IP Library Granted Patent US 10,801,026
Granted Patent B2
US 10,801,026 · App. 15/768,405 · Granted Oct 13, 2020

Compounds and compositions including phosphorothioated oligodeoxynucleotide, and methods of use thereof

Inventors: Marcin Tomasz Kortylewski (Monrovia, CA); Piotr Marek Swiderski (San Dimas, CA); Guido Marcucci (Azusa, CA); Bin Zhang (Duarte, CA); Ya-Huei Kuo (Duarte, CA)
Assignee: CITY OF HOPE
C12N15/113A61K31/506A61K31/7004A61K31/704A61K31/7125A61K45/06A61K47/549A61P35/02C12N15/111C12N2310/113C12N2310/141C12N2310/17C12N2310/315C12N2310/3519
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Quick Facts
Patent No.
US 10,801,026
App. No.
15/768,405
Granted
Oct 13, 2020
Kind
B2
Abstract

The present disclosure relates to a compound including a nucleic acid sequence conjugated to an anti-microRNA or a microRNA-mimic or a compound including a modified anti-microRNA sequence, compositions of such a compound, and method of treatment of a disease, and method of suppressing microRNA activity by the disclosed compound or composition.

Claims (15)

1. A pharmaceutical composition comprising a pharmaceutically acceptable excipient, a compound comprising a phosphorothioated CpG oligodeoxynucleotide (CpG-ODN) conjugated to an anti-miR126 nucleic acid, and an anti-tumor or anti-cancer agent.

2. The pharmaceutical composition compound of claim 1 , further comprising a covalent linker between the CpG-ODN and anti-miR126 nucleic acid.

3. The pharmaceutical composition of claim 2 , wherein the linker is a substituted or unsubstituted alkylene, substituted or unsubstituted heteroalkylene, substituted or unsubstituted cycloalkylene, substituted or unsubstituted heterocycloalkylene, substituted or unsubstituted arylene, or substituted or unsubstituted heteroarylene.

4. The pharmaceutical composition of claim 2 , wherein the linker is a substituted or unsubstituted C 1 -C 40 alkylene, substituted or unsubstituted 2 to 40 membered heteroalkylene, substituted or unsubstituted C 3 -C 8 cycloalkylene, substituted or unsubstituted 3 to 8 membered heterocycloalkylene, substituted or unsubstituted C 6 -C 10 arylene, or substituted or unsubstituted 5 to 10 membered heteroarylene.

5. The pharmaceutical composition of claim 2 , wherein the linker is an unsubstituted C 1 -C 40 alkylene, unsubstituted 2 to 40 membered heteroalkylene, unsubstituted C 3 -C 8 cycloalkylene, unsubstituted 3 to 8 membered heterocycloalkylene, unsubstituted C 6 -C 10 arylene, or unsubstituted 5 to 10 membered heteroarylene.

6. The pharmaceutical composition of claim 2 , wherein the linker is a substituted 2 to 40 membered heteroalkylene.

7. The pharmaceutical composition of claim 1 , wherein said anti-miR126 nucleic acid is chemically modified.

8. The pharmaceutical composition of claim 7 , wherein said anti-miR126 nucleic acid comprises a chemical modification selected for the group consisting of a 2′ O-Methyl, 2′-deoxy-2′fluoro, 2′-deoxy, a universal base, 5-C-methyl, an inverted deoxy abasic residue incorporation, and a locked nucleic acid.

9. The pharmaceutical composition of claim 8 , wherein said modification is positioned at the terminal nucleobase of said anti-miR126 nucleic acid.

10. The pharmaceutical composition of claim 8 , wherein the modification is not positioned at the terminal nucleobase of said anti-miR126 nucleic acid.

11. The pharmaceutical composition of claim 8 , wherein said modification protects against serum-derived nucleases.

12. The pharmaceutical composition of claim 1 , wherein said CpG-ODN nucleic acid sequence is selected from the group consisting of a Class A CpG-ODN nucleic acid sequence, a Class B CpG-ODN nucleic acid sequence, and a Class C CpG-ODN nucleic acid sequence.

13. The pharmaceutical composition of claim 1 , wherein said CpG-ODN comprises phosphodiester derivative linkage selected from the group consisting of a phosphoramidate linkage, phosphorodiamidate linkage, phosphorodithioate linkage, phosphonocarboxylic acid linkage, phosphonocarboxylate linkage, phosphonoacetic acid linkage, phosphonoformic acid linkage, methyl phosphonate linkage, boron phosphonate linkage, and O-methylphosphoroamidite linkage.

14. The pharmaceutical composition of claim 1 , wherein said anti-cancer agent is a cell death promoting agent.

15. The pharmaceutical composition of claim 1 , wherein said anti-cancer agent is selected from the group consisting of: Nilotinib, Actinomycin D / Dactinomycin, Bleomycin, Daunorubicin, Doxorubicin, Doxorubicin (pegylated liposomal), Epirubicin, Idarubicin, Mitomycin, Mitoxantrone, Etoposide, Docetaxel, Irinotecan, Paclitaxel, Topotecan, Vinblastine, Vincristine, Vinorelbine, Carboplatin, Cisplantin, Oxaliplatin, Alemtuzamab, BCG, Bevacizumab, Cetuximab, Denosumab, Erlotinib, Gefitinib, Imatinib, Interferon, Ipilimumab, Lapatinib, Monomethyl auristatin E (MMEA), Mertansine (DM1), Rituximab, Sunitinib, Sorafenib, Temsirolimus, and Trastuzumab, or any combination(s) thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2019
From: KORTYLEWSKI, MARCIN TOMASZ; SWIDERSKI, PIOTR MAREK; MARCUCCI, GUIDO; ZHANG, BIN; KUO, YA-HUEI
To: CITY OF HOPE
Reel/Frame 047985/0400 →
Continuity (2)
Provisional Application 62242189 · Oct 15, 2015
Related Publication 20180312837A1 · Nov 1, 2018
Cited By (3)
US 12,227,745 US 12,404,509 US 12,655,429