IP Library Granted Patent US 10,004,814
Granted Patent B2
US 10,004,814 · App. 15/035,950 · Granted Jun 26, 2018

Systemic delivery of myostatin short interfering nucleic acids (siNA) conjugated to a lipophilic moiety

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Quick Facts
Patent No.
US 10,004,814
App. No.
15/035,950
Granted
Jun 26, 2018
Kind
B2
Abstract

The present invention provides methods comprising the in vivo delivery of small nucleic acid molecules capable of mediating RNA interference and reducing the expression of myostatin, wherein the small nucleic acid molecules are introduced to a subject by systemic administration. Specifically, the invention relates to methods comprising the in vivo delivery of short interfering nucleic acid (siNA) molecules that target a myostatin gene expressed by a subject, wherein the siNA molecule is conjugated to a lipophilic moiety, such as cholesterol. The myostatin siNA conjugates that are delivered as per the methods disclosed are useful to modulate the in vivo expression of myostatin, increase muscle mass and/or enhance muscle performance. Use of the disclosed methods is further indicated for treating musculoskeletal diseases or disorders and/or diseases or disorders that result in conditions in which muscle is adversely affected.

Claims (25)

1. A double-stranded short interfering nucleic acid (siNA) molecule that inhibits the expression of myostatin, wherein:

(a) the siNA comprises a sense strand and an antisense strand;

(b) each strand is independently 19 to 30 nucleotides in length; and

(c) the antisense strand comprises nucleotide sequence of:

(SEQ ID NO: 18)

5′- AUUAUUUGUUCUUUGCCAU -3′;

and wherein one or more of the nucleotides are chemically modified.

2. A double-stranded siNA molecule of claim 1 , wherein the siNA molecule comprises:

(SEQ ID NO: 1)

5′- AUGGCAAAGAACAAAUAAU -3′

and

(SEQ ID NO: 18)

5′- AUUAUUUGUUCUUUGCCAU -3′.

3. The double-stranded siNA molecule of claim 2 , wherein the siNA molecule is linked to a lipophilic moiety.

4. The double-stranded siNA molecule of claim 3 , wherein the lipophilic moiety is cholesterol.

5. The double-stranded siNA molecule of claim 4 , wherein the lipophilic moiety is attached to a 3′-end of the siNA molecule.

6. The double-stranded siNA molecule of claim 4 , wherein the lipophilic moiety is attached to a 5′-end of the siNA molecule.

7. The double-stranded siNA molecule of claim 2 , which comprises one or more chemically-modified nucleotides.

8. The double-stranded siNA molecule of claim 2 , which comprises one or more 3′-overhanging nucleotides on one or both strands.

9. The double-stranded siNA molecule of claim 1 , wherein the siNA molecule is linked to a lipophilic moiety.

10. The double-stranded siNA molecule of claim 9 , wherein the lipophilic moiety is cholesterol.

11. The double-stranded siNA molecule of claim 10 , wherein the lipophilic moiety is attached to a 3′-end of the siNA molecule.

12. The double-stranded siNA molecule of claim 10 , wherein the lipophilic moiety is attached to a 5′-end of the siNA molecule.

13. The double-stranded siNA molecule of claim 1 , which comprises one or more chemically-modified nucleotides.

14. The double-stranded siNA molecule of claim 1 , which comprises one or more 3′-overhanging nucleotides on one or both strands.

Assignments (3)
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 Apr 3, 2017
From: TADIN-STRAPPS, MARIJA; KHAN, TAYEBA; STRAPPS, WALTER RICHARD; SEPP-LORENZINO, LAURA; JADHAV, VASANT R.; BROWN, DUNCAN
To: MERCK SHARP & DOHME CORP,
Reel/Frame 041833/0539 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 3, 2017
From: MERCK SHARP & DOHME CORP.
To: SIRNA THERAPEUTICS, INC.
Reel/Frame 041833/0592 →