IP Library Granted Patent US 10,287,582
Granted Patent B2
US 10,287,582 · App. 15/359,894 · Granted May 14, 2019

Organic compositions to treat HSF1-related diseases

Inventors: Gregory Hinkle (Cambridge, MA); Satyanarayana Kuchimanchi (Cambridge, MA); Stuart Milstein (Cambridge, MA); Markus Warmuth (Cambridge, MA); Wenlai Zhou (Cambridge, MA); Ping Zhu (Cambridge, MA); Tracy S. Zimmermann (Cambridge, MA)
Assignee: Arrowhead Pharmaceuticals, Inc.
C12N15/113A61K31/713A61K45/06C07H21/02C12N2310/14C12N2310/321C12N2310/322C12N2320/31C12N2320/51C12N2320/53Y02A50/467
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Quick Facts
Patent No.
US 10,287,582
App. No.
15/359,894
Granted
May 14, 2019
Kind
B2
Abstract

The present disclosure relates to methods of treating heat shock factor 1 (HSF1)-related diseases such as cancer and viral diseases, using a therapeutically effective amount of a RNAi agent to HSF.

Claims (18)

1. A composition comprising an RNAi agent to HSF1 comprising a first strand and a second strand, wherein the sequence of the first strand comprises SEQ ID NO: 678, wherein the first and/or second strand comprises at least one modified sugar backbone or 2′-modified nucleotide, wherein the first and/or second strand are no more than about 49 nt long, and wherein the first strand and the second strand are at least substantially complementary to each other.

2. The composition of claim 1 , wherein the composition further comprises a second RNAi agent to HSF1.

3. The composition of claim 1 , wherein the first strand and the second strand are both about 19 to about 23 nucleotides in length.

4. The composition of claim 1 , wherein the RNAi agent comprises a phosphorothioate linkage.

5. The composition of claim 1 , wherein the RNAi agent comprises a 2′-modification selected from the group consisting of: 2′-deoxy, 2′-deoxy-2′-fluoro, 2′-O-methyl, 2′-O-methoxyethyl (2′-O-MOE), 2′-O-aminopropyl (2′-O-AP), 2′-O-dimethylaminoethyl (2′-O-DMAOE), 2′-O-dimethylaminopropyl (2′-O-DMAP), 2′-O-dimethylaminoethyloxyethyl (2′-O-DMAEOE), and 2′-O—N-methylacetamido (2′-O-NMA).

6. The composition of claim 1 , wherein the RNAi agent comprises a blunt end or an overhang having 1 to 4 unpaired nucleotides.

7. The composition of claim 1 , wherein the RNAi agent is ligated to one or more 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/or transferrin.

8. A composition comprising an RNAi agent to HSF1 comprising a first strand and a second strand, wherein the sequence of the first strand comprises the sequence of SEQ ID NO: 678, and the sequence of the second strand comprises the sequence of SEQ ID NO: 166, wherein the first and/or second strand comprises at least one modified sugar backbone or 2′-modified nucleotide, wherein the first and/or second strand are no more than about 49 nt long, and wherein the composition further comprises and a pharmaceutically acceptable carrier.

9. The composition of claim 8 , wherein the composition further comprises a second RNAi agent to HSF1.

10. The composition of claim 8 , wherein the first strand and the second strand are both 19 to 23 nucleotides in length.

11. The composition of claim 8 , wherein the RNAi agent comprises a phosphorothioate linkage.

12. The composition of claim 8 , wherein the RNAi agent comprises a 2′-modification selected from the group consisting of: 2′-deoxy, 2′-deoxy-2′-fluoro, 2′-O-methyl, 2′-O-methoxyethyl (2′-O-MOE), 2′-O-aminopropyl (2′-O-AP), 2′-O-dimethylaminoethyl (2′-O-DMAOE), 2′-O-dimethylaminopropyl (2′-O-DMAP), 2′-O-dimethylaminoethyloxyethyl (2′-O-DMAEOE), and 2′-O—N-methylacetamido (2′-O-NMA).

13. The composition of claim 8 , wherein the RNAi agent comprises a blunt end or an overhang having 1 to 4 unpaired nucleotides.

14. The composition of claim 8 , wherein the RNAi agent is ligated to one or more 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/or transfenin.

15. A method of inhibiting the expression of HSF1 in an individual afflicted with an HSF1-related cancer, the method comprising administering to the individual a composition comprising a pharmaceutically acceptable carrier and a therapeutically effective amount of an RNAi agent to HSF1 comprising a first strand and a second strand, wherein the sequence of the first strand comprises SEQ ID NO: 678, wherein the first and/or second strand comprises at least one modified sugar backbone or 2′-modified nucleotide, wherein the first and/or second strand are no more than about 49 nucleotides long, wherein the first strand and the second strand are at least substantially complementary to each other, and wherein the method optionally further comprises administering a second RNAi agent to HSF1.

16. The method of claim 15 , wherein the HSF1-related disease is cancer selected from the list of bladder, bone, breast, cervical, colon, colorectal, endometrial, fibrosarcoma, gastric, haematopoietic, intestine, kidney, liver, lung, lymphoma, neuroectodermal, neuroblastoma, Ewing's sarcoma, osteosarcoma, ovary, pancreas, pleura, prostate, skin, squamous cell, stomach, and testicular cancers, leukemia, promyelocytic leukemia, and Hodgkin's disease.

17. The method of claim 15 , wherein the method further comprises the step of administering one or more additional pharmaceutical agents.

18. The composition of claim 1 , further comprising one or more additional pharmaceutical agents.

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, 2017
From: HINKLE, GREGORY; KUCHMANCHI, SATYANARAYANA; MILSTEIN, STUART; ZIMMERMANN, TRACY S.
To: ALNYLAM PHARMACEUTICALS, INC.
Reel/Frame 041264/0213 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2017
From: ALNYLAM PHARMACEUTICALS, INC.
To: NOVARTIS AG
Reel/Frame 041264/0412 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2017
From: NOVARTIS AG
To: ARROWHEAD RESEARCH CORPORATION
Reel/Frame 041264/0494 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2017
From: WARMUTH, MARKUS; ZHOU, WENLAI; ZHU, PING
To: NOVARTIS AG
Reel/Frame 041727/0632 →
CHANGE OF NAME Recorded Feb 15, 2017
From: ARROWHEAD RESEARCH CORPORATION
To: ARROWHEAD PHARMACEUTICALS, INC.
Reel/Frame 041727/0714 →
Continuity (6)
Division 14746148 · Jun 22, 2015
Division 14054166 · Oct 15, 2013
Division 13363504 · Feb 1, 2012
Division 12970268 · Dec 16, 2010
Provisional Application 61288137 · Dec 18, 2009
Related Publication 20170073678A1 · Mar 16, 2017