Methods for inhibiting atherosclerosis by administering an anti-PCSK9 antibody
The present invention provides methods and compositions for inhibiting atherosclerotic plaque formation in a subject. In certain embodiments, the methods of the present invention comprise selecting a subject who has, or is at risk of developing, atherosclerosis, and administering to the subject a pharmaceutical composition comprising a proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor. In certain embodiments, the PCSK9 inhibitor is an anti-PCSK9 antibody, or antigen binding protein.
1. A method of inhibiting progression of atherosclerosis comprising:
administering to a subject in need thereof a therapeutically effective amount of a proprotein convertase subtilisin/kexin type 9 (PCSK9) antibody or antigen-binding fragment thereof, wherein the PCSK9 antibody or antigen-binding fragment thereof comprises heavy and light chain complementarity determining regions (CDR) amino acid sequences having SEQ ID NOs: 2, 3, 4, 7, 8, and 10; and
wherein the subject has suffered a stroke or myocardial infarction.
2. The method of claim 1 , wherein the subject is nonhyperlipidemic.
3. The method of claim 1 , wherein the subject is nonhypercholesterolemic.
4. The method of claim 1 , wherein the subject is nonhypertriglyceridemic.
5. The method of claim 1 , wherein the subject has a disease or disorder selected from the group consisting of type I diabetes mellitus, type II diabetes mellitus, Kawasaki disease, chronic inflammatory disease, and hypertension.
6. The method of claim 1 , wherein the subject has elevated levels of an inflammatory marker.
7. The method of claim 6 , wherein the inflammatory marker is C-reactive protein.
8. The method of claim 6 , wherein the inflammatory marker is an inflammatory cytokine.
9. The method of claim 1 , wherein the subject has heterozygous Familial Hypercholesterolemia (heFH).
10. The method of claim 1 , wherein the subject has a form of hypercholesterolemia that is not Familial Hypercholesterolemia (nonFH).
11. The method of claim 1 , wherein the subject is on another lipid-modifying agent before or during administration of the antibody or antigen-binding protein.
12. The method of claim 11 , wherein the therapeutic lipid-modifying agent is a statin, ezetimibe, a fibrate, niacin, an omega-3 fatty acid, or a bile acid resin.
13. The method of claim 12 , wherein the statin is cerivastatin, atorvastatin, simvastatin, pitavastatin, rosuvastatin, fluvastatin, lovastatin, or pravastatin.
14. The method of claim 1 , wherein the subject is not on another lipid-modifying agent before or during administration of the antibody or antigen-binding protein.
15. The method of claim 1 , wherein the subject has an LDL-C level greater than or equal to 70 mg/dL.
16. The method of claim 1 , wherein the antibody or antigen-binding protein comprises a heavy chain variable region (HCVR) having the amino acid sequence of SEQ ID NO:1 and a light chain variable region (LCVR) having the amino acid sequence of SEQ ID NO:6.
17. The method of claim 1 , wherein the antibody or antigen-binding protein reduces atherosclerotic plaque formation in the subject by at least 10%.
18. The method of claim 1 , wherein the antibody or antigen binding protein is administered subcutaneously.
19. The method of claim 1 , wherein the administering step comprises administering to the subject one or more doses of 150 mg of the antibody or antigen-binding fragment thereof about every two weeks.