IP Library › Granted Patent US 8,436,026
Granted Patent B2
US 8,436,026 · App. 12/034,614 · Granted May 7, 2013

Endogeneous repair factor production promoters

Inventors: Yoshiki Sakai (Mishima-gun, JP); Akio Nishiura (Mishima-gun, JP); Teppei Ogata (Mishima-gun, JP)
Assignee: Ono Pharmaceutical Co., Ltd.
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Quick Facts
Patent No.
US 8,436,026
App. No.
12/034,614
Granted
May 7, 2013
Kind
B2
Abstract

It relates to an endogenous repair factor production accelerator which comprises one or at least two selected from prostaglandin (PG) 12 agonist, EP2 agonist and EP4 agonist. Since prostaglandin (PG) 12 agonist, EP2 agonist or EP4 agonist has various endogenous repair factor production accelerating action, angiogenesis acceleration action and stem cell differentiation induction action, it is useful as preventive and/or therapeutic agents for ischemic organ diseases (e.g., arteriosclerosis obliterans, Buerger disease, Raynaud disease, myocardial infarction, angina pectoris, diabetic neuropathy, spinal canal stenosis, cerebrovascular accidents, cerebral infarction, pulmonary hypertension, bone fracture, Alzheimer disease, etc.) and various cell and organ diseases.

Claims (26)

1. A method of treating diseases, said diseases selected from the group consisting of:

ischemic organ disease selected from the group consisting of arteriosclerosis obliterans and cerebral infarction;

liver disease selected from the group consisting of fluminant hepatitis, acute hepatitis and fatty liver;

kidney disease selected from the group consisting of acute renal insufficiency and chronic renal insufficiency;

pancreas disease selected from the group consisting of diabetes mellitus and chronic pancreatitis;

digestive organ disease selected from the group consisting of duodenal ulcer;

nerve degeneration disease selected from the group consisting of stroke;

diabetic complication selected from the group consisting of diabetic nerve disorder and diabetic nephropathy;

vascular endothelial cell disease which is restenosis after PTCA (percutaneous transluminal coronary angiopathy); and

heart disease selected from the group consisting of dilated cardiomyopathy;

comprising administering to a patient in need of treatment an effective amount of (E)-[5-[2-[1-phenyl-1-(3-pyridyl)methylideneaminoxy]ethyl]-7, 8-dihydronaphthalen-1-yloxy]acetic acid or a salt thereof.

2. A method of treating chronic renal insufficiency, comprising administering to a patient in need of treatment an effective amount of (E)-[5-[2-[1-phenyl-1-(3-pyridyl)methylideneaminoxy]ethyl]-7,8-dihydronaphthalen-1-yloxy]acetic acid or a salt thereof.

3. A method of treating dilated cardiomyopathy, comprising administering to a patient in need of treatment an effective amount of (E)[-5-[2-[1-phenyl-1-(3-pyridyl)methylideneaminoxy]ethyl]-7,8-dihydronaphthalen-1-yloxy]acetic acid or a salt thereof.

4. A method of treating diseases, said diseases selected from the group consisting of:

ischemic organ disease selected from the group consisting of arteriosclerosis obliterans and cerebral infarction;

liver disease selected from the group consisting of fluminant hepatitis, acute hepatitis and fatty liver;

kidney disease selected from the group consisting of acute renal insufficiency and chronic renal insufficiency;

pancreas disease selected from the group consisting of diabetes mellitus and chronic pancreatitis;

digestive organ disease selected from the group consisting of duodenal ulcer;

nerve degeneration disease selected from the group consisting of stroke;

diabetic complication selected from the group consisting of diabetic nerve disorder and diabetic nephropathy;

vascular endothelial cell disease which is restenosis after PTCA (percutaneous transluminal coronary angiopathy); and

heart disease selected from the group consisting of dilated cardiomyopathy;

comprising administering to a patient in need of treatment an effective amount of (E)-[5-[2-[1-phenyl-1-(3-pyridyl)methylideneaminoxy]ethyl]-7,8-dihydronaphthalen-1-yloxy]acetic acid or a salt thereof whereby production of VEGF and/or HGF is accelerated.

5. A method of treating chronic renal insufficiency, comprising administering to a patient in need of treatment an effective amount of (E)-[5-[2-[1-phenyl-1-(3-pyridyl)methylideneaminoxy]ethyl]-7,8-dihydronaphthalen-1-yloxy]acetic acid or a salt thereof whereby production of VEGF and/or HGF is accelerated.

6. A method of treating dilated cardiomyopathy, comprising administering to a patient in need of treatment an effective amount of (E)-[5-[2-[1-phenyl-1-(3-pyridyl)methylideneaminoxy]ethyl]-7,8-dihydronaphthalen-1-yloxy]acetic acid or a salt thereof whereby production of VEGF and/or HGF is accelerated.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 18, 2021
From: ONO PHARMACEUTICAL CO., LTD.
To: CUORIPS INC.
Reel/Frame 058152/0931 →
Priority Claims (3)
JP 2002-298079 · Oct 10, 2002 · national
JP 2002-318830 · Oct 31, 2002 · national
JP 2003-117604 · Apr 22, 2003 · national
Continuity (2)
Division 10530685 · Apr 8, 2005
Related Publication 20080299089A1 · Dec 4, 2008