Branched oligonucleotides

US10799591B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10799591-B2
Application numberUS-201916390712-A
CountryUS
Kind codeB2
Filing dateApr 22, 2019
Priority dateJan 31, 2016
Publication dateOct 13, 2020
Grant dateOct 13, 2020

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  1. Title

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  2. Abstract

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

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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.

First claim

Opening claim text (preview).

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.

Assignees

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Classifications

  • C12N15/113Primary

    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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What does patent US10799591B2 cover?
Provided herein are branched oligonucleotides exhibiting efficient and specific tissue distribution, cellular uptake, minimum immune response and off-target effects, without formulation.
Who is the assignee on this patent?
Univ Massachusetts
What technology area does this patent fall under?
Primary CPC classification C12N15/113. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Oct 13 2020 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 6 related publications on this page (citations in our corpus or others sharing the same primary CPC).