IP Library Granted Patent US 11,873,493
Granted Patent B2
US 11,873,493 · App. 17/157,803 · Granted Jan 16, 2024

Methods and compositions for the specific inhibition of glycolate oxidase (HAO1) by double-stranded RNA

Inventors: Bob D. Brown (Lexington, MA); Henryk T. Dudek (Lexington, MA)
Assignee: Dicerna Pharmaceuticals, Inc.
C12N15/1137C12N9/0006C12Y101/03015C12N2310/11C12N2310/14
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Quick Facts
Patent No.
US 11,873,493
App. No.
17/157,803
Granted
Jan 16, 2024
Kind
B2
Abstract

This invention relates to compounds, compositions, and methods useful for reducing Glycolate Oxidase (HAO1) target RNA and protein levels via use of dsRNAs, e.g., Dicer substrate siRNA (DsiRNA) agents.

Claims (20)

1. A method for treating a subject having excessive urinary excretion of oxalate, the method comprising: administering to the subject in need thereof an effective amount of a nucleic acid comprising a first strand and a second strand forming a duplex structure, wherein the first strand is 21 nucleotides in length and the second strand is 23 nucleotides in length, wherein the second strand is 100% complementary with the sequence as set forth in SEQ ID NO: 1823, wherein the second strand has a 3′ overhang of 2 nucleotides in length, wherein a GalNac moiety is conjugated to the 3′ terminal nucleotide of the first strand, and wherein administration of the nucleic acid to the subject results in a reduction of HAO1 mRNA levels in the subject.

2. The method of claim 1 , wherein the excessive urinary excretion of oxalate causes urolithiasis in the subject.

3. The method of claim 1 , wherein the excessive urinary excretion of oxalate causes nephrocalcinosis in the subject.

4. The method of claim 1 , wherein the excessive urinary excretion of oxalate causes kidney stone in the subject.

5. The method of claim 1 , wherein the subject is treated for urolithiasis, nephrocalcinosis or kidney stones.

6. The method of claim 1 , wherein the second strand comprises at least two phosphorothioate internucleotide linkages.

7. The method of claim 1 , wherein the first strand and/or second strands comprise one or more modified nucleotides.

8. The method of claim 7 , wherein each residue of the first strand and/or each residue of the second strand is a modified nucleotide.

9. The method of claim 7 , wherein each modified nucleotide is independently a 2′-O-methyl or 2′-fluoro modified nucleotide.

10. The method of claim 9 , wherein at least one nucleotide of the first strand is conjugated with one or more GalNac moieties.

11. The method of claim 9 , wherein the at least one nucleotide is conjugated to the 3′ terminal nucleotide of the first strand.

12. The method of claim 1 , wherein the second strand is a guide strand that complexes with RISC, binds a target mRNA as a component of the RISC complex, and promotes cleavage of a target RNA by RISC.

13. The method of claim 1 , wherein administration of the nucleic acid to the subject results in a reduction in glycolate oxidase in the subject.

14. The method of claim 1 , wherein administration of the nucleic acid to the subject results in a decrease in an accumulation of calcium oxalate deposits in the subject.

15. The method of claim 1 , wherein administration of the nucleic acid to the subject results in a decrease in an accumulation of calcium precipitates in the kidney in the subject.

16. The method of claim 1 , wherein administration of the nucleic acid to the subject results in an increase in a glycolate/creatinine ratio in urine of the subject.

17. The method of claim 1 , wherein administration of the nucleic acid to the subject is performed at a dose in a range of 0.3 to 10 mg/kg.

18. The method of claim 1 , wherein administration of the nucleic acid to the subject results in at least an 80% reduction of HAO1 mRNA levels.

19. The method of claim 1 , wherein administration of the nucleic acid to the subject is performed subcutaneously.

20. The method of claim 19 , wherein administration of the nucleic acid to the subject results in a reduction of HAO1 mRNA levels in the subject that are detectable at 29 days post-administration.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 14, 2025
From: DICERNA PHARMACEUTICALS, INC.
To: NOVO NORDISK A/S
Reel/Frame 070837/0034 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2021
From: BROWN, BOB DALE; DUDEK, HENRYK
To: DICERNA PHARMACEUTICALS, INC.
Reel/Frame 056090/0275 →
Continuity (7)
Continuation 16545149 · Aug 20, 2019
Continuation 15793441 · Oct 25, 2017
Continuation 15616254 · Jun 7, 2017
Division 14583200 · Dec 26, 2014
Provisional Application 61937838 · Feb 10, 2014
Provisional Application 61921181 · Dec 27, 2013
Related Publication 20210230604A1 · Jul 29, 2021