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filingDate 2021-02-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4297a2728d010e4074d44a8060e8c980
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ee362cb90b638615a747328af969f902
publicationDate 2022-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2021158814-A9
titleOfInvention Gene therapy systems and related methods for treatment of hearing loss
abstract The present disclosure describes gene therapy systems, and related methods, useful for treating and/or preventing deafness caused by genetic mutation of the TMPRSS3 gene or the LOXHD1 gene. The compositions and methods disclosed herein use adeno-associated viral (AAV) vector gene delivery of TRMPSS3 or LOXHD1 into the inner ear to restore activity of the TMPRSS3 gene or the LOXHD1 gene, respectively, promote hair cell survival and restore hearing in patients suffering from hearing loss. As disclosed herein, the systems and methods may utilize a combination of gene therapy (e.g., molecular therapeutics) for hearing loss caused by a genetic mutation together with implantation of a cochlear implant.
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