Claims for Patent: 10,612,024

Summary for Patent: 10,612,024

Title:	Modified double-stranded RNA agents
Abstract:	One aspect of the present invention relates to double-stranded RNA (dsRNA) agent capable of inhibiting the expression of a target gene. The sense strand of the dsRNA agent comprises at least one thermally destabilizing nucleotide, and at least one said thermally destabilizing nucleotide occurring at a site opposite to the seed region (positions 2-8) of the antisense strand; and the antisense strand of the dsRNA agent comprises at least two modified nucleotides that provide the nucleotide a steric bulk that is less than or equal to the steric bulk of a 2'-OMe modification, wherein said modified nucleotides are separated by 11 nucleotides in length. Other aspects of the invention relates to pharmaceutical compositions comprising these dsRNA agents suitable for therapeutic use, and methods of inhibiting the expression of a target gene by administering these dsRNA agents, e.g., for the treatment of various disease conditions.
Inventor(s):	Maier; Martin (Cambridge, MA), Foster; Don (Cambridge, MA), Milstein; Stuart (Cambridge, MA), Kuchimanchi; Satya (Cambridge, MA), Jadhav; Vasant (Cambridge, MA), Rajeev; Kallanthottathil (Cambridge, MA), Manoharan; Muthiah (Cambridge, MA), Parmar; Rubina (Cambridge, MA)
Assignee:	ALNYLAM PHARMACEUTICALS, INC. (Cambridge, MA)
Application Number:	16/272,721
Patent Claims:	1. A double-stranded RNA (dsRNA) agent capable of inhibiting the expression of a target gene, comprising a sense strand and an antisense strand complementary to at least one portion of a mRNA corresponding to the target gene, each strand having 14 to 40 nucleotides, wherein the dsRNA agent is represented by formula (I): ##STR00059## wherein: B1, B1', B2', B3', and B4' each independently represent a nucleotide containing a modification selected from the group consisting of 2'-Oalkyl, 2'-substituted alkoxy, 2'-substituted alkyl, 2'-halo, ENA, and BNA/LNA; C1 is a thermally destabilizing nucleotide, selected from the group consisting of i) a nucleotide that forms a mismatch pair with the opposing nucleotide in the antisense strand, ii) a nucleotide having an abasic modification, and iii) a nucleotide having a sugar modification, and placed at a site opposite to the seed region (positions 2-8) of the antisense strand; T1', T2', and T3' each independently represent a nucleotide comprising a modification providing the nucleotide a steric bulk that is less than or equal to the steric bulk of a 2'-OMe modification, wherein the modification is at the 2'-position of a ribose sugar of the nucleotide or at a position of a non-ribose nucleotide similar to the 2'-position of a ribose sugar; each n.sup.1, and q.sup.1 is independently 4 to 15 nucleotides in length; each q.sup.3, and q.sup.7 is independently 1-6 nucleotide(s) in length; each q.sup.2 and q.sup.6 is independently 1-3 nucleotide(s) in length; q.sup.5 is independently 0-10 nucleotide(s) in length; each n.sup.4, and q.sup.4 is independently 0-3 nucleotide(s) in length; n.sup.2 is 3 nucleotides in length, and T1 each are 2'-F; n.sup.3 is 7 nucleotides in length, and B2 each are 2'-OMe; and n.sup.5 is 3 nucleotides in length, and B3 each are 2'-OMe. 2. The dsRNA agent of claim 1, wherein n.sup.4 is 0. 3. The dsRNA agent of claim 1, wherein T1' and T3' are separated by 11 nucleotides in length. 4. The dsRNA agent of claim 1, wherein T1' is at position 14 from the 5' end of the antisense strand, and q.sup.2 is 1. 5. The dsRNA agent of claim 1, wherein T3' is at position 2 from the 5' end of the antisense strand, and q.sup.6 is 1. 6. The dsRNA agent of claim 1, wherein one of the T1 nucleotides is at position 11 from the 5' end of the sense strand, when the sense strand is 19-22 nucleotides in length. 7. The dsRNA agent of claim 1, wherein T2' is at positions 6-10 from the 5' end of the antisense strand. 8. The dsRNA agent of claim 1, wherein B1, B1', B2', B3', and B4' each contain 2'-OMe modifications. 9. The dsRNA agent of claim 1, wherein q.sup.2 is 1, and T1' is 2'-F; q.sup.6 is 1, and T3' is 2'-F; and q.sup.7 is 1, and B4' is 2'-OMe. 10. The dsRNA agent of claim 1, wherein n.sup.1 is 8, and each B1 is 2'-OMe or 2'-F; n.sup.2 is 3, and each T1 is 2'-F; n.sup.3 is 7, and each B2 is 2'-OMe; n.sup.4 is 0; n.sup.5 is 3, and each B3 is 2'OMe; q.sup.1 is 9, and each B1' is 2'-OMe or 2'-F; q.sup.2 is 1, and T1' is 2'-F; q.sup.3 is 4, and each B2' is 2'-OMe or 2'-F; q.sup.4 is 0; q.sup.5 is 7, and each B3' is 2'-OMe or 2'-F; q.sup.6 is 1, and T3' is 2'-F; and q.sup.7 is 1, and B4' is 2'-OMe. 11. The dsRNA agent of claim 1, wherein n.sup.1 is 8, and each B1 is 2'-OMe or 2'-F; n.sup.2 is 3, and each T1 is 2'-F; n.sup.3 is 7, and each B2 is 2'-OMe; n.sup.4 is 0; n.sup.5 is 3, and each B3 is 2'OMe; q.sup.1 is 9, and each B1' is 2'-OMe or 2'-F; q.sup.2 is 1, and T1' is 2'-F; q.sup.3 is 4, and each B2' is 2'-OMe or 2'-F; q.sup.4 is 2, and each T2' is 2'-F; q.sup.5 is 5, and each B3' is 2'-OMe or 2'-F; q.sup.6 is 1, and T3' is 2'-F; and q.sup.7 is 1, and B4' is 2'-OMe. 12. The dsRNA agent of claim 1, wherein each of the sense and antisense strands is independently modified with acyclic nucleotides, LNA, HNA, CeNA, 2'-methoxyethyl, 2'-O-methyl, 2'-O-allyl, 2'-C-allyl, 2'-deoxy, 2'-fluoro, 2'-O-N-methylacetamido (2'-O-NMA), a 2'-O-dimethylaminoethoxyethyl (2'-O-DMAEOE), 2'-O-aminopropyl (2'-O-AP), or 2'-ara-F. 13. The dsRNA agent of claim 1, wherein each of the sense and antisense strands contains at least two different modifications. 14. The dsRNA agent of claim 1, wherein the antisense strand comprises two blocks of two phosphorothioate or methylphosphonate internucleotide linkages separated by 16-18 phosphate internucleotide linkages. 15. The dsRNA agent of claim 14, wherein the antisense strand comprises two phosphorothioate internucleotide linkage modifications at positions 1 and 2 and two phosphorothioate internucleotide linkage modifications within positions 18-23 of the antisense strand, counting from the 5'-end of the antisense strand. 16. The dsRNA agent of claim 1, wherein the sense strand comprises two phosphorothioate internucleotide linkage modifications within position 1-5 of the sense strand, counting from the 5'-end of the sense strand. 17. The dsRNA agent of claim 1, wherein the sense strand comprises 2'-F modifications at positions 7 and 9-11, counting from the 5'-end of the sense strand; and the antisense strand comprises 2'-F modifications at positions 2, 6, 14, and 16, counting from the 5'-end of the antisense strand; and wherein the sense and antisense strands comprise six phosphorothioate internucleotide linkage modifications. 18. The dsRNA agent of claim 1, wherein the sense strand comprises 2'-F modifications at positions 7 and 9-11, counting from the 5'-end of the sense strand; and the antisense strand comprises 2'-F modifications at positions 2, 6, 8-9, 14, and 16, counting from the 5'-end of the antisense strand; and wherein the sense and antisense strand comprise six phosphorothioate internucleotide linkage modifications. 19. The dsRNA agent of claim 1, wherein the sense strand has 19-22 nucleotides, and the antisense strand has 19-25 nucleotides. 20. The dsRNA agent of claim 1, wherein the sense strand has 21 nucleotides, and the antisense strand has 23 nucleotides. 21. The dsRNA agent of claim 1, wherein the dsRNA agent has a 3' and/or 5' overhang(s) of 1-10 nucleotides in length. 22. The dsRNA agent of claim 20, wherein the dsRNA agent has a two nucleotide overhang at the 3'-end of the antisense strand, and a blunt end at the 5'-end of the antisense strand. 23. The dsRNA agent of claim 1, wherein the nucleotide at position 1 of the 5'-end of the antisense strand in the duplex is selected from the group consisting of A, dA, dU, U, and dT. 24. The dsRNA agent of claim 1, further comprising at least one ASGPR ligand. 25. The dsRNA agent of claim 24, wherein the ASGPR ligand is attached to the 3' end of the sense strand. 26. The dsRNA agent of claim 24, wherein the ASGPR ligand is one or more GalNAc derivatives attached through a bivalent or trivalent branched linker. 27. The dsRNA agent of claim 26, wherein the ASGPR ligand is: ##STR00060## 28. The dsRNA agent of claim 1, wherein formula (I) further comprises a 5'-vinyl phosphonate (VP). 29. The dsRNA agent of claim 1, wherein formula (I) further comprises a 2'-deoxythymidine linked via a phosphorodithioate (PS.sub.2) linkage at the 5'-end of the antisense strand or sense strand. 30. A pharmaceutical composition comprising the dsRNA agent according to claim 1, in combination with a pharmaceutically acceptable carrier or excipient. 31. A method for inhibiting the expression of a target gene comprising the step of administering the dsRNA agent of claim 1, in an amount sufficient to inhibit expression of the target gene. 32. The method of claim 31, wherein the dsRNA agent is administered through subcutaneous or intravenous administration. 33. A method for delivering polynucleotide to specific target in a subject by administering the dsRNA agent of claim 1. 34. The method of claim 33, wherein said administering step is carried out by an administration means comprising intramuscular, intrabronchial, intrapleural, intraperitoneal, intraarterial, lymphatic, intravenous, subcutaneous, cerebrospinal, or combinations thereof. 35. A method for delivering a polynucleotide to specific target of a subject, the method comprising: delivering a dsRNA agent of claim 1 by subcutaneous administration into the subject, such that the polynucleotide is delivered into specific target of the subject.