Widespread gene delivery to the retina using systemic administration of AAV vectors
US9114161B2 · kind B2 · utility
4Cited by
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25Claims
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Key dates
| Filing date | Jul 30, 2010 |
| Grant date | Aug 25, 2015 |
| Priority date | — |
| Expiry date | Jul 30, 2030 |
Classification
- Technology area (CPC C)Chemistry; Metallurgy
- CPC primaryC12N2750/14143
- WIPO fieldPharmaceuticals
- WIPO sectorChemistry
Abstract
The present invention relates to compositions and methods, in particular to methods based on systemic administration of scAAV, for delivering genes to cells of the retina of mammals, and in particular to photoreceptor cells, ganglion cells, glial cells, inner nuclear layer cells or cells of the retinal pigmented epithelium.
Source: USPTO / EPO open patent data. Objective bibliographic and citation counts.