IP Library Granted Patent US 10,858,656
Granted Patent B2
US 10,858,656 · App. 15/476,102 · Granted Dec 8, 2020

KRAS nucleic acids and uses thereof

Inventor: Hanhua Huang (San Diego, CA)
Assignee: AVIDITY BIOSCIENCES, INC.
C12N15/1137C12N15/1135C12N2310/11C12N2310/14C12N2310/31C12N2310/313C12N2310/315C12N2310/321C12N2310/3231
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Quick Facts
Patent No.
US 10,858,656
App. No.
15/476,102
Granted
Dec 8, 2020
Kind
B2
Abstract

Disclosed herein are molecules and pharmaceutical compositions that mediate RNA interference against KRAS. Also described herein include methods for treating a disease or disorder that comprises a molecule or a pharmaceutical composition that mediate RNA interference against KRAS.

Claims (24)

1. A polynucleic acid molecule that mediates RNA interference against Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS), comprising a sense strand and an antisense strand that hybridizes to a KRAS target sequence selected from SEQ ID NOs: 3, 4, 9, and 15, wherein:

the polynucleic acid molecule comprises 100% modification of nucleotides, wherein the sense strand comprises nnN′nN′n at the 5′ end, and the antisense strand comprises N′N′nN′nN′ at the 5′ end, and wherein n is 2′-O′-methyl modified nucleotide and N′ is 2′-F modified nucleotide; and

the sense strand and the antisense strand are each at least 19, 20, 21, 22, 23, 24, or 25 nucleotides in length.

2. The polynucleic acid molecule of claim 1 , wherein the 2′ O-Me modified nucleotide comprises locked nucleic acid (LNA) or ethylene nucleic acid (ENA).

3. The polynucleic acid molecule of claim 1 , further comprising at least one inverted abasic moiety at at least one terminus.

4. The polynucleic acid molecule of claim 1 , wherein the sense strand and the antisense strand are each 19, 20, or 21 nucleotides in length.

5. The polynucleic acid molecule of claim 1 , wherein the sense strand or the antisense strand comprises at least 45% 2′-O-methyl modification.

6. The polynucleic acid molecule of claim 1 , wherein the sense strand and the antisense strand each independently comprises RNA molecules.

7. The polynucleic acid molecule of claim 1 , wherein the sense strand comprises a sequence having at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 100% sequence identity to a sequence selected from SEQ ID NOs: 20-23, 32, 33, 44, 45, 50-53, 62, 63, 74, and 75.

8. The polynucleic acid molecule of claim 1 , wherein the antisense strand comprises a sequence having at least 80%, 85%, 90%, 95%, 96%, 97%, 98%, 99%, or 100% sequence identity to a sequence selected from SEQ ID NOs: 20-23, 32, 33, 44, 45, 50-53, 62, 63, 74, and 75.

9. The polynucleic acid molecule of claim 1 , wherein the polynucleic acid molecule comprises two contiguous modified T or U residues at the 3′ terminus.

10. The polynucleic acid molecule of claim 1 , wherein the polynucleic acid molecule comprises at least one inverted abasic moiety.

11. The polynucleic acid molecule of claim 1 , wherein the sense strand comprises at least one inverted abasic moiety.

12. The polynucleic acid molecule of claim 11 , wherein the at least one inverted abasic moiety is at the 5′ terminus of the sense strand.

13. The polynucleic acid molecule of claim 11 , wherein the at least one inverted abasic moiety is at the 3′ terminus of the sense strand.

14. A pharmaceutical composition comprising:

a) a molecule of claim 1 ; and

b) a pharmaceutically acceptable excipient.

15. The pharmaceutical composition of claim 14 , wherein the pharmaceutical composition is formulated as a nanoparticle formulation.

16. The pharmaceutical composition of claim 14 , wherein the pharmaceutical composition is formulated for parenteral, oral, intranasal, buccal, rectal, or transdermal administration.

17. A polynucleic acid molecule that mediates RNA interference against Kirsten Rat Sarcoma Viral Oncogene Homolog (KRAS), comprising a sense strand and an antisense strand that hybridizes to a KRAS target sequence selected from SEQ ID NOs: 3, 4, 9, and 15, wherein:

the polynucleic acid molecule comprises 100% modification of nucleotides, wherein the sense strand comprises nnN′nN′n at the 5′ end, and the antisense strand comprises N′N′nN′nN′ at the 5′ end, and wherein n is 2′-O′-methyl modified nucleotide and N′ is 2′-F modified nucleotide;

the sense strand comprises an inverted abasic moiety at the 3′ terminus and the 5′ terminus of the sense strand; and

the polynucleic acid molecule comprises at least one phosphorodithioate linkages at the 3′ terminus of the sense strand and the antisense strand.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY PREVIOUSLY RECORDED AT REEL: 050018 FRAME: 0456. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Sep 12, 2019
From: AVIDITY BIOSCIENCES LLC
To: AVIDITY BIOSCIENCES, INC.
Reel/Frame 050371/0483 →
CHANGE OF NAME Recorded Aug 9, 2019
From: AVIDITY BIOSCIENCES LLC
To: AVIDITY BIOSCIENCES LLC; AVIDITY BIOSCIENCES, INC.
Reel/Frame 050018/0456 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 24, 2017
From: HUANG, HANHUA
To: AVIDITY BIOSCIENCES LLC
Reel/Frame 042553/0090 →
Continuity (2)
Provisional Application 62316937 · Apr 1, 2016
Related Publication 20170283806A1 · Oct 5, 2017