发明公开
EP1597377A2 METHOD OF USING ADENOVIRAL VECTORS WITH INCREASED PERSISTENCE IN VIVO
审中-公开
腺病毒载体使用方法延长体内作用
- 专利标题: METHOD OF USING ADENOVIRAL VECTORS WITH INCREASED PERSISTENCE IN VIVO
- 专利标题(中): 腺病毒载体使用方法延长体内作用
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申请号: EP04712409.4申请日: 2004-02-18
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公开(公告)号: EP1597377A2公开(公告)日: 2005-11-23
- 发明人: WICKHAM, Thomas, J. , AKIYAMA, Masaki
- 申请人: GenVec, Inc. , FUSO PHARMACEUTICAL INDUSTRIES LTD.
- 申请人地址: 65 West Watkins Mill Road Gaithersburg,Maryland 20878 US
- 专利权人: GenVec, Inc.,FUSO PHARMACEUTICAL INDUSTRIES LTD.
- 当前专利权人: GenVec, Inc.,FUSO PHARMACEUTICAL INDUSTRIES LTD.
- 当前专利权人地址: 65 West Watkins Mill Road Gaithersburg,Maryland 20878 US
- 代理机构: Wössner, Gottfried
- 优先权: US374271 20030225
- 国际公布: WO2004076627 20040910
- 主分类号: C12N15/861
- IPC分类号: C12N15/861 ; C12N15/86 ; A61K48/00
摘要:
The invention provides a method of expressing an exogenous nucleic acid in a mammal. The method comprises slowly releasing into the bloodstream a dose of replication-deficient or conditionally-replicating adenoviral vector having reduced ability to transduce mesothelial cells and hepatocytes. The normalized average bloodstream concentration of the adenovirus over 24 hours post-administration is at least about 1%. Alternatively, the normalized average bloodstream concentration over 24 hours post-administration is at least about 5-fold greater than the normalized average bloodstream concentration for an equivalent dose of a wild-type adenoviral vector. A method of destroying tumor cells in a mammal also is provided.
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