IP Library Granted Patent US 10,413,542
Granted Patent B2
US 10,413,542 · App. 15/950,965 · Granted Sep 17, 2019

Methods and compositions for killing senescent cells and for treating senescence-associated diseases and disorders using an inhibitor of Akt kinase

Inventors: Remi-Martin Laberge (San Francisco, CA); Nathaniel David (Brisbane, CA); Alain Philippe Vasserot (Carlsbad, CA); Darren J. Baker (Rochester, MN); Bennett G. Childs (Rochester, MN); James L. Kirkland (Rochester, MN); Tamar Tchkonia (Rochester, MN); Jan M. A. van Deursen (Rochester, MN); Yi Zhu (Rochester, MN)
Assignees: Buck Institute for Research on Aging; Unity Biotechnology, Inc.; Mayo Foundation for Medical Education and Research
A61K31/496A61K9/0048A61K9/0073A61K31/404A61K31/4178A61K31/428A61K31/4375A61K31/495A61K31/5377A61K31/728A61K45/06A61K47/36A61P9/10A61P11/00A61P27/02C12N5/0081C12N2501/999C12N2503/02C12Q1/485
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Quick Facts
Patent No.
US 10,413,542
App. No.
15/950,965
Granted
Sep 17, 2019
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 (25)

1. A method for treating a disease or disorder that is not a cancer in a target tissue in a subject,

wherein symptoms of the disease or disorder are caused at least in part by senescent cells that are located in or around the target tissue,

wherein the senescent cells are defined as non-cancerous cells that express p16,

the method comprising administering in or around the target tissue a course of therapy with a pharmaceutical composition,

wherein the pharmaceutical composition includes a formulation of an amount of senolytic agent that is less than 10,000 mol. wt., the senolytic agent being a means for binding to Akt kinase, thereby directly inhibiting Akt kinase activity,

wherein the amount of the senolytic agent and the formulation of the composition configure the composition such that upon administration to the target tissue in the subject, the senolytic agent contacts the senescent cells located in or around the target tissue, and selectively removes such senescent cells in preference to adjacent non-senescent cells,

wherein the course of therapy includes a treatment period during which the pharmaceutical composition is administered to the subject in one or a plurality of doses, followed by a therapeutic period of at least two weeks during which the pharmaceutical composition is not administered but one or more signs or symptoms of the disease or disorder in the target tissue are alleviated.

2. The method of claim 1 , wherein the means for directly inhibiting Akt kinase is selected from CCT128930, GDC-0068, GSK2110183 (afuresertib), GSK690693, AT7867, Perifosine (KRX-0401), AKTide-2T, GST-anti-Akt1-MTS, PX-316, GSK-2141795, VQD-002 (Triciribine), AZD5363, API-1, and pharmaceutically acceptable salts thereof.

3. The method of claim 1 , wherein the means for directly inhibiting Akt kinase is MK-2206 (8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-2H-[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3-one dihydrochloride), or a pharmaceutically acceptable salt thereof.

4. The method of claim 1 , wherein a single dose of the pharmaceutical composition is administered to the subject during the treatment period.

5. The method of claim 1 , wherein the therapeutic period during which the composition is not administered lasts at least one month.

6. The method of claim 1 , wherein the disease or disorder is osteoarthritis.

7. The method of claim 1 , wherein the disease or disorder is a lung disease.

8. The method of claim 1 , wherein the disease or disorder is atherosclerosis.

9. The method of claim 1 , wherein the disease or disorder is cardiac stress, a side effect of chemotherapy in a cancer patient, or diabetes.

10. A method for treating a disease or disorder that is not a cancer in a target tissue in a subject,

wherein symptoms of the disease or disorder are caused at least in part by senescent cells that are located in or around the target tissue,

wherein the senescent cells are defined as non-cancerous cells that express p16,

the method comprising administering in or around the target tissue a course of therapy with a pharmaceutical composition, and

monitoring senescent cells in or around the target tissue during or following the therapy;

wherein the pharmaceutical composition includes a formulation of an amount of senolytic agent that is less than 10,000 mol. wt., the senolytic agent being a means for binding to Akt kinase, thereby directly inhibiting Akt kinase activity,

wherein the senolytic agent is a means for inhibiting Akt kinase, and

wherein the amount of the senolytic agent and the formulation of the composition configure the composition such that upon administration to the target tissue in the subject, the senolytic agent contacts the senescent cells located in or around the target tissue, and selectively removes such senescent cells from the target tissue in preference to adjacent non-senescent cells.

11. The method of claim 10 , wherein the means for directly inhibiting Akt kinase is selected from CCT128930, GDC-0068, GSK2110183 (afuresertib), GSK690693, AT7867, Perifosine (KRX-0401), AKTide-2T, GST-anti-Akt1-MTS, PX-316, GSK-2141795, VQD-002 (Triciribine), AZD5363, API-1, and pharmaceutically acceptable salts thereof.

12. The method of claim 10 , wherein the means for directly inhibiting Akt kinase is MK-2206 (8-[4-(1-aminocyclobutyl)phenyl]-9-phenyl-2H-[1,2,4]triazolo[3,4-f][1,6]naphthyridin-3-one dihydrochloride), or a pharmaceutically acceptable salt thereof.

Assignments (5)
CONFIRMATORY LICENSE Recorded Jul 5, 2018
From: MAYO CLINIC ROCHESTER
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 046499/0259 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2018
From: BAKER, DARREN J.; CHILDS, BENNETT G.; KIRKLAND, JAMES L.; TCHKONIA, TAMAR; VAN DEURSEN, JAN M.A.; PALMER, ALLYSON K.; ZHU, YI
To: MAYO FOUNDATION FOR MEDICAL EDUCATION AND RESEARCH
Reel/Frame 045580/0028 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2018
From: ELISSEEFF, JENNIFER; KIM, CHAEKYU; JEON, OKHEE
To: THE JOHNS HOPKINS UNIVERSITY
Reel/Frame 045580/0134 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2018
From: LABERGE, REMI-MARTIN; CAMPISI, JUDITH; DAVALOS, ALBERT; DEMARIA, MARCO
To: BUCK INSTITUTE FOR RESEARCH ON AGING
Reel/Frame 045580/0220 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 18, 2018
From: DAVID, NATHANIEL; VASSEROT, ALAIN PHILIPPE
To: UNITY BIOTECHNOLOGY, INC.
Reel/Frame 045580/0254 →
Continuity (13)
Continuation 15114762
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Provisional Application 62057828 · Sep 30, 2014
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