Method of reducing titers of antibodies specific for a therapeutic agent
AssigneeDuke University
InventorsPriya S. Kishnani, Suhrad G. Banugaria, Dwight D. Koeberl, Sean N. Prater
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AssigneeDuke University
InventorsPriya S. Kishnani, Suhrad G. Banugaria, Dwight D. Koeberl, Sean N. Prater
Estimating the term…
The present invention relates, in general, to a method of treating patients undergoing enzyme replacement therapy (ERT) or other therapy involving the administration of a proteinaceous therapeutic agent as well gene replacement therapy with non-viral or viral vectors, or other therapeutic modality or modalities, used alone or in combination, which involve the administration of exogenous substances for potential therapeutic benefit, including, but not limited to DNA vaccines, siRNA, splice-site switching oligomers (SSOs) as well as RNA-based nanoparticles (RNPs) and nanovaccines. The invention further relates to compounds and compositions suitable for use in such methods.
A method of improving the efficacy of gene replacement therapy, the method comprising:
A method of reducing the risk of developing high sustained antibody titers (HSAT), the method comprising:
Dependencies are inferred from the claim text.