IP Library Granted Patent US 10,273,478
Granted Patent B2
US 10,273,478 · App. 15/643,346 · Granted Apr 30, 2019

Compositions and methods for inhibition of expression of protein C (PROC) genes

Inventors: Ivanka Toudjarska (Medford, MA); John M. Maraganore (Charleston, MA); Brian Bettencourt (Groton, MA); Stuart Milstein (Cambridge, MA); Martin A. Maier (Belmont, MA); Klaus Charisse (Acton, MA); Kallanthottathil Rajeev (Wayland, MA); Satyanarayana Kuchimanchi (Acton, MA)
Assignee: Alnylam Pharmaceuticals, Inc.
C12N15/113C12N2310/14C12N2310/315C12N2310/321C12N2310/3515C12N2310/3521
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Quick Facts
Patent No.
US 10,273,478
App. No.
15/643,346
Granted
Apr 30, 2019
Kind
B2
Abstract

The invention relates to double-stranded ribonucleic acid (dsRNA) targeting a PROC gene, and methods of using the dsRNA to inhibit expression of PROC.

Claims (30)

1. A double-stranded ribonucleic acid (dsRNA) for inhibiting expression of a Protein C (PROC) gene, wherein the dsRNA comprises a sense strand and an antisense strand each 30 nucleotides or less in length, wherein the antisense strand is complementary to at least 15 contiguous nucleotides of SEQ ID NO: 158.

2. The dsRNA of claim 1 , wherein at least one nucleotide of the dsRNA is a modified nucleotide.

3. The dsRNA of claim 2 , wherein the modified nucleotide is chosen from the group consisting of: a 2′-O-methyl modified nucleotide, a nucleotide comprising a 5′-phosphorothioate group, and a terminal nucleotide linked to a cholesteryl derivative or dodecanoic acid bisdecylamide group.

4. The dsRNA of claim 2 , wherein the modified nucleotide is chosen from the group consisting of: a 2′-deoxy-2′-fluoro modified nucleotide, a 2′-deoxy-modified nucleotide, a locked nucleotide, an abasic nucleotide, 2′-amino-modified nucleotide, 2′-alkyl-modified nucleotide, morpholino nucleotide, a phosphoramidate, and a non-natural base comprising nucleotide.

5. The dsRNA of claim 1 , wherein at least one strand comprises a 3′ overhang of at least 1 nucleotide.

6. The dsRNA of claim 1 , wherein each strand comprises a 3′ overhang of at 2 nucleotides.

7. The dsRNA of claim 1 , further comprising a ligand.

8. The dsRNA of claim 7 , wherein the ligand is conjugated to the 3′ end of the sense strand of the dsRNA.

9. The dsRNA of claim 1 , further comprising at least one N-Acetyl-Galactosamine.

10. An isolated cell comprising the dsRNA of claim 1 .

11. A vector encoding at least one strand of the dsRNA of claim 1 .

12. An isolated cell comprising the vector of claim 11 .

13. A pharmaceutical composition for inhibiting expression of a PROC gene comprising the dsRNA of claim 1 .

14. The pharmaceutical composition of claim 13 , comprising a lipid formulation.

15. The pharmaceutical composition of claim 13 , comprising a lipid formulation comprising (6Z,9Z,28Z,31Z)-heptatriaconta-6,9,28,31-tetraen-19-yl 4-(dimethylamino)butanoate (MC3).

16. A method of inhibiting Protein C (PROC) expression in a cell, the method comprising:

(a) contacting the cell with the dsRNA of claim 1 ; and

(b) maintaining the cell produced in step (a) for a time sufficient to obtain degradation of the mRNA transcript of a PROC gene, thereby inhibiting expression of the PROC gene in the cell.

17. The method of claim 16 , wherein the PROC expression is inhibited by at least 30%.

18. A method of treating a disorder mediated by PROC expression comprising administering to a human in need of such treatment a therapeutically effective amount of the PROC dsRNA of claim 1 .

19. The method of claim 18 , wherein the disorder is a bleeding disorder.

20. The method of claim 18 , wherein the disorder is hemophilia.

21. The method of claim 18 , wherein administration causes an increase in blood clotting and/or a decrease in PROC protein accumulation.

22. The method of claim 18 , wherein the dsRNA or the pharmaceutical composition is administered at a dose of about 0.01 mg/kg to about 10 mg/kg or about 0.5 mg/kg to about 50 mg/kg.

23. The dsRNA of claim 1 , wherein the sense strand comprises SEQ ID NO: 158.

24. The dsRNA of claim 1 , wherein the antisense strand comprises SEQ ID NO: 212.

25. The dsRNA of claim 1 , wherein the sense strand comprises SEQ ID NO: 158 and the antisense strand comprises SEQ ID NO: 212.

26. The dsRNA of claim 1 , wherein the sense strand consists of SEQ ID NO: 158.

27. The dsRNA of claim 1 , wherein the antisense strand consists of SEQ ID NO: 212.

28. The dsRNA of claim 1 , wherein the sense strand consists of SEQ ID NO: 158 and the antisense strand consists of SEQ ID NO: 212.

Assignments (2)
SECURITY INTEREST Recorded Oct 1, 2025
From: ALNYLAM PHARMACEUTICALS, INC.; SIRNA THERAPEUTICS, INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 072996/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 6, 2017
From: TOUDJARSKA, IVANKA; MARAGANORE, JOHN M.; BETTENCOURT, BRIAN; MILSTEIN, STUART; MAIER, MARTIN A.; CHARISSE, KLAUS; RAJEEV, KALLANTHOTTATHIL; KUCHIMANCHI, SATYANARAYANA
To: ALNYLAM PHARMACEUTICALS, INC.
Reel/Frame 042927/0154 →
Continuity (6)
Continuation 14730100 · Jun 3, 2015
Continuation 14127090
Provisional Application 61615010 · Mar 23, 2012
Provisional Application 61542729 · Oct 3, 2011
Provisional Application 61499620 · Jun 21, 2011
Related Publication 20180066255A1 · Mar 8, 2018