IP Library Granted Patent US 10,465,194
Granted Patent B2
US 10,465,194 · App. 15/176,231 · Granted Nov 5, 2019

Complement component iRNA compositions and methods of use thereof

Inventors: Anna Borodovsky (Melrose, MA); Brian Bettencourt (Groton, MA)
Assignee: Alnylam Pharmaceuticals, Inc.
C12N15/1137A61K31/713A61K38/12A61K39/3955C07K16/18C12N15/111C12N15/1138C12N2310/14C12N2310/315C12N2310/321C12N2310/343C12N2310/346C12N2310/351C12N2320/51C12Y304/21047Y02A50/473
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Quick Facts
Patent No.
US 10,465,194
App. No.
15/176,231
Granted
Nov 5, 2019
Kind
B2
Abstract

The invention relates to iRNA, e.g., double-stranded ribonucleic acid (dsRNA), compositions targeting the complement factor B (CFB) gene, the complement component C3 gene, and the complement component C9 gene and methods of using such iRNA, e.g., dsRNA, compositions to inhibit expression of CFB, C9 and/or C3 and to treat subjects having a complement component-associated disease, e.g., paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome.

Claims (18)

1. A double stranded ribonucleic acid (dsRNA) agent for inhibiting expression of complement factor B (CFB) in a cell, wherein said dsRNA agent comprises a sense strand and an antisense strand forming a double stranded region, wherein the sense strand comprises the nucleotide sequence 5′-AfsgsCfaAfcAfuGfUfGfuUfcAfaAfgUfcAf-3′ (SEQ ID NO:482) and the antisense strand comprises the nucleotide sequence 5′-usGfsaCfuUfuGfaAfcacAfuGfuUfgCfuscsa-3′ (SEQ ID NO:485),

wherein a, c, g, and u are 2′-O-methyl (2′-OMe) A, C, G, and U; Af, Cf, Gf, and Uf are 2′-fluoro A, C, G, and U; and s is a phosphorothioate linkage, and

wherein the sense strand is conjugated to a ligand attached at the 3′-terminus.

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

3. The dsRNA agent of claim 1 , wherein the ligand is

4. An isolated cell containing the dsRNA agent of claim 1 .

5. A pharmaceutical composition for inhibiting expression of complement factor B (CFB) comprising the dsRNA agent of claim 1 .

6. The dsRNA agent of claim 3 , wherein the dsRNA agent is conjugated to the ligand as shown in the following schematic

7. The pharmaceutical composition of claim 5 , wherein dsRNA agent is formulated in a buffered solution.

8. The dsRNA agent of claim 1 , wherein the sense strand consists of the nucleotide sequence 5′-AfsgsCfaAfcAfuGfUfGfuUfcAfaAfgUfcAfL96-3′ (SEQ ID NO:482) and the antisense strand consists of the nucleotide sequence 5′-usGfsaCfuUfuGfaAfcacAfuGfuUfgCfuscsa-3′ (SEQ ID NO:485),

wherein a, c, g, and u are 2′-O-methyl (2′-OMe) A, C, G, and U; Af, Cf, Gf, and Uf are 2′-fluoro A, C, G, and U; s is a phosphorothioate linkage; and L96 is N-[tris(GalNAc-alkyl)-amidodecanoyl)]-4-hydroxyprolinol.

9. The pharmaceutical composition of claim 5 , wherein dsRNA agent is formulated in an unbuffered solution.

10. A pharmaceutical composition for inhibiting expression of complement factor B (CFB), comprising a double stranded ribonucleic acid (dsRNA) agent comprising a sense strand and an antisense strand forming a double stranded region,

wherein the sense strand comprises the nucleotide sequence 5′-AfsgsCfaAfcAfuGfUfGfuUfcAfaAfgUfcAfL96-3′ (SEQ ID NO:482) and the antisense strand comprises the nucleotide sequence 5′-usGfsaCfuUfuGfaAfcacAfuGfuUfgCfuscsa-3′ (SEQ ID NO:485),

wherein a, c, g, and u are 2′-O-methyl (2′-OMe) A, C, G, and U; Af, Cf, Gf, and Uf are 2′-fluoro A, C, G, and U; s is a phosphorothioate linkage; and L96 is N-[tris(GalNAc-alkyl)-amidodecanoyl)]-4-hydroxyprolinol.

11. A pharmaceutical composition for inhibiting expression of complement factor B (CFB), comprising a double stranded ribonucleic acid (dsRNA) agent comprising a sense strand and an antisense strand forming a double stranded region,

wherein the sense strand consists of the nucleotide sequence 5′-AfsgsCfaAfcAfuGfUfGfuUfcAfaAfgUfcAfL96-3′ (SEQ ID NO:482) and the antisense strand consists of the nucleotide sequence 5′-usGfsaCfuUfuGfaAfcacAfuGfuUfgCfuscsa-3′ (SEQ ID NO:485),

wherein a, c, g, and u are 2′-O-methyl (2′-OMe) A, C, G, and U; Af, Cf, Gf, and Uf are 2′-fluoro A, C, G, and U; s is a phosphorothioate linkage; and L96 is N-[tris(GalNAc-alkyl)-amidodecanoyl)]-4-hydroxyprolinol.

Assignments (2)
SECURITY INTEREST Recorded Oct 1, 2025
From: ALNYLAM PHARMACEUTICALS, INC.; SIRNA THERAPEUTICS, INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 072996/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 30, 2016
From: BETTENCOURT, BRIAN; BORODOVSKY, ANNA
To: ALNYLAM PHARMACEUTICALS, INC.
Reel/Frame 039056/0164 →
Cited By (4)
US 12,258,565 US 12,365,896 US 12,680,099 US 12,703,865