PLYMOUTH MEETING, Pa., May 31, 2018 (GLOBE NEWSWIRE) — Inovio Pharmaceuticals, Inc. (NASDAQ:INO) today announced that Dr. J. Joseph Kim, President and CEO, will address Inovio’s ability to respond to emerging viral threats at the Biotechnology Industry Organization’s annual international convention, June 4-7 in Boston, MA. Dr. Kim will join other world leaders in pandemic response on a panel:
From One Epidemic to the Next: Learning from Ebola and Zika
June 5, 2018 at 11 AM ET
The panel will use the most recent experiences with Ebola and Zika to discuss the challenges of vaccine development in the midst of a global public health emergency with experts from industry, government and partner organizations. Experts from industry, government and partner organizations will consider whether existing systems, mechanisms and incentives for vaccine development are sufficient to prepare us for the next epidemic threat. Joining Dr. Kim on the panel are these government, non-government and commercial leaders: Richard Hatchett, CEO, CEPI; Rick Bright, Director, BARDA; Julia Spencer, Executive Director, Global Vaccines Public Policy, Merck & Co.; and Nima Farzan, CEO, PaxVax.
Inovio was the first organization to develop, manufacture and report positive human data from a Zika vaccine in less than seven months – when traditional vaccines take several years to reach this point. These results were published in the October 2017 – New England Journal of Medicine. By utilizing both the capabilities and versatility of Inovio’s DNA-based immunotherapies and vaccines, Inovio is poised to combat well-established pathogens with significant unmet needs to new and emerging threats around the world, while also offering treatment alternatives and prevention of multiple cancers and infectious diseases.
In addition to the recent Zika publication, Inovio recently announced a $56 million partnership with the Coalition for Epidemic Preparedness Innovations (CEPI) under which Inovio will develop vaccine candidates against two emerging viral threats: Lassa fever and Middle East Respiratory Syndrome (MERS). Inovio is also advancing its vaccines in clinical trials against HIV, Ebola and hepatitis B infection, in both preventive and therapeutic modalities.
About Inovio Pharmaceuticals, Inc.
Inovio is a late-stage biotechnology company focused on the discovery, development, and commercialization of DNA immunotherapies that transform the treatment of cancer and infectious diseases. Inovio’s proprietary platform technology, ASPIRE, applies next-generation antigen sequencing and DNA delivery to activate potent immune responses to targeted diseases. The technology functions exclusively in vivo, and has been demonstrated to consistently activate robust and fully functional T cell and antibody responses against targeted cancers and pathogens. Inovio is the only immunotherapy company that has reported generating T cells whose killing capacity correlates with relevant clinical outcomes. Inovio’s most advanced clinical program, VGX-3100, is in Phase 3 for the treatment of HPV-related cervical precancer. Also in development are Phase 2 immuno-oncology programs targeting head and neck cancer, bladder cancer, and glioblastoma, as well as platform development programs in hepatitis B, Zika, Ebola, MERS, and HIV. Partners and collaborators include MedImmune, Regeneron, Roche/Genentech, ApolloBio Corporation, The Wistar Institute, University of Pennsylvania, the Parker Institute for Cancer Immunotherapy, CEPI, DARPA, GeneOne Life Science, Plumbline Life Sciences, Drexel University, NIH, HIV Vaccines Trial Network, National Cancer Institute, U.S. Military HIV Research Program, and Laval University. For more information, visit www.inovio.com.
This press release contains certain forward-looking statements relating to our business, including our plans to develop electroporation-based drug and gene delivery technologies and DNA vaccines, our expectations regarding our research and development programs, including the planned initiation and conduct of clinical trials and the availability and timing of data from those trials, and our plans and expectations regarding partnerships. Actual events or results may differ from the expectations set forth herein as a result of a number of factors, including uncertainties inherent in pre-clinical studies, clinical trials and product development programs, the availability of funding to support continuing research and studies in an effort to prove safety and efficacy of electroporation technology as a delivery mechanism or develop viable DNA vaccines, our ability to support our pipeline of SynCon® active immunotherapy and vaccine products, the ability of our collaborators to attain development and commercial milestones for products we license and product sales that will enable us to receive future payments and royalties, the adequacy of our capital resources, the availability or potential availability of alternative therapies or treatments for the conditions targeted by us or our collaborators, including alternatives that may be more efficacious or cost effective than any therapy or treatment that we and our collaborators hope to develop, issues involving product liability, issues involving patents and whether they or licenses to them will provide us with meaningful protection from others using the covered technologies, whether such proprietary rights are enforceable or defensible or infringe or allegedly infringe on rights of others or can withstand claims of invalidity and whether we can finance or devote other significant resources that may be necessary to prosecute, protect or defend them, the level of corporate expenditures, assessments of our technology by potential corporate or other partners or collaborators, capital market conditions, the impact of government healthcare proposals and other factors set forth in our Annual Report on Form 10-K for the year ended December 31, 2017, our Quarterly Report on Form 10-Q for the quarter ended March 31, 2018 and other regulatory filings we make from time to time. There can be no assurance that any product candidate in our pipeline will be successfully developed, manufactured or commercialized, that final results of clinical trials will be supportive of regulatory approvals required to market licensed products, or that any of the forward-looking information provided herein will be proven accurate. Forward-looking statements speak only as of the date of this release, and we undertake no obligation to update or revise these statements, except as may be required by law.