IP Library Granted Patent US 10,081,811
Granted Patent B2
US 10,081,811 · App. 15/661,132 · Granted Sep 25, 2018

Organic compositions to treat Beta-ENaC-related diseases

Inventors: Antonin De Fougerolles (Cambridge, MA); John Diener (Cambridge, MA); Emma Hickman (Horsham, GB); Gregory Hinkle (Cambridge, MA); Stuart Milstein (Cambridge, MA); Anne-Marie Pulichino (Cambridge, MA); Andrew Griffin Sprague (Cambridge, MA)
Assignee: Arrowhead Pharmaceuticals, Inc.
C12N15/1138A61K31/713C12N2310/111C12N2310/14C12N2310/31C12N2310/315C12N2310/321C12N2310/322C12N2310/344C12N2310/351C12N2310/3513C12N2310/3515C12N2310/3517
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Quick Facts
Patent No.
US 10,081,811
App. No.
15/661,132
Granted
Sep 25, 2018
Kind
B2
Abstract

The present disclosure relates to RNAi agents useful in methods of treating Beta-ENaC-related diseases such as cystic fibrosis, pseudohypoaldosteronism type 1 (PHA1), Liddle's syndrome, hypertension, alkalosis, hypokalemia, and obesity-associated hypertension, using a therapeutically effective amount of a RNAi agent to Beta-ENaC.

Claims (15)

1. A composition comprising a RNAi agent comprising a first strand and a second strand, wherein the first strand comprises the base sequence AGACGCUGACCUCCCAGCU (SEQ ID NO: 126), wherein the length of the first and the second strand are each no more than about 30 nucleotides, wherein the second strand is at least substantially complementary to the first strand, and wherein the first and/or the second strand comprises at least one modified nucleotide.

2. The composition of claim 1 , wherein the composition further comprises a second RNAi agent to Beta-ENaC.

3. The composition of claim 1 , wherein the RNAi agent comprises a phosphorothioate and/or at least one 2′-modified nucleotide.

4. The composition of claim 1 , wherein the RNAi agent is ligated to one or more agents, wherein the one or more agents are selected from: diagnostic compound, reporter group, cross-linking agent, nuclease-resistance conferring moiety, natural or unusual nucleobase, lipophilic molecule, cholesterol, lipid, lectin, steroid, uvaol, hecigenin, diosgenin, terpene, triterpene, sarsasapogenin, Friedelin, epifriedelanol-derivatized lithocholic acid, vitamin, carbohydrate, dextran, pullulan, chitin, chitosan, synthetic carbohydrate, oligo lactate 15-mer, natural polymer, low- or medium-molecular weight polymer, inulin, cyclodextrin, hyaluronic acid, protein, protein-binding agent, integrin-targeting molecule, polycationic, peptide, polyamine, peptide mimic, and transferrin.

5. A method of reducing the level and/or expression of Beta-ENaC in an individual, the method comprising the step of administering to the individual a therapeutically effective amount of a composition comprising a pharmaceutically acceptable carrier and a composition comprising the RNAi agent of claim 1 .

6. The method of claim 5 , wherein the composition further comprises a second RNAi agent to Beta-ENaC.

7. The method of claim 5 , wherein the RNAi agent comprises a phosphorothioate and/or a 2′-modified nucleotide.

8. The method of claim 5 , wherein the RNAi agent is ligated to one or more agents, wherein the one or more agents are selected from: diagnostic compound, reporter group, cross-linking agent, nuclease-resistance conferring moiety, natural or unusual nucleobase, lipophilic molecule, cholesterol, lipid, lectin, steroid, uvaol, hecigenin, diosgenin, terpene, triterpene, sarsasapogenin, Friedelin, epifriedelanol-derivatized lithocholic acid, vitamin, carbohydrate, dextran, pullulan, chitin, chitosan, synthetic carbohydrate, oligo lactate 15-mer, natural polymer, low- or medium-molecular weight polymer, inulin, cyclodextrin, hyaluronic acid, protein, protein-binding agent, integrin-targeting molecule, polycationic, peptide, polyamine, peptide mimic, and transferrin.

9. The composition of claim 1 , wherein the second strand comprises the base sequence AGCUGGGAGGUCAGCGUCU (SEQ ID NO: 125), and wherein both the first strand and the second strand each comprise at least one modified nucleotide.

10. The composition of claim 9 , wherein the RNAi agent comprises one or more 2′-modified nucleotides selected from the group consisting of: 2′-deoxy, 2′-deoxy-2′-fluoro, 2′-O-methyl, 2′-O-methoxyethyl (2′-O-M0E), 2′-O-aminopropyl (2′-O-AP), 2′-O-dimethylaminoethyl (2′-O-DMAOE), 2′-O-dimethylaminopropyl (21-O-DMAP), 2′-O-dimethylaminoethyloxyethyl (2′-O-DMAEOE), and 2′-O—N-methylacetamido (2′-O-NMA).

11. The composition of claim 9 , wherein the RNAi agent is ligated to one or more agents, wherein the one or more agents are selected from: diagnostic compound, reporter group, cross-linking agent, nuclease-resistance conferring moiety, natural or unusual nucleobase, lipophilic molecule, cholesterol, lipid, lectin, steroid, uvaol, hecigenin, diosgenin, terpene, triterpene, sarsasapogenin, Friedelin, epifriedelanol-derivatized lithocholic acid, vitamin, carbohydrate, dextran, pullulan, chitin, chitosan, synthetic carbohydrate, oligo lactate 15-mer, natural polymer, low- or medium-molecular weight polymer, inulin, cyclodextrin, hyaluronic acid, protein, protein-binding agent, integrin-targeting molecule, polycationic, peptide, polyamine, peptide mimic, and transferrin.

12. The composition of claim 9 , wherein the composition comprises a second RNAi agent targeted to Beta-ENaC.

13. The composition of claim 9 , wherein the RNAi agent comprises a phosphorothioate and/or a 2′-modified nucleotide.

14. A composition comprising a therapeutically effective amount of a composition of claim 1 and a pharmaceutically acceptable carrier.

15. A composition comprising a therapeutically effective amount of a composition of claim 9 and a pharmaceutically acceptable carrier.

Assignments (6)
SECURITY INTEREST Recorded Aug 7, 2024
From: ARROWHEAD PHARMACEUTICALS, INC.
To: SIXTH STREETLENDING PARTNERS, AS THE ADMINISTRATIVE AGENT
Reel/Frame 068510/0363 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2018
From: DIENER, JOHN L.; PULICHINO, ANNE-MARIE; HICKMAN, EMMA
To: NOVARTIS AG
Reel/Frame 044945/0414 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2018
From: DE FOUGEROLLES, ANTONIN; HINKLE, GREGORY; MILSTEIN, STUART; SPRAGUE, ANDREW
To: ALNYLAM PHARMACEUTICALS, INC.
Reel/Frame 044945/0881 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2018
From: ALNYLAM PHARMACEUTICALS, INC.
To: NOVARTIS AG
Reel/Frame 044945/0925 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2018
From: NOVARTIS AG
To: ARROWHEAD RESEARCH CORPORATION
Reel/Frame 044945/0979 →
CHANGE OF NAME Recorded Feb 15, 2018
From: ARROWHEAD RESEARCH CORPORATION
To: ARROWHEAD PHARMACEUTICALS, INC.
Reel/Frame 045346/0681 →
Continuity (9)
Division 15166576 · May 27, 2016
Division 14723555 · May 28, 2015
Division 14042924 · Oct 1, 2013
Division 13614836 · Sep 13, 2012
Division 13355930 · Jan 23, 2012
Division 13090580 · Apr 20, 2011
Provisional Application 61333398 · May 11, 2010
Provisional Application 61327379 · Apr 23, 2010
Related Publication 20170327829A1 · Nov 16, 2017