Methods and compositions for treating a proprotein convertase subtilisin kexin (PCSK9) gene-associated disorder
The invention relates to methods of inhibiting the expression of a PCSK9 gene in a subject, as well as therapeutic and prophylactic methods for treating subjects having a lipid disorder, such as a hyperlipidemia using RNAi agents, e.g., double-stranded RNAi agents, targeting the PCSK9 gene.
1. A method of inhibiting the expression of a Proprotein convertase subtilisin kexin 9 (PCSK9) gene in a human subject, comprising subcutaneously administering to the subject a fixed dose of 275 mg to 325 mg of a double stranded ribonucleic acid (RNAi) agent, or salt thereof,
wherein the double stranded RNAi agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises the nucleotide sequence of 5′-csusagacCfuGfudTuugcuuuugu-3′ (SEQ ID NO: 687) and the antisense strand comprises the nucleotide sequence of 5′-asCfsaAfAfAfgCfaAfaAfcAfgGfuCfuagsasa-3′ (SEQ ID NO: 688),
wherein a, g, c and u are 2′-O-methyl (2′-OMe) A, G, C, and U; Af, Gf, Cf and Uf are 2′-fluoro A, G, C and U; dT is 2′-deoxythymidine; and s is a phosphorothioate linkage, and
wherein the double stranded RNAi agent is conjugated to a N-acetylgalactosamine (GalNAc)3 ligand.
2. A method of treating a human subject having a hyperlipidemia, comprising subcutaneously administering to the subject a fixed dose of 275 mg to 325 mg of a double stranded ribonucleic acid (RNAi) agent, or salt thereof,
wherein the double stranded RNAi agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises the nucleotide sequence of 5′-csusagacCfuGfudTuugcuuuugu-3′ (SEQ ID NO: 687) and the antisense strand comprises the nucleotide sequence of 5′-asCfsaAfAfAfgCfaAfaAfcAfgGfuCfuagsasa-3′ (SEQ ID NO: 688),
wherein a, g, c and u are 2′-O-methyl (2′-OMe) A, G, C, and U; Af, Gf, Cf and Uf are 2′-fluoro A, G, C and U; dT is 2′-deoxythymidine; and s is a phosphorothioate linkage, and
wherein the double stranded RNAi agent is conjugated to a N-acetylgalactosamine (GalNAc)3 ligand.
3. The method of claim 1 , wherein the subject is administered a fixed dose of 300 mg.
4. The method of claim 2 , wherein the subject is administered a fixed dose of 300 mg.
5. The method of claim 1 , wherein the subject is administered a fixed dose of 300 mg once a quarter.
6. The method of claim 2 , wherein the subject is administered a fixed dose of 300 mg once a quarter.
7. The method of claim 1 , wherein the subject is administered a fixed dose of 300 mg biannually.
8. The method of claim 2 , wherein the subject is administered a fixed dose of 300 mg biannually.
9. The method of claim 1 , wherein the double stranded RNAi agent or salt thereof is administered to the subject in a dosing regimen that includes a loading phase followed by a maintenance phase.
10. The method of claim 2 , wherein the double stranded RNAi agent or salt thereof is administered to the subject in a dosing regimen that includes a loading phase followed by a maintenance phase.
11. The method of claim 9 , wherein the dose administered to the subject during the loading phase is the same as the dose administered to the subject during the maintenance phase.
12. The method of claim 10 , wherein the dose administered to the subject during the loading phase is the same as the dose administered to the subject during the maintenance phase.
13. The method of claim 1 , further comprising administering an additional therapeutic agent to the subject.
14. The method of claim 2 , further comprising administering an additional therapeutic agent to the subject.
15. The method of claim 2 , wherein the hyperlipidemia is hypercholesterolemia.
16. The method of claim 1 , wherein the double stranded RNAi agent or salt thereof is administered in a pharmaceutical composition.
17. The method of claim 2 , wherein the double stranded RNAi agent or salt thereof is administered in a pharmaceutical composition.
18. The method of claim 1 , wherein the (GalNAc)3 ligand is
19. The method of claim 2 , wherein the (GalNAc)3 ligand is
20. The method of claim 1 , wherein the double stranded RNAi agent is conjugated to the (GalNAc)3 ligand as shown in the following schematic
wherein X is O.
21. The method of claim 2 , wherein the double stranded RNAi agent is conjugated to the (GalNAc)3 ligand as shown in the following schematic
wherein X is O.
22. The method of claim 1 , wherein the sense strand consists of the nucleotide sequence of 5′-csusagacCfuGfudTuugcuuuugu-3′ (SEQ ID NO: 687) and the antisense strand consists of the nucleotide sequence of 5′-asCfsaAfAfAfgCfaAfaAfcAfgGfuCfuagsasa-3′ (SEQ ID NO: 688), wherein a, g, c and u are 2′-O-methyl (2′-OMe) A, G, C, and U; Af, Gf, Cf, and Uf are 2′-fluoro A, G, C, and U; dT is 2′-deoxythymidine; s is a phosphorothioate linkage; and
wherein the (GalNAc)3 ligand is conjugated to the 3′ end of the sense strand as shown in the following schematic:
wherein X is O.
23. The method of claim 2 , wherein the sense strand consists of the nucleotide sequence of 5′-csusagacCfuGfudTuugcuuuugu-3′ (SEQ ID NO: 687) and the antisense strand consists of the nucleotide sequence of 5′-asCfsaAfAfAfgCfaAfaAfcAfgGfuCfuagsasa-3′ (SEQ ID NO: 688), wherein a, g, c and u are 2′-O-methyl (2′-OMe) A, G, C, and U; Af, Gf, Cf, and Uf are 2′-fluoro A, G, C, and U; dT is 2′-deoxythymidine; s is a phosphorothioate linkage; and
wherein the (GalNAc)3 ligand is conjugated to the 3′ end of the sense strand as shown in the following schematic:
wherein X is O.
24. The method of claim 22 , wherein the double stranded RNAi agent is in a salt form.
25. The method of claim 23 , wherein the double stranded RNAi agent is in a salt form.
26. A method of decreasing levels of low density lipoprotein (LDLc) in serum of a human subject, comprising subcutaneously administering to the subject a fixed dose of 275 mg to 325 mg of a double stranded ribonucleic acid (RNAi) agent, or salt thereof,
wherein the double stranded RNAi agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises the nucleotide sequence of 5′-csusagacCfuGfudTuugcuuuugu-3′ (SEQ ID NO: 687) and the antisense strand comprises the nucleotide sequence of 5′-asCfsaAfAfAfgCfaAfaAfcAfgGfuCfuagsasa-3′ (SEQ ID NO: 688),
wherein a, g, c and u are 2′-O-methyl (2′-OMe) A, G, C, and U; Af, Gf, Cf and Uf are 2′-fluoro A, G, C and U; dT is 2′-deoxythymidine; and s is a phosphorothioate linkage, and
wherein the double stranded RNAi agent is conjugated to a N-acetylgalactosamine (GalNAc)3 ligand.
27. The method of claim 26 , wherein the subject has hypercholesterolemia.
28. The method of claim 26 , wherein the subject has heterozygous LDL receptor genotype.
29. A method of decreasing levels of low density lipoprotein (LDLc) in serum of a human subject having one or more risk factors associated with cardiovascular disease, comprising subcutaneously administering to the subject a fixed dose of 275 mg to 325 mg of a double stranded ribonucleic acid (RNAi) agent, or salt thereof,
wherein the double stranded RNAi agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises the nucleotide sequence of 5′-csusagacCfuGfudTuugcuuuugu-3′ (SEQ ID NO: 687) and the antisense strand comprises the nucleotide sequence of 5′-asCfsaAfAfAfgCfaAfaAfcAfgGfuCfuagsasa-3′ (SEQ ID NO: 688),
wherein a, g, c and u are 2′-O-methyl (2′-0Me) A, G, C, and U; Af, Gf, Cf and Uf are 2′-fluoro A, G, C and U; dT is 2′-deoxythymidine; and s is a phosphorothioate linkage, and
wherein the double stranded RNAi agent is conjugated to a N-acetylgalactosamine (GalNAc)3 ligand,
wherein said one or more risk factors comprise diabetes, previous personal history of coronary heart disease (CHD) or noncoronary atherosclerosis, family history of cardiovascular disease, tobacco use, hypertension and/or obesity.
30. The method of claim 29 , wherein the cardiovascular disease is selected from the group consisting of arteriosclerosis, coronary artery disease, heart valve disease, arrhythmia, heart failure, hypertension, orthostatic hypotension, shock, endocarditis, diseases of the aorta and its branches, disorders of the peripheral vascular system, heart attack, cardiomyopathy, and congenital heart disease.