TMPRSS6 iRNA COMPOSITIONS AND METHODS OF USE THEREOF

Patent metadata

Field	Value
Publication number	US-2024309387-A1
Application number	US-202318376217-A
Country	US
Kind code	A1
Filing date	Oct 3, 2023
Priority date	May 22, 2013
Publication date	Sep 19, 2024
Grant date	—

Abstract

The invention relates to RNAi agents, e.g., double-stranded RNAi agents, targeting the TMPRSS6 gene, and methods of using such RNAi agents to inhibit expression of TMPRSS6 and methods of treating subjects having a TMPRSS6 associated disorder, e.g., an iron overload associated disorder, such as β-thalassemia or hemochromatosis.

First claim

1 . A double stranded ribonucleic acid (dsRNA) agent, or a pharmaceutically acceptable salt thereof, capable of inhibiting expression of TMPRSS6 in a cell, wherein said dsRNA agent, or a pharmaceutically acceptable salt thereof, comprises a sense strand and an antisense strand forming a double-stranded region, wherein said sense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the nucleotide sequences of SEQ ID NO:1, SEQ ID NO:2, or SEQ ID NO:3, SEQ ID NO:4, or SEQ ID NO:5, and said antisense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the nucleotide sequences of SEQ ID NO:6, SEQ ID NO:7, or SEQ ID NO:8, SEQ ID NO:9, or SEQ ID NO:10,
wherein substantially all of the nucleotides of said sense strand and substantially all of the nucleotides of said antisense strand are modified nucleotides, and wherein said sense strand is conjugated to a ligand attached at the 3′- terminus.

2 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 , wherein all of the nucleotides of said sense strand and all of the nucleotides of said antisense strand are modified nucleotides.

3 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 , wherein said sense strand and said antisense strand comprise a region of complementarity which comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the antisense sequences listed in any one of Tables 1, 2,4, 5, 8, 10, and 12.

4 . (canceled)

5 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of any claim 1 , wherein at least one strand comprises a 3′ overhang of at least 1 nucleotide or at least 2 nucleotides.

6 - 17 . (canceled)

18 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 , wherein the double-stranded region is 15-30 nucleotide pairs in length.

19 - 23 . (canceled)

24 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 , wherein each strand is 15-30 nucleotides in length.

25 . (canceled)

26 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 , wherein the modifications on the nucleotides are selected from the group consisting of LNA, HNA, CeNA, 2′-methoxyethyl, 2′-O-alkyl, 2′-O-allyl, 2′-C-allyl, 2′-fluoro, 2′-deoxy, 2′-hydroxyl, and combinations thereof.

27 . (canceled)

28 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 , wherein the ligand is one or more GalNAc derivatives attached through a bivalent or trivalent branched linker.

29 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 , wherein the ligand is

30 . (canceled)

31 . (canceled)

32 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 , wherein said agent further comprises at least one phosphorothioate or methylphosphonate intemucleotide linkage.

33 - 40 . (canceled)

41 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 32 , wherein dsRNA agent, or a pharmaceutically acceptable salt thereof, comprises 6-8 phosphorothioate intemucleotide linkages.

42 - 52 . (canceled)

53 . The dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 , wherein said dsRNA agent, or a pharmaceutically acceptable salt thereof, is selected from the group of dsRNA agents listed in any one of Tables 1, 2, 4, 5, 8, 10, and 12.

54 . (canceled)

55 . (canceled)

56 . A double stranded ribonucleic acid (dsRNA) agent, or a pharmaceutically acceptable salt thereof, capable of inhibiting expression of TMPRSS6 in a cell,
wherein said dsRNA agent, or a pharmaceutically acceptable salt thereof, comprises a sense strand and an antisense strand forming a double stranded region, wherein said sense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the nucleotide sequences of SEQ ID NO:1, SEQ ID NO:2, or SEQ ID NO:3, SEQ ID NO:4, or SEQ ID NO:5, and said antisense strand comprises at least 15 contiguous nucleotides differing by no more than 3 nucleotides from any one of the nucleotide sequences of SEQ ID NO:6, SEQ ID NO:7, or SEQ ID NO:8, SEQ ID NO:9, or SEQ ID NO: 10, wherein substantially all of the nucleotides of said sense strand comprise a modification selected from the group consisting of a 2′-O-methyl modification and a 2′-fluoro modification, wherein said sense strand comprises two phosphorothioate internucleotide linkages at the 5′-terminus, wherein substantially all of the nucleotides of said antisense strand comprise a modification selected from the group consisting of a 2′-O-methyl modification and a 2′-fluoro modification, wherein said antisense strand comprises two phosphorothioate internucleotide linkages at the 5′-terminus and two phosphorothioate internucleotide linkages at the 3′-terminus, and wherein said sense strand is conjugated to one or more GalNAc derivatives attached through a branched bivalent or trivalent linker at the 3′-terminus.

57 - 67 . (canceled)

68 . A pharmaceutical composition comprising the dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 .

69 - 73 . (canceled)

74 . A method of inhibiting TMPRSS6 expression in a cell, the method comprising:
(a) contacting the cell with the dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 ; and (b) maintaining the cell produced in step (a) for a time sufficient to obtain degradation of the mRNA transcript of a TMPRSS6 gene, thereby inhibiting expression of the TMPRSS6 gene in the cell.

75 - 81 . (canceled)

82 . A method of treating a subject having a TMPRSS6 associated disorder, comprising administering to the subject a therapeutically effective amount of the dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 , thereby treating said subject.

83 - 100 . (canceled)

101 . An isolated cell containing the dsRNA agent, or a pharmaceutically acceptable salt thereof, of claim 1 .

Assignees

• Alnylam Pharmaceuticals Inc

Inventors

• Butler James
• Bettencourt Brian
• Rajeev Kallanthottathil G
• Maier Martin A
• Charisse Klaus

Classifications

• C12N2310/32

  of the sugar · CPC title

• A61K31/713

  Double-stranded nucleic acids or oligonucleotides · CPC title

• A61K48/00

  Medicinal preparations containing genetic material which is inserted into cells of the living body to treat genetic diseases; Gene therapy · CPC title

• A61P3/00 Primary

  Drugs for disorders of the metabolism (of the blood or the extracellular fluid A61P7/00) · CPC title

• C12N15/1138 Primary

  against receptors or cell surface proteins · CPC title