Oligonucleotide compounds for targeting huntingtin mRNA
US-9809817-B2 · Nov 7, 2017 · US
US10799591B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10799591-B2 |
| Application number | US-201916390712-A |
| Country | US |
| Kind code | B2 |
| Filing date | Apr 22, 2019 |
| Priority date | Jan 31, 2016 |
| Publication date | Oct 13, 2020 |
| Grant date | Oct 13, 2020 |
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Provided herein are branched oligonucleotides exhibiting efficient and specific tissue distribution, cellular uptake, minimum immune response and off-target effects, without formulation.
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The invention claimed is: 1. A method of delivering double-stranded nucleic acids to one or both of the brain and spinal cord of a patient, comprising administering to the patient a branched oligonucleotide compound comprising two siRNA duplexes connected to one another by a linker, wherein each siRNA duplex comprises a sense strand of at least 15 contiguous nucleotides and an antisense strand of at least 15 contiguous nucleotides having complementarity to the sense strand, wherein each sense strand and each antisense strand has a 5′ end and a 3′ end, and wherein the branched oligonucleotide compound is administered to the patient by intrastriatal (IS) injection, intrathecal (IT) injection, or intracerebroventricular (ICV) injection, thereby delivering the double-stranded nucleic acids to the brain and/or spinal cord of the patient. 2. The method of claim 1 , wherein the branched oligonucleotide compound comprises 5-20 phosphorothioated bonds. 3. The method of claim 1 , wherein the nucleotides at positions 1-6 from the 3′ end of the antisense strand, or positions 1-7 from the 3′ end of the antisense strand, are connected to adjacent nucleotides via phosphorothioate linkages. 4. The method of claim 1 , wherein the nucleotides at positions 1 and 2 from the 5′ end of the sense and antisense strands are connected to adjacent nucleotides via phosphorothioate linkages. 5. The method of claim 1 , wherein each siRNA duplex comprises an unpaired overhang of at least 2 nucleotides. 6. The method of claim 5 , wherein the nucleotides of the overhang are connected via phosphorothioate linkages. 7. The method of claim 1 , wherein each of the sense and antisense strands comprise >80% chemically-modified nucleotides. 8. The method of claim 1 , wherein each strand of the siRNA duplex has a length of 16-20 contiguous nucleotides. 9. The method of claim 1 , wherein each sense strand of the siRNA duplex has a length of 16 contiguous nucleotides. 10. The method of claim 1 , wherein each antisense strand has a length of 20 contiguous nucleotides. 11. The method of claim 1 , wherein the nucleic acid further comprises a hydrophobic moiety attached to a 5′end of at least one of the siRNA duplexes. 12. The method of claim 11 , wherein the hydrophobic moiety comprises an alkyl, alkenyl, or aryl moiety; a vitamin or cholesterol derivative; a lipophilic amino acid; or a combination thereof. 13. The method of claim 1 , wherein the branched oligonucleotide compound is delivered to the brain of the patient. 14. The method of claim 13 , wherein the branched oligonucleotide compound is delivered to one or both of the striatum of the brain and the cortex of the brain. 15. The method of claim 1 , wherein the branched oligonucleotide compound is delivered to the cerebrospinal fluid (CSF) of the patient. 16. The method of claim 1 , wherein the antisense strand has complementarity to a target mRNA in a neuronal cell.
Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; {Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing (when used in plants C12N15/8218)} · CPC title
Sugars, nucleosides, nucleotides or nucleic acids · CPC title
for treating abnormal movements, e.g. chorea, dyskinesia · CPC title
branched · CPC title
Compounds having two nucleosides or nucleotides, e.g. nicotinamide-adenine dinucleotide, flavine-adenine dinucleotide · CPC title
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