The DOI matches its Crossref record; 1 of the 1 references it cites were found in a registry or an index.
Gene therapy clinical trials worldwide 1989–2004—an overview
Abstract
In 1989, Rosenberg et al. performed the first human gene therapy trial when they used a retrovirus to introduce the gene coding for resistance to neomycin into human tumor‐infiltrating lymphocytes before infusing them into five patients with advanced melanoma. This study demonstrated the feasibility of using retroviral gene transduction in humans and set the stage for further studies. Since then, over 900 clinical trials have been completed, are ongoing or have been approved worldwide. These trials have been designed to establish feasibility and safety, to demonstrate the reality of expression of therapeutic protein(s) in vivo by the genes transferred and, in some cases, to show therapeutic benefit. There is no single source of information that presents an overview of all the clinical trials undertaken worldwide. In 1997 we set up a database to bring all the information on clinical trials together as comprehensively and as globally as possible. The data were compiled and are regularly updated from official agency sources, the published literature, presentations at conferences and from information kindly provided by investigators or trial sponsors themselves. As of January 31, 2004, we have identified 918 trials in 24 countries. The USA accounts for two‐thirds of these trials. Cancer is by far the most common disease indication, followed by inherited monogenic diseases, and cardiovascular diseases. Viral vectors have been the most frequently used vehicles for transferring genes into human cells, with retroviruses and adenoviruses representing the vast majority. Plasmid (naked) DNA and other non‐viral vectors have been used in one‐quarter of the trials. Over 100 distinct genes have been transferred. This article aims to provide a descriptive overview of the clinical trials that, to the best of our knowledge, have been or are being performed worldwide. Details of the data presented, including an interactive, searchable database that currently holds information on 918 trials, can be found on The Journal of Gene Medicine clinical trials website 1. Copyright © 2004 John Wiley & Sons, Ltd.
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Citations
Cites
A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency
Hacein-Bey-Abina, S., von Kalle, C., Schmidt, M., Le Deist, F., Wulffraat, N., McIntyre, E., Radford, I., Villeval, J.-L., Fraser, C. C., Cavazzana-Calvo, M., et al. (2003) · New England Journal of Medicine · doi:10.1056/nejm200301163480314 · Cited by 1,867 · cited 3×
“The excitement gave way to alarm at the end of 2002, when two of the ten children treated developed a leukemia-like condition [6], subsequently shown to be related to retrovirus vector integration near the LMO2 proto-oncogene promoter, leading to aberrant transcription and expression of LMO2 [13].”
Background
Cited by
Nonviral vectors for gene delivery
Mintzer, M. A., & Simanek, E. E. (2009) · Chemical Reviews · doi:10.1021/cr800409e · Cited by 2,366
Gene therapy clinical trials worldwide to 2017: An update
Ginn, S. L., Amaya, A. K., Alexander, I. E., Edelstein, M., & Abedi, M. R. (2018) · The Journal of Gene Medicine · doi:10.1002/jgm.3015 · Cited by 903
Self-citationThe approved gene therapy drugs worldwide: from 1998 to 2019
Ma, C.-C., Wang, Z.-L., Xu, T., He, Z.-Y., & Wei, Y.-Q. (2020) · Biotechnology Advances · doi:10.1016/j.biotechadv.2019.107502 · Cited by 310
Viral vector‐based gene therapies in the clinic
Zhao, Z., Anselmo, A. C., & Mitragotri, S. (2022) · Bioengineering & Translational Medicine · doi:10.1002/btm2.10258 · Cited by 269
Non-viral is superior to viral gene delivery
Li, S.-D., & Huang, L. (2007) · Journal of Controlled Release · doi:10.1016/j.jconrel.2007.09.004 · Cited by 225
Metadata
- Authors
- Edelstein, M. L., Abedi, M. R., Wixon, J., & Edelstein, R. M.
- Venue
- The Journal of Gene Medicine
- Publisher
- Wiley
- Published
- 2004-05-26
- Volume
- 6
- Issue
- 6
- Pages
- 597-602
- ISSN
- 1099-498X (ISSN-L)
- 1521-2254
- OpenAlex
- W2077462718
- Cited by
- 350
- References
- 1
- FWCI
- 20.20
- Type
- journal article
- Language
- en
- Open access
- closed
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