IP Library Patent Application 17264905
Patent Application
App. No. 17/264,905

MUSCLE TARGETING COMPLEXES AND USES THEREOF FOR TREATING MYOTONIC DYSTROPHY

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Patent No.
US None
App. No.
17/264,905
Abstract

Aspects of the disclosure relate to complexes comprising a muscle-targeting agent covalently linked to a molecular payload. In some embodiments, the muscle-targeting agent specifically binds to an internalizing cell surface receptor on muscle cells. In some embodiments, the molecular payload inhibits expression or activity of a DMPK allele comprising a disease-associated-repeat. In some embodiments, the molecular payload is an oligonucleotide, such as an antisense oligonucleotide or RNAi oligonucleotide.

Claims (27)

1 .- 79 . (canceled)

80 . A complex comprising an anti-transferrin receptor antibody covalently linked to an oligonucleotide that targets a DMPK RNA,

wherein the oligonucleotide is 15 to 25 nucleotides in length and comprises a region of complementarity to a DMPK sequence as set forth in SEQ ID NO: 15, wherein the region of complementarity is at least 12 nucleotides in length; and

wherein the anti-transferrin receptor antibody binds in the range of C89 to F760 of human transferrin receptor protein 1 (TfR1) having an amino acid sequence as set forth in SEQ ID NO: 1.

81 . The complex of claim 80 , wherein the anti-transferrin receptor antibody is in the form of a ScFv, Fab fragment, Fab′ fragment, F(ab′)2 fragment, or Fv fragment.

82 . The complex of claim 80 , wherein the anti-transferrin receptor antibody binds human TfR1 with a K D of 10 −11 M to 10 −6 M.

83 . The complex of claim 80 , wherein the anti-transferrin receptor antibody is a humanized antibody.

84 . The complex of claim 80 , wherein the oligonucleotide targets a non-repeat region of the DMPK RNA.

85 . The complex of claim 80 , wherein the oligonucleotide comprises one or more modified nucleosides.

86 . The complex of claim 85 , wherein the one or more modified nucleosides are 2′-modified nucleosides selected from the group consisting of: 2′-O-methyl, 2′-fluoro, 2′-O-methoxyethyl, and 2′,4′-bridged nucleosides.

87 . The complex of claim 80 , wherein the oligonucleotide directs RNAse H cleavage mediated degradation of a DMPK RNA transcript in a cell.

88 . The complex of claim 87 , wherein the oligonucleotide comprises a central portion of 5 to 15 deoxyribonucleosides flanked by wings of 2 to 8 modified nucleosides.

89 . The complex of claim 88 , wherein the modified nucleosides of the wings are 2′-modified nucleosides selected from the group consisting of: 2′-O-methyl, 2′-fluoro, 2′-O-methoxyethyl, and 2′,4′-bridged nucleosides.

90 . The complex of claim 80 , wherein the oligonucleotide comprises one or more modified internucleoside linkages.

91 . The complex of claim 90 , wherein the one or more modified internucleoside linkage are phosphorothioate linkages.

92 . The complex of claim 80 , wherein the oligonucleotide comprises a region of complementarity to at least 15 consecutive nucleotides of any one of SEQ ID NOs: 281-516.

93 . The complex of claim 80 , wherein the oligonucleotide comprises at least 15 consecutive nucleotides of any one of SEQ ID NO: 45-280.

94 . The complex of claim 80 , wherein the anti-transferrin receptor is covalently linked to the oligonucleotide via a cleavable linker.

95 . The complex of claim 94 , wherein the cleavable linker comprises a valine-citrulline sequence.

96 . The complex of claim 80 , wherein the anti-transferrin receptor antibody is covalently linked to the oligonucleotide via conjugation to a lysine residue or a cysteine residue of the anti-transferrin receptor antibody.

97 . The complex of claim 80 , wherein the complex is configured to promote transferrin receptor mediated internalization of the oligonucleotide into a muscle cell.

98 . A method of reducing expression level of DMPK in a muscle cell, the method comprising contacting the muscle cell with a complex comprising an anti-transferrin receptor antibody covalently linked to an oligonucleotide that targets a DMPK RNA,

wherein the oligonucleotide is 15 to 25 nucleotides in length and comprises a region of complementarity to a DMPK sequence as set forth in SEQ ID NO: 15, wherein the region of complementarity is at least 12 nucleotides in length; and

wherein the anti-transferrin receptor antibody binds in the range of C89 to F760 of human transferrin receptor protein 1 (TfR1) having an amino acid sequence as set forth in SEQ ID NO: 1.

99 . A method of treating myotonic dystrophy type 1 (DM1) in a subject expressing a DMPK RNA containing a disease-associated repeat sequence, the method comprising administering to the subject a complex comprising an anti-transferrin receptor antibody covalently linked to an oligonucleotide that targets the DMPK RNA,

wherein the oligonucleotide is 15 to 25 nucleotides in length and comprises a region of complementarity to a DMPK sequence as set forth in SEQ ID NO: 15, wherein the region of complementarity is at least 12 nucleotides in length; and

wherein the anti-transferrin receptor antibody binds in the range of C89 to F760 of human transferrin receptor protein 1 (TfR1) having an amino acid sequence as set forth in SEQ ID NO: 1.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE SECOND ASSIGNOR'S NAME PREVIOUSLY RECORDED AT REEL: 055585 FRAME: 0650. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT . Recorded Apr 6, 2021
From: SUBRAMANIAN, ROMESH R.; QATANANI, MOHAMMED T.; WEEDEN, TIMOTHY; DESJARDINS, CODY A.
To: DYNE THERAPEUTICS, INC.
Reel/Frame 055828/0273 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2021
From: SUBRAMANIAN, ROMESH R.; Q, MOHAMMED T.; WEEDEN, TIMOTHY; DESJARDINS, CODY A.
To: DYNE THERAPEUTICS, INC.
Reel/Frame 055585/0650 →