IP Library Patent Application 16157726
Patent Application
App. No. 16/157,726

RNAi-Mediated Inhibition of Tumor Necrosis Factor Alpha-Related Conditions

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Quick Facts
Patent No.
US None
App. No.
16/157,726
Abstract

RNA interference is provided for inhibition of tumor necrosis factor α (TNFα) by silencing TNFα cell surface receptor TNF receptor-1 (TNFR1) mRNA expression, or by silencing TNFα converting enzyme (TACE/ADAM17) mRNA expression. Silencing such TNFα targets, in particular, is useful for treating patients having a TNFα-related condition or at risk of developing a TNFα-related condition such as the ocular conditions dry eye, allergic conjunctivitis, or ocular inflammation, or such as dermatitis, rhinitis, or asthma, for example.

Claims (22)

1 . An interfering RNA for inhibiting the expression of a tumor necrosis factor α converting enzyme (TACE) gene, wherein the interfering RNA comprises a sense strand and an antisense strand each 19-49 nucleotides in length, wherein the antisense strand comprises a nucleotide sequence that is complementary to any of SEQ ID NO:3, SEQ ID NO:14-SEQ ID NO:58, or SEQ ID NO:155-SEQ ID NO:201.

2 . The compositions of claim 1 , wherein each strand of the interfering RNA molecule is 19 to 27 nucleotides in length.

3 . The interfering RNA of claim 1 , wherein the interfering RNA comprises one or more chemically modified nucleotides, one or more deoxyribonucleotides, and/or one or more non-phosphodiester linkages.

4 . The interfering RNA of claim 3 , wherein one or more of the chemically modified nucleotides have a sugar modification selected from the group consisting of: a 2′ amino group, a 2′ O-methyl group, and a 2′ methoxyethyl group.

5 . The interfering RNA of claim 3 , wherein the interfering RNA comprises one or more chemically modified nucleotides and one or more non-phosphodiester linkages.

6 . The interfering RNA of claim 3 , wherein non-nucleotide material is bound to the 5′ end and/or 3′ end of the sense strand and/or the antisense strand.

7 . The interfering RNA of claim 3 , wherein the non-nucleotide material is bound internally to the sense strand and/or the antisense strand.

8 . The interfering RNA of claim 6 , wherein the non-nucleotide material improves cellular uptake, enhances cellular targeting, assists in tracing, improves stability, and/or reduces activation of the interferon pathway.

9 . The interfering RNA of claim 3 , wherein the sense strand and/or the antisense strand contains a 3′ overhang.

10 . The interfering RNA of claim 3 , wherein the sense strand and/or the antisense strand contains a 5′ overhang.

11 . The interfering RNA of claim 3 , wherein the interfering RNA molecule at least one blunt end.

12 . A composition for inhibiting the expression of a tumor necrosis factor α converting enzyme (TACE) gene comprising:

an interfering RNA that comprises a sense strand and an antisense strand, wherein the sense strand comprises a nucleotide sequence of any of SEQ ID NO:3, SEQ ID NO:14-SEQ ID NO:58, or SEQ ID NO:155-SEQ ID NO:201 except that the T's can be T's or U's, and the antisense strand comprises a nucleotide sequence that is complementary to any of SEQ ID NO:59-SEQ ID NO:154, SEQ ID NO:202-SEQ ID NO:204; and

a pharmaceutically acceptable carrier.

13 . The composition of claim 12 , wherein the interfering RNA comprises one or more chemically modified nucleotides, one or more deoxyribonucleotides, and/or one or more non-phosphodiester linkages.

14 . The composition of claim 13 , wherein one or more of the chemically modified nucleotides have a sugar modification selected from the group consisting of: a 2′ amino group, a 2′ O-methyl group, and a 2′ methoxyethyl group.

15 . The composition of claim 13 , wherein the interfering RNA comprises one or more chemically modified nucleotides and one or more non-phosphodiester linkages.

16 . The composition of claim 13 , wherein non-nucleotide material is bound to the 5′ end and/or 3′ end of the sense strand and/or the antisense strand.

17 . The composition of claim 13 , wherein the non-nucleotide material is bound internally to the sense strand and/or the antisense strand.

18 . The composition of claim 16 , wherein the non-nucleotide material improves cellular uptake, enhances cellular targeting, assists in tracing, improves stability, and/or reduces activation of the interferon pathway.

19 . The composition of claim 14 , wherein the sense strand and/or the antisense strand contains a 3′ overhang and/or a 5′ overhang.

20 . An interfering RNA for inhibiting the expression of a tumor necrosis factor α receptor-1 (TNFR1) wherein the interfering RNA comprises a sense strand and an antisense strand, wherein said antisense strand is complementary to any of any of SEQ ID NO:59-SEQ ID NO:154, or SEQ ID NO:202-SEQ ID NO:204.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 10, 2019
From: YANNI, JOHN M.; CHATTERTON, JON E.; SENCHYNA, DIANE MICHELLE; GAMACHE, DANIEL A.; MILLER, STEVEN T.
To: ALCON MANUFACTURING, LTD.
Reel/Frame 050681/0708 →
MERGER AND CHANGE OF NAME Recorded Oct 10, 2019
From: ALCON MANUFACTURING, LTD.; ALCON RESEARCH, LTD.
To: ALCON RESEARCH, LTD.
Reel/Frame 050681/0850 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 10, 2019
From: ALCON RESEARCH, LTD.
To: ARROWHEAD RESEARCH CORPORATION
Reel/Frame 050681/0920 →
CHANGE OF NAME Recorded Oct 10, 2019
From: ARROWHEAD RESEARCH CORPORATION
To: ARROWHEAD PHARMACEUTICALS, INC.
Reel/Frame 050704/0486 →