Methods of administering adenoviral vectors
The present invention provides methods for administering an adenoviral gene transfer vector comprising an exogenous gene to an animal. One method involves utilizing systemic neutralizing antibodies to neutralize the adenoviral gene transfer vector outside a targeted muscle. Another method involves t...
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| Main Authors | , |
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| Format | Patent |
| Language | English |
| Published |
22.07.2003
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| Edition | 7 |
| Subjects | |
| Online Access | Get full text |
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| Abstract | The present invention provides methods for administering an adenoviral gene transfer vector comprising an exogenous gene to an animal. One method involves utilizing systemic neutralizing antibodies to neutralize the adenoviral gene transfer vector outside a targeted muscle. Another method involves the repeat administration of an adenoviral gene transfer vector to a skeletal muscle. |
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| AbstractList | The present invention provides methods for administering an adenoviral gene transfer vector comprising an exogenous gene to an animal. One method involves utilizing systemic neutralizing antibodies to neutralize the adenoviral gene transfer vector outside a targeted muscle. Another method involves the repeat administration of an adenoviral gene transfer vector to a skeletal muscle. |
| Author | BRUDER JOSEPH T KOVESDI IMRE |
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| Notes | Application Number: US20010835683 |
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| Snippet | The present invention provides methods for administering an adenoviral gene transfer vector comprising an exogenous gene to an animal. One method involves... |
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| Title | Methods of administering adenoviral vectors |
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