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| Inventor(s) | Ronald Vogels · Abraham Bout · |
| Assignee(s) |
Crucell Holland B.V. ·
|
| Attorney/Agent(s) | TraskBritt · |
| Primary Examiner | David Guzo · |
| Application Number | US10396548 |
| Filing date | 03/25/2003 |
| Issue date | 05/02/2006 |
| Prior Publication Data |
|
| Predicted expiration date | 12/29/2018 |
| Patent term adjustment | 249 |
| U.S. Classifications | 435/320.1 · 536/237.2 · 536/241 · 536/231 · |
| International Classifications | C12N1500 · |
| Kind Code | B2 |
| Related U.S. Application Data | CROSS-REFERENCE TO RELATED APPLICATION This application is a continuation of application Ser. No. 09/900,062, filed Jul. 6, 2001, now abandoned, which was a divisional of application Ser. No. 09/065,752, filed Apr. 24, 1998, now U.S. Pat. No. 6,670,188, issued Dec. 30, 2003. |
| Document Number | Assignees | Inventors | Issue/Pub Date |
|---|---|---|---|
| AUA2853395 | Mar 1996 | ||
| CA2053187 | CANADA MAJESTY IN RIGHT OF | Apr 1993 | |
| CA2117668 | SUMITOMO PHARMA | Sep 1995 | |
| EP95201611.1 | Jun 1995 | ||
| EP95201728.3 | Jun 1995 | ||
| FR2707664 | CENTRE NAT RECH SCIENT | Jan 1995 | |
| WO199102804* | Mar 1991 | ||
| WO199412649 | Jun 1994 | ||
| WO199423582 | Oct 1994 | ||
| WO199426914 | Nov 1994 | ||
| WO199428152 | Dec 1994 | ||
| WO199500655 | Jan 1995 | ||
| WO199502697 | Jan 1995 | ||
| WO199527071 | Oct 1995 | ||
| WO199616676 | Jun 1996 | ||
| WO199618418 | Jun 1996 | ||
| WO199633280 | Oct 1996 | ||
| WO199640955 | Dec 1996 | ||
| WO199700326 | Jan 1997 | ||
| WO199700947 | Jan 1997 | ||
| WO199704119 | Feb 1997 | ||
| WO199705255 | Feb 1997 |
| Amalfitano et al., “Improved adenovirus packaging cell lines to support the growth of replication-defective gene-delivery vectors,” Proc. Natl. Acad. Sci. USA, 93:3352-3356, Apr. 1996. |
| Amalfitano et al., “Isolation and characterization of packaging cell lines that coexpress the adenovirus E1, DNA polymerase, and preterminal proteins: implications for gene therapy,” Gene Therapy, 4:258-263,1997. |
| Armentano et al., “Characterization of an Adenovirus Gene Transfer Vector Containing an E4 Deletion,” Human Gene Therapy, 6:1343-1353, Oct. 1995. |
| Berkner, Expression of Heterologous Sequences in Adenoviral Vectors, Current Topics in Microbiology and Immunology, vol. 158, Springer-Verlag Berlin Heidelberg 1992. |
| Blaese et al., Vectors in Cancer therapy: how will they deliver?, Cancer Gene Therapy, vol. 2, No. 4, 1995, pp. 291-297. |
| Bout et al., “In vivo adenovirus-mediated transfer of human CFTR cDNA to Rhesus monkey airway epithelium: efficacy, toxicity and safety,” Gene Therapy 1, pp. 385-394, 1994. |
| Bout et al., “Lung Gene Therapy: In Vivo Adenovirus-Mediated Gene Transfer to Rhesus Monkey Airway Epithelium,” Human Gene Therapy, 5:3-10, 1994. |
| Brough et al., “A Gene Transfer Vector-Cell Line System for Complete Functional Complementation of Adenovirus Early Regions E1 and E4,” Journal of Virology, 70(9):6497-6501, Sep. 1996. |
| Brough et al., Stable Cell Lines for Complementation of Adenovirus Early Regions E1, E2A and E4; Abstract Book CSH Conference on Gene Therapy, 42, 1996. |
| Brough et al., “Construction, Characterization, and Utilization of Cell Lines Which Inducibly Express the Adenovirus DNA-Binding Protein,” Virology, 190:624-634, 1992. |
| Caravokyri et al., “Constitutive Episomal Expression of Polypeptide IX (pIX) in a 293-Based Cell Line Complements the Deficiency of pIX Mutant Adenovirus Type 5,” Journal of Virology, 69(11):6627-6633, Nov. 1995. |
| Fallaux et al., “Characterization of 911: A New Helper Cell Line for the Titration and Propagation of Early Region 1-Deleted Adenoviral Vectors,” Human Gene Therapy, 7:215-222, 1996. |
| Fisher et al., “Recombinant Adenovirus Deleted of All Viral Genes for Gene Therapy of Cystic Fibrosis,” Virology, 217:11-22, 1996. |
| Gao et al., “Biology of Adenovirus Vectors with E1 and E4 Deletions for Liver-Directed Gene Therapy,” Journal of Virology, 70(12):8934-8943, Dec. 1996. |
| Gorziglia et al., “Elimination of both E1 and E2a from Adenovirus Vectors Further Improves Prospects for In Vivo Human Gene Therapy,” Journal of Virology, 70(6):4173-4178, Jun. 1996. |
| Haddada et al., “Adenoviral Interleukin-2 Gene Transfer into P815 Tumor Cells Abrogates Tumorigenicity and Induces Antitumoral Immunity in Mice,” Human Gene Therapy, 4:703-711, 1993. |
| Hardy et al., “Construction of Adenovirus Vectors through Cre-Iox Recombination,” Journal of Virology, 71(3):1842-1849, Mar. 1997. |
| Hehir et al., “Molecular Characterization of Replication-Competent Variants of Adenovirus Vectors and Genome Modifications to Prevent Their Occurrence,” Journal of Virology, 70(12):8459-8467, Dec. 1996. |
| Imler et al., “Novel complementation cell lines derived from human lung carcinoma A549 cells support the growth of E1-deleted adenovirus vectors,” Gene Therapy, 3:75-84, 1996. |
| Kornberg, Arthur, “DNA Replication,” W.H.Freeman and Company, San Francisco, 4 pages (double sided). |
| Krougliak et al., “Development of Cell Lines Capable of Complementing E1, E4, and Protein IX Defective Adenovirus Type 5 Mutants,” Human Gene Therapy, 6:1575-1586, Dec. 1995. |
| Lieber et al., “Recombinant Adenoviruses with Large Deletions Generated by Cre-Mediated Excision Exhibit Different Biological Properties Compared with First-Generation Vectors In Vitro and In Vivo,” Journal of Virology, 70:8944-8960, Dec. 1996. |
| Ngo et al., “Computational Complexity, Protein Structure Prediction, and the Levinthal Paradox,” The Protein Folding Problem and Tertiary Structure Prediction, 5 pages. |
| Sabatie et al., “Process Development for the Production of Second Generation Adenovirus Vectors for Gene Transfer in Clinical Protocols,” Abstract Book 14th Meeting on Animal Cell Technolgoy, BI3, 1996. |
| Schaack et al., “Adenivorus Type 5 Precursor Terminal Protein-Expressing 293 and HeLa Cell Lines,” Journal of Virology, 69(7):4079-4085, Jul. 1995. |
| Stratford-Perricaudet et al., Gene transfer into animals: the promise of adenovirus, Human Gene Transfer, 1991, vol. 219, pp. 51-61. |
| Vanhaesebroeck et al., “Modulation of Cellular Susceptibility to the Cytotoxic/Cytostatic Action of Tumor Necrosis Factor by Adenovirus E1 Gene Expression Is Cell Type-Dependent,” Virology, 176(2), pp. 362-368, Jun. 1990. |
| Vincent et al., “Herpes Simplex Virus Thymidine Kinase Gene Therapy for Rat Malignant Brain Tumors,” Human Gene Therapy 7:197-205, Jan. 20, 1996. |
| Vincent et al., “Treatment of leptomeningeal metastases in a rat model using a recombinant adenovirus containing the HSV-tk gene,” J. Neurosurg., vol. 85, pp. 648-654, 1996. |
| Wang et al., “A packaging cell line for propagation of recombinant adenovirus vectors containing two lethal gene-region deletions,” Gene Therapy, 2:775-783, 1995. |
| Yeh et al., “Efficient Dual Transcomplementation of Adenovirus E1 and E4 Regions from a 293-Derived Cell Line Expressing a Minimal E4 Functional Unit”, Journal of Virology, 70(1):559-565, Jan. 1996. |
| Zhou et al., “Development of a Complementing Cell Line and a System for Construction of Adenovirus Vectors with E1 and E2a Deleted,” Journal of Virology, 70(1):7030-7038, Oct. 1996. |
| McKinnon et al., Tn5 mutagenesis of the transforming genes of human adenovirus type 5. Gene, 1982, pp. 33-42, vol. 19. |
| Document Number | Assignee | Inventors | Issue/Pub Date |
|---|---|---|---|
| US20050074885 | Ronald Vogels et al. | Apr 2005 | |
| US7037716 | Crucell Holland B.V. | Ronald Vogels et al. | May 2006 |
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