 and Y 2 are both chloride.

4. The method of claim 1 , wherein X 1 and X 2 are —O—CH—(CH 3 ) 2 and —O—CH 3 respectively.

5. The method of claim 1 , wherein the compound is administered intra-articularly to an osteoarthritic joint in the subject.

6. The method of claim 1 , wherein the compound is formulated in a pharmaceutical composition that contains a hyaluronan.

7. The method of claim 1 , wherein the compound is formulated in a sustained release formulation that includes a gel, a polymeric matrix, or a microparticle.

8. The method of claim 1 , wherein the compound is administered as a single dose, followed by a non-treatment interval of at least two weeks.

9. The method of claim 5 , whereby erosion of a proteoglycan layer is inhibited in the osteoarthritic joint.

10. The method of claim 5 , whereby production of collagen Type II is promoted in the osteoarthritic joint.

11. The method of claim 5 , whereby symptoms of osteoarthritis being experienced by the subject in the joint are relieved.

12. The method of claim 5 , whereby pain being experienced by the subject in the joint is relieved.

13. The method of claim 1 , wherein the compound is 4-[[(4S,5R)-4,5-bis(4-chlorophenyl)-4,5-dihydro-2-[4-methoxy-2-(1-methylethoxy)phenyl]-1H-imidazol-1-yl]carbonyl]-2-piperazinone.

14. The method of any of claims 2 to 12 , wherein the compound is 4-[[(4S,5R)-4,5-bis(4-chlorophenyl)-4,5-dihydro-2-[4-methoxy-2-(1-methylethoxy)phenyl]-1H-imidazol-1-yl]carbonyl]-2-piperazinone.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2017
From: ZHU, YI
To: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
Reel/Frame 043997/0162 →
CONFIRMATORY LICENSE Recorded May 12, 2017
From: MAYO CLINIC ROCHESTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 042456/0970 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2017
From: ELISSEEFF, JENNIFER; KIM, CHAEKYU; JEON, OKHEE
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 041970/0698 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2017
From: BAKER, DARREN J.; CHILDS, BENNETT G.; KIRKLAND, JAMES L.; TCHKONIA, TAMAR; VAN DEURSEN, JAN M.A.; PALMER, ALLYSON K.
To: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
Reel/Frame 041970/0831 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2017
From: DAVID, NATHANIEL; VASSEROT, ALAIN PHILIPPE
To: UNITY BIOTECHNOLOGY, INC.
Reel/Frame 041970/0864 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2017
From: LABERGE, REMI-MARTIN; CAMPISI, JUDITH; DAVALOS, ALBERT; DEMARIA, MARCO
To: BUCK INSTITUTE FOR RESEARCH ON AGING
Reel/Frame 041970/0968 →
Continuity (13)
Continuation 15114762
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Provisional Application 62002709 · May 23, 2014
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Provisional Application 62044664 · Sep 2, 2014
Provisional Application 62057820 · Sep 30, 2014
Provisional Application 62057825 · Sep 30, 2014
Provisional Application 62057828 · Sep 30, 2014
Provisional Application 62061627 · Oct 8, 2014
Provisional Application 62061629 · Oct 8, 2014
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