Oncolytic adenovirus

Drug – bio-affecting and body treating compositions – Whole live micro-organism – cell – or virus containing – Genetically modified micro-organism – cell – or virus

Reexamination Certificate

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Details

C435S320100, C435S325000, C435S457000

Reexamination Certificate

active

07078030

ABSTRACT:
Viral vectors and methods of making such vectors are described that preferentially kill neoplastic but not normal cells, the preferred vector being an adenovirus that has the endogenous promoters in the E1A and/or E4 regions substituted with a tumor specific promoter which is preferably E2F responsive.

REFERENCES:
Parr MJ, Tumor-selective transgene expression in vivo mediated by an E2F-responsive adenoviral vector, 1997, Nature, Medicine, vol. 3, pp. 1145-1149.
Parekh-Olmedo H, Gene therapy progress and prospects: targeted gene repair, 2005, Gene Therapy, vol. 12, pp. 639-646.
Verma IM, Gene Therapy: Twenty-first century medicine, 2005, Annu. Rev. Biochem. vol. 74, pp. 711-738.
Concalves M, A concise peer into the background, initial thoughts, and practices of human gene therapy, 2005, BioEssays, vol. 27, pp. 506-517.
Schmid, SI, Bipartite structure and functional independence of adenovirus type 5 packaging elements, 1997, J. of Virology, vol. 71, pp. 3375-3384.

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