Viral Genomix Inc. was founded in April of 2000 ; In 2006, it changed its name to , VGX Pharmaceuticals Inc. . This is the "root" of the corporation that eventually becomes known as Inovio Pharmaceuticals, Incorporated.
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In 2005, Genetronics Biomedical Corporation purchased a Norwegian company called Inovio AS ( Source: [HW009F][GDrive] ); shortly afterwards, this combined corporation was renamed to Inovio Biomedical Corporation .
In Feb 2007, VGX Pharmaceuticals Inc. purchases/merges with ADViSYS Inc. .
In June 2009, VGX Pharmaceuticals Inc. purchased Inovio Biomedical Corporation , and the combined company was retained the name Inovio Biomedical Corporation . In May 2010, Inovio Biomedical Corporation was renamed to Inovio Pharmaceuticals, Incorporated.
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1999 - https://www.pnas.org/doi/full/10.1073/pnas.96.11.6417
Gabriella Rizzuto, Manuela Cappelletti, Domenico Maione, +8, and Elena FattoriAuthors Info & Affiliations
May 25, 1999
96 (11) 6417-6422
Authors
S Tollefsen, M Vordermeier, I Olsen, AK Storset, LJ Reitan, D Clifford, DB Lowrie, HG Wiker, K Huygen, G Hewinson, I Mathiesen, TE Tjelle
Publication date
2003/3
Source
Scandinavian journal of immunology
Volume
57
Issue
3
Pages
229-238
Publisher
Blackwell Science Ltd
Description
Injection of plasmid DNA encoding antigens into rodents followed by electroporation improved the immune response when compared with injection without electroporation (Widera et al. J Immunol 2000;164:4635–40; Zucchelli et al. J Virol 2000;74:11598–607; Kadowaki et al. Vaccine 2000;18:2779–88). The present study describes the extension of this technology to farm animals, by injecting plasmid DNA encoding mycobacterial antigens (MPB70, Ag85B and Hsp65) into the muscles of goats and cattle using two different types of electrodes, both allowing DNA delivery at the site of electroporation. The animals were vaccinated under local anaesthesia without any observed immediate or long‐term distress or discomfort, or any behavioural signs of muscle damage or pathological changes after the electroporation. DNA‐injected and electroporated goats showed increased humoral response after the primary …
2003 - Estimated time Inovio AS was created in Norway ...
2003 - Inovio AS
https://pubmed.ncbi.nlm.nih.gov/14533200/
J Gene Med
. 2003 Oct;5(10):909-917. doi: 10.1002/jgm.416.
Eirik Grønevik 1, Stig Tollefsen 2, Liv Ingunn Bjoner Sikkeland 3, Terje Haug 3, Torunn Elisabeth Tjelle 4, Iacob Mathiesen 4
Affiliations collapse
1
Department of Physiology, University of Oslo, Box 1103 Blindern, 0316 Oslo, Norway.
2
Immunological institute, Rikshospitalet, 0027 Oslo, Norway.
3
Centre for Occupational and Environmental Medicine, Rikshospitalet, 0027 Oslo, Norway.
4
Inovio AS, Oslo Research Park, Gaustadalleen 21, 0349 Oslo, Norway.
PMID: 14533200
DOI: 10.1002/jgm.416
Background: Genes encoding non-self proteins may be injected into skeletal muscles in vivo to obtain induction of cellular and humoral immune responses against the encoded antigens (DNA vaccination). Bone marrow derived professional antigen-presenting cells (APCs) play a key role in the induction of immunity by DNA vaccination. In the present work we have investigated whether the APCs are transfected by DNA injection into muscle.
Methods: DNA encoding green fluorescent protein (GFP) was injected into rat and mouse limb muscle and followed by electroporation. Whole mount muscle tissue with GFP-positive mononuclear cells (MNCs) were treated with immunocytochemical markers specific for leukocytes, and studied with fluorescent microscopy. To detect transfected cells migrating to peripheral lymphoid tissue RT-PCR was applied on RNA isolated from the draining popliteal lymph node and spleen. Lymphoid tissue was also analyzed with real-time PCR for distribution of the injected plasmid.
Results: MNCs were transfected after intramuscular DNA injection, and, following DNA injection with electroporation, the number of GFP-positive MNCs increased 6-fold in rats and 14-fold in mice. None of the GFP-positive MNCs were stained with leukocyte-specific antibodies. Even though GFP encoding DNA was detected in the popliteal lymph node, no RNA encoding GFP was found in the lymph node or spleen. However, MHC II-positive cells in the muscle tissue appeared preferentially around the transfected MNCs.
Conclusions: Many MNCs in the muscle are transfected after intramuscular DNA injection. Electroporation significantly increases the number of transfected MNCs. None of the observed transfected MNCs however were leukocytes. MHC II-positive cells accumulated around transfected MNCs; this suggests that transfer of antigen from transfected MNCs to APCs may contribute to the immune response.
2004 - Inovio AS
ARTICLE| VOLUME 9, ISSUE 3, P328-336, MARCH 2004Download Full Issue
Open ArchiveDOI:https://doi.org/10.1016/j.ymthe.2003.12.007
Mentioned - Inovio AS / Genetronics Biomedical Corporation / Dr. Avtar Singh Dhillon (born 1961) /
SAN DIEGO and OSLO, Norway, Jan. 26 /PRNewswire-FirstCall/ -- [ Genetronics Biomedical Corporation]. , a late stage developer of oncology and other therapies using electroporation to deliver drugs and nucleic acids, announced today the acquisition of Oslo-based [Inovio AS ], a leader in patented gene delivery technology for the most efficient, nonviral method for gene transfer to skeletal muscles. Inovio's use of electroporation for gene therapy and DNA vaccines is a complement to Genetronics' existing electroporation therapy program. The acquisition expands Genetronics' intellectual property in electroporation, expands the number of agreements with major pharmaceutical companies, and provides for the near-term initiation of a Phase I/II DNA vaccine clinical trial.
The deal includes cash in Inovio's treasury of approximately $775,000 and approximately $2.0M in current and anticipated appropriations for biodefense research from the US Army and other committed grants. The share purchase agreement consists of $3M in cash, $7M in Genetronics stock, and potential additional share payments given the achievement of certain revenue milestones. In addition, Iacob Mathiesen, Ph.D., Inovio's CEO, will serve as Executive Director, Gene Delivery of Genetronics.
"This is a perfect strategic fit as we increase our licensing activities in the area of DNA therapies involving intramuscular electroporation for application to vaccines and immunotherapy," said [Dr. Avtar Singh Dhillon (born 1961)], Genetronics' President and CEO. "Together with Dr. Mathiesen and his team, we will promote and advance gene-based collaborations with existing and new partners. We anticipate that license revenue from our DNA delivery technology will be increasingly important in creating additional value for our shareholders."
"I am delighted to bring our technology and products to [ Genetronics Biomedical Corporation], the market leader in electroporation-based therapies," noted Iacob Mathiesen, Ph.D., [the CEO of Inovio AS]. "Genetronics is in an enviable position to enable the advancement of DNA vaccinations and gene therapy, and I am certain that the company will play a prominent role in this promising and rapidly growing area."