Treatment with anti-pcsk9 antibodies
US-2016152734-A1 · Jun 2, 2016 · US
US10494442B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10494442-B2 |
| Application number | US-201414896196-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jun 6, 2014 |
| Priority date | Jun 7, 2013 |
| Publication date | Dec 3, 2019 |
| Grant date | Dec 3, 2019 |
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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.
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We claim: 1. A method of inhibiting atherosclerotic plaque formation, the method comprising: (a) selecting a subject who has atherosclerosis; and (b) administering to the subject a pharmaceutical composition comprising an antibody or antigen-binding fragment thereof that specifically binds to proprotein convertase subtilisin/kexin type 9 (PCSK9), wherein the antibody or antigen-binding fragment thereof comprises heavy and light chain CDR amino acid sequences having SEQ ID NOs:2, 3, 4, 7, 8, and 10, such that the administration of the antibody or antigen-binding fragment thereof inhibits an increase in the number, total area, severity, or instability of atherosclerotic plaques in the subject. 2. The method of claim 1 , wherein the subject has suffered a stroke or myocardial infarction. 3. The method of claim 1 , wherein the subject has one or more of the following conditions: a) 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; b) heterozygous Familial Hypercholesterolemia (heFH); and c) a form of hypercholesterolemia that is not Familial Hypercholesterolemia (nonFH). 4. The method of claim 1 , wherein the subject has an elevated level of an inflammatory marker. 5. The method of claim 4 , wherein the inflammatory marker is C-reactive protein or an inflammatory cytokine. 6. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof comprises an HCVR having the amino acid sequence of SEQ ID NO:1 and an LCVR having the amino acid sequence of SEQ ID NO:6. 7. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof inhibits the increase of the number, total area, severity, or instability of atherosclerotic plaques in the subject by at least 10%, 20%, 30%, 40%, 50%, 60%, 70%, 80%, or 90%. 8. The method of claim 1 , wherein the subject is on another lipid-modifying agent before and/or during administration of the antibody or antigen-binding fragment thereof. 9. The method of claim 8 , wherein the therapeutic lipid-modifying agent is selected from the group consisting of a statin, ezetimibe, a fibrate, niacin, an omega-3 fatty acid, and a bile acid resin. 10. The method of claim 9 , wherein the statin is selected from the group consisting of cerivastatin, atorvastatin, simvastatin, pitavastatin, rosuvastatin, fluvastatin, lovastatin and pravastatin. 11. The method of claim 1 , wherein the subject is not on another lipid-modifying agent before and/or during administration of the antibody or antigen-binding fragment thereof. 12. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof is administered subcutaneously. 13. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof inhibits an increase in the number of atherosclerotic plaques. 14. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof inhibits an increase in the total area of atherosclerotic plaques. 15. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof inhibits an increase in the severity of atherosclerotic plaques. 16. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof inhibits an increase in the instability of atherosclerotic plaques. 17. The method of claim 1 , wherein the antibody or antigen-binding fragment thereof inhibits an increase in the number, total area, severity, and instability of atherosclerotic plaques. 18. A method of inhibiting atherosclerotic plaque formation, the method comprising: (a) selecting a subject who has atherosclerosis and hypercholesterolemia; and (b) administering to the subject a pharmaceutical composition comprising an antibody or antigen-binding fragment thereof that specifically binds to PCSK9, wherein the antibody or antigen-binding fragment thereof comprises heavy and light chain CDR amino acid sequences having SEQ ID NOs:2, 3, 4, 7, 8, and 10, such that the administration of the antibody or antigen-binding fragment thereof inhibits an increase in the number, total area, severity, or instability of atherosclerotic plaques in the subject. 19. The method of claim 18 , wherein the antibody or antigen-binding fragment thereof comprises an HCVR having the amino acid sequence of SEQ ID NO:1 and an LCVR having the amino acid sequence of SEQ ID NO:6. 20. A method of inhibiting atherosclerotic plaque formation, the method comprising: (a) selecting a subject who has atherosclerosis and hypercholesterolemia; and (b) administering to the subject subcutaneously a pharmaceutical composition comprising an antibody or antigen-binding fragment thereof that specifically binds to PCSK9, wherein the antibody or antigen-binding fragment thereof comprises an HCVR having the amino acid sequence of SEQ ID NO:1 and an LCVR having the amino acid sequence of SEQ ID NO:6, such that the administration of the antibody or antigen-binding fragment thereof inhibits an increase in the number, total area, severity, or instability of atherosclerotic plaques in the subject.
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