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US Patent 9228187 Antisense molecules and methods for treating pathologies

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US Patent 12128109 Muscle targeting complexes and formulations for treating dystrophinopathies
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US Patent 12104156 Compositions and methods of treating facioscapulohumeral muscular dystrophy
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US Patent 12071621 Anti-transferrin receptor antibody-PMO conjugates for inducing DMD exon 44 skipping
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US Patent 12064483 Nucleic acid-polypeptide compositions and methods of inducing exon skipping
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US Patent 12005124 Muscle targeting complexes and uses thereof for treating dystrophinopathies
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US Patent 11999955 Compositions and methods of treating facioscapulohumeral muscular dystrophy
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US Patent 11986537 Muscle targeting complexes and uses thereof for treating dystrophinopathies
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US Patent 11932851 Exon skipping compositions for treating muscular dystrophy
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US Patent 11872287 Compositions and methods of treating muscle atrophy and myotonic dystrophy
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US Patent 11833217 Muscle targeting complexes and uses thereof for treating dystrophinopathies
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Patent abstract

An antisense molecule capable of binding to a selected target site to induce exon skipping in the dystrophin gene, as set forth in SEQ ID NO: 1 to 59.

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US Patent 11771776 Muscle targeting complexes and uses thereof for treating dystrophinopathies
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Patent Inventor Names
Abbie Adams0
Penny Meloni0
Stephen Donald Wilton0
Sue Fletcher0
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US Patent 11712478 Compositions and methods of treating muscle atrophy and myotonic dystrophy
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US Patent 09228187 Antisense molecules and methods for treating pathologies US Patent 9228187 Antisense molecules and methods for treating pathologies

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Patent Number
09228187
Patent Number
9228187
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Official Website
https://pdfpiw.uspto.gov/.piw?Docid=09228187

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