US2017137505A1PendingUtilityA1

Treatment of congestive heart failure and other cardiac dysfunction using a gdf15 modulator

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Assignee: AVEO PHARMACEUTICALS INCPriority: Jun 20, 2014Filed: Jun 19, 2015Published: May 18, 2017
Est. expiryJun 20, 2034(~7.9 yrs left)· nominal 20-yr term from priority
A61P 9/04C07K 2317/56C07K 2317/24C07K 2317/565C07K 2317/76C07K 16/22A61K 2039/505
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Claims

Abstract

The invention provides methods and compositions of treating a subject having a cardiac-related disorder such as congestive or chronic heart failure (CHF), cardiac hypertrophy, cardiac hypotrophy, and other cardiac myopathies/dystrophies. The methods comprise administering an effective amount of a composition that modulates, for example, reduces or inhibits, GDF 15 activity in the subject.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of increasing cardiac function in a subject in need thereof, the method comprising administering an effective amount of a composition comprising a GDF15 modulator thereby to increase cardiac function in said subject. 
     
     
         2 . The method of  claim 1 , wherein the subject has elevated GDF15 activity in a body fluid. 
     
     
         3 . A method of treating a subject having a cardiac disorder or dysfunction, the method comprising administering an effective amount of a composition comprising a GDF15 modulator thereby to ameliorate a symptom of the cardiac disorder or dysfunction. 
     
     
         4 . The method of  claim 3 , wherein the subject has elevated GDF15 activity in a body fluid. 
     
     
         5 . A method of reducing or reversing cardiac hypotrophy in a subject exhibiting one or more symptoms of congestive heart failure, the method comprising administering an effective amount of a composition comprising a GDF15 modulator, wherein the composition ameliorates at least one symptom of cardiac hypotrophy in the subject. 
     
     
         6 . The method of  claim 5 , wherein the subject has elevated GDF15 activity in a body fluid. 
     
     
         7 . A method of treating or preventing congestive heart failure (CHF) in a subject in need thereof, the method comprising administering an effective amount of a composition that reduces or inhibits a GDF15 activity in the subject, thereby to treat or prevent CHF in the subject. 
     
     
         8 . The method of  claim 7 , wherein the subject has elevated GDF15 activity in a body fluid. 
     
     
         9 . A method of reducing cardiac hypotrophy in a subject exhibiting one or more characteristics of congestive heart failure, the method comprising administering an effective amount of a composition that modulates the activity of GDF15, thereby to reduce cardiac hypotrophy in the subject. 
     
     
         10 . The method of  claim 9 , wherein the subject has elevated GDF15 activity in a body fluid. 
     
     
         11 . The method of any one of  claims 1 - 10 , wherein the subject exhibits a peak VO 2  of less than less than 14 mL/kg/min. 
     
     
         12 . The method of any one of  claims 1 - 11 , wherein the subject exhibits an LVEF of less than 40%. 
     
     
         13 . The method of any one of  claims 1 - 12 , wherein the subject exhibits BNP levels in excess of 100 pg/ml. 
     
     
         14 . The method of any one of  claims 1 - 13 , wherein the subject exhibits serum cardiac troponin I (cTnI) levels in excess of 1.5 ng/mL. 
     
     
         15 . The method of any one of  claims 1 - 14 , wherein the subject has been diagnosed as having congestive heart failure. 
     
     
         16 . The method of any one of  claims 1 - 15 , wherein the GDF15 modulator reduces or inhibits GDF15 activity in the subject. 
     
     
         17 . The method of  claim 16 , wherein the GDF15 modulator binds GDF15. 
     
     
         18 . The method of  claim 17 , wherein the GDF15 inhibitor is an anti-GDF15 antibody. 
     
     
         19 . The method of  claim 18 , wherein the antibody is humanized or human. 
     
     
         20 . The method of any one of  claims 1 - 19 , wherein the subject exhibits above normal levels of a marker selected from the group consisting of cardiac troponin I, cardiac troponin T, brain natriuretic protein (BNP), N-terminal peptides derived from BNP (NT-proBNP), and cardiac fatty acid binding protein (cFABP). 
     
     
         21 . The method of any one of  claim 2 ,  4 ,  6 ,  8 , or  10 , wherein the body fluid is plasma or serum.

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