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US Patent 9617540 Compounds and methods for modulating gene expression

Patent 9617540 was granted and assigned to Ionis Pharmaceuticals on April, 2017 by the United States Patent and Trademark Office.

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Is a
Patent
Patent
0

Patent attributes

Patent Applicant
Ionis Pharmaceuticals
Ionis Pharmaceuticals
Current Assignee
Ionis Pharmaceuticals
Ionis Pharmaceuticals
Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
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Patent Number
96175400
Patent Inventor Names
Punit P. Seth0
Andrew M. Siwkowski0
Brett P. Monia0
Edward Wancewicz0
Eric E. Swayze0
Richard S. Geary0
Robert McKay0
Sanjay Bhanot0
Date of Patent
April 11, 2017
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Patent Application Number
146985540
Date Filed
April 28, 2015
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Patent Citations Received
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US Patent 12012460 Muscle-targeting complexes comprising an anti-transferrin receptor antibody linked to an oligonucleotide
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US Patent 12018087 Muscle-targeting complexes comprising an anti-transferrin receptor antibody linked to an oligonucleotide and methods of delivering oligonucleotide to a subject
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US Patent 12102687 Muscle targeting complexes and uses thereof for treating myotonic dystrophy
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US Patent 11679161 Muscle targeting complexes and uses thereof for treating facioscapulohumeral muscular dystrophy
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US Patent 11787869 Methods of using muscle targeting complexes to deliver an oligonucleotide to a subject having facioscapulohumeral muscular dystrophy or a disease associated with muscle weakness
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US Patent 11879125 GalNAc compositions for improving siRNA bioavailability
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US Patent 11911484 Muscle targeting complexes and uses thereof for treating myotonic dystrophy
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US Patent 11931421 Muscle targeting complexes and formulations for treating myotonic dystrophy
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Patent Primary Examiner
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Tracy Vivlemore
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Patent abstract

The present disclosure describes short antisense compounds, including such compounds comprising chemically-modified high-affinity monomers 8-16 monomers in length. Certain such short antisense compound are useful for the reduction of target nucleic acids and/or proteins in cells, tissues, and animals with increased potency and improved therapeutic index. Thus, provided herein are short antisense compounds comprising high-affinity nucleotide modifications useful for reducing a target RNA in vivo. Such short antisense compounds are effective at lower doses than previously described antisense compounds, allowing for a reduction in toxicity and cost of treatment. In addition, the described short antisense compounds have greater potential for oral dosing.

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